Pub Date : 2025-12-30DOI: 10.1007/s00404-025-08277-z
Danni Zhou, Xinglin Wang, Huali Deng, Xiu Luo, Dongyun Liu, Hong Ye
Objective
The purpose of this study was to compare oral estradiol valerate and estradiol transdermal gel for clinical pregnancy outcomes in patients undergoing frozen–thaw embryo transfer (FET).
Methods
This was a prospective study performed between March 1, 2017 and October 30, 2019. Totally 244 HR FET cycles were included, with 123 cycles using oral estrogen tablets (oral group) and 121 applying estradiol transdermal gel (gel group). The primary aim of this study was to compare implantation (IR), clinical pregnancy (CPR), miscarriage (MR) and live birth (LBR) rates between the two groups. The secondary aim was to assess liver function, specifically measuring alanine transaminase (ALT) and aspartate transaminase (AST) levels at 12 weeks of gestation.
Results
There were no significant differences in EPR, IR, and CPR between the two groups. Meanwhile, the gel group had a higher live birth rate (55.37% versus 51.20%, p = 0.302) and a lower miscarriage rate (5.79% versus 10.57%, p = 0.173) compared with the oral group, but statistical significance was not reached. The oral group had higher ALT (16.58 ± 6.13 versus 23.78 ± 7.17, p < 0.001) and AST (19.70 ± 3.58 versus 23.78 ± 7.17, p = 0.001) levels at 12 weeks of gestation.
Conclusion
Estradiol transdermal gel is a safe and feasible alternative for endometrial preparation in frozen embryo transfer cycles, yielding comparable ongoing pregnancy rates to the standard oral regimen.
{"title":"Comparison of clinical outcomes between use of estradiol transdermal gel and oral estradiol valerate in patients undergoing frozen–thaw embryo transfer: an observational study","authors":"Danni Zhou, Xinglin Wang, Huali Deng, Xiu Luo, Dongyun Liu, Hong Ye","doi":"10.1007/s00404-025-08277-z","DOIUrl":"10.1007/s00404-025-08277-z","url":null,"abstract":"<div><h3>Objective</h3><p>The purpose of this study was to compare oral estradiol valerate and estradiol transdermal gel for clinical pregnancy outcomes in patients undergoing frozen–thaw embryo transfer (FET).</p><h3>Methods</h3><p>This was a prospective study performed between March 1, 2017 and October 30, 2019. Totally 244 HR FET cycles were included, with 123 cycles using oral estrogen tablets (oral group) and 121 applying estradiol transdermal gel (gel group). The primary aim of this study was to compare implantation (IR), clinical pregnancy (CPR), miscarriage (MR) and live birth (LBR) rates between the two groups. The secondary aim was to assess liver function, specifically measuring alanine transaminase (ALT) and aspartate transaminase (AST) levels at 12 weeks of gestation.</p><h3>Results</h3><p>There were no significant differences in EPR, IR, and CPR between the two groups. Meanwhile, the gel group had a higher live birth rate (55.37% versus 51.20%, <i>p</i> = 0.302) and a lower miscarriage rate (5.79% versus 10.57%, <i>p</i> = 0.173) compared with the oral group, but statistical significance was not reached. The oral group had higher ALT (16.58 ± 6.13 versus 23.78 ± 7.17, <i>p</i> < 0.001) and AST (19.70 ± 3.58 versus 23.78 ± 7.17, <i>p</i> = 0.001) levels at 12 weeks of gestation.</p><h3>Conclusion</h3><p>Estradiol transdermal gel is a safe and feasible alternative for endometrial preparation in frozen embryo transfer cycles, yielding comparable ongoing pregnancy rates to the standard oral regimen.</p></div>","PeriodicalId":8330,"journal":{"name":"Archives of Gynecology and Obstetrics","volume":"313 1","pages":""},"PeriodicalIF":2.5,"publicationDate":"2025-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s00404-025-08277-z.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145852627","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-01DOI: 10.1007/s00404-025-08217-x
Irena Rohr, Anna Sophie Skof, Michaela Heinrich-Rohr, Fabian Weiss, Jan-Peter Siedentopf, Katharina von Weizsäcker, Irene Alba Alejandre, Wolfgang Henrich, Jalid Sehouli, Charlotte K Metz
{"title":"Correction: Impact of HIV infection on cervical intraepithelial neoplasia detection in pregnant and non-pregnant women in Germany: a cross-sectional study.","authors":"Irena Rohr, Anna Sophie Skof, Michaela Heinrich-Rohr, Fabian Weiss, Jan-Peter Siedentopf, Katharina von Weizsäcker, Irene Alba Alejandre, Wolfgang Henrich, Jalid Sehouli, Charlotte K Metz","doi":"10.1007/s00404-025-08217-x","DOIUrl":"10.1007/s00404-025-08217-x","url":null,"abstract":"","PeriodicalId":8330,"journal":{"name":"Archives of Gynecology and Obstetrics","volume":" ","pages":"2355"},"PeriodicalIF":2.5,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12705712/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145312399","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-29DOI: 10.1007/s00404-025-08179-0
Bing Wang, Meng Wang, Huili Xu, Yu Liu, Tengteng Kang, Yang Cao
Objectives
This meta-analysis seeks to clarify the relationship between hysterectomy, oophorectomy, and the subsequent risk of developing breast cancer.
Methods
A comprehensive literature search was conducted across PubMed, the Cochrane Library, and Embase to identify relevant studies. The quality of the included studies was assessed using the Newcastle–Ottawa Scale (NOS). Statistical analyses were performed using Stata software (version 14.0), with hazard ratios (HRs) and their corresponding 95% confidence intervals (CIs) calculated. Publication bias was assessed using funnel plots and Egger’s test.
Results
A total of 12 studies were included, comprising 9 cohort studies and 3 case–control studies, with publication years ranging from 1988 to 2023, involving 5,868,660 participants, predominantly from the United States. The analysis revealed that both hysterectomy and oophorectomy are associated with a reduced risk of breast cancer, lowering the risk by 16% (HR 0.84; 95% CI: 0.76–0.92; I2 = 76.5%; P < 0.001). Standalone hysterectomy was associated with a 13% reduction in breast cancer risk (HR 0.87; 95% CI: 0.77–0.99; I2 = 82.3%; P = 0.033), while bilateral oophorectomy reduced the risk by approximately 19% (HR 0.81; 95% CI: 0.68–0.96; I2 = 61.7%; P = 0.016). In contrast, unilateral oophorectomy did not significantly affect the risk of breast cancer (HR 0.89; 95% CI: 0.71–1.11; I2 = 45.5%; P = 0.288). Patients who underwent bilateral oophorectomy and received hormone therapy experienced a 20% reduction in breast cancer risk (HR 0.80; 95% CI: 0.68–0.93; I2 = 38.5%; P = 0.005), whereas those who did not receive hormone therapy showed no significant risk reduction (HR 0.87; 95% CI: 0.69–1.10; I2 = 48.5%; P = 0.254). Premenopausal bilateral oophorectomy was associated with a 13% decrease in breast cancer incidence risk (HR 0.87; 95% CI: 0.79–0.96; I2 = 0%; P = 0.004), while postmenopausal bilateral oophorectomy had no significant impact (HR 0.95; 95% CI: 0.88–1.03; I2 = 1.2%; P = 0.196).
Conclusions
This meta-analysis suggests that both hysterectomy and oophorectomy are significantly associated with a reduction in breast cancer risk. The effectiveness of bilateral oophorectomy appears to be modulated by hormone therapy and menopausal status. Further research is needed to clarify these associations and to explore the underlying biological mechanisms.
目的:本荟萃分析旨在阐明子宫切除术、卵巢切除术与随后发生乳腺癌风险之间的关系。方法:通过PubMed、Cochrane图书馆和Embase进行全面的文献检索,以确定相关研究。纳入研究的质量采用纽卡斯尔-渥太华量表(NOS)进行评估。采用Stata软件(14.0版)进行统计分析,计算风险比(hr)及其相应的95%置信区间(ci)。采用漏斗图和Egger检验评估发表偏倚。结果:共纳入12项研究,包括9项队列研究和3项病例对照研究,发表年份从1988年到2023年,涉及5,868,660名受试者,主要来自美国。分析显示,子宫切除术和卵巢切除术与乳腺癌风险降低相关,风险降低16% (HR 0.84; 95% CI: 0.76-0.92; I2 = 76.5%; P = 82.3%; P = 0.033),而双侧卵巢切除术风险降低约19% (HR 0.81; 95% CI: 0.68-0.96; I2 = 61.7%; P = 0.016)。相比之下,单侧卵巢切除术对乳腺癌的风险无显著影响(HR 0.89; 95% CI: 0.71-1.11; I2 = 45.5%; P = 0.288)。接受双侧卵巢切除术并接受激素治疗的患者乳腺癌风险降低20% (HR 0.80; 95% CI: 0.68-0.93; I2 = 38.5%; P = 0.005),而未接受激素治疗的患者风险无显著降低(HR 0.87; 95% CI: 0.69-1.10; I2 = 48.5%; P = 0.254)。绝经前双侧卵巢切除术与乳腺癌发病率降低13%相关(HR 0.87; 95% CI: 0.79-0.96; I2 = 0%; P = 0.004),而绝经后双侧卵巢切除术无显著影响(HR 0.95; 95% CI: 0.88-1.03; I2 = 1.2%; P = 0.196)。结论:这项荟萃分析表明,子宫切除术和卵巢切除术与乳腺癌风险的降低显著相关。双侧卵巢切除术的有效性似乎受到激素治疗和绝经状态的调节。需要进一步的研究来澄清这些关联并探索潜在的生物学机制。
{"title":"Association between hysterectomy, oophorectomy, and risk of breast cancer: a meta-analysis","authors":"Bing Wang, Meng Wang, Huili Xu, Yu Liu, Tengteng Kang, Yang Cao","doi":"10.1007/s00404-025-08179-0","DOIUrl":"10.1007/s00404-025-08179-0","url":null,"abstract":"<div><h3>Objectives</h3><p>This meta-analysis seeks to clarify the relationship between hysterectomy, oophorectomy, and the subsequent risk of developing breast cancer.</p><h3>Methods</h3><p>A comprehensive literature search was conducted across PubMed, the Cochrane Library, and Embase to identify relevant studies. The quality of the included studies was assessed using the Newcastle–Ottawa Scale (NOS). Statistical analyses were performed using Stata software (version 14.0), with hazard ratios (HRs) and their corresponding 95% confidence intervals (CIs) calculated. Publication bias was assessed using funnel plots and Egger’s test.</p><h3>Results</h3><p>A total of 12 studies were included, comprising 9 cohort studies and 3 case–control studies, with publication years ranging from 1988 to 2023, involving 5,868,660 participants, predominantly from the United States. The analysis revealed that both hysterectomy and oophorectomy are associated with a reduced risk of breast cancer, lowering the risk by 16% (HR 0.84; 95% CI: 0.76–0.92; <i>I</i><sup><i>2</i></sup> = 76.5%; <i>P</i> < 0.001). Standalone hysterectomy was associated with a 13% reduction in breast cancer risk (HR 0.87; 95% CI: 0.77–0.99; <i>I</i><sup><i>2</i></sup> = 82.3%; <i>P</i> = 0.033), while bilateral oophorectomy reduced the risk by approximately 19% (HR 0.81; 95% CI: 0.68–0.96; <i>I</i><sup><i>2</i></sup> = 61.7%; <i>P</i> = 0.016). In contrast, unilateral oophorectomy did not significantly affect the risk of breast cancer (HR 0.89; 95% CI: 0.71–1.11; <i>I</i><sup><i>2</i></sup> = 45.5%; <i>P</i> = 0.288). Patients who underwent bilateral oophorectomy and received hormone therapy experienced a 20% reduction in breast cancer risk (HR 0.80; 95% CI: 0.68–0.93; <i>I</i><sup><i>2</i></sup> = 38.5%; <i>P</i> = 0.005), whereas those who did not receive hormone therapy showed no significant risk reduction (HR 0.87; 95% CI: 0.69–1.10; <i>I</i><sup><i>2</i></sup> = 48.5%; <i>P</i> = 0.254). Premenopausal bilateral oophorectomy was associated with a 13% decrease in breast cancer incidence risk (HR 0.87; 95% CI: 0.79–0.96; <i>I</i><sup><i>2</i></sup> = 0%; <i>P</i> = 0.004), while postmenopausal bilateral oophorectomy had no significant impact (HR 0.95; 95% CI: 0.88–1.03; <i>I</i><sup><i>2</i></sup> = 1.2%; <i>P</i> = 0.196).</p><h3>Conclusions</h3><p>This meta-analysis suggests that both hysterectomy and oophorectomy are significantly associated with a reduction in breast cancer risk. The effectiveness of bilateral oophorectomy appears to be modulated by hormone therapy and menopausal status. Further research is needed to clarify these associations and to explore the underlying biological mechanisms.</p></div>","PeriodicalId":8330,"journal":{"name":"Archives of Gynecology and Obstetrics","volume":"312 6","pages":"2031 - 2042"},"PeriodicalIF":2.5,"publicationDate":"2025-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s00404-025-08179-0.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145628210","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Up to 60% of breast cancer patients achieve pathological complete response (pCR) and factors associated with breast pCR have been extensively investigated. In patients with initially node-positive disease predicting axillary response to treatment remains challenging. Our study examines a biomarker panel assessed on core-biopsy lymph-node metastatic tissue with the goal to establish predictive markers for nodal positive breast cancer.
Materials and methods
Forty women with core biopsy-proven node-positive breast cancer scheduled to receive neoadjuvant treatment at the certified Breast Cancer Center of the University Hospital Schleswig–Holstein Campus Lübeck were included. The expressions of CAIX, PD-L1, TROP2, MSH2, MSH6, MLH1, and PMS2 as well as p53 mutation were assessed. Biomarkers were chosen based on their association with tumorigenesis and tumor progression. Statistical analysis was performed using SPSS 29. This investigator-initiated study was supported by a research grant from Gilead (Gilead Förderprogramm).
Results
Higher CAIX levels were associated with triple-negative and Her2-positive receptor status (p = 0.003), Ki67 ≥ 50% in breast core biopsy (p = 0.005), as well as postmenopausal status (p = 0.007). P53 mutation was more frequent in G3 tumors (p = 0.025). All lymph-node metastases were microsatellite stable (MSS). None of the markers could significantly predict pathological response (complete, breast, or nodal).
Conclusion
Our study shows upregulated CAIX in lymph-node metastasis frequently occurs in aggressive and highly proliferative tumors. However, none of the examined biomarkers could predict nodal response to therapy. Further research is necessary to better identify patients most likely to achieve nodal response through neoadjuvant chemotherapy.
{"title":"AXINEO: AXIllary response to NEOadjuvant chemotherapy for breast cancer: can we predict response based on a biomarker panel?","authors":"Franziska Fick, Florian Lenz, Verena-Wilbeth Sailer, Achim Rody, Nikolas Tauber, Kerstin Muras, Natalia Krawczyk, Julika Ribbat-Idel, Franziska Hemptenmacher, Maggie Banys-Paluchowski","doi":"10.1007/s00404-025-08209-x","DOIUrl":"10.1007/s00404-025-08209-x","url":null,"abstract":"<div><h3>Background</h3><p>Up to 60% of breast cancer patients achieve pathological complete response (pCR) and factors associated with breast pCR have been extensively investigated. In patients with initially node-positive disease predicting axillary response to treatment remains challenging. Our study examines a biomarker panel assessed on core-biopsy lymph-node metastatic tissue with the goal to establish predictive markers for nodal positive breast cancer.</p><h3>Materials and methods</h3><p>Forty women with core biopsy-proven node-positive breast cancer scheduled to receive neoadjuvant treatment at the certified Breast Cancer Center of the University Hospital Schleswig–Holstein Campus Lübeck were included. The expressions of CAIX, PD-L1, TROP2, MSH2, MSH6, MLH1, and PMS2 as well as p53 mutation were assessed. Biomarkers were chosen based on their association with tumorigenesis and tumor progression. Statistical analysis was performed using SPSS 29. This investigator-initiated study was supported by a research grant from Gilead (Gilead Förderprogramm).</p><h3>Results</h3><p>Higher CAIX levels were associated with triple-negative and Her2-positive receptor status (<i>p</i> = 0.003), Ki67 ≥ 50% in breast core biopsy (<i>p</i> = 0.005), as well as postmenopausal status (<i>p</i> = 0.007). P53 mutation was more frequent in G3 tumors (<i>p</i> = 0.025). All lymph-node metastases were microsatellite stable (MSS). None of the markers could significantly predict pathological response (complete, breast, or nodal).</p><h3>Conclusion</h3><p>Our study shows upregulated CAIX in lymph-node metastasis frequently occurs in aggressive and highly proliferative tumors. However, none of the examined biomarkers could predict nodal response to therapy. Further research is necessary to better identify patients most likely to achieve nodal response through neoadjuvant chemotherapy.</p></div>","PeriodicalId":8330,"journal":{"name":"Archives of Gynecology and Obstetrics","volume":"312 6","pages":"2211 - 2219"},"PeriodicalIF":2.5,"publicationDate":"2025-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s00404-025-08209-x.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145538286","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Idiopathic granulomatous mastitis (IGM) is a chronic, relapsing inflammatory breast disease of unknown etiology. Its unpredictable course and unclear pathogenesis have made treatment a persistent clinical challenge. This study aimed to evaluate treatment outcomes in patients with IGM, focusing on extending remission periods and reducing relapse rates after discontinuation of therapy.
Methods
This retrospective cohort study included 200 patients with histopathological confirmed idiopathic granulomatous mastitis who were referred to the Teaching and Therapeutic Center at the Central Hospital of Mazandaran University of Medical Sciences. Patient demographics, pathological characteristics, treatment regimens, remission duration, and recurrence rates were analyzed.
Results
From January 2018 to December 2024, a total of 200 patients were enrolled in the study, with a mean age of 33 years (range: 18–54 years) and a mean follow-up duration of 34 months (range: 8–51 months). Patients were divided into two treatment groups: Group A received high-dose prednisolone combined with abscess drainage (n = 99), while Group B received low-dose prednisolone, abscess drainage, and methotrexate (n = 101). Group B demonstrated a significantly shorter treatment duration (11.56 ± 2.15 months) compared to Group A (14.86 ± 3.42 months; P < 0.001). The mean time to follow-up was significantly longer in Group B (35.97 ± 6.96 months) than in Group A (20.00 ± 7.02 months; P < 0.001). The recurrence rate was lower in Group B (4.9%) than in Group A (23.2%), with the difference approaching statistical significance (P = 0.057). In addition, the mean time to relapse in Group B (34.46 ± 6.50 months) was significantly longer than that of Group A (16.96 ± 5.34 months), indicating that patients receiving the combined regimen of low-dose prednisolone, drainage, and methotrexate experienced a more sustained remission period.
Conclusions
According to the results, the treatment of idiopathic granulomatous mastitis, especially the moderate to severe form of the disease, using combination therapy with low-dose prednisolone and methotrexate can be associated with a reduction in treatment duration, and increase in remission duration, and a reduction in relapse, and drug side effects.
{"title":"Methotrexate plus low-dose prednisolone compared with high-dose corticosteroid therapy in the management of idiopathic granulomatous mastitis","authors":"Leyla Shojaee, Nahid Nafissi, Fatemeh Niksolat Roodposhti, Kiana Shakeriastani, Kiarash Shakeriastani","doi":"10.1007/s00404-025-08220-2","DOIUrl":"10.1007/s00404-025-08220-2","url":null,"abstract":"<div><h3>Purpose</h3><p>Idiopathic granulomatous mastitis (IGM) is a chronic, relapsing inflammatory breast disease of unknown etiology. Its unpredictable course and unclear pathogenesis have made treatment a persistent clinical challenge. This study aimed to evaluate treatment outcomes in patients with IGM, focusing on extending remission periods and reducing relapse rates after discontinuation of therapy.</p><h3>Methods</h3><p>This retrospective cohort study included 200 patients with histopathological confirmed idiopathic granulomatous mastitis who were referred to the Teaching and Therapeutic Center at the Central Hospital of Mazandaran University of Medical Sciences. Patient demographics, pathological characteristics, treatment regimens, remission duration, and recurrence rates were analyzed.</p><h3>Results</h3><p>From January 2018 to December 2024, a total of 200 patients were enrolled in the study, with a mean age of 33 years (range: 18–54 years) and a mean follow-up duration of 34 months (range: 8–51 months). Patients were divided into two treatment groups: Group A received high-dose prednisolone combined with abscess drainage (<i>n</i> = 99), while Group B received low-dose prednisolone, abscess drainage, and methotrexate (<i>n</i> = 101). Group B demonstrated a significantly shorter treatment duration (11.56 ± 2.15 months) compared to Group A (14.86 ± 3.42 months; <i>P</i> < 0.001). The mean time to follow-up was significantly longer in Group B (35.97 ± 6.96 months) than in Group A (20.00 ± 7.02 months; <i>P</i> < 0.001). The recurrence rate was lower in Group B (4.9%) than in Group A (23.2%), with the difference approaching statistical significance (<i>P</i> = 0.057). In addition, the mean time to relapse in Group B (34.46 ± 6.50 months) was significantly longer than that of Group A (16.96 ± 5.34 months), indicating that patients receiving the combined regimen of low-dose prednisolone, drainage, and methotrexate experienced a more sustained remission period.</p><h3>Conclusions</h3><p>According to the results, the treatment of idiopathic granulomatous mastitis, especially the moderate to severe form of the disease, using combination therapy with low-dose prednisolone and methotrexate can be associated with a reduction in treatment duration, and increase in remission duration, and a reduction in relapse, and drug side effects.</p></div>","PeriodicalId":8330,"journal":{"name":"Archives of Gynecology and Obstetrics","volume":"312 6","pages":"2251 - 2258"},"PeriodicalIF":2.5,"publicationDate":"2025-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s00404-025-08220-2.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145538345","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Current data regarding prognostic factors for malignant tumors arising from mature cystic teratomas (MT-MCTs) and effective treatments are insufficient. This study aimed to identify risk factors for MT-MCTs of the ovary.
Methods
Tumor samples diagnosed as MT-MCTs were collected from 13 institutions that participated in the Kansai Clinical Oncology Group. Based on the clinicopathological features and prognoses of the tumors, risk factors for progression and death were statistically assessed using univariable and multivariable analyses.
Results
Among the 60 tumor samples collected, 56 were diagnosed as MT-MCTs. Four samples were excluded based on the results of a central pathological review. Nine histological types, including squamous cell carcinoma, were diagnosed. Thirty of the 56 included samples were classified as International Federation of Gynecology and Obstetrics (FIGO) stage I, seven were classified as FIGO stage II, 18 were classified as FIGO stage III, and one was classified as FIGO stage IV. The 5-year progression-free survival and overall survival probabilities for stage I disease were significantly higher than those for stages II–IV disease (p < 0.001). In the multivariable analysis, surgery with residual tumor margins was a prognostic factor for progression, and FIGO stages I–IV and the absence of adjuvant therapy were prognostic factors for death.
Conclusion
Surgery without residual tumor margins and adjuvant therapy may be promising treatments for advanced-stage MT-MCTs.
{"title":"Prognostic factors for malignant tumors arising from mature cystic teratomas: a study involving the Kansai Clinical Oncology Group (KCOG-G1305s study)","authors":"Fuminori Ito, Mototsugu Shimokawa, Atsushi Sugiura, Yoshio Itani, Atsushi Arakawa, Kayo Inoue, Mamiko Onuki, Tadahiro Shoji, Tomomi Egawa-Takata, Yuji Takei, Kazuhiro Takehara, Takashi Motohashi, Hiroaki Nagano, Toshiaki Nakamura, Satoru Munakata, Takashi Yamada, Naoto Furukawa, Tsunekazu Kita, Kimihiko Ito","doi":"10.1007/s00404-025-08194-1","DOIUrl":"10.1007/s00404-025-08194-1","url":null,"abstract":"<div><h3>Purpose</h3><p>Current data regarding prognostic factors for malignant tumors arising from mature cystic teratomas (MT-MCTs) and effective treatments are insufficient. This study aimed to identify risk factors for MT-MCTs of the ovary.</p><h3>Methods</h3><p>Tumor samples diagnosed as MT-MCTs were collected from 13 institutions that participated in the Kansai Clinical Oncology Group. Based on the clinicopathological features and prognoses of the tumors, risk factors for progression and death were statistically assessed using univariable and multivariable analyses.</p><h3>Results</h3><p>Among the 60 tumor samples collected, 56 were diagnosed as MT-MCTs. Four samples were excluded based on the results of a central pathological review. Nine histological types, including squamous cell carcinoma, were diagnosed. Thirty of the 56 included samples were classified as International Federation of Gynecology and Obstetrics (FIGO) stage I, seven were classified as FIGO stage II, 18 were classified as FIGO stage III, and one was classified as FIGO stage IV. The 5-year progression-free survival and overall survival probabilities for stage I disease were significantly higher than those for stages II–IV disease (p < 0.001). In the multivariable analysis, surgery with residual tumor margins was a prognostic factor for progression, and FIGO stages I–IV and the absence of adjuvant therapy were prognostic factors for death.</p><h3>Conclusion</h3><p>Surgery without residual tumor margins and adjuvant therapy may be promising treatments for advanced-stage MT-MCTs.</p></div>","PeriodicalId":8330,"journal":{"name":"Archives of Gynecology and Obstetrics","volume":"312 6","pages":"2333 - 2340"},"PeriodicalIF":2.5,"publicationDate":"2025-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s00404-025-08194-1.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145538312","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-16DOI: 10.1007/s00404-025-08190-5
T. Engler, M. Nägele, D. Dannehl, A. Englisch, S. Gerstner, M. Henes
Background
In 2020, Germany implemented a revised cervical cancer screening program, incorporating co-testing with cytology and human papillomavirus (HPV) testing for women aged 35 and older. This study describes patient characteristics, referral patterns, and follow-up outcomes of histologically confirmed cervical intraepithelial neoplasia (CIN) 1 and CIN 2 lesions before and after the introduction of the organized cervical cancer screening program in Germany.
Methods
In a hybrid prospective-retrospective study, we analyzed two consecutive cohorts of patients with histologically confirmed CIN 1 or CIN 2 at the Department of Women’s Health, University Hospital Tuebingen, between 2013 and 2022. Patient characteristics, referral indications, and follow-up outcomes were described and compared.
Results
Patients post-2020 were older (median 41 vs. 31 years), more often hrHPV-positive (93.4% vs. 63.3%), and more frequently presented with CIN 1 (62% vs. 51%). Immediate intervention was less common post-2020 (CIN 1: 7% vs. 25%; CIN 2: 37% vs. 67%). Among those followed, remission was higher in the post-2020 cohort (CIN 1: 63.5% vs. 42.2%; CIN 2: 61.6% vs. 41.0%). Progression to CIN 3 remained rare in both cohorts. Multivariable regression indicated that CIN 2 diagnosis and smoking reduced remission, while the post-2020 period was associated with increased remission odds.
Conclusion
The differences in remission and persistence between cohorts likely reflect changes in referral pathways, patient age rather than causal program effects. These data provide a descriptive benchmark for clinicians, supporting conservative management of CIN 1 and selected CIN 2 under the new screening program.
{"title":"Management and natural course of CIN 1 and CIN 2 before and after implementation of the revised cervical cancer screening in Germany","authors":"T. Engler, M. Nägele, D. Dannehl, A. Englisch, S. Gerstner, M. Henes","doi":"10.1007/s00404-025-08190-5","DOIUrl":"10.1007/s00404-025-08190-5","url":null,"abstract":"<div><h3>Background</h3><p>In 2020, Germany implemented a revised cervical cancer screening program, incorporating co-testing with cytology and human papillomavirus (HPV) testing for women aged 35 and older. This study describes patient characteristics, referral patterns, and follow-up outcomes of histologically confirmed cervical intraepithelial neoplasia (CIN) 1 and CIN 2 lesions before and after the introduction of the organized cervical cancer screening program in Germany.</p><h3>Methods</h3><p>In a hybrid prospective-retrospective study, we analyzed two consecutive cohorts of patients with histologically confirmed CIN 1 or CIN 2 at the Department of Women’s Health, University Hospital Tuebingen, between 2013 and 2022. Patient characteristics, referral indications, and follow-up outcomes were described and compared.</p><h3>Results</h3><p>Patients post-2020 were older (median 41 vs. 31 years), more often hrHPV-positive (93.4% vs. 63.3%), and more frequently presented with CIN 1 (62% vs. 51%). Immediate intervention was less common post-2020 (CIN 1: 7% vs. 25%; CIN 2: 37% vs. 67%). Among those followed, remission was higher in the post-2020 cohort (CIN 1: 63.5% vs. 42.2%; CIN 2: 61.6% vs. 41.0%). Progression to CIN 3 remained rare in both cohorts. Multivariable regression indicated that CIN 2 diagnosis and smoking reduced remission, while the post-2020 period was associated with increased remission odds.</p><h3>Conclusion</h3><p>The differences in remission and persistence between cohorts likely reflect changes in referral pathways, patient age rather than causal program effects. These data provide a descriptive benchmark for clinicians, supporting conservative management of CIN 1 and selected CIN 2 under the new screening program.</p></div>","PeriodicalId":8330,"journal":{"name":"Archives of Gynecology and Obstetrics","volume":"312 6","pages":"2053 - 2061"},"PeriodicalIF":2.5,"publicationDate":"2025-11-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s00404-025-08190-5.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145530306","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
<div><h3>Objective</h3><p>First-trimester fetal malformation screening via ultrasound has become increasingly important. This study aims to establish a standardized expert consensus on the ultrasound anatomical examination of fetuses during the first trimester.</p><h3>Methods</h3><p>A comprehensive literature review was conducted on first-trimester fetal anatomical examinations and malformation screening. A draft of the <i>Chinese Expert Consensus on Fetal Anatomical Examination at 11</i> + <i>0 to 13</i> + <i>6 Weeks of Gestation</i> was initially prepared by eight core committee members. Using the Delphi method, three rounds of online voting were conducted by 35 expert panel members, and feedback was solicited from 122 experts across 27 representative medical institutions of various levels and regions in China. If three-fourths of the expert panel members agreed to categorize the first-trimester fetal anatomical ultrasound examination into three types, these classification methods were adopted. Similarly, if three-fourths of the experts agreed that a specific item or plane in the consensus should be a mandatory component of the examination, it was designated as a recommended item or plane; otherwise, it was classified as a suggested item or plane.</p><h3>Results</h3><p>This expert consensus categorizes the first-trimester fetal ultrasound anatomical examination into basic (Class I), detailed (Class II), and targeted (Class III) examinations. The examination includes one measurement item (with six sub-items) and nine anatomical examination items (with 26 sub-items). The basic and detailed fetal anatomical examinations involve largely consistent measurement parameters and target organs. However, the detailed examination includes a greater number of sub-items. In the basic examination, biometric parameters such as biparietal diameter (BPD), head circumference (HC), and abdominal circumference (AC) are considered suggested items (not mandatory). Similarly, sub-items such as the primary palate, kidneys, and genital tubercle are also classified as suggested items. In contrast, all of these parameters are regarded as recommended items (mandatory) in the detailed examination. Both the basic and detailed fetal anatomical examinations are indicated for low-risk pregnancies. The primary distinction between the two lies in the level of healthcare facility where they are conducted. Basic examinations are suitable for county-level hospitals with screening qualifications, whereas detailed examinations should be performed at municipal-level hospitals with equivalent screening credentials. In the targeted examination of the fetal central nervous system (FCNS), a total of 11 ultrasound planes are included. Among these, 4 are designated as recommended planes, and the remaining 7 as suggested planes. In the targeted fetal cardiac examination, 5 planes are evaluated, with 4 being recommended and the bilateral subclavian artery plane classified as a suggested plane.
{"title":"Chinese Expert Consensus on ultrasound anatomical examination of fetuses at 11 + 0 to 13 + 6 weeks of gestation based on the Delphi method","authors":"Guorong Lyu, Ruibi Liao, Qiuxia Jiang, Xiaoqin He, Zongjie Weng","doi":"10.1007/s00404-025-08231-z","DOIUrl":"10.1007/s00404-025-08231-z","url":null,"abstract":"<div><h3>Objective</h3><p>First-trimester fetal malformation screening via ultrasound has become increasingly important. This study aims to establish a standardized expert consensus on the ultrasound anatomical examination of fetuses during the first trimester.</p><h3>Methods</h3><p>A comprehensive literature review was conducted on first-trimester fetal anatomical examinations and malformation screening. A draft of the <i>Chinese Expert Consensus on Fetal Anatomical Examination at 11</i> + <i>0 to 13</i> + <i>6 Weeks of Gestation</i> was initially prepared by eight core committee members. Using the Delphi method, three rounds of online voting were conducted by 35 expert panel members, and feedback was solicited from 122 experts across 27 representative medical institutions of various levels and regions in China. If three-fourths of the expert panel members agreed to categorize the first-trimester fetal anatomical ultrasound examination into three types, these classification methods were adopted. Similarly, if three-fourths of the experts agreed that a specific item or plane in the consensus should be a mandatory component of the examination, it was designated as a recommended item or plane; otherwise, it was classified as a suggested item or plane.</p><h3>Results</h3><p>This expert consensus categorizes the first-trimester fetal ultrasound anatomical examination into basic (Class I), detailed (Class II), and targeted (Class III) examinations. The examination includes one measurement item (with six sub-items) and nine anatomical examination items (with 26 sub-items). The basic and detailed fetal anatomical examinations involve largely consistent measurement parameters and target organs. However, the detailed examination includes a greater number of sub-items. In the basic examination, biometric parameters such as biparietal diameter (BPD), head circumference (HC), and abdominal circumference (AC) are considered suggested items (not mandatory). Similarly, sub-items such as the primary palate, kidneys, and genital tubercle are also classified as suggested items. In contrast, all of these parameters are regarded as recommended items (mandatory) in the detailed examination. Both the basic and detailed fetal anatomical examinations are indicated for low-risk pregnancies. The primary distinction between the two lies in the level of healthcare facility where they are conducted. Basic examinations are suitable for county-level hospitals with screening qualifications, whereas detailed examinations should be performed at municipal-level hospitals with equivalent screening credentials. In the targeted examination of the fetal central nervous system (FCNS), a total of 11 ultrasound planes are included. Among these, 4 are designated as recommended planes, and the remaining 7 as suggested planes. In the targeted fetal cardiac examination, 5 planes are evaluated, with 4 being recommended and the bilateral subclavian artery plane classified as a suggested plane.","PeriodicalId":8330,"journal":{"name":"Archives of Gynecology and Obstetrics","volume":"312 6","pages":"1937 - 1954"},"PeriodicalIF":2.5,"publicationDate":"2025-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s00404-025-08231-z.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145522753","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
This study aimed to evaluate the impact of repeated cesarean deliveries on isthmocele formation and to investigate the diagnostic value and clinical presentation of morphometric parameters, including niche depth, width, length, residual myometrial thickness (RMT), adjacent myometrial thickness (AMT), and the depth/AMT ratio.
Methods
A cross-sectional study was conducted with 116 symptomatic and asymptomatic women aged 18–45 years who had undergone one or more cesarean sections. The presence and dimensions of the isthmocele were assessed via transvaginal ultrasonography using Delphi consensus criteria. Morphometric and obstetric data were analyzed using descriptive statistics, correlation analysis, and binary logistic regression.
Results
Isthmocele was identified in 71.6% of participants, with prevalence rising from 42.9% after the first cesarean to 100% after the fourth. The isthmocele group had significantly higher gravidity, parity, and cesarean numbers (p < 0.001). Niche depth, length, and the depth/AMT ratio were significantly elevated, while RMT was reduced (p < 0.001). The number of cesareans showed a strong negative correlation with RMT (r = –0.499, p < 0.001) and a strong positive correlation with the depth/RMT ratio (r = 0.615, p < 0.001). Multivariate analysis identified having three or more cesareans as an independent predictor of isthmocele (OR = 15.6; 95% CI 3.27–74.4; p < 0.001). Niche length had the highest diagnostic accuracy for symptomatic isthmocele (AUC 0.700; 95% CI 0.589–0.796; cutoff 5 mm).
Conclusion
Repeated cesarean deliveries significantly increase both the risk and severity of isthmocele. In women with four cesareans, isthmocele was detected in 100% of cases. A niche length of ≥ 5 mm proved to be the most reliable morphometric marker in identifying symptomatic cases.
Implications for clinical practice
These findings emphasize the importance of routine transvaginal ultrasound screening post-cesarean—especially in women with multiple cesarean sections—and the incorporation of morphometric assessment (including RMT and depth/RMT ratio) into clinical decision-making.
{"title":"Isthmocele risk in repeated cesarean: the diagnostic and clinical role of morphometric parameters","authors":"Gülhan Özüm, Hakan Güraslan, Levent Deniz, Tuğba Demirtaş","doi":"10.1007/s00404-025-08238-6","DOIUrl":"10.1007/s00404-025-08238-6","url":null,"abstract":"<div><h3>Objective</h3><p>This study aimed to evaluate the impact of repeated cesarean deliveries on isthmocele formation and to investigate the diagnostic value and clinical presentation of morphometric parameters, including niche depth, width, length, residual myometrial thickness (RMT), adjacent myometrial thickness (AMT), and the depth/AMT ratio.</p><h3>Methods</h3><p>A cross-sectional study was conducted with 116 symptomatic and asymptomatic women aged 18–45 years who had undergone one or more cesarean sections. The presence and dimensions of the isthmocele were assessed via transvaginal ultrasonography using Delphi consensus criteria. Morphometric and obstetric data were analyzed using descriptive statistics, correlation analysis, and binary logistic regression.</p><h3>Results</h3><p>Isthmocele was identified in 71.6% of participants, with prevalence rising from 42.9% after the first cesarean to 100% after the fourth. The isthmocele group had significantly higher gravidity, parity, and cesarean numbers (<i>p</i> < 0.001). Niche depth, length, and the depth/AMT ratio were significantly elevated, while RMT was reduced (<i>p</i> < 0.001). The number of cesareans showed a strong negative correlation with RMT (<i>r</i> = –0.499, <i>p</i> < 0.001) and a strong positive correlation with the depth/RMT ratio (<i>r</i> = 0.615, <i>p</i> < 0.001). Multivariate analysis identified having three or more cesareans as an independent predictor of isthmocele (OR = 15.6; 95% CI 3.27–74.4; <i>p</i> < 0.001). Niche length had the highest diagnostic accuracy for symptomatic isthmocele (AUC 0.700; 95% CI 0.589–0.796; cutoff 5 mm).</p><h3>Conclusion</h3><p>Repeated cesarean deliveries significantly increase both the risk and severity of isthmocele. In women with four cesareans, isthmocele was detected in 100% of cases. A niche length of ≥ 5 mm proved to be the most reliable morphometric marker in identifying symptomatic cases.</p><h3>Implications for clinical practice</h3><p>These findings emphasize the importance of routine transvaginal ultrasound screening post-cesarean—especially in women with multiple cesarean sections—and the incorporation of morphometric assessment (including RMT and depth/RMT ratio) into clinical decision-making.</p></div>","PeriodicalId":8330,"journal":{"name":"Archives of Gynecology and Obstetrics","volume":"312 6","pages":"2321 - 2332"},"PeriodicalIF":2.5,"publicationDate":"2025-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s00404-025-08238-6.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145470352","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-04DOI: 10.1007/s00404-025-08205-1
Amparo García-Tejedor, Rodrigo Guevara-Peralta, Jose Manuel Martinez-Garcia, Shiana Corbalán, Mauricio Agüero, Maria Gomez-Romero, Marta Cararach, Marta Castellarnau, Mariví Rodríguez, Ana Cristina Lou-Mercadé, Laura Costa, Maria Jose Rodríguez, Eva Huguet, Manuel Carreras, Ana Belen Castel-Segui, Maria Font-Roig, Susana Royo, Nuria Sarasa, Beatriz Candas, Samuel Perez-Carton, Carlos Ortega, Maria Jesus Pla, Jordi Ponce
Purpose
To compare the efficacy of ultrasound-guided alcohol sclerotherapy versus laparoscopic cystectomy for the management of ovarian endometriomas, focusing on complications, recurrence, pain relief, and healthcare costs.
Methods
We conducted a multicentre, randomized clinical trial across 20 centers in Spain. A total of 167 women aged 18–40 years with ovarian endometriomas (35–100 mm) were recruited between June 2018 and June 2022. Participants were randomized to receive either ultrasound-guided aspiration with ethanol sclerotherapy or standard laparoscopic cystectomy. Complications were graded using the Clavien–Dindo classification. Pain was assessed using a visual analogue scale (VAS) before and six months after treatment. Recurrence was defined as the reappearance of a cystic lesion at the treated site and analyzed using Kaplan–Meier curves and log-rank tests. The primary analysis followed an intention-to-treat approach and included 158 patients (sclerotherapy: n = 84; cystectomy: n = 74). The per-protocol analysis included 92 patients (sclerotherapy: n = 57; cystectomy: n = 37). Direct hospital costs, complication rates, recurrence, and pain relief were compared between groups.
Results
Intention-to-treat analyses show that complications were low in both groups (12%), most of which were Grade I–II, although 4.1% were Grade III in the surgery group. The cost of sclerotherapy was significantly lower (€472 vs. €2128, p < 0.001). In per-protocol analyses, the cyst recurrence or reappearance was similar between the two groups, with rates of 25.7% (9 of 35) in the surgery group and 22.8% (13 of 57) in the sclerotherapy group (p = 0.16). Pain was improved or completely resolved in 49 of 55 cases (89.1%) in the sclerotherapy group and in 21 of 32 cases (65.7%) in the laparoscopic surgery group (p = 0.05).
Conclusions
Ultrasound-guided alcohol sclerotherapy is a safe, cost-effective alternative to laparoscopic cystectomy for the treatment of endometriomas, with comparable recurrence rates and pain relief. Clinical Trial Registration: https://clinicaltrials.gov/search?term=NCT03571776. Registered May 5, 2018.
{"title":"Ultrasound-guided ethanol sclerotherapy versus laparoscopic surgery for endometriomas: a randomized clinical trial in a real-world setting","authors":"Amparo García-Tejedor, Rodrigo Guevara-Peralta, Jose Manuel Martinez-Garcia, Shiana Corbalán, Mauricio Agüero, Maria Gomez-Romero, Marta Cararach, Marta Castellarnau, Mariví Rodríguez, Ana Cristina Lou-Mercadé, Laura Costa, Maria Jose Rodríguez, Eva Huguet, Manuel Carreras, Ana Belen Castel-Segui, Maria Font-Roig, Susana Royo, Nuria Sarasa, Beatriz Candas, Samuel Perez-Carton, Carlos Ortega, Maria Jesus Pla, Jordi Ponce","doi":"10.1007/s00404-025-08205-1","DOIUrl":"10.1007/s00404-025-08205-1","url":null,"abstract":"<div><h3>Purpose</h3><p>To compare the efficacy of ultrasound-guided alcohol sclerotherapy versus laparoscopic cystectomy for the management of ovarian endometriomas, focusing on complications, recurrence, pain relief, and healthcare costs.</p><h3>Methods</h3><p>We conducted a multicentre, randomized clinical trial across 20 centers in Spain. A total of 167 women aged 18–40 years with ovarian endometriomas (35–100 mm) were recruited between June 2018 and June 2022. Participants were randomized to receive either ultrasound-guided aspiration with ethanol sclerotherapy or standard laparoscopic cystectomy. Complications were graded using the Clavien–Dindo classification. Pain was assessed using a visual analogue scale (VAS) before and six months after treatment. Recurrence was defined as the reappearance of a cystic lesion at the treated site and analyzed using Kaplan–Meier curves and log-rank tests. The primary analysis followed an <i>intention-to-treat</i> approach and included 158 patients (sclerotherapy: <i>n</i> = 84; cystectomy: <i>n</i> = 74). The <i>per-protocol</i> analysis included 92 patients (sclerotherapy: <i>n</i> = 57; cystectomy: <i>n</i> = 37). Direct hospital costs, complication rates, recurrence, and pain relief were compared between groups.</p><h3>Results</h3><p>Intention-to-treat analyses show that complications were low in both groups (12%), most of which were Grade I–II, although 4.1% were Grade III in the surgery group. The cost of sclerotherapy was significantly lower (€472 vs. €2128, <i>p</i> < 0.001). In per-protocol analyses, the cyst recurrence or reappearance was similar between the two groups, with rates of 25.7% (9 of 35) in the surgery group and 22.8% (13 of 57) in the sclerotherapy group (<i>p</i> = 0.16). Pain was improved or completely resolved in 49 of 55 cases (89.1%) in the sclerotherapy group and in 21 of 32 cases (65.7%) in the laparoscopic surgery group (<i>p</i> = 0.05).</p><h3>Conclusions</h3><p>Ultrasound-guided alcohol sclerotherapy is a safe, cost-effective alternative to laparoscopic cystectomy for the treatment of endometriomas, with comparable recurrence rates and pain relief. Clinical Trial Registration: https://clinicaltrials.gov/search?term=NCT03571776. Registered May 5, 2018.</p></div>","PeriodicalId":8330,"journal":{"name":"Archives of Gynecology and Obstetrics","volume":"312 6","pages":"2199 - 2210"},"PeriodicalIF":2.5,"publicationDate":"2025-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s00404-025-08205-1.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145437240","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}