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Patterns of treatment and outcome in patients with unresectable or inoperable esophageal cancer: A real world data 不可切除或不可手术食管癌患者的治疗模式和结果:一个真实世界的数据
Pub Date : 2022-01-27 DOI: 10.1101/2022.01.26.22269828
R. Chauhan, V. Trivedi, R. Rani, U. Singh
Background: Esophageal cancer is the eighth most common cancer in the world with a high mortality rate. Surgery radiation and chemotherapy have been tried in various combinations to improve on the survival rates. Our study provides real world data from a South Asian country on patterns of treatment and outcome in patients with unresectable or inoperable esophageal cancer. Materials and Methods: This study is a retrospective analysis of all consecutive esophageal cancer patients with medically inoperable or unresectable disease and treated with conformal radical radiotherapy at a tertiary cancer center from January 2016 to December 2017. Data regarding patients age histology location pretreatment imaging disease stage treatment details compliance and response to treatment and status at last followup were retrieved from their file. Continuous and categorical variables were summarized by descriptive statistics. Results: A total of 100 esophageal cancer patients with a mean age of 60.24 years were included in the study. 60% of the patients were male and upper onethird was the most common site involved. Squamous cell carcinoma was reported in 83% of the patients. About 70% of the patients had a T3/T4 disease and 44% also had nodal metastasis. The radiation dose ranged from 45Gy 63Gy (median = 59.4Gy). Further 15% and 54% of the patients received neoadjuvant and concurrent chemotherapy respectively. Radiation compliance was seen in 90% of the patients. With a median follow-up of 7 months (range 3 58 months) 80% of the patients were alive with 32.22% having no evidence of disease. Distant metastases and loco regional failure was seen in 32.22% and 28% of the patients respectively. Conclusion: Our study showed that esophageal cancer is more common in elderly males. Adherence to a uniform treatment protocol using concurrent chemo radiation is difficult in clinical practice especially in resource constrained set up. Both distant metastases and loco regional failure continues to be a matter of concern. Further improvement in local control must be evaluated by either radiation dose escalation or novel combinations with chemotherapy and immunotherapy in large multi centric trial settings.
背景:食管癌是世界上第八大常见癌症,死亡率高。为了提高生存率,已经尝试了手术、放疗和化疗的各种组合。我们的研究提供了来自南亚国家的真实数据,关于不可切除或不可手术食管癌患者的治疗模式和结果。材料与方法:本研究回顾性分析2016年1月至2017年12月在某三级肿瘤中心连续接受适形根治性放疗的食管癌患者。从他们的档案中检索患者的年龄、组织学、位置、预处理、影像学、疾病分期、治疗细节、依从性和对治疗的反应以及最后随访状态等数据。用描述性统计对连续变量和分类变量进行汇总。结果:共纳入100例食管癌患者,平均年龄60.24岁。60%的患者为男性,上三分之一是最常见的部位。83%的患者为鳞状细胞癌。约70%的患者有T3/T4病变,44%的患者有淋巴结转移。放射剂量为45Gy ~ 63Gy,中位数为59.4Gy。另外15%和54%的患者分别接受了新辅助化疗和同期化疗。90%的患者接受了放射治疗。中位随访7个月(范围358个月),80%的患者存活,32.22%的患者无疾病证据。远处转移和局部衰竭分别占32.22%和28%。结论:食管癌多见于老年男性。在临床实践中,特别是在资源有限的情况下,坚持使用同步化疗放疗的统一治疗方案是困难的。远处转移和局部区域失败仍然是值得关注的问题。局部控制的进一步改善必须在大型多中心试验环境中通过增加辐射剂量或与化疗和免疫治疗的新组合来评估。
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引用次数: 0
Ulcerative Budding Skin Tumor Revealing Malignant Pleural Mesothelioma 溃疡性出芽皮肤肿瘤显示恶性胸膜间皮瘤
Pub Date : 2022-01-19 DOI: 10.31487/j.ijcst.2021.03.03
S. Niang, Fatimata Binetou Rassoul Mbaye, Maimouna Fafa Cisse, Justin Eca, K. Thiam, El Hadji Mamadou Ndiaye, A. Diop Dia, Y. Dia Kane, A. Diatta, N. O. Toure Badiane
Pleural mesothelioma is a malignant tumor, which develops from the pleural mesothelial lining. We report a clinical observation of a 24-year-old young man who presented with a right serohematic pleurisy and ulcerative budding skin lesion of the right abdominal wall. Through this case, we highlight a very rare, atypical metastatic localization that can be clinically confused with a primary skin tumor.
胸膜间皮瘤是一种恶性肿瘤,由胸膜间皮层发展而来。我们报告一个临床观察的24岁的年轻人谁提出了一个右血清性胸膜炎和溃疡萌芽皮肤损害的右腹壁。通过这个病例,我们强调了一个非常罕见的,非典型的转移性定位,它在临床上可能与原发性皮肤肿瘤混淆。
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引用次数: 0
Case Studies of Postoperative Cognitive Dysfunction in Elderly Patients 老年患者术后认知功能障碍病例分析
Pub Date : 2021-11-26 DOI: 10.31487/j.ijcst.2021.03.02
Kalliopi Megari
Background and Objective: Postoperative cognitive dysfunction (POCD) involves decline in several cognitive domains after surgery and is particularly common after cardiac surgery. Given the potential effects of such cognitive dysfunction on quality of life, it is important to study it in multiple populations in order to limit its occurrence. Recent advances in surgical technology may assist in achieving this goal.Methods: We present the long-term neuropsychological outcome of two elderly patients, one of whom had off pump heart surgery and the other oncological surgery. We administered a series of neuropsychological tests assessing attention, complex scanning, verbal working memory, executive functioning, short-term and long-term memory, and visuospatial perception before surgery, prior to discharge, at 3-month follow-up and 6 years after surgery. We compared the performance of these two patients to normative datasets.Results: Despite equivalent levels of pre-surgery performance between the two patients, the oncology patient exceeded his preoperative neurocognitive levels, suggesting less postoperative cognitive dysfunction in the heart patient overall, on all neuropsychological domains at 6-year follow-up, except short-term retention. In contrast, the heart patient showed no improvement, and, instead, showed some cognitive decline which remained consistent over time.Conclusion: Our findings highlight the critical role of the type of surgery utilized in the development of POCD and have implications for clinical management and patients’ quality of life in the very long term.
背景与目的:术后认知功能障碍(POCD)涉及手术后多个认知领域的下降,在心脏手术后尤为常见。鉴于这种认知功能障碍对生活质量的潜在影响,在多个人群中进行研究以限制其发生是很重要的。外科技术的最新进展可能有助于实现这一目标。方法:报告两例老年患者的长期神经心理结果,其中一例接受了无泵心脏手术,另一例接受了肿瘤手术。我们在手术前、出院前、随访3个月和术后6年进行了一系列神经心理测试,评估注意力、复杂扫描、言语工作记忆、执行功能、短期和长期记忆以及视觉空间感知。我们将这两名患者的表现与规范数据集进行了比较。结果:尽管两名患者的术前表现相当,但肿瘤患者的神经认知水平超过了术前水平,这表明在6年随访期间,除短期保留外,心脏患者在所有神经心理领域的总体术后认知功能障碍较少。相比之下,心脏病患者没有表现出任何改善,相反,随着时间的推移,他们的认知能力有所下降。结论:我们的研究结果强调了手术类型在POCD发展中的关键作用,并对临床管理和患者的长期生活质量具有重要意义。
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引用次数: 0
1-(4-Methoxyphenyl)-3-(3-phenoxyphenyl) prop-2-en-1-one: A Diphenyl Chalcone Derivative with Potent Antitumor Activity Via Up-Regulation of p21 Gene 1-(4-甲氧基苯基)-3-(3-phenoxyphenyl) prop-2-en-1-one:一种通过上调p21基因而具有抗肿瘤活性的二苯查尔酮衍生物
Pub Date : 2021-11-08 DOI: 10.31487/j.ijcst.2021.02.04
Litty Joseph, Lakshmi Ps
Background and Aim: Cancer is a disease of complex aetiology and is characterised by uncontrolled growth of abnormal cells. It is a major worldwide health problem. Many natural and synthetic chalcone or their derivatives showed anticancer activities. The aim of the present study is to evaluate the anticancer activity of novel chalcone derivatives and also to establish possible mechanism of action.Materials and Methods: A series of chalcones 3-(3-phenoxyphenyl)-1-phenylprop-2-en-1-one (2a); 1-(4-chlorophenyl)-3-(3-phenoxyphenyl) prop-2-en-1-one (2b); 1-(4-fluorophenyl)-3-(3-phenoxyphenyl) prop-2-en-1-one (2c); 1-(4-Nitro-phenyl)-3-(3-phenoxy-phenyl)prop-2-en-1-one (2d); 1-(4-methoxyphenyl)-3-(3-phenoxyphenyl) prop-2-en-1-one(2e) were evaluated for the cytotoxic activity both in vitro and in vivo. The in vivo antitumor activity of these compounds was estimated on Daltons Ascites Lymphoma induced solid tumor model. The effect of promising compound was further analysed by flow cytometer and RT- PCR analysis.Results and Conclusion: 1-(4-methoxyphenyl)-3-(3-phenoxyphenyl) prop-2-en-1-one and 1-(4- chlorophenyl)-3-(3-phenoxyphenyl) prop-2-en-1-one was showed in vitro cytotoxic activity, DNA damage and antiproliferative activity. DLA induced solid tumor model suggested that 1-(4-methoxyphenyl)-3-(3- phenoxy phenyl) prop-2-en-1-one significantly reduced the tumor volume, increase the percentage tumor inhibition and reverse the haematological parameters. Flow cytometry analysis concluded that the compound induces cell cycle arrest at G0/G1 phase due to the over expression of p21. 1-(4-methoxyphenyl)-3-(3- phenoxy phenyl) prop-2-en-1-one may be a potential agent for cancer treatment.
背景与目的:癌症是一种病因复杂的疾病,其特点是异常细胞不受控制地生长。这是一个世界性的重大健康问题。许多天然和合成查尔酮或其衍生物显示出抗癌活性。本研究的目的是评价新型查尔酮衍生物的抗癌活性,并探讨其可能的作用机制。材料与方法:一系列查尔酮3-(3-phenoxyphenyl)-1-苯丙-2-en-1-one (2a);1-(4-氯苯基)-3-(3-phenoxyphenyl) pro- 2-en-1-one (2b);1-(4-氟苯基)-3-(3-phenoxyphenyl) pro- 2-en-1-one (2c);(1 - (4-Nitro-phenyl) 3) - 3-phenoxy-phenyl prop-2-en-1-one (2 d);体外和体内评价了1-(4-甲氧基苯基)-3-(3-苯氧基)prop-2-en-1-one(2e)的细胞毒活性。在道尔顿腹水淋巴瘤诱导的实体瘤模型上测定了这些化合物的体内抗肿瘤活性。通过流式细胞仪和RT- PCR分析进一步分析了有希望的化合物的作用。结果与结论:1-(4-甲氧基苯基)-3-(3-phenoxyphenyl) prop-2-en-1和1-(4-氯苯基)-3-(3-phenoxyphenyl) prop-2-en-1具有体外细胞毒活性、DNA损伤和抗增殖活性。DLA诱导实体瘤模型显示,1-(4-甲氧基苯基)-3-(3-苯氧基苯基)prop-2-en-1-one显著减小肿瘤体积,提高肿瘤抑制率,逆转血液学参数。流式细胞术分析表明,该化合物由于p21过表达导致细胞周期阻滞在G0/G1期。1-(4-甲氧基苯基)-3-(3-苯氧基苯基)pro- 2-en-1-one可能是一种潜在的癌症治疗药物。
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引用次数: 0
A Combination of Formoterol and the Histone Deacetylase Inhibitor AR42 has No Effects on Muscle Mass in Tumor-Bearing Rats 福莫特罗联合组蛋白去乙酰化酶抑制剂AR42对荷瘤大鼠肌肉质量无影响
Pub Date : 2021-11-05 DOI: 10.31487/j.ijcst.2021.02.02
S. Busquets, Marta-Inés Castillejo, Queralt Jové, Alina Noguera, F. López‐Soriano, J. M. Argiles
Background: Accelerated muscle and adipose tissue loss are two of the main aspects of cancer cachexia. β2-agonists seem to be successful in the treatment of cachexia in experimental animals. The aim if the present investigation was to study the effects on body weight loss in tumor-bearing animals of a combination of formoterol and AR-42, an inhibitor of histone deacetylase (HDAC).Methods: Rats were divided into two groups, namely controls (C) and tumor-bearing (T). TB group was further divided into four subgroups: untreated (saline as a vehicle), treated with Formoterol (F) (0,3 mg/kg body weight in saline, subcutaneous (s.c.), daily), treated with AR-42 (A) (20 mg/kg body weight in olive oil, intragastric (i.g.), only the last 4 days). and double-treated treated (TFA) with Formoterol (0,3 mg/kg body weight, subcutaneous (s.c.), daily) and AR-42 (20 mg/kg body weight in olive oil, intragastric (i.g.), only the last 4 days). 7 days after tumor transplantation, muscle weights, grip force and total physical activity were determined in all experimental groups.Results: The presence of the Yoshida AH-130 ascites hepatoma induced severe muscle wasting in rats. Treatment of the tumor-bearing animals with the beta2-agonist formoterol (0,3 mg/kg), resulted in a significant improvement in the cachectic state of the animals. Treatment of the tumor-bearing animals with AR42 did not result in any effects on muscle wasting in the cachectic rats. Furthermore, the combination of formoterol and AR42 showed no additional effects to those observed with just formoterol.Conclusion: The results presented question the previously described effects of AR42 on cancer cachexia, probably due to its effect on tumor growth.
背景:加速肌肉和脂肪组织的损失是癌症恶病质的两个主要方面。β2激动剂在实验动物中治疗恶病质似乎是成功的。本研究的目的是研究福莫特罗和组蛋白去乙酰化酶(HDAC)抑制剂AR-42联合使用对荷瘤动物体重减轻的影响。方法:将大鼠分为对照组(C)和荷瘤组(T), TB组进一步分为4个亚组:未治疗组(生理盐水为对照)、福莫特罗(F)组(0.3 mg/kg体重生理盐水,皮下(s.c),每日)、AR-42 (a)组(20 mg/kg体重橄榄油,灌胃(ig),仅最后4天)。福莫特罗(0.3 mg/kg体重,皮下(s.c),每日)和AR-42 (20 mg/kg体重,橄榄油中,灌胃(ig),仅在最近4天)双重处理(TFA)。肿瘤移植后7 d,测定各组肌肉重量、握力和总体力活动。结果:吉田AH-130腹水型肝癌引起大鼠严重肌肉萎缩。用β 2激动剂福莫特罗(0.3 mg/kg)治疗荷瘤动物,可显著改善动物的病毒质状态。用AR42治疗荷瘤动物对恶病质大鼠的肌肉萎缩没有任何影响。此外,福莫特罗和AR42的联合治疗没有显示出与仅使用福莫特罗相比的额外效果。结论:研究结果对AR42对肿瘤恶病质的作用提出了质疑,这可能与它对肿瘤生长的影响有关。
{"title":"A Combination of Formoterol and the Histone Deacetylase Inhibitor AR42 has No Effects on Muscle Mass in Tumor-Bearing Rats","authors":"S. Busquets, Marta-Inés Castillejo, Queralt Jové, Alina Noguera, F. López‐Soriano, J. M. Argiles","doi":"10.31487/j.ijcst.2021.02.02","DOIUrl":"https://doi.org/10.31487/j.ijcst.2021.02.02","url":null,"abstract":"Background: Accelerated muscle and adipose tissue loss are two of the main aspects of cancer cachexia. β2-agonists seem to be successful in the treatment of cachexia in experimental animals. The aim if the present investigation was to study the effects on body weight loss in tumor-bearing animals of a combination of formoterol and AR-42, an inhibitor of histone deacetylase (HDAC).\u0000Methods: Rats were divided into two groups, namely controls (C) and tumor-bearing (T). TB group was further divided into four subgroups: untreated (saline as a vehicle), treated with Formoterol (F) (0,3 mg/kg body weight in saline, subcutaneous (s.c.), daily), treated with AR-42 (A) (20 mg/kg body weight in olive oil, intragastric (i.g.), only the last 4 days). and double-treated treated (TFA) with Formoterol (0,3 mg/kg body weight, subcutaneous (s.c.), daily) and AR-42 (20 mg/kg body weight in olive oil, intragastric (i.g.), only the last 4 days). 7 days after tumor transplantation, muscle weights, grip force and total physical activity were determined in all experimental groups.\u0000Results: The presence of the Yoshida AH-130 ascites hepatoma induced severe muscle wasting in rats. Treatment of the tumor-bearing animals with the beta2-agonist formoterol (0,3 mg/kg), resulted in a significant improvement in the cachectic state of the animals. Treatment of the tumor-bearing animals with AR42 did not result in any effects on muscle wasting in the cachectic rats. Furthermore, the combination of formoterol and AR42 showed no additional effects to those observed with just formoterol.\u0000Conclusion: The results presented question the previously described effects of AR42 on cancer cachexia, probably due to its effect on tumor growth.","PeriodicalId":13867,"journal":{"name":"International Journal of Cancer Science and Therapy","volume":"57 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91374748","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Epidemiological Survey of Central Nervous System Tumors Admitted in a Reference Hospital in the North Fluminense Region in Brazil 巴西北弗鲁米嫩塞地区某参考医院中枢神经系统肿瘤的流行病学调查
Pub Date : 2021-10-25 DOI: 10.31487/j.ijcst.2021.02.03
L. A. Buexm, Danielli Aparecida de Souza Silva, Bruna Areas Ribeiro, Rayane Figueiredo Silva Moreira Carvalho, Julia Moraes Ferreira, Marina S. Teixeira, Alessandra Oliveira Ferrari Gomes, Frederico P. Barbosa
Cancer is a major worldwide health problem, being an important cause of morbidity and mortality to population. In global scale, nervous system cancers represent around 1.8% of all malignant tumors in the planet. From 2020 to 2022, it’s estimated around 11.090 new cases of this type of cancer in Brazil. This study aims to raise epidemiological data on central nervous system tumors admitted to the oncology department of a reference hospital in the North Fluminense region in Brazil. Forty-four patients were included in this study, who were predominant males (56.8%), aged between 41 to 60 years old (47.7%), with tumors located primarily in the brain (65.9%) and histopathologically classified as glioblastomas (38.6%). Patients had no family history of cancer (64.3%), were non-smokers (68.2%), non-alcoholics (70%), undergoing primary surgical treatment (34.1%), who did not undergo adjuvant treatment (84.1%) and who died from the disease (66.7%). Glioblastoma was the most incident malignant neoplasm, followed by astrocytoma for both sexes, corroborating with literature data. In summary, this work contributes to a better understanding of these tumors, focusing on their prevention, early diagnosis and treatment.
癌症是世界范围内的一个重大健康问题,是人类发病和死亡的一个重要原因。在全球范围内,神经系统癌症约占地球上所有恶性肿瘤的1.8%。从2020年到2022年,巴西估计会有大约11.090例这种癌症的新病例。本研究旨在提高巴西北弗鲁米嫩塞地区一家参考医院肿瘤科收治的中枢神经系统肿瘤的流行病学数据。本研究纳入44例患者,以男性为主(56.8%),年龄41 - 60岁(47.7%),肿瘤主要位于脑部(65.9%),组织病理学分类为胶质母细胞瘤(38.6%)。患者无癌症家族史(64.3%),不吸烟(68.2%),不酗酒(70%),接受初级手术治疗(34.1%),未接受辅助治疗(84.1%),死于疾病(66.7%)。恶性肿瘤中胶质母细胞瘤发生率最高,其次为星形细胞瘤,两性发生率均较高,与文献资料一致。总之,这项工作有助于更好地了解这些肿瘤,重点关注其预防,早期诊断和治疗。
{"title":"Epidemiological Survey of Central Nervous System Tumors Admitted in a Reference Hospital in the North Fluminense Region in Brazil","authors":"L. A. Buexm, Danielli Aparecida de Souza Silva, Bruna Areas Ribeiro, Rayane Figueiredo Silva Moreira Carvalho, Julia Moraes Ferreira, Marina S. Teixeira, Alessandra Oliveira Ferrari Gomes, Frederico P. Barbosa","doi":"10.31487/j.ijcst.2021.02.03","DOIUrl":"https://doi.org/10.31487/j.ijcst.2021.02.03","url":null,"abstract":"Cancer is a major worldwide health problem, being an important cause of morbidity and mortality to population. In global scale, nervous system cancers represent around 1.8% of all malignant tumors in the planet. From 2020 to 2022, it’s estimated around 11.090 new cases of this type of cancer in Brazil. This study aims to raise epidemiological data on central nervous system tumors admitted to the oncology department of a reference hospital in the North Fluminense region in Brazil. Forty-four patients were included in this study, who were predominant males (56.8%), aged between 41 to 60 years old (47.7%), with tumors located primarily in the brain (65.9%) and histopathologically classified as glioblastomas (38.6%). Patients had no family history of cancer (64.3%), were non-smokers (68.2%), non-alcoholics (70%), undergoing primary surgical treatment (34.1%), who did not undergo adjuvant treatment (84.1%) and who died from the disease (66.7%). Glioblastoma was the most incident malignant neoplasm, followed by astrocytoma for both sexes, corroborating with literature data. In summary, this work contributes to a better understanding of these tumors, focusing on their prevention, early diagnosis and treatment.","PeriodicalId":13867,"journal":{"name":"International Journal of Cancer Science and Therapy","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-10-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76063528","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Vaginal Dilator Use to Promote Sexual Wellbeing After Radiotherapy in Gynaecological Cancer Survivors: A Prospective Observational Study 阴道扩张器用于促进妇科癌症幸存者放疗后的性健康:一项前瞻性观察研究
Pub Date : 2021-10-14 DOI: 10.31487/j.ijcst.2021.03.01
Dimitra Charatsi, P. Vanakara, M. Nikolaou, Aikaterini Evaggelopoulou, D. Korfias, F. Simopoulou, N. Charalampakis, D. Schizas, A. Daponte, G. Kyrgias, M. Tolia
Background: Since continuing advances in radiotherapy technology broaden the role of radiotherapy in the treatment of gynaecologic malignancies, the use of vaginal dilators has been introduced in order to mitigate the risk of vaginal stenosis. The main aims of this study were to investigate the vaginal dilator use efficacy in the treatment of radiation-induced vaginal stenosis and the vaginal dilator effect on sexual quality of life. Methods: We studied fifty-three patients with endometrial or cervical cancer. The participants were treated with radical or adjuvant external beam radiotherapy and/or brachytherapy. They were routinely examined at four time points post-radiotherapy when also they were asked to fill in a validated sexual function-vaginal changes questionnaire. A p-value less than 0.05 was considered statistically significant.Results: The vaginal stenosis grading score was decreased and the size of the vaginal dilator comfortably insertable was gradually increased throughout the year of vaginal dilator use while radiation-induced vaginal and sexual symptoms were improved throughout the year of VD use. All patients with initial grade 3 showed vaginal stenosis of grade 2 after 12 months of vaginal dilator use and 65.8% of the patients with grade 2 initial vaginal stenosis demonstrated final vaginal stenosis grade 1 while 77.8% of the participants with initial 1st size of vaginal dilators reached the 3rd vaginal dilator size after 12 months. Starting time of dilator therapy <= 3 months after the end of radiotherapy was associated with a significant decrease in vaginal stenosis. Additionally, there was an overall upward trend regarding patients’ satisfaction with their sexual life.Conclusion: Endometrial and cervical cancer survivors should be encouraged to use vaginal dilators for the treatment of vaginal stenosis and sexual rehabilitation after radiotherapy.
背景:由于放射治疗技术的不断进步扩大了放射治疗在妇科恶性肿瘤治疗中的作用,为了减轻阴道狭窄的风险,阴道扩张器的使用已经被引入。本研究的主要目的是探讨阴道扩张器在治疗放射性阴道狭窄中的应用效果以及阴道扩张器对性生活质量的影响。方法:对53例子宫内膜癌或宫颈癌患者进行研究。参与者接受根治性或辅助性外束放疗和/或近距离放疗。他们在放疗后的四个时间点接受常规检查,同时他们被要求填写一份有效的性功能阴道变化问卷。p值小于0.05被认为具有统计学意义。结果:在阴道扩张器使用的一年中,阴道狭窄分级评分降低,阴道扩张器舒适插入的尺寸逐渐增加,而在VD使用的一年中,辐射引起的阴道和性症状得到改善。所有初始尺寸为3级的患者在使用阴道扩张器12个月后阴道狭窄程度达到2级,初始尺寸为2级的患者中65.8%的患者最终阴道狭窄程度达到1级,而初始尺寸为1的患者中77.8%的患者在12个月后阴道扩张器尺寸达到3级。放疗结束后开始使用扩张器治疗时间<= 3个月与阴道狭窄明显减少相关。此外,患者对性生活的满意度总体呈上升趋势。结论:应鼓励子宫内膜癌和宫颈癌幸存者使用阴道扩张器治疗阴道狭窄和放疗后的性康复。
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引用次数: 0
Potential Biomarkers in Diagnosis, Prognosis and Prediction of Treatment Response in Malignant Glioma 恶性胶质瘤诊断、预后及治疗反应预测的潜在生物标志物
Pub Date : 2021-09-29 DOI: 10.31487/j.ijcst.2021.02.05
P. Shokrani, M. Heidari
Gliomas are the most common type of primary central nervous system malignancies with poor prognosis in adults. There are several challenges in developing a treatment protocol for this malignancy including presence of blood-brain barrier that inhibit drug delivery to brain tissue, drug and radiation resistance of tumor cells, and inter and intra-tumor heterogeneity of glioma. In addition, early treatment assessment is difficult for glioma patients because of phenomenon of pseudo-progression. Due to the challenges involved in treatment and monitoring of treatment response for glioma, it is very helpful to identify specific and non-invasive molecular and imaging markers in order to provide useful prognostic information. The aim of this article is to summarize several potential biological and imaging markers regarding malignant glioma. A brief description of the proteins involved in the glioma signaling pathways is provided in order to introduce potential biological markers. Furthermore, the role of imaging techniques in treatment management is discussed. Finally, correlation between tumor characteristics and values of angiogenesis and physiological factors measured in perfusion magnetic resonance imaging techniques as well as metabolites in MRS, and PET tracer’s uptake is investigated.
胶质瘤是成人最常见的原发性中枢神经系统恶性肿瘤,预后较差。在开发这种恶性肿瘤的治疗方案中存在一些挑战,包括血脑屏障的存在,抑制药物向脑组织的传递,肿瘤细胞的药物和辐射抗性,以及胶质瘤之间和肿瘤内部的异质性。此外,由于胶质瘤患者存在假进展现象,早期治疗评估困难。由于胶质瘤的治疗和治疗反应监测所涉及的挑战,识别特异性和非侵入性的分子和成像标记以提供有用的预后信息是非常有帮助的。本文的目的是总结几种潜在的生物学和影像学标记与恶性胶质瘤。为了介绍潜在的生物标记物,简要介绍了胶质瘤信号通路中涉及的蛋白质。此外,还讨论了成像技术在治疗管理中的作用。最后,研究了肿瘤特征与血管生成值、灌注磁共振成像技术测量的生理因素、MRS代谢物和PET示踪剂摄取之间的相关性。
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引用次数: 0
BDE-209 and TCDD Modulate the Expression and Activity of ATP-Binding Cassette (ABC) Transporters in Murine Melanoma Cells (B16-F1) BDE-209和TCDD调节小鼠黑色素瘤细胞(B16-F1)中atp结合盒(ABC)转运体的表达和活性
Pub Date : 2021-09-02 DOI: 10.31487/j.ijcst.2021.02.01
C. Ribeiro, M. De Marchi, Erick E. Moggio, F. Filipak Neto, P. E. Brito, Benisio F. Silva Filho
Persistent organic pollutants (POPs) may alter tumor cells phenotype, possibly increasing malignancy, but there is a lack of studies investigating the mechanisms by which POPs may affect tumor cells. The ATP-Binding Cassette (ABC) transporter proteins are a widely studied component of drug resistance and tumor progression. We hypothesized that the levels of BDE-209 and TCDD detected in human serum can modulate the gene expression or activity of ATP-binding cassette (ABC) transporters in murine melanoma (B16-F1) cells. In this study, we observed an upregulation of the ABCB1 and ABCC4 (24 h) genes followed by an increased protein activity after BDE-209 15 day-exposure. We also observed that cells exposed to TCDD showed an upregulation of ABCB5, ABCC1 and ABCC4 genes (24 h) and change of protein activity after 15 days of exposure. These findings suggest that BDE-209 and TCDD can regulate the phenotype of B16-F1 cells by interfering with the expression and activity of ATP-binding cassette (ABC) transporters. Thisinvestigation revealed that environmental pollutants might intervene and modify cells’ resistance to chemotherapy and cancer prognosis.
持久性有机污染物(POPs)可能改变肿瘤细胞的表型,可能增加恶性肿瘤,但缺乏关于持久性有机污染物影响肿瘤细胞的机制的研究。atp结合盒(ABC)转运蛋白是一个广泛研究的耐药和肿瘤进展的组成部分。我们假设在人血清中检测到的BDE-209和TCDD水平可以调节小鼠黑色素瘤(B16-F1)细胞中atp结合盒(ABC)转运体的基因表达或活性。在这项研究中,我们观察到BDE-209暴露15天后,ABCB1和ABCC4基因(24小时)上调,随后蛋白质活性增加。我们还观察到,暴露于TCDD的细胞显示ABCB5、ABCC1和ABCC4基因(24 h)上调,暴露15天后蛋白质活性发生变化。这些结果表明,BDE-209和TCDD可以通过干扰atp结合盒(ABC)转运体的表达和活性来调节B16-F1细胞的表型。本研究揭示了环境污染物可能干预和改变细胞对化疗的耐药性和肿瘤预后。
{"title":"BDE-209 and TCDD Modulate the Expression and Activity of ATP-Binding Cassette (ABC) Transporters in Murine Melanoma Cells (B16-F1)","authors":"C. Ribeiro, M. De Marchi, Erick E. Moggio, F. Filipak Neto, P. E. Brito, Benisio F. Silva Filho","doi":"10.31487/j.ijcst.2021.02.01","DOIUrl":"https://doi.org/10.31487/j.ijcst.2021.02.01","url":null,"abstract":"Persistent organic pollutants (POPs) may alter tumor cells phenotype, possibly increasing malignancy, but \u0000there is a lack of studies investigating the mechanisms by which POPs may affect tumor cells. The ATP-Binding Cassette (ABC) transporter proteins are a widely studied component of drug resistance and tumor \u0000progression. We hypothesized that the levels of BDE-209 and TCDD detected in human serum can modulate \u0000the gene expression or activity of ATP-binding cassette (ABC) transporters in murine melanoma (B16-F1) \u0000cells. In this study, we observed an upregulation of the ABCB1 and ABCC4 (24 h) genes followed by an \u0000increased protein activity after BDE-209 15 day-exposure. We also observed that cells exposed to TCDD \u0000showed an upregulation of ABCB5, ABCC1 and ABCC4 genes (24 h) and change of protein activity after 15 \u0000days of exposure. These findings suggest that BDE-209 and TCDD can regulate the phenotype of B16-F1 \u0000cells by interfering with the expression and activity of ATP-binding cassette (ABC) transporters. This\u0000investigation revealed that environmental pollutants might intervene and modify cells’ resistance to \u0000chemotherapy and cancer prognosis.","PeriodicalId":13867,"journal":{"name":"International Journal of Cancer Science and Therapy","volume":"109 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78781596","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
The Pivotal Role of PAO in CDK Inhibitors (Roscovitine and Purvalanol)- Triggered Apoptosis in PUMA Null HCT116 Colon Cancer Cells PAO在CDK抑制剂(罗斯科维汀和普缬烷醇)引发PUMA缺失HCT116结肠癌细胞凋亡中的关键作用
Pub Date : 2021-08-04 DOI: 10.31487/j.ijcst.2021.01.03
Ajda Coker-Gurkan, Burcu Ayhan-Sahin
Background: Cycline-dependent kinase inhibitors (CDKi); roscovitine and purvalanol, are promising anti-cancer drugs due to their strong anti-proliferative effectiveness due to activation of PA catabolism. Besides transforming acetylated spermine and spermidine into spermidine and putrescine, respectively, polyamine oxidase (PAO) also generates hydrogen peroxide in high concentrations as a by-product. PAO was assumed as a pivotal key molecule during drug-induced apoptosis in cancer cells. Our aim is to reveal the role of PAO action in CDKi-triggered apoptosis in Puma knock-out HCT116 colon cancer cells. Methods: HCT116 wt and HCT116 Puma-/-cells were treated with Roscovitine and Purvalanol and cell viability and apoptosis were determined. Protein was isolated from treated and untreated cells and key molecules of cell cycle control and polyamine pathways were investigated at translational level. Polyamine content was determined by HPLC for all conditions. MDL-72527 was used as a PAO inhibitor and apoptotic cell death was analysed. Results: Roscovitine and purvalanol induced apoptosis and increased the cytotoxic responses in HCT116 wt and HCT116 Puma-/-colon carcinoma cell lines by modulating CDK1, 4, cyclin-B1, D3. Both, CDKi altered intrinsic apoptotic pathways in HCT116 wt. Whereas, drug-induced apoptosis occurred caspase-independent in Puma-/-colon cancer cells. Roscovitine and purvalanol up-regulated polyamine catabolic enzymes, whereas CDK inhibitors decreased the polyamine levels in HCT116 wt and HCT116 Puma-/-colon cancer cells. In addition, PAO inhibitor MDL72527 prevented drug-induced apoptosis. Conclusion: PAO expression profile might be a critical target in CDK inhibitors-triggered apoptosis in HCT116 colorectal cancer cells. Thus, MAPK signaling pathway relations with cell cycle and polyamine catabolic pathway investigations are in progress.
背景:周期素依赖性激酶抑制剂;rosscovitine和purvalanol是很有前景的抗癌药物,因为它们通过激活PA分解代谢而具有很强的抗增殖作用。多胺氧化酶(PAO)除了将乙酰化的精胺和亚精胺分别转化为亚精胺和腐胺外,还产生高浓度过氧化氢作为副产物。PAO被认为是药物诱导癌细胞凋亡的关键分子。我们的目的是揭示PAO在cdki引发的Puma敲除HCT116结肠癌细胞凋亡中的作用。方法:将HCT116 wt和HCT116 Puma-/-细胞分别用罗斯科维汀和普缬烷醇处理,观察细胞活力和凋亡情况。从处理和未处理的细胞中分离蛋白质,并在翻译水平上研究细胞周期控制和多胺途径的关键分子。采用高效液相色谱法测定各条件下多胺含量。以MDL-72527作为PAO抑制剂,观察凋亡细胞的死亡情况。结果:罗scovitine和purvalanol通过调节CDK1, 4, cyclin-B1, D3,诱导HCT116 wt和HCT116 Puma-/-结肠癌细胞株凋亡,增加细胞毒反应。CDKi改变了HCT116 wt中固有的凋亡途径。然而,在Puma-/-结肠癌细胞中,药物诱导的凋亡不依赖于caspase。Roscovitine和purvalanol上调多胺分解代谢酶,而CDK抑制剂降低HCT116 wt和HCT116 Puma-/-结肠癌细胞中的多胺水平。此外,PAO抑制剂MDL72527可阻止药物诱导的细胞凋亡。结论:PAO表达谱可能是CDK抑制剂引发HCT116结直肠癌细胞凋亡的关键靶点。因此,MAPK信号通路与细胞周期和多胺分解代谢通路的关系研究正在进行中。
{"title":"The Pivotal Role of PAO in CDK Inhibitors (Roscovitine and Purvalanol)- Triggered Apoptosis in PUMA Null HCT116 Colon Cancer Cells","authors":"Ajda Coker-Gurkan, Burcu Ayhan-Sahin","doi":"10.31487/j.ijcst.2021.01.03","DOIUrl":"https://doi.org/10.31487/j.ijcst.2021.01.03","url":null,"abstract":"Background: Cycline-dependent kinase inhibitors (CDKi); roscovitine and purvalanol, are promising anti-cancer drugs due to their strong anti-proliferative effectiveness due to activation of PA catabolism. Besides \u0000transforming acetylated spermine and spermidine into spermidine and putrescine, respectively, polyamine \u0000oxidase (PAO) also generates hydrogen peroxide in high concentrations as a by-product. PAO was assumed \u0000as a pivotal key molecule during drug-induced apoptosis in cancer cells. Our aim is to reveal the role of \u0000PAO action in CDKi-triggered apoptosis in Puma knock-out HCT116 colon cancer cells. \u0000Methods: HCT116 wt and HCT116 Puma-/-\u0000cells were treated with Roscovitine and Purvalanol and cell \u0000viability and apoptosis were determined. Protein was isolated from treated and untreated cells and key \u0000molecules of cell cycle control and polyamine pathways were investigated at translational level. Polyamine \u0000content was determined by HPLC for all conditions. MDL-72527 was used as a PAO inhibitor and apoptotic \u0000cell death was analysed. \u0000Results: Roscovitine and purvalanol induced apoptosis and increased the cytotoxic responses in HCT116 \u0000wt and HCT116 Puma-/-\u0000colon carcinoma cell lines by modulating CDK1, 4, cyclin-B1, D3. Both, CDKi \u0000altered intrinsic apoptotic pathways in HCT116 wt. Whereas, drug-induced apoptosis occurred caspase-independent in Puma-/-\u0000colon cancer cells. Roscovitine and purvalanol up-regulated polyamine catabolic \u0000enzymes, whereas CDK inhibitors decreased the polyamine levels in HCT116 wt and HCT116 Puma-/-\u0000colon \u0000cancer cells. In addition, PAO inhibitor MDL72527 prevented drug-induced apoptosis. \u0000Conclusion: PAO expression profile might be a critical target in CDK inhibitors-triggered apoptosis in \u0000HCT116 colorectal cancer cells. Thus, MAPK signaling pathway relations with cell cycle and polyamine \u0000catabolic pathway investigations are in progress.","PeriodicalId":13867,"journal":{"name":"International Journal of Cancer Science and Therapy","volume":"21 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-08-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79128613","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
International Journal of Cancer Science and Therapy
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