Pub Date : 2026-02-01Epub Date: 2025-05-06DOI: 10.1007/s00066-025-02400-4
Mike Wenzel, Katrin Burdenski, Nikolaos Tselis, Claus Rödel, Christian Brandts, Marit Ahrens, Jens Koellermann, Markus Graefen, Clara Humke, Carolin Siech, Benedikt Hoeh, Severine Banek, Felix K H Chun, Philipp Mandel
Purpose: Outcomes of adjuvant (aRT) or salvage radiation therapy (sRT) after radical prostatectomy are under investigation regarding cancer-control outcomes.
Methods: Relying on the University Cancer Center database elaborating differences in metastasis-free (MFS), cancer-specific (CSS) and overall survival (OS) of aRT vs. sRT-treated patients between 2014-2024. Sensitivity analyses addressed high-risk patients with pN1 and/or Gleason score 8-10 and/or pT3-4 stage.
Results: Of 1862 patients, 7.1% underwent aRT and 93% were in the sRT group. Median PSA at sRT was 0.33 ng/ml. Patients with aRT harbored significantly worse baseline tumor and pathological characteristics such as PSA level (12.0 vs. 7.6 ng/ml), Gleason score 9-10 (30% vs. 9.8%), D'Amico high risk prostate cancer (97% vs. 56%), as well as pT3-4, pN1 and positive surgical margins rates (all p < 0.001). Similar observations were made for high-risk patients. No differences were observed for aRT vs. sRT with 60-month MFS rates of 85.1% vs. 95.4% (hazard ratio [HR] 0.60, p = 0.18). 60-months CSS-rates of 96.8% vs. 99.1% and 60-month OS-rates of 91.0% vs. 89.1% respectively (all p ≥ 0.15). Neither sensitivity analyses of high-risk patients nor multivariable adjusted Cox regression models revealed significant differences regarding MFS, CSS or OS in aRT vs. SRT comparison (all p ≥ 0.05), despite aRT showing qualitatively better OS results.
Conclusion: Within real-world setting, patients undergoing aRT harbor wore tumor characteristics. However, these differences did not translate into significant differences of mid-term oncological outcomes, relative to sRT patients. Similar observations were made within analyses of high-risk patients with pT3-4 and/or Gleason 8-10 and/or pN1 stage, nevertheless aRT showed slightly higher OS rates within this subgroup.
目的:研究根治性前列腺切除术后的辅助(aRT)或补救性放射治疗(sRT)对癌症控制结果的影响。方法:依托大学癌症中心数据库,详细阐述2014-2024年间aRT与srt治疗患者的无转移(MFS)、癌症特异性(CSS)和总生存(OS)的差异。敏感性分析针对pN1和/或Gleason评分为8-10和/或pT3-4期的高危患者。结果:1862例患者中,接受aRT治疗的占7.1%,接受sRT治疗的占93%。sRT时中位PSA为0.33 ng/ml。aRT患者的基线肿瘤和病理特征明显更差,如PSA水平(12.0 vs. 7.6 ng/ml), Gleason评分9-10 (30% vs. 9.8%), D'Amico高危前列腺癌(97% vs. 56%),以及pT3-4, pN1和阳性手术切界率(均p 结论:在现实环境中,接受aRT治疗的患者具有肿瘤特征。然而,这些差异并没有转化为中期肿瘤预后的显著差异,相对于sRT患者。在pT3-4期和/或Gleason 8-10期和/或pN1期的高危患者的分析中也有类似的观察结果,尽管aRT在该亚组中显示出略高的OS率。
{"title":"Real world comparison of adjuvant vs. salvage radiation therapy on cancer-control outcomes after radical prostatectomy.","authors":"Mike Wenzel, Katrin Burdenski, Nikolaos Tselis, Claus Rödel, Christian Brandts, Marit Ahrens, Jens Koellermann, Markus Graefen, Clara Humke, Carolin Siech, Benedikt Hoeh, Severine Banek, Felix K H Chun, Philipp Mandel","doi":"10.1007/s00066-025-02400-4","DOIUrl":"10.1007/s00066-025-02400-4","url":null,"abstract":"<p><strong>Purpose: </strong>Outcomes of adjuvant (aRT) or salvage radiation therapy (sRT) after radical prostatectomy are under investigation regarding cancer-control outcomes.</p><p><strong>Methods: </strong>Relying on the University Cancer Center database elaborating differences in metastasis-free (MFS), cancer-specific (CSS) and overall survival (OS) of aRT vs. sRT-treated patients between 2014-2024. Sensitivity analyses addressed high-risk patients with pN1 and/or Gleason score 8-10 and/or pT3-4 stage.</p><p><strong>Results: </strong>Of 1862 patients, 7.1% underwent aRT and 93% were in the sRT group. Median PSA at sRT was 0.33 ng/ml. Patients with aRT harbored significantly worse baseline tumor and pathological characteristics such as PSA level (12.0 vs. 7.6 ng/ml), Gleason score 9-10 (30% vs. 9.8%), D'Amico high risk prostate cancer (97% vs. 56%), as well as pT3-4, pN1 and positive surgical margins rates (all p < 0.001). Similar observations were made for high-risk patients. No differences were observed for aRT vs. sRT with 60-month MFS rates of 85.1% vs. 95.4% (hazard ratio [HR] 0.60, p = 0.18). 60-months CSS-rates of 96.8% vs. 99.1% and 60-month OS-rates of 91.0% vs. 89.1% respectively (all p ≥ 0.15). Neither sensitivity analyses of high-risk patients nor multivariable adjusted Cox regression models revealed significant differences regarding MFS, CSS or OS in aRT vs. SRT comparison (all p ≥ 0.05), despite aRT showing qualitatively better OS results.</p><p><strong>Conclusion: </strong>Within real-world setting, patients undergoing aRT harbor wore tumor characteristics. However, these differences did not translate into significant differences of mid-term oncological outcomes, relative to sRT patients. Similar observations were made within analyses of high-risk patients with pT3-4 and/or Gleason 8-10 and/or pN1 stage, nevertheless aRT showed slightly higher OS rates within this subgroup.</p>","PeriodicalId":21998,"journal":{"name":"Strahlentherapie und Onkologie","volume":" ","pages":"129-138"},"PeriodicalIF":2.5,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12872771/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144046601","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 : 2026-02-01Epub Date: 2025-09-23DOI: 10.1007/s00066-025-02445-5
Anne Caroline Knöchelmann, Roland Merten, Hans Christiansen, Elna Kuehnle, Daniela Meinecke
Purpose: Locally advanced breast cancer in frail and inoperable patients often causes tumor-associated pain, bleeding, or discharge. These patients may not be suitable for therapeutic options like surgery or potentially toxic systemic treatment. Local radiotherapy with little impact on treatment time may be beneficial in this patient subgroup. We evaluated an ultra-hypofractionated definitive irradiation concept in five fractions (5 × 5 Gy with a simultaneous integrated boost of 5 × 6 Gy) for these patients, focusing on tolerability and clinical outcome.
Methods: A total of 29 patients were retrospectively sampled. They were treated by irradiation to the breast with 25 Gy in five fractions with a simultaneous integrated boost (SIB) of 6 Gy per fraction. Tumor response and clinical outcome were evaluated by clinical examination.
Results: In total, 27 patients with a median age of 82 years were assessed. Median follow-up was 7.4 months. All patients completed radiotherapy with 25 Gy in five fractions with a simultaneous integrated boost of 30 Gy (6 Gy per fraction) without any high-grade toxicity (≥ grade 2). Within the first 90 days after irradiation, 15 patients (56%) exhibited a clinical response and 12 showed stable disease. Only 7 patients reported low-grade acute dermatotoxicity grade 1 (CTCAE) within the first 90 days, and only one experienced toxicity later (fibrosis grade 1, LENT-SOMA).
Conclusion: Radiotherapy in five consecutive daily fractions is sufficient. The studied regimen proved to be a safe, effective palliative treatment in inoperable and frail patients not suitable for surgery or toxic systemic therapy.
{"title":"Locally advanced breast cancer: primary ultra-hypofractionated radiotherapy for inoperable or frail patients.","authors":"Anne Caroline Knöchelmann, Roland Merten, Hans Christiansen, Elna Kuehnle, Daniela Meinecke","doi":"10.1007/s00066-025-02445-5","DOIUrl":"10.1007/s00066-025-02445-5","url":null,"abstract":"<p><strong>Purpose: </strong>Locally advanced breast cancer in frail and inoperable patients often causes tumor-associated pain, bleeding, or discharge. These patients may not be suitable for therapeutic options like surgery or potentially toxic systemic treatment. Local radiotherapy with little impact on treatment time may be beneficial in this patient subgroup. We evaluated an ultra-hypofractionated definitive irradiation concept in five fractions (5 × 5 Gy with a simultaneous integrated boost of 5 × 6 Gy) for these patients, focusing on tolerability and clinical outcome.</p><p><strong>Methods: </strong>A total of 29 patients were retrospectively sampled. They were treated by irradiation to the breast with 25 Gy in five fractions with a simultaneous integrated boost (SIB) of 6 Gy per fraction. Tumor response and clinical outcome were evaluated by clinical examination.</p><p><strong>Results: </strong>In total, 27 patients with a median age of 82 years were assessed. Median follow-up was 7.4 months. All patients completed radiotherapy with 25 Gy in five fractions with a simultaneous integrated boost of 30 Gy (6 Gy per fraction) without any high-grade toxicity (≥ grade 2). Within the first 90 days after irradiation, 15 patients (56%) exhibited a clinical response and 12 showed stable disease. Only 7 patients reported low-grade acute dermatotoxicity grade 1 (CTCAE) within the first 90 days, and only one experienced toxicity later (fibrosis grade 1, LENT-SOMA).</p><p><strong>Conclusion: </strong>Radiotherapy in five consecutive daily fractions is sufficient. The studied regimen proved to be a safe, effective palliative treatment in inoperable and frail patients not suitable for surgery or toxic systemic therapy.</p>","PeriodicalId":21998,"journal":{"name":"Strahlentherapie und Onkologie","volume":" ","pages":"178-186"},"PeriodicalIF":2.5,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12872697/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145125965","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 : 2026-02-01Epub Date: 2025-10-06DOI: 10.1007/s00066-025-02474-0
Georg Wurschi, Thomas Ernst
{"title":"[Non-operative management through immune-checkpoint inhibition in mismatch repair-deficient tumors].","authors":"Georg Wurschi, Thomas Ernst","doi":"10.1007/s00066-025-02474-0","DOIUrl":"10.1007/s00066-025-02474-0","url":null,"abstract":"","PeriodicalId":21998,"journal":{"name":"Strahlentherapie und Onkologie","volume":" ","pages":"233-235"},"PeriodicalIF":2.5,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145233399","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2025-11-04DOI: 10.1007/s00066-025-02487-9
Aysenur Elmali, Birhan Demirhan, Ozan Cem Guler, Cem Onal
Purpose: To evaluate genitourinary (GU) toxicity in patients with prostate cancer receiving conventional radiotherapy (RT) with a simultaneous integrated boost (SIB) to intraprostatic lesions (IPL), with a specific focus on those with a history of transurethral resection of the prostate (TURP).
Methods: This retrospective study initially included 606 patients with localized prostate cancer treated with definitive image-guided external beam RT between 2012 and 2023. Of these, 79 patients (13%) had a history of TURP. To reduce potential bias and balance baseline characteristics, 1:1 propensity score matching (PSM) was performed based on age, cardiac disease, diabetes mellitus, RT field, and androgen deprivation therapy (ADT) use. After matching, 158 patients (79 TURP vs. 79 no-TURP) were included in the final analysis. SIB was delivered to IPLs up to 86 Gy in 39 fractions. Toxicities were recorded according to CTCAE v4.03, and logistic regression was used to identify predictors of late GU toxicity.
Results: In the matched cohort, baseline urinary function, α‑blocker use, prostate and IPL volumes, and IPL localisation were well balanced between groups. After a median follow-up of 78 months, late Grade ≥ 2 GU toxicity occurred in 21.5% of TURP vs. 7.6% of non-TURP patients (p = 0.02). The median time to late toxicity was significantly shorter among TURP patients (16 vs. 47 months, p = 0.007). On multivariable analysis, prior TURP and diabetes mellitus were independently associated with increased risk of late grade ≥ 2 GU toxicity.
Conclusion: Prior TURP is independently associated with higher and earlier-onset late GU toxicity in patients with prostate cancer receiving modern SIB-based RT. These results suggest that TURP status should be incorporated into personalized RT planning.
{"title":"Does transurethral resection of prostate increase toxicity risk after simultaneous integrated boost radiotherapy? A matched cohort study with long-term follow-up.","authors":"Aysenur Elmali, Birhan Demirhan, Ozan Cem Guler, Cem Onal","doi":"10.1007/s00066-025-02487-9","DOIUrl":"10.1007/s00066-025-02487-9","url":null,"abstract":"<p><strong>Purpose: </strong>To evaluate genitourinary (GU) toxicity in patients with prostate cancer receiving conventional radiotherapy (RT) with a simultaneous integrated boost (SIB) to intraprostatic lesions (IPL), with a specific focus on those with a history of transurethral resection of the prostate (TURP).</p><p><strong>Methods: </strong>This retrospective study initially included 606 patients with localized prostate cancer treated with definitive image-guided external beam RT between 2012 and 2023. Of these, 79 patients (13%) had a history of TURP. To reduce potential bias and balance baseline characteristics, 1:1 propensity score matching (PSM) was performed based on age, cardiac disease, diabetes mellitus, RT field, and androgen deprivation therapy (ADT) use. After matching, 158 patients (79 TURP vs. 79 no-TURP) were included in the final analysis. SIB was delivered to IPLs up to 86 Gy in 39 fractions. Toxicities were recorded according to CTCAE v4.03, and logistic regression was used to identify predictors of late GU toxicity.</p><p><strong>Results: </strong>In the matched cohort, baseline urinary function, α‑blocker use, prostate and IPL volumes, and IPL localisation were well balanced between groups. After a median follow-up of 78 months, late Grade ≥ 2 GU toxicity occurred in 21.5% of TURP vs. 7.6% of non-TURP patients (p = 0.02). The median time to late toxicity was significantly shorter among TURP patients (16 vs. 47 months, p = 0.007). On multivariable analysis, prior TURP and diabetes mellitus were independently associated with increased risk of late grade ≥ 2 GU toxicity.</p><p><strong>Conclusion: </strong>Prior TURP is independently associated with higher and earlier-onset late GU toxicity in patients with prostate cancer receiving modern SIB-based RT. These results suggest that TURP status should be incorporated into personalized RT planning.</p>","PeriodicalId":21998,"journal":{"name":"Strahlentherapie und Onkologie","volume":" ","pages":"149-159"},"PeriodicalIF":2.5,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145439333","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2025-06-17DOI: 10.1007/s00066-025-02419-7
Ann-Katrin Exeli, Andreas Lurtz, Linda Agolli, Daniel Habermehl
Purpose: The healthcare sector is a large greenhouse gas producer. Especially in radiotherapy (RT), a lot of electricity is consumed by the medical linear accelerator (linac) and associated patient travel. Our aim was to ascertain by how much electrical energy consumption and patient travel can be reduced by replacing normofractionated (NF) with emerging moderately hypofractionated (UF) or ultra-hypofractionated (UHF) concepts.
Results: This study measured the energy consumption of a linac (in kWh) and its impact on CO2 emissions for various radiotherapy fractionation concepts. Ultra-hypofractionated regimens consistently showed the lowest energy consumption and variability across prostate, breast, and bone metastasis treatment courses, while NF regimens had significantly higher energy consumption and variability. Transitioning from NF to UHF regimens reduced CO2 emissions by up to 75%, driven by fewer patient visits and lower electricity consumption. These findings highlight the environmental and logistical benefits of HF and UHF treatment protocols.
Conclusion: The adoption of HF and UHF treatment concepts can significantly reduce energy consumption and CO2 emissions, achieving an up to 75% reduction per treatment course. This is primarily due to decreased patient travel and electricity consumption at the linac. Extrapolated globally, these changes offer further potential to mitigate climate change.
Pub Date : 2026-02-01Epub Date: 2025-05-19DOI: 10.1007/s00066-025-02412-0
Lukas Goerdt, Janina Pömsl, Uta Kraus-Tiefenbacher, Viktoria Brück, Christina Kaiser, Ralf Keymer, Yasser Abo-Madyan, Katharina Fleckenstein, Sebastian Berlit, Benjamin Tuschy, Marc Sütterlin, Frederik Wenz, Elena Sperk
Purpose: The TARGIT BQR (boost quality registry) phase IV trial investigates clinical outcomes of breast cancer patients with standard external-beam radiotherapy (EBRT) of the whole breast and intraoperative radiotherapy (IORT) with low-kV x‑rays as an anticipated tumor bed boost in a real-world setting.
Methods: Intraoperative radiotherapy was performed immediately after breast-conserving surgery in one fraction. External-beam radiotherapy and systemic treatment were given according to the German S3 guideline for breast cancer and local tumor board recommendations. Outcome parameters were death, local recurrence, metastasis, local lymph node recurrence, and ipsilateral and contralateral invasive breast cancer. Kaplan-Meier estimates were used to calculate overall survival, metastasis-free survival, local recurrence-free survival, and disease-free survival.
Results: From 10 centers, 1133 patients were recruited. This analysis included 871 patients with 879 cancers, with a median follow-up of 36 months (up to 12 years). An IORT boost was performed in 82% and whole-breast irradiation in 84%. Overall survival was 98.4% after 3 years, 96.8% after 5 years, and 95.4% after 10 years (16 deaths; 1.8%). Metastasis and local recurrence occurred in 11 patients each (1.3%). At 5 years, the local control rate was 97.4% and local recurrence-free survival was 94.4%. Ipsilateral breast cancer occurred in 2 patients, contralateral breast cancer in 3 patients, and local lymph node recurrence in 2 patients. Disease-free survival was 92.9% after 5 years and 82.6% after 10 years.
Conclusion: This phase IV trial confirms previously reported outcomes on upfront IORT boost, with excellent disease-control outcomes.
{"title":"Oncological outcomes of breast cancer patients after planned IORT boost with low-kV x-rays-results of the TARGIT BQR prospective phase IV trial.","authors":"Lukas Goerdt, Janina Pömsl, Uta Kraus-Tiefenbacher, Viktoria Brück, Christina Kaiser, Ralf Keymer, Yasser Abo-Madyan, Katharina Fleckenstein, Sebastian Berlit, Benjamin Tuschy, Marc Sütterlin, Frederik Wenz, Elena Sperk","doi":"10.1007/s00066-025-02412-0","DOIUrl":"10.1007/s00066-025-02412-0","url":null,"abstract":"<p><strong>Purpose: </strong>The TARGIT BQR (boost quality registry) phase IV trial investigates clinical outcomes of breast cancer patients with standard external-beam radiotherapy (EBRT) of the whole breast and intraoperative radiotherapy (IORT) with low-kV x‑rays as an anticipated tumor bed boost in a real-world setting.</p><p><strong>Methods: </strong>Intraoperative radiotherapy was performed immediately after breast-conserving surgery in one fraction. External-beam radiotherapy and systemic treatment were given according to the German S3 guideline for breast cancer and local tumor board recommendations. Outcome parameters were death, local recurrence, metastasis, local lymph node recurrence, and ipsilateral and contralateral invasive breast cancer. Kaplan-Meier estimates were used to calculate overall survival, metastasis-free survival, local recurrence-free survival, and disease-free survival.</p><p><strong>Results: </strong>From 10 centers, 1133 patients were recruited. This analysis included 871 patients with 879 cancers, with a median follow-up of 36 months (up to 12 years). An IORT boost was performed in 82% and whole-breast irradiation in 84%. Overall survival was 98.4% after 3 years, 96.8% after 5 years, and 95.4% after 10 years (16 deaths; 1.8%). Metastasis and local recurrence occurred in 11 patients each (1.3%). At 5 years, the local control rate was 97.4% and local recurrence-free survival was 94.4%. Ipsilateral breast cancer occurred in 2 patients, contralateral breast cancer in 3 patients, and local lymph node recurrence in 2 patients. Disease-free survival was 92.9% after 5 years and 82.6% after 10 years.</p><p><strong>Conclusion: </strong>This phase IV trial confirms previously reported outcomes on upfront IORT boost, with excellent disease-control outcomes.</p>","PeriodicalId":21998,"journal":{"name":"Strahlentherapie und Onkologie","volume":" ","pages":"169-177"},"PeriodicalIF":2.5,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12872669/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144094851","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 : 2026-02-01Epub Date: 2025-06-24DOI: 10.1007/s00066-025-02417-9
Felix Ehret, Michael Oertel, Alexander Rühle
{"title":"Tenth anniversary of the Young DEGRO Team Trial-reflecting on the past, shaping the future.","authors":"Felix Ehret, Michael Oertel, Alexander Rühle","doi":"10.1007/s00066-025-02417-9","DOIUrl":"10.1007/s00066-025-02417-9","url":null,"abstract":"","PeriodicalId":21998,"journal":{"name":"Strahlentherapie und Onkologie","volume":" ","pages":"123-128"},"PeriodicalIF":2.5,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12872678/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144476698","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 : 2026-02-01Epub Date: 2025-09-23DOI: 10.1007/s00066-025-02470-4
Caglayan Selenge Beduk Esen, Aysenur Elmali, Birhan Demirhan, Ozan Cem Guler, Selvi Tabak Dincer, Ilknur Alsan Cetin, Meral Kurt, Mustafa Akin, Ertugrul Senturk, Serap Akyurek, Halil Cumhur Yildirim, Gulhan Guler Avci, Pelin Altinok, Hamit Basaran, Gokhan Ozyigit, Pervin Hurmuz, Cem Onal
Purpose: Evidence on the use of definitive radiotherapy (RT) in younger prostate cancer (PCa) patients is limited, with no national-level studies systematically evaluating oncologic outcomes and treatment-related toxicity in this population. This study aimed to assess oncologic outcomes and toxicity of definitive prostate RT in patients aged 55 years or younger.
Methods: Records of 180 PCa patients aged ≤ 55 years treated with definitive RT ± androgen deprivation therapy across 12 cancer centers were retrospectively reviewed. Primary endpoints included freedom from biochemical failure (FFBF) and PCa-specific survival (PCSS). Secondary endpoints were overall survival (OS), acute/late genitourinary (GU) and gastrointestinal (GI) toxicities, local recurrence (LR), and distant metastasis (DM).
Results: Median age was 54 years; median PSA at diagnosis was 10.4 ng/mL. Risk group distribution was 29% low-, 29% intermediate-, and 42% high-risk. Median RT dose was 76 Gy delivered in 38 fractions. After a median follow-up of 106.2 months, local recurrence (9%), distant metastasis (7%), and isolated PSA progression (3%) were noted. The 8‑year FFBF, PCSS, and OS were 85.7%, 93.8%, and 90.3%, respectively. Univariate analysis identified PSA, clinical T stage, Gleason score (GS), and risk group as significant prognostic factors for FFBF and PCSS. Multivariate analysis showed advanced stage and high GS independently predicted worse FFBF and PCSS. Acute and late grade ≥ 2 GU toxicity occurred in 12% and 6%, and GI toxicity in 11% and 3%.
Conclusion: Definitive radiotherapy is a safe and effective treatment for prostate cancer patients aged ≤ 55 years. Prospective studies are needed to confirm these findings.
{"title":"Long term outcomes of prostate cancer patients aged 55 years or younger treated with definitive radiotherapy: Trod 09-005 study.","authors":"Caglayan Selenge Beduk Esen, Aysenur Elmali, Birhan Demirhan, Ozan Cem Guler, Selvi Tabak Dincer, Ilknur Alsan Cetin, Meral Kurt, Mustafa Akin, Ertugrul Senturk, Serap Akyurek, Halil Cumhur Yildirim, Gulhan Guler Avci, Pelin Altinok, Hamit Basaran, Gokhan Ozyigit, Pervin Hurmuz, Cem Onal","doi":"10.1007/s00066-025-02470-4","DOIUrl":"10.1007/s00066-025-02470-4","url":null,"abstract":"<p><strong>Purpose: </strong>Evidence on the use of definitive radiotherapy (RT) in younger prostate cancer (PCa) patients is limited, with no national-level studies systematically evaluating oncologic outcomes and treatment-related toxicity in this population. This study aimed to assess oncologic outcomes and toxicity of definitive prostate RT in patients aged 55 years or younger.</p><p><strong>Methods: </strong>Records of 180 PCa patients aged ≤ 55 years treated with definitive RT ± androgen deprivation therapy across 12 cancer centers were retrospectively reviewed. Primary endpoints included freedom from biochemical failure (FFBF) and PCa-specific survival (PCSS). Secondary endpoints were overall survival (OS), acute/late genitourinary (GU) and gastrointestinal (GI) toxicities, local recurrence (LR), and distant metastasis (DM).</p><p><strong>Results: </strong>Median age was 54 years; median PSA at diagnosis was 10.4 ng/mL. Risk group distribution was 29% low-, 29% intermediate-, and 42% high-risk. Median RT dose was 76 Gy delivered in 38 fractions. After a median follow-up of 106.2 months, local recurrence (9%), distant metastasis (7%), and isolated PSA progression (3%) were noted. The 8‑year FFBF, PCSS, and OS were 85.7%, 93.8%, and 90.3%, respectively. Univariate analysis identified PSA, clinical T stage, Gleason score (GS), and risk group as significant prognostic factors for FFBF and PCSS. Multivariate analysis showed advanced stage and high GS independently predicted worse FFBF and PCSS. Acute and late grade ≥ 2 GU toxicity occurred in 12% and 6%, and GI toxicity in 11% and 3%.</p><p><strong>Conclusion: </strong>Definitive radiotherapy is a safe and effective treatment for prostate cancer patients aged ≤ 55 years. Prospective studies are needed to confirm these findings.</p>","PeriodicalId":21998,"journal":{"name":"Strahlentherapie und Onkologie","volume":" ","pages":"139-148"},"PeriodicalIF":2.5,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145125995","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2025-10-09DOI: 10.1007/s00066-025-02471-3
Muath Suliman, Farag M A Altalbawy, Malathi H, Syeda Wajida Kazmi, Ashish Sharma, M Ravi Kumar, Hassan Thoulfikar A Alamir, Faraj Mohammed, Abed J Kadhim, Merwa Alhadrawi
Chemo-/radiotherapy-induced cardiomyopathy is a clinical challenge for patients with cancer, characterized by detrimental effects on cardiac structure and function. To date, numerous experimental and clinical investigations have revealed that numerous mechanisms, such as oxidative damage, contribute to chemo-/radiotherapy-induced cardiomyopathy. Chronic oxidative stress and reactive oxygen species (ROS) production following damage to mitochondria and the endoplasmic reticulum (ER) play a fundamental role in the progression of cell death, inflammation, and fibrosis, leading to heart failure and unusual changes in the heart structure. This review delves into the mechanisms of cardiotoxicity induced by chemotherapy and radiotherapy, highlighting the pivotal role of mitochondrial dysfunction and subsequent oxidative stress and cell death. The interplay between mitochondrial and ER dysfunction can also be offered as a paramount factor in the development of cardiomyopathy. We review how damage to these organelles may trigger cardiac injury through crosstalk with other mechanisms such as activation of pro-oxidant enzymes, inflammation, fibrosis, and other important processes.
{"title":"Chemo-/radiotherapy-induced cardiomyopathy: roles of mitochondria and endoplasmic reticulum.","authors":"Muath Suliman, Farag M A Altalbawy, Malathi H, Syeda Wajida Kazmi, Ashish Sharma, M Ravi Kumar, Hassan Thoulfikar A Alamir, Faraj Mohammed, Abed J Kadhim, Merwa Alhadrawi","doi":"10.1007/s00066-025-02471-3","DOIUrl":"10.1007/s00066-025-02471-3","url":null,"abstract":"<p><p>Chemo-/radiotherapy-induced cardiomyopathy is a clinical challenge for patients with cancer, characterized by detrimental effects on cardiac structure and function. To date, numerous experimental and clinical investigations have revealed that numerous mechanisms, such as oxidative damage, contribute to chemo-/radiotherapy-induced cardiomyopathy. Chronic oxidative stress and reactive oxygen species (ROS) production following damage to mitochondria and the endoplasmic reticulum (ER) play a fundamental role in the progression of cell death, inflammation, and fibrosis, leading to heart failure and unusual changes in the heart structure. This review delves into the mechanisms of cardiotoxicity induced by chemotherapy and radiotherapy, highlighting the pivotal role of mitochondrial dysfunction and subsequent oxidative stress and cell death. The interplay between mitochondrial and ER dysfunction can also be offered as a paramount factor in the development of cardiomyopathy. We review how damage to these organelles may trigger cardiac injury through crosstalk with other mechanisms such as activation of pro-oxidant enzymes, inflammation, fibrosis, and other important processes.</p>","PeriodicalId":21998,"journal":{"name":"Strahlentherapie und Onkologie","volume":" ","pages":"209-232"},"PeriodicalIF":2.5,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145252806","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2025-05-06DOI: 10.1007/s00066-025-02409-9
Cezara Cheptea, Youlia Kirova, Jeremy Baude, Fatima Laki, Alain Fourquet, Pierre Loap
Background: Isolated nodal recurrence (INR) after localized breast cancer is rare, with an incidence of less than 1%. Curative management typically includes surgical resection, often with axillary lymph node dissection (ALND), followed by regional nodal radiotherapy. However, evidence-based guidelines remain limited due to the rarity of this clinical scenario. The aim of this study was to evaluate survival determinants and the acute and long-term toxicities associated with second-course regional nodal irradiation as part of curative strategies for INR after localized breast cancer.
Materials and methods: This retrospective study included 11 patients with localized breast cancer who developed ipsilateral, nonmetastatic INR between 2003 and 2019. All patients were treated with curative intent, including regional nodal irradiation. Overall survival (OS), cancer-specific survival (CSS), metastasis-free survival (MFS), local control, and treatment toxicities were analyzed. Survival probabilities were calculated using the Kaplan-Meier method, and Cox regression was used to assess prognostic factors.
Results: The 5‑year OS and CSS were 71.6%, while MFS was 62.3%. Inclusion of internal mammary chain (IMC) irradiation significantly improved OS, CSS, and MFS (p < 0.01). Triple-negative breast cancer (TNBC) INRs were associated with worse survival outcomes. Acute grade 2 toxicities included radiodermatitis (36.4%), and late grade 2 toxicities were limited to fibrosis (18.2%). No cardiac, pulmonary, or grade 3 or higher toxicities were reported.
Conclusion: This study highlights the favorable survival outcomes and safety profile of contemporary curative strategies for INRs following localized breast cancer, with a 5-year OS rate exceeding historical benchmarks. Internal mammary chain irradiation appears to improve survival without increased toxicity. However, the poor prognosis associated with TNBC INR underscores the need for effective systemic therapies. Prospective multicenter trials are essential to validate these findings and optimize treatment protocols.
{"title":"Survival determinants and toxicity of second-course radiotherapy for isolated nodal recurrences in breast cancer.","authors":"Cezara Cheptea, Youlia Kirova, Jeremy Baude, Fatima Laki, Alain Fourquet, Pierre Loap","doi":"10.1007/s00066-025-02409-9","DOIUrl":"10.1007/s00066-025-02409-9","url":null,"abstract":"<p><strong>Background: </strong>Isolated nodal recurrence (INR) after localized breast cancer is rare, with an incidence of less than 1%. Curative management typically includes surgical resection, often with axillary lymph node dissection (ALND), followed by regional nodal radiotherapy. However, evidence-based guidelines remain limited due to the rarity of this clinical scenario. The aim of this study was to evaluate survival determinants and the acute and long-term toxicities associated with second-course regional nodal irradiation as part of curative strategies for INR after localized breast cancer.</p><p><strong>Materials and methods: </strong>This retrospective study included 11 patients with localized breast cancer who developed ipsilateral, nonmetastatic INR between 2003 and 2019. All patients were treated with curative intent, including regional nodal irradiation. Overall survival (OS), cancer-specific survival (CSS), metastasis-free survival (MFS), local control, and treatment toxicities were analyzed. Survival probabilities were calculated using the Kaplan-Meier method, and Cox regression was used to assess prognostic factors.</p><p><strong>Results: </strong>The 5‑year OS and CSS were 71.6%, while MFS was 62.3%. Inclusion of internal mammary chain (IMC) irradiation significantly improved OS, CSS, and MFS (p < 0.01). Triple-negative breast cancer (TNBC) INRs were associated with worse survival outcomes. Acute grade 2 toxicities included radiodermatitis (36.4%), and late grade 2 toxicities were limited to fibrosis (18.2%). No cardiac, pulmonary, or grade 3 or higher toxicities were reported.</p><p><strong>Conclusion: </strong>This study highlights the favorable survival outcomes and safety profile of contemporary curative strategies for INRs following localized breast cancer, with a 5-year OS rate exceeding historical benchmarks. Internal mammary chain irradiation appears to improve survival without increased toxicity. However, the poor prognosis associated with TNBC INR underscores the need for effective systemic therapies. Prospective multicenter trials are essential to validate these findings and optimize treatment protocols.</p>","PeriodicalId":21998,"journal":{"name":"Strahlentherapie und Onkologie","volume":" ","pages":"160-168"},"PeriodicalIF":2.5,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144032432","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}