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Effect of neoadjuvant chemoradiation on anorectal function assessed with anorectal manometry: A systematic review and meta-analysis. 用肛门直肠测压法评估新辅助化疗对肛门直肠功能的影响:系统回顾和荟萃分析。
IF 2 4区 医学 Q3 ONCOLOGY Pub Date : 2024-08-01 Epub Date: 2024-05-31 DOI: 10.1177/03008916241256544
Pamela Milito, Guglielmo Niccolò Piozzi, Mohammad Iqbal Hussain, Tommaso A Dragani, Luca Sorrentino, Maurizio Cosimelli, Marcello Guaglio, Luigi Battaglia

Aim: Improvement in oncological survival for rectal cancer increases attention to anorectal dysfunction. Diagnostic questionnaires can evaluate quality of life but are subjective and dependent on patients' compliance. Anorectal manometry can objectively assess the continence mechanism and identify functional sphincter weakness and rectal compliance. Neoadjuvant chemoradiotherapy is presumed to affect anorectal function. We aim to assess anorectal function in rectal cancer patients who undergo total mesorectal excision, with or without neoadjuvant chemoradiation, using anorectal manometry measurements.

Method: MEDLINE, Embase, and Cochrane databases were searched for studies comparing perioperative anorectal manometry between neoadjuvant chemoradiation and upfront surgery for rectal cancers. Primary outcomes were resting pressure, squeeze pressure, sensory threshold volume and maximal tolerable volume.

Results: Eight studies were included in the systematic review, of which seven were included for metanalysis. 155 patients (45.3%) had neoadjuvant chemoradiation before definitive surgery, and 187 (54.6%) underwent upfront surgery. Most patients were male (238 vs. 118). The standardized mean difference of mean resting pressure, mean and maximum squeeze pressure, maximum resting pressure, sensory threshold volume, and maximal tolerable volume favored the upfront surgery group but without statistical significance.

Conclusion: Currently available evidence on anorectal manometry protocols failed to show any statistically significant differences in functional outcomes between neoadjuvant chemoradiation and upfront surgery. Further large-scale prospective studies with standardized neoadjuvant chemoradiation and anorectal manometry protocols are needed to validate these findings.

目的:直肠癌肿瘤生存率的提高增加了对肛门直肠功能障碍的关注。诊断问卷可以评估生活质量,但比较主观,而且取决于患者的依从性。肛门直肠测压法可客观评估排便机制,识别功能性括约肌无力和直肠顺应性。新辅助化放疗被认为会影响肛门直肠功能。我们的目的是通过肛门直肠测压测量,评估接受全直肠系膜切除术、新辅助化放疗或未接受新辅助化放疗的直肠癌患者的肛门直肠功能:方法:在 MEDLINE、Embase 和 Cochrane 数据库中搜索比较直肠癌新辅助化疗和前期手术围手术期肛门直肠测压的研究。主要结果为静息压、挤压压、感觉阈值容积和最大可耐受容积:系统综述共纳入八项研究,其中七项纳入荟萃分析。155名患者(45.3%)在明确手术前接受了新辅助化疗,187名患者(54.6%)接受了前期手术。大多数患者为男性(238 对 118)。平均静息压、平均和最大挤压压、最大静息压、感觉阈值容积和最大可耐受容积的标准化平均差有利于前期手术组,但无统计学意义:结论:目前关于肛门直肠测压方案的现有证据未能显示新辅助化疗和前期手术在功能结果上存在任何统计学意义上的显著差异。需要进一步开展大规模的前瞻性研究,采用标准化的新辅助化疗和肛门直肠测压方案来验证这些研究结果。
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引用次数: 0
Adjuvant treatment in hormone receptor-positive early breast cancer: New approaches of endocrine therapy. 激素受体阳性早期乳腺癌的辅助治疗:内分泌治疗的新方法。
4区 医学 Q3 ONCOLOGY Pub Date : 2024-06-01 Epub Date: 2023-12-19 DOI: 10.1177/03008916231216830
Simone Nardin, Tommaso Ruelle, Irene Giannubilo, Lucia Del Mastro

Breast cancer is the most common cancer in women, and luminal breast cancer is the predominant subtype, characterized by the presence of estrogen receptors and/or progesterone receptors in tumor cells. Adjuvant endocrine therapy is the pivotal approach in the management of luminal early breast cancer. Hence, new therapeutic approaches have been studied during the last few years, especially in patients with high risk of recurrence.Here we provide a summary of the most recent clinical trials evaluating adjuvant treatment in hormone-receptors-positive early breast cancer. First, the main cornerstone is related to the role of extended endocrine treatment, which has been widely investigated to access a benefit in disease-free survival and overall survival (only the GIM4 trial has positive feedback about survival) and to tailor the treatment according to patient compliance. The results highlighted an advantage in extending the use of endocrine treatment for at least seven full years, considering aromatase inhibitors as principal drugs. Second, the shift of CDK4/6 inhibitors (CDK4/6i) from advanced to early setting reported positive outcomes, with favorable results from MonarchE and NATALEE trials, using Abemaciclib and Ribociclib respectively, even if non-negligible toxicities have been reported. Last, the use of PARP inhibitors for BRCA1/2 mutated patients has been evaluated in the OlympiA trial (Olaparib), observing a comparable benefit between hormone-receptors-positive and triple-negative early breast cancer.However, more data are still required to better select patients that could benefit more from CDK4/6i considering side effects too, and sequential treatments are still not codified.

乳腺癌是女性最常见的癌症,腔隙性乳腺癌是最主要的亚型,其特点是肿瘤细胞中存在雌激素受体和/或孕酮受体。辅助内分泌治疗是治疗早期管腔型乳腺癌的关键方法。因此,在过去几年中,人们一直在研究新的治疗方法,尤其是针对复发风险较高的患者。在此,我们总结了评估激素受体阳性早期乳腺癌辅助治疗的最新临床试验。首先,主要基石与延长内分泌治疗的作用有关,延长内分泌治疗已被广泛研究,以获得无病生存期和总生存期的益处(只有 GIM4 试验对生存期有积极反馈),并根据患者的依从性进行定制治疗。结果凸显了将芳香化酶抑制剂作为主要药物,延长内分泌治疗至少整整七年的优势。其次,CDK4/6 抑制剂(CDK4/6i)从晚期治疗转向早期治疗取得了积极的成果,分别使用 Abemaciclib 和 Ribociclib 的 MonarchE 和 NATALEE 试验取得了良好的结果,尽管也有不可忽视的毒性报道。最后,OlympiA 试验(Olaparib)评估了对 BRCA1/2 基因突变患者使用 PARP 抑制剂的情况,观察到激素受体阳性和三阴性早期乳腺癌患者的获益相当。
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引用次数: 0
Management of cancer treatment-induced bone loss in patients with breast and hormone sensitive prostate cancer: AIOM survey. 乳腺癌和对激素敏感的前列腺癌患者因癌症治疗导致骨质流失的管理:AIOM 调查。
4区 医学 Q3 ONCOLOGY Pub Date : 2024-06-01 Epub Date: 2024-03-10 DOI: 10.1177/03008916241236279
Anna Amela Valsecchi, Vittorio Fusco, Massimo Di Maio, Daniele Santini, Marcello Tucci, Ugo De Giorgi, Rossana Dionisio, Francesca Vignani, Saverio Cinieri

Purpose: Cancer treatment-induced bone loss is a side effect of hormonal therapy that can severely affect patients' quality of life. The aim of this survey was to obtain an updated picture of management of bone health in patients with breast cancer undergoing adjuvant hormonal therapy and in patients with hormone sensitive prostate cancer according to Italian oncologists.

Methods: Our survey was made up of 21 multiple-choice questions: the first part dealt with the respondents' characteristics, while the second with management of bone health in the described setting. An invitation to complete the survey was sent by e-mail to 2336 oncologists, members of Italian Association of Medical Oncology, in October 2022.

Results: Overall, 121 (5.2%) Italian oncologists completed the survey. In most cases (57%) the oncologist personally took charge of the management of bone health in patients at risk for cancer treatment-induced bone loss. At the beginning of hormonal therapy, most respondents reported to require bone health diagnostic exams, such as dual-energy X-ray absorptiometry (89%), repeated with different timing. Main reported reasons (not mutually exclusive) for prescribing antiresorptive drugs were modifying fracture risk (87%), densitometry values (75%) or prognosis (34%). Answers about the management of antiresorptive therapy were heterogeneous.

Conclusion: A heterogeneous approach on the management of cancer treatment-induced bone loss in Italy arises from this survey. This scenario highlights the need for a major consensus of the Italian scientific community on the diagnostic and therapeutic approach of cancer treatment-induced bone loss and for a greater awareness of this topic among Italian oncologists.

目的:癌症治疗引起的骨质流失是激素治疗的副作用之一,会严重影响患者的生活质量。本调查旨在了解意大利肿瘤专家对接受激素辅助治疗的乳腺癌患者和激素敏感性前列腺癌患者骨健康管理的最新情况:我们的调查由 21 道选择题组成:第一部分涉及受访者的特征,第二部分涉及所述环境中的骨健康管理。2022 年 10 月,我们通过电子邮件向 2336 名肿瘤学家(意大利肿瘤内科协会会员)发出了完成调查的邀请:共有 121 名(5.2%)意大利肿瘤学家完成了调查。在大多数情况下(57%),肿瘤学家亲自负责管理有癌症治疗诱发骨质流失风险的患者的骨骼健康。在激素治疗开始时,大多数受访者表示需要进行骨健康诊断检查,如双能 X 射线吸收测量(89%),并在不同时间重复进行。据报告,处方抗骨质吸收药物的主要原因(不相互排斥)是改变骨折风险(87%)、骨密度测量值(75%)或预后(34%)。关于抗骨质吸收治疗的管理,答案各不相同:结论:本次调查显示,意大利对癌症治疗引起的骨质流失的管理方法存在差异。这种情况突出表明,意大利科学界需要就癌症治疗诱发骨质流失的诊断和治疗方法达成重要共识,意大利肿瘤学家也需要提高对这一主题的认识。
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引用次数: 0
I was only sixteen. 那时我只有十六岁。
4区 医学 Q3 ONCOLOGY Pub Date : 2024-06-01 Epub Date: 2023-11-30 DOI: 10.1177/03008916231214220
Andrea Ferrari, Matteo Silva, Alice Patriccioli, Stefano Signoroni, Maura Massimino

This short piece describes a new project developed by the adolescent patients with cancer involved in the Youth Project at the Istituto Nazionale dei Tumori in Milan, Italy. This is a scheme dedicated to young cancer patients with the dual aim of optimizing medical aspects of their care and promoting a holistic approach to their needs. "I was only sixteen" is a ballad, written in English by the patients, that became a song with the help of professional musicians (and among them international star Tony Hadley, former frontman of Spandau Ballet). This song sounds like hymn to life for teenagers with cancer in the world. It emphasizes again the value of giving young patients novel creative ways to express themselves.

这篇短文描述了一个新项目,由参与意大利米兰国家肿瘤研究所青年项目的青少年癌症患者开发。这是一项专门针对年轻癌症患者的计划,其双重目标是优化他们的医疗方面的护理,并促进对他们的需求的整体方法。“我只有16岁”是一首由病人用英语写的民谣,在专业音乐家的帮助下成为了一首歌(其中包括国际明星托尼·哈德利,他是Spandau芭蕾舞团的前主唱)。这首歌听起来像是世界上患有癌症的青少年对生命的赞美诗。它再次强调了为年轻患者提供新颖的创造性方式来表达自己的价值。
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引用次数: 0
Nivolumab in pretreated pleural mesothelioma: Results from an observational real-world study of patients treated within the AIFA 5% Fund. Nivolumab治疗预处理胸膜间皮瘤:在 AIFA 5% 基金范围内接受治疗的患者的真实世界观察研究结果。
IF 2 4区 医学 Q3 ONCOLOGY Pub Date : 2024-06-01 Epub Date: 2024-02-19 DOI: 10.1177/03008916241229287
Luigi Cerbone, Sara Delfanti, Stefania Crivellari, Antonina Maria De Angelis, Laura Mazzeo, Claudia Proto, Mario Occhipinti, Giuseppe Lo Russo, Chiara Dellepiane, Federica Biello, Irene Alabiso, Francesco Verderame, Roberta Gauna, Irene De Simone, Federica Cuppone, Sandra Petraglia, Giulia Pasello, Giovanni Luca Ceresoli, Marina Chiara Garassino, Valter Torri, Federica Grosso

Background: Pleural mesothelioma is a rare cancer with a dismal prognosis and few therapeutic options, especially in the pretreated setting. Immunotherapy with checkpoint inhibitors as single agents yielded interesting results in refractory pleural mesothelioma, achieving a response rate between 10-20%, median progression-free survival of 2-5 months and median overall survival of 7-13 months.

Patients and methods: A retrospective, multi-institutional study of pleural mesothelioma patients treated with nivolumab in second and further line was performed. The endpoints of the study are response rate, disease control rate, progression free survival and overall survival.

Results: Sixty-five patients with pleural mesothelioma treated with nivolumab in second and further line were enrolled at seven Italian institutions. The response rate was 8%, disease control rate was 37%, median progression free survival was 5.7 months (95% CI: 2.9-9.0) and median overall survival was 11.1 (95% CI 6.2-19.9) months. A higher neutrophils and neutrophils to lymphocytes ratio at baseline were associated with worse prognosis.

Conclusion: Nivolumab as a single agent is fairly active in a cohort of unselected pretreated pleural mesothelioma patients. Further investigations on clinical and translational factors are needed to define which patient might benefit most from nivolumab treatment in pleural mesothelioma.

背景:胸膜间皮瘤是一种罕见的癌症,其预后很差,治疗方案很少,尤其是在预处理的情况下。以检查点抑制剂为单药的免疫疗法在难治性胸膜间皮瘤中取得了令人感兴趣的结果,反应率在10%-20%之间,中位无进展生存期为2-5个月,中位总生存期为7-13个月:对胸膜间皮瘤患者进行了一项多机构回顾性研究,研究对象为接受二线及二线以上nivolumab治疗的胸膜间皮瘤患者。研究终点为反应率、疾病控制率、无进展生存期和总生存期:意大利七家机构共招募了65名胸膜间皮瘤患者,对他们进行了二线和三线nivolumab治疗。应答率为8%,疾病控制率为37%,中位无进展生存期为5.7个月(95% CI:2.9-9.0),中位总生存期为11.1个月(95% CI:6.2-19.9)。基线中性粒细胞和中性粒细胞与淋巴细胞比值越高,预后越差:结论:Nivolumab作为一种单药,在未经选择的预处理胸膜间皮瘤患者队列中具有相当的活性。需要进一步研究临床和转化因素,以确定哪些胸膜间皮瘤患者可从尼伐单抗治疗中获益最多。
{"title":"Nivolumab in pretreated pleural mesothelioma: Results from an observational real-world study of patients treated within the AIFA 5% Fund.","authors":"Luigi Cerbone, Sara Delfanti, Stefania Crivellari, Antonina Maria De Angelis, Laura Mazzeo, Claudia Proto, Mario Occhipinti, Giuseppe Lo Russo, Chiara Dellepiane, Federica Biello, Irene Alabiso, Francesco Verderame, Roberta Gauna, Irene De Simone, Federica Cuppone, Sandra Petraglia, Giulia Pasello, Giovanni Luca Ceresoli, Marina Chiara Garassino, Valter Torri, Federica Grosso","doi":"10.1177/03008916241229287","DOIUrl":"10.1177/03008916241229287","url":null,"abstract":"<p><strong>Background: </strong>Pleural mesothelioma is a rare cancer with a dismal prognosis and few therapeutic options, especially in the pretreated setting. Immunotherapy with checkpoint inhibitors as single agents yielded interesting results in refractory pleural mesothelioma, achieving a response rate between 10-20%, median progression-free survival of 2-5 months and median overall survival of 7-13 months.</p><p><strong>Patients and methods: </strong>A retrospective, multi-institutional study of pleural mesothelioma patients treated with nivolumab in second and further line was performed. The endpoints of the study are response rate, disease control rate, progression free survival and overall survival.</p><p><strong>Results: </strong>Sixty-five patients with pleural mesothelioma treated with nivolumab in second and further line were enrolled at seven Italian institutions. The response rate was 8%, disease control rate was 37%, median progression free survival was 5.7 months (95% CI: 2.9-9.0) and median overall survival was 11.1 (95% CI 6.2-19.9) months. A higher neutrophils and neutrophils to lymphocytes ratio at baseline were associated with worse prognosis.</p><p><strong>Conclusion: </strong>Nivolumab as a single agent is fairly active in a cohort of unselected pretreated pleural mesothelioma patients. Further investigations on clinical and translational factors are needed to define which patient might benefit most from nivolumab treatment in pleural mesothelioma.</p>","PeriodicalId":23349,"journal":{"name":"Tumori","volume":" ","pages":"168-173"},"PeriodicalIF":2.0,"publicationDate":"2024-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139900438","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A five-year review of chemoradiotherapy practice in anal cancer: Radiotherapy audit results from a cancer centre in Wales, UK. 肛门癌化放疗五年回顾:英国威尔士一家癌症中心的放疗审计结果。
4区 医学 Q3 ONCOLOGY Pub Date : 2024-06-01 Epub Date: 2024-03-29 DOI: 10.1177/03008916241241424
Mutahar A Tunio, Nicki Davies, Elliot Caparros, Janis Davies, Stuart Foyle

Aim: To review a five-year clinical practice of radical chemoradiotherapy (CRT) for anal cancers at a cancer centre in Wales.

Methods: A retrospective audit examined the quality of radical CRT for anal cancers treated between November 2016 and November 2021 by investigating seven critical indicators set by Radiation Therapy Oncology Group and ACT II trials, (1) 95% completion of computed tomography simulation within 14 days of consent, (2) 100% CRT delivery within 28 days of computed tomography simulation, (3) 100% CRT delivery within 28 days of consent, (4) overall treatment time of RT 38 days with > 2 days breaks <5%, (5) 75% completion of concurrent chemotherapy, (6) <2% CRT related colostomies, and (7) <2% the 30-days mortality rate.

Results: A total of 80 anal cancers received CRT over five years. Around 95.0% underwent computed tomography simulation within 14 days of consent. The observed slight deviation was related to the Covid pandemic in 2020. About 96.3% started CRT within 28 days of computed tomography simulation. The mean duration of CRT was 37.9 days. Radiotherapy (RT) interruptions > 2 days were about 5%, and 67.5% started CRT within 28 days of consent. About 92.5% and 76.2% completed mitomycin and capecitabine without breaks, respectively. The colostomy rate was 1.2%, and the 30-day mortality was 1.2%.

Conclusion: Audit results matched with the standards in six domains. Overall treatment time of 37.9 days, colostomy rates of 1.2%, and the 30-day mortality rate of 1.2% were commendable. Overall time interval between consent and CRT delivery can be achieved by time-constrained measures.

目的:回顾威尔士一家癌症中心五年来肛门癌根治性化学放疗(CRT)的临床实践:方法:通过回顾性审计检查2016年11月至2021年11月期间肛门癌根治性CRT的治疗质量,调查放射治疗肿瘤学组和ACT II试验设定的七项关键指标:(1)95%的患者在同意后14天内完成计算机断层扫描模拟;(2)100%的患者在同意后28天内完成计算机断层扫描模拟;(3)100%的患者在同意后28天内完成CRT;(4)RT的总体治疗时间为38天,休息时间大于2天 结果:五年内共有80例肛门癌患者接受了CRT治疗:五年来,共有 80 例肛门癌接受了 CRT 治疗。约 95.0% 的患者在获得同意后 14 天内接受了计算机断层扫描模拟治疗。观察到的轻微偏差与 2020 年 Covid 大流行有关。约96.3%的患者在计算机断层扫描模拟后28天内开始接受CRT治疗。CRT 的平均持续时间为 37.9 天。放疗(RT)中断时间大于 2 天的患者约占 5%,67.5% 的患者在获得同意后 28 天内开始 CRT。分别约有 92.5% 和 76.2% 的患者在没有中断的情况下完成了丝裂霉素和卡培他滨治疗。结肠造瘘率为1.2%,30天死亡率为1.2%:审计结果在六个方面符合标准。总体治疗时间为 37.9 天,结肠造瘘率为 1.2%,30 天死亡率为 1.2%,值得称赞。从同意到提供 CRT 的总体时间间隔可以通过有时间限制的措施来实现。
{"title":"A five-year review of chemoradiotherapy practice in anal cancer: Radiotherapy audit results from a cancer centre in Wales, UK.","authors":"Mutahar A Tunio, Nicki Davies, Elliot Caparros, Janis Davies, Stuart Foyle","doi":"10.1177/03008916241241424","DOIUrl":"10.1177/03008916241241424","url":null,"abstract":"<p><strong>Aim: </strong>To review a five-year clinical practice of radical chemoradiotherapy (CRT) for anal cancers at a cancer centre in Wales.</p><p><strong>Methods: </strong>A retrospective audit examined the quality of radical CRT for anal cancers treated between November 2016 and November 2021 by investigating seven critical indicators set by Radiation Therapy Oncology Group and ACT II trials, (1) 95% completion of computed tomography simulation within 14 days of consent, (2) 100% CRT delivery within 28 days of computed tomography simulation, (3) 100% CRT delivery within 28 days of consent, (4) overall treatment time of RT 38 days with > 2 days breaks <5%, (5) 75% completion of concurrent chemotherapy, (6) <2% CRT related colostomies, and (7) <2% the 30-days mortality rate.</p><p><strong>Results: </strong>A total of 80 anal cancers received CRT over five years. Around 95.0% underwent computed tomography simulation within 14 days of consent. The observed slight deviation was related to the Covid pandemic in 2020. About 96.3% started CRT within 28 days of computed tomography simulation. The mean duration of CRT was 37.9 days. Radiotherapy (RT) interruptions > 2 days were about 5%, and 67.5% started CRT within 28 days of consent. About 92.5% and 76.2% completed mitomycin and capecitabine without breaks, respectively. The colostomy rate was 1.2%, and the 30-day mortality was 1.2%.</p><p><strong>Conclusion: </strong>Audit results matched with the standards in six domains. Overall treatment time of 37.9 days, colostomy rates of 1.2%, and the 30-day mortality rate of 1.2% were commendable. Overall time interval between consent and CRT delivery can be achieved by time-constrained measures.</p>","PeriodicalId":23349,"journal":{"name":"Tumori","volume":" ","pages":"186-192"},"PeriodicalIF":0.0,"publicationDate":"2024-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140327205","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A new era after a long wait: Vorasidenib, an inhibitor of mutant IDH1 and IDH2 enzymes in patients with IDH-mutant glioma. 漫长等待后的新纪元IDH突变胶质瘤患者的IDH1和IDH2突变酶抑制剂Vorasetinib。
4区 医学 Q3 ONCOLOGY Pub Date : 2024-06-01 Epub Date: 2024-01-02 DOI: 10.1177/03008916231217583
Antonio Silvani, Enrico Franceschi
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引用次数: 0
Muscle-invasive bladder cancer in elderly and frail people: Is hypofractionated radiotherapy a feasible approach when no other local options are available? 年老体弱者的肌肉浸润性膀胱癌:在没有其他局部选择的情况下,低分次放射治疗是一种可行的方法吗?
4区 医学 Q3 ONCOLOGY Pub Date : 2024-06-01 Epub Date: 2024-05-10 DOI: 10.1177/03008916241252326
Giulia Marvaso, Angelo Vitullo, Giulia Corrao, Maria Giulia Vincini, Mattia Zaffaroni, Riccardo Villa, Federico Mastroleo, Lukasz Kuncman, Dario Zerini, Ilaria Repetti, Chiara Lorubbio, Gennaro Musi, Ottavio De Cobelli, Barbara Alicja Jereczek-Fossa

Aim: The study aims to report the feasibility and safety of palliative hypofractionated radiotherapy targeting macroscopic bladder tumors in a monocentric cohort of frail and elderly bladder cancer patients not eligible for curative treatments.

Methods: Patients who underwent hypofractionated radiotherapy to the gross disease or to the tumor bed after transurethral resection of bladder tumor from 2017 to 2021 at the European Institute of Oncology IRCCS, were retrospectively considered. Schedules of treatment were 30 and 25 Gy in 5 fractions (both every other day, and consecutive days). Treatment response was evaluated with radiological investigation and/or cystoscopy. Toxicity assessment was carried out according to RTOG/EORTC v2.0 criteria.

Results: A total of 16 patients were included in the study, of these 11 received hypofractionated radiotherapy on the macroscopic target volume and five on the tumor bed after transurethral resection of bladder tumor. No grade (G) >2 acute toxicities were described after treatment for both groups. Only one patient in the group receiving radiotherapy on the macroscopic disease reported G4 GU late toxicity. Ten patients had available follow-up status (median FU time 18 months), of them six had complete response, one had stable disease, and three had progression of disease. The overall response rate and disease control rate were 60% and 70%, respectively.

Conclusion: Our preliminary data demonstrate that palliative hypofractionated radiotherapy for bladder cancer in a frail and elderly population is technically feasible, with an acceptable toxicity profile. These outcomes emphasize the potential of this approach in a non-radical setting and could help to provide more solid indications in this underrepresented setting of patients.

目的:该研究旨在报告在不符合根治性治疗条件的体弱老年膀胱癌患者单中心队列中针对大体膀胱肿瘤进行姑息性低分量放疗的可行性和安全性:回顾性研究了2017年至2021年期间在欧洲肿瘤研究所(European Institute of Oncology IRCCS)接受经尿道膀胱肿瘤切除术后对大体病变或肿瘤床进行低分次放疗的患者。治疗计划为5次分次30 Gy和25 Gy(隔天和连续两天)。治疗反应通过放射学检查和/或膀胱镜检查进行评估。毒性评估根据RTOG/EORTC v2.0标准进行:共有16名患者参与了研究,其中11名患者接受了经尿道膀胱肿瘤切除术后的宏观靶体积低分次放疗,5名患者接受了肿瘤床低分次放疗。两组患者治疗后均未出现急性毒性反应(G)>2 级的情况。只有一名接受大病灶放疗组患者出现了 G4 GU 级晚期毒性反应。10 名患者有随访记录(中位随访时间为 18 个月),其中 6 人完全应答,1 人病情稳定,3 人病情进展。总反应率和疾病控制率分别为60%和70%:我们的初步数据表明,对年老体弱的人群进行膀胱癌姑息性低分量放射治疗在技术上是可行的,而且毒性也是可以接受的。这些结果强调了这种方法在非根治性环境中的潜力,有助于为这种代表性不足的患者提供更可靠的适应症。
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引用次数: 0
The Italian Rare Biliary tract Cancer initiative (IRaBiCa): A multicentric observational study of Gruppo Oncologico dell'Italia Meridionale (GOIM) in collaboration with Gruppo Italiano Colangiocarcinoma (GICO). 意大利罕见胆道癌症倡议(IRaBiCa):由 Gruppo Oncologico dell'Italia Meridionale (GOIM) 与 Gruppo Italiano Colangiocarcinoma (GICO) 合作开展的一项多中心观察研究。
IF 2 4区 医学 Q3 ONCOLOGY Pub Date : 2024-06-01 Epub Date: 2024-02-07 DOI: 10.1177/03008916231222761
Desirèe Speranza, Elena Sapuppo, Giuseppe Aprile, Alessandra Auriemma, Francesca Bergamo, Roberto Bianco, Roberto Bordonaro, Giovanni Brandi, Oronzo Brunetti, Carlo Carnaghi, Domenico Ciliberto, Saverio Cinieri, Salvatore Corallo, Ferdinando De Vita, Samantha Di Donato, Francesco Ferraù, Lorenzo Fornaro, Viola Barucca, Elisa Giommoni, Claudio Lotesoriere, Claudio Luchini, Cristina Masini, Monica Niger, Salvatore Pisconti, Ilario Giovanni Rapposelli, Lorenza Rimassa, Chiara Rognone, Maria Grazia Rodriquenz, Lidia Rita Corsini, Daniele Santin, Aldo Scarpa, Mario Scartozzi, Hector Soto Parra, Giuseppe Tonini, Giampaolo Tortora, Paolo Tralongo, Nicola Silvestris

Introduction: About 90% of cholangiocarcinomas are adenocarcinomas with glandular or tubular structures lined by epithelial cells, with no bile production and with a variable degree of differentiation, arising in the background of desmoplastic stroma. The remaining 10% is represented by rarer histological variants of which there is little knowledge regarding the biological behavior, molecular characterization, and sensitivity to the various possible therapies, including molecular-based treatments. Such rare tumors are described only in case reports or small retrospective series because of their exclusion from clinical trials. This national initiative, here presented, aims to address the following knowledge gap: a) how much does histological diversity translate into clinical manifestation variety? b) are those chemotherapy regimens, recommended for conventional biliary tract cancers, potentially active in rare variants?Therefore, epidemiological, pathological, and clinical characterization of series of rare biliary histotypes/variants, for which therapeutic and follow-up data are available, will be collected.

Methods: An Italian task force on rare tumors of the biliary tract (IRaBiCa) has been created, whose initiative is a multicenter retrospective study involving 34 Italian cancer centers.Clinical data from approximately 100 patients will be collected and analyzed. Continuous variables will be presented as median ± standard deviation, while categorical variables will be expressed in terms of frequency. Kaplan-Maier analyses will be used to compare disease free, progression free and overall survival, according to the different histotypes.

Conclusions: We expect to gather novel data on rare histotypes of biliary tract cancer that will be useful to support their molecular and immunological characterization.

导言约 90% 的胆管癌是腺癌,具有腺状或管状结构,内衬上皮细胞,不产生胆汁,分化程度不一,发生在脱鳞基质的背景下。其余 10%的肿瘤属于较罕见的组织学变异,人们对其生物学行为、分子特征以及对各种可能疗法(包括分子疗法)的敏感性知之甚少。由于这些罕见肿瘤被排除在临床试验之外,因此仅在病例报告或小型回顾性系列研究中有所描述。因此,我们将收集一系列有治疗和随访数据的罕见胆道组织类型/变异的流行病学、病理学和临床特征:方法:意大利成立了一个胆道罕见肿瘤工作组(IRaBiCa),该工作组发起了一项多中心回顾性研究,涉及 34 个意大利癌症中心。连续变量将以中位数±标准差表示,而分类变量将以频率表示。卡普兰-迈尔(Kaplan-Maier)分析法将用于比较不同组织类型的无病生存期、无进展生存期和总生存期:我们希望能收集到有关胆道癌罕见组织型的新数据,这些数据将有助于支持胆道癌的分子和免疫学特征描述。
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引用次数: 0
How many Italian cancer patients are eligible for, and may respond to, Italian Medicines Agency-approved immune checkpoint inhibitors? 有多少意大利癌症患者有资格使用意大利药品管理局批准的检查点免疫抑制药,并可能对其产生反应?
4区 医学 Q3 ONCOLOGY Pub Date : 2024-04-01 Epub Date: 2024-02-19 DOI: 10.1177/03008916241229649
Emanuele Crocetti, Alessandra Ravaioli, Fabio Falcini, Rosa Vattiato, Silvia Mancini, Flavia Baldacchini, Federica Zamagni, Benedetta Vitali, Chiara Balducci, Lauro Bucchi, Orietta Giuliani

Introduction: This cross-sectional study was aimed at estimating the number of Italian incident cancer patients in 2020 eligible for, and respondent to, immune checkpoint inhibitors (ICI).

Methods: The study is based on publicly available data: the ICI approved until August 2022 by the Italian Medicines Agency (AIFA) with their specific indications and overall observed responses, rther details can be found in the Online Supplementary Materi cancer incidence estimates at 2020 and observed cancer deaths, and published papers with estimates on the frequency of different cancer stage/histology/markers etc. corresponding to AIFA authorizations.

Results: In the analyzed period, a total of seven ICI were authorized in Italy for 20 cancer types. The estimated number of ICI-eligible patients in 2020 was 48,400, 14.3% of those tumors (including skin epitheliomas) that may fit AIFA-indications, and 10.5% of all the incident malignant tumors, including skin epitheliomas. The number of patients who may benefit from ICI therapy was 24,052, 49.7% of the ICI-eligible ones, or 5.2% of the overall estimated incident cancers in 2020.

Conclusions: In conclusion, although the number of ICI-eligible patients is a relatively small proportion of the yearly burden of cancers, about half of them may respond to ICI-treatment.

导言:这项横断面研究旨在估算 2020 年有资格使用免疫检查点抑制剂(ICI)的意大利癌症患者人数:这项横断面研究旨在估算 2020 年符合免疫检查点抑制剂(ICI)治疗条件和应答的意大利癌症患者人数:研究基于公开数据:意大利药品管理局(AIFA)批准的2022年8月前的ICI及其具体适应症和总体观察反应,更多详情可参见在线补充材料:2020年癌症发病率估计值和观察到的癌症死亡人数,以及与AIFA授权相对应的不同癌症分期/组织学/标志物等频率估计值的已发表论文:在分析期内,意大利共批准了 7 种 ICI,用于治疗 20 种癌症。据估计,2020 年符合 ICI 治疗条件的患者人数为 48,400 人,占可能符合 AIFA 适应症的肿瘤(包括皮肤上皮瘤)的 14.3%,占所有恶性肿瘤(包括皮肤上皮瘤)的 10.5%。可能从 ICI 治疗中获益的患者人数为 24,052 人,占符合 ICI 治疗条件的患者人数的 49.7%,或占 2020 年预计发生的癌症总数的 5.2%:总之,虽然符合 ICI 治疗条件的患者人数在每年的癌症发病率中所占比例较小,但其中约有一半的患者可能会对 ICI 治疗产生反应。
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