贝伐单抗治疗复发性上皮性卵巢癌:来自印度三级肿瘤医院的真实世界经验。

IF 1.2 Q4 ONCOLOGY
ecancermedicalscience Pub Date : 2025-04-23 eCollection Date: 2025-01-01 DOI:10.3332/ecancer.2025.1897
Ranti Ghosh, Debarshi Lahiri, Debjit Ghosh, Kushal Sen, Debanjan Chakraborty, Tapas Maji, Suparna Mazumder, Ranajit Mandal, Arit Bhattacharjee, Jayanta Chakrabarti
{"title":"贝伐单抗治疗复发性上皮性卵巢癌:来自印度三级肿瘤医院的真实世界经验。","authors":"Ranti Ghosh, Debarshi Lahiri, Debjit Ghosh, Kushal Sen, Debanjan Chakraborty, Tapas Maji, Suparna Mazumder, Ranajit Mandal, Arit Bhattacharjee, Jayanta Chakrabarti","doi":"10.3332/ecancer.2025.1897","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>In combination with chemotherapy, bevacizumab, a humanised monoclonal antibody against angiogenesis, significantly increases progression-free survival (PFS) in recurrent epithelial ovarian cancer (EOC). However, due to financial constraints, real-world experience with bevacizumab in EOC is lacking in Indian populations. This study assessed bevacizumab's efficacy with chemotherapy in platinum-sensitive and resistant EOC in resource-limited Indian populations.</p><p><strong>Method and materials: </strong>This retrospective study was conducted at a regional cancer hospital in eastern India. Platinum-sensitive and resistant recurrent EOC patients were enrolled between 2021 and 2024. Patients' demographic and treatment details were retrieved from hospital medical records. All patients received bevacizumab 7.5 mg/kg IV dose with chemotherapy followed by maintenance till disease progression or inadvertent toxicity occurred. Primary endpoints were PFS and objective response rate (ORR); secondary endpoints were overall survival (OS) and safety. Kaplan-Meier plot generated PFS and OS survival curves.</p><p><strong>Results: </strong>48 patients were enrolled. With a median follow-up of 37 months, 46% of patients progressed on bevacizumab. The median duration of PFS was 17 months (95% CI, 14.31-19.68); it was slightly higher in platinum-sensitive patients at 18 months (95% CI, 14.25-21.74). Half of the patients achieved partial response, with an ORR of 66%. Median OS was not reached due to fewer events. The 3-year OS rate was 83%. About 15 patients who progressed on bevacizumab were able to receive further chemotherapy lines. No new safety concerns were noted. Only 4.2% of patients developed grade 3 proteinuria, one developed arterial thrombosis and two had grade 3 thrombocytopenia. Only one patient died due to a GI fistula.</p><p><strong>Conclusion: </strong>Bevacizumab plus chemotherapy followed by bevacizumab maintenance till disease progression significantly improved PFS in recurrent EOC. This real-world finding suggests a crucial insight into effective treatment options for financially compromised Indian populations with recurrent EOC.</p>","PeriodicalId":11460,"journal":{"name":"ecancermedicalscience","volume":"19 ","pages":"1897"},"PeriodicalIF":1.2000,"publicationDate":"2025-04-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12149230/pdf/","citationCount":"0","resultStr":"{\"title\":\"Bevacizumab in recurrent epithelial ovarian cancer: real-world experience from a tertiary cancer hospital in India.\",\"authors\":\"Ranti Ghosh, Debarshi Lahiri, Debjit Ghosh, Kushal Sen, Debanjan Chakraborty, Tapas Maji, Suparna Mazumder, Ranajit Mandal, Arit Bhattacharjee, Jayanta Chakrabarti\",\"doi\":\"10.3332/ecancer.2025.1897\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>In combination with chemotherapy, bevacizumab, a humanised monoclonal antibody against angiogenesis, significantly increases progression-free survival (PFS) in recurrent epithelial ovarian cancer (EOC). However, due to financial constraints, real-world experience with bevacizumab in EOC is lacking in Indian populations. This study assessed bevacizumab's efficacy with chemotherapy in platinum-sensitive and resistant EOC in resource-limited Indian populations.</p><p><strong>Method and materials: </strong>This retrospective study was conducted at a regional cancer hospital in eastern India. Platinum-sensitive and resistant recurrent EOC patients were enrolled between 2021 and 2024. Patients' demographic and treatment details were retrieved from hospital medical records. All patients received bevacizumab 7.5 mg/kg IV dose with chemotherapy followed by maintenance till disease progression or inadvertent toxicity occurred. Primary endpoints were PFS and objective response rate (ORR); secondary endpoints were overall survival (OS) and safety. Kaplan-Meier plot generated PFS and OS survival curves.</p><p><strong>Results: </strong>48 patients were enrolled. With a median follow-up of 37 months, 46% of patients progressed on bevacizumab. The median duration of PFS was 17 months (95% CI, 14.31-19.68); it was slightly higher in platinum-sensitive patients at 18 months (95% CI, 14.25-21.74). Half of the patients achieved partial response, with an ORR of 66%. Median OS was not reached due to fewer events. The 3-year OS rate was 83%. About 15 patients who progressed on bevacizumab were able to receive further chemotherapy lines. No new safety concerns were noted. Only 4.2% of patients developed grade 3 proteinuria, one developed arterial thrombosis and two had grade 3 thrombocytopenia. Only one patient died due to a GI fistula.</p><p><strong>Conclusion: </strong>Bevacizumab plus chemotherapy followed by bevacizumab maintenance till disease progression significantly improved PFS in recurrent EOC. This real-world finding suggests a crucial insight into effective treatment options for financially compromised Indian populations with recurrent EOC.</p>\",\"PeriodicalId\":11460,\"journal\":{\"name\":\"ecancermedicalscience\",\"volume\":\"19 \",\"pages\":\"1897\"},\"PeriodicalIF\":1.2000,\"publicationDate\":\"2025-04-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12149230/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ecancermedicalscience\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3332/ecancer.2025.1897\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q4\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ecancermedicalscience","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3332/ecancer.2025.1897","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

背景:贝伐单抗是一种抗血管生成的人源化单克隆抗体,联合化疗可显著提高复发性上皮性卵巢癌(EOC)的无进展生存期(PFS)。然而,由于财政限制,在印度人群中缺乏贝伐单抗治疗EOC的实际经验。本研究评估了贝伐单抗与化疗在资源有限的印度人群中铂敏感和耐药EOC的疗效。方法和材料:本回顾性研究在印度东部的一家区域性肿瘤医院进行。在2021年至2024年期间招募了铂敏感和耐药的复发EOC患者。患者的人口统计和治疗细节从医院医疗记录中检索。所有患者均接受贝伐单抗7.5 mg/kg静脉剂量化疗,随后维持治疗,直至疾病进展或发生意外毒性。主要终点为PFS和客观缓解率(ORR);次要终点是总生存期(OS)和安全性。Kaplan-Meier图生成PFS和OS生存曲线。结果:48例患者入组。中位随访37个月,46%的患者在贝伐单抗治疗中进展。PFS的中位持续时间为17个月(95% CI, 14.31-19.68);铂敏感患者18个月时略高(95% CI, 14.25-21.74)。一半的患者达到部分缓解,ORR为66%。由于事件较少,未达到OS中值。3年生存率为83%。约有15名接受贝伐单抗治疗的患者能够接受进一步的化疗。没有发现新的安全隐患。只有4.2%的患者发生3级蛋白尿,1例发生动脉血栓形成,2例发生3级血小板减少症。只有一名患者死于胃肠道瘘。结论:贝伐单抗加化疗后再维持贝伐单抗直至疾病进展,可显著改善复发性EOC的PFS。这一现实世界的发现为经济困难的印度复发性EOC患者提供了有效的治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bevacizumab in recurrent epithelial ovarian cancer: real-world experience from a tertiary cancer hospital in India.

Background: In combination with chemotherapy, bevacizumab, a humanised monoclonal antibody against angiogenesis, significantly increases progression-free survival (PFS) in recurrent epithelial ovarian cancer (EOC). However, due to financial constraints, real-world experience with bevacizumab in EOC is lacking in Indian populations. This study assessed bevacizumab's efficacy with chemotherapy in platinum-sensitive and resistant EOC in resource-limited Indian populations.

Method and materials: This retrospective study was conducted at a regional cancer hospital in eastern India. Platinum-sensitive and resistant recurrent EOC patients were enrolled between 2021 and 2024. Patients' demographic and treatment details were retrieved from hospital medical records. All patients received bevacizumab 7.5 mg/kg IV dose with chemotherapy followed by maintenance till disease progression or inadvertent toxicity occurred. Primary endpoints were PFS and objective response rate (ORR); secondary endpoints were overall survival (OS) and safety. Kaplan-Meier plot generated PFS and OS survival curves.

Results: 48 patients were enrolled. With a median follow-up of 37 months, 46% of patients progressed on bevacizumab. The median duration of PFS was 17 months (95% CI, 14.31-19.68); it was slightly higher in platinum-sensitive patients at 18 months (95% CI, 14.25-21.74). Half of the patients achieved partial response, with an ORR of 66%. Median OS was not reached due to fewer events. The 3-year OS rate was 83%. About 15 patients who progressed on bevacizumab were able to receive further chemotherapy lines. No new safety concerns were noted. Only 4.2% of patients developed grade 3 proteinuria, one developed arterial thrombosis and two had grade 3 thrombocytopenia. Only one patient died due to a GI fistula.

Conclusion: Bevacizumab plus chemotherapy followed by bevacizumab maintenance till disease progression significantly improved PFS in recurrent EOC. This real-world finding suggests a crucial insight into effective treatment options for financially compromised Indian populations with recurrent EOC.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
3.80
自引率
5.60%
发文量
138
审稿时长
27 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信