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每周使用紫杉醇和顺铂进行确定性同步放化疗治疗局部晚期食管癌和交界性癌的临床疗效

Clinical Outcome in Definitive Concurrent Chemoradiation With Weekly Paclitaxel and Carboplatin for Locally Advanced Esophageal and Junctional Cancer.

作者信息

Noronha Vanita, Prabhash Kumar, Joshi Amit, Patil Vijay Maruti, Talole Sanjay, Nakti Dipti, Sahu Arvind, Shah Srushti, Ghosh-Laskar Sarbani, Patil Prachi S, Mehta Shaesta A, Jambhekar Nirmala, Mahajan Abhishek, Purandare Nilendu

机构信息

Department of Medical Oncology, Tata Memorial Hospital, Mumbai, India.

出版信息

Oncol Res. 2016;23(4):183-95. doi: 10.3727/096504016X14537290676865.

Abstract

There are little data on the efficacy and safety of taxane/platinum with definitive radiotherapy (RT) for esophageal/GEJ cancer. This article is a retrospective analysis of patients who received weekly paclitaxel 50 mg/m(2) and carboplatin AUC 2 with radical definitive RT for locally advanced esophageal/GEJ cancer. Between February 2011 and July 2014, 179 patients were included. The median age was 54 years. Ninety-two percent of patients had squamous histology. Mean RT dose was 58.7 Gy in 32 fractions over 53 days, with mean of six chemotherapy cycles. Fifty-six percent of patients developed ≥grade 3 acute toxicities, commonly febrile neutropenia (12%) and infection (11%); ≥grade 3 laboratory abnormalities included hyponatremia (38%), leukopenia (49%), neutropenia (27%), and anemia (16%). Twelve percent of patients developed ≥grade 3 chronic toxicity. Fatal toxicities included six during CRT, eight within 30 days of completing CRT, and three chronic. Radiologic response was 49% (CR 5.6%, PR 43%). Follow-up endoscopy showed remission in 53% and residual disease in 14%. At a median follow-up of 28 months, median PFS was 11 months (95% CI: 8-13.9), median OS was 19 months (95% CI: 15.4-22.6), and estimated 1-year, 2-year, and 3-year survivals were 70%, 47%, and 39%, respectively. Weekly paclitaxel-carboplatin concurrently with definitive RT is efficacious with manageable toxicity. [The trial was registered with the Clinical Trials Registry-India (CTRI), registration number: CTRI/2014/07/004776.].

摘要

关于紫杉烷/铂类联合根治性放疗(RT)治疗食管/胃食管交界部癌的疗效和安全性的数据较少。本文是一项对接受每周50mg/m²紫杉醇和AUC 2卡铂联合根治性RT治疗局部晚期食管/胃食管交界部癌患者的回顾性分析。2011年2月至2014年7月期间,纳入了179例患者。中位年龄为54岁。92%的患者为鳞状组织学类型。平均放疗剂量为58.7Gy,分32次在53天内完成,平均化疗周期数为6个。56%的患者发生≥3级急性毒性反应,常见的有发热性中性粒细胞减少(12%)和感染(11%);≥3级实验室异常包括低钠血症(38%)、白细胞减少(49%)、中性粒细胞减少(27%)和贫血(16%)。12%的患者发生≥3级慢性毒性反应。致命毒性反应包括同步放化疗期间6例、完成同步放化疗后30天内8例和慢性期3例。放射学缓解率为49%(完全缓解5.6%,部分缓解43%)。随访内镜检查显示缓解率为53%,残留病灶率为14%。中位随访28个月时,中位无进展生存期为11个月(95%CI:8 - 13.9),中位总生存期为19个月(95%CI:15.4 - 22.6),估计1年、2年和3年生存率分别为70%、47%和39%。每周紫杉醇 - 卡铂同步联合根治性放疗有效且毒性可控。[该试验已在印度临床试验注册中心(CTRI)注册,注册号:CTRI/2014/07/004776。]

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deee/7838643/bd56a75df7e6/OR-23-183-g001.jpg

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