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多西他赛、铂类和氟尿嘧啶(DCF)联合诱导化疗用于局部晚期食管癌和食管交界癌时的高病理完全缓解率。

High pathologic complete remission rate from induction docetaxel, platinum and fluorouracil (DCF) combination chemotherapy for locally advanced esophageal and junctional cancer.

作者信息

Noronha Vanita, Joshi Amit, Jandyal Sunny, Jambhekar Nirmala, Prabhash Kumar

机构信息

Department of Medical Oncology, Tata Memorial Hospital, Dr. E Borges Marg, Parel, Mumbai, 400012, India.

出版信息

Med Oncol. 2014 Sep;31(9):188. doi: 10.1007/s12032-014-0188-0. Epub 2014 Aug 23.

Abstract

Adding docetaxel to the cisplatin/5-fluorouracil induction regimen for locally advanced esophageal and GEJ cancer may increase the pathologic complete remission (pCR) rate, leading to an improved outcome. Institutional ethics committee approved the protocol of retrospective analysis of patients with locally advanced esophageal and GEJ carcinoma, who received 2-3 cycles of docetaxel, cisplatin and 5-fluorouracil (DCF) induction chemotherapy with primary growth factors and prophylactic antibiotics. Following chemotherapy, a restaging scan was performed. If disease was deemed resectable, surgery was performed. Between February 2010 and October 2013, 31 patients received induction DCF. Ninety-four percent patients had squamous histology. Response rate was 81 %: complete remission (CR)-23 % and partial remission-58 %. Eighty-seven percent patients underwent surgery; R0 resection rate was 67 %. pCR occurred in 26 %. Common grade 3/4 toxicities included anemia-23 %, neutropenia-42 %, febrile neutropenia-39 %, diarrhea-39 %, hyponatremia-55 % and hypokalemia-39 %. There were no toxic deaths. At a median follow-up of 34 months (95 % CI 31.3-36.6), estimated median progression-free survival (PFS) was 27 months (95 % CI 11-39) and the overall survival (OS) at 1 year, 2 years and 3 years was 80, 68 and 55 %, respectively. Patients who attained pCR had a significant longer PFS and OS; median PFS and OS were not reached in patients with pCR and were 15 months (95 %CI 8.4-21.5 months), P = 0.012 and 25 months (95 %CI 10.3-39.7), P = 0.023, respectively, in patients who did not attain a pCR. DCF induction chemotherapy leads to pCR of 26 %, which rivals that obtained from chemoradiotherapy. Toxicity is substantial but manageable with adequate supportive care.

摘要

在局部晚期食管癌和胃食管交界部癌的顺铂/5-氟尿嘧啶诱导方案中加入多西他赛可能会提高病理完全缓解(pCR)率,从而改善预后。机构伦理委员会批准了对局部晚期食管癌和胃食管交界部癌患者进行回顾性分析的方案,这些患者接受了2 - 3周期的多西他赛、顺铂和5-氟尿嘧啶(DCF)诱导化疗,并使用了主要生长因子和预防性抗生素。化疗后,进行重新分期扫描。如果疾病被认为可切除,则进行手术。在2010年2月至2013年10月期间,31例患者接受了诱导DCF化疗。94%的患者为鳞状组织学类型。缓解率为81%:完全缓解(CR)占23%,部分缓解占58%。87%的患者接受了手术;R0切除率为67%。pCR发生率为26%。常见的3/4级毒性包括贫血(23%)、中性粒细胞减少(42%)、发热性中性粒细胞减少(39%)、腹泻(39%)、低钠血症(55%)和低钾血症(39%)。无毒性死亡病例。中位随访34个月(95%CI 31.3 - 36.6),估计中位无进展生存期(PFS)为27个月(95%CI 11 - 39),1年、2年和3年的总生存期(OS)分别为80%、68%和55%。达到pCR的患者PFS和OS显著更长;达到pCR的患者未达到中位PFS和OS,未达到pCR的患者中位PFS和OS分别为15个月(95%CI 8.4 - 21.5个月),P = 0.012和25个月(95%CI 10.3 - 39.7),P = 0.023。DCF诱导化疗导致26%的pCR率,与放化疗获得的pCR率相当。毒性较大,但通过充分的支持治疗可控制。

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