北京大学学报(医学版) ›› 2014, Vol. 46 ›› Issue (1): 144-148.

• 论著 • 上一篇    下一篇

注射用紫杉醇(白蛋白结合型)治疗进展期胃癌

龚继芳,陆明,李洁,李燕,周军,鲁智豪,王晰程,李健,张小田,沈琳△   

  1. (北京大学肿瘤医院暨北京市肿瘤防治研究所消化肿瘤内科,恶性肿瘤发病机制及转化研究教育部重点实验室,北京100142)
  • 出版日期:2014-02-18 发布日期:2014-02-18

Efficacy of albumin-bound paclitaxel in advanced gastric cancer patients

GONG Ji-fang, LU Ming, LI Jie, LI Yan, ZHOU Jun, LU Zhi-hao, WANG Xi-cheng, LI Jian, ZHANG Xiao-tian, SHEN Lin△   

  1. (Key Laboratory of Carcinogenesis and Translational Research, Ministry of Education; Department of Gastrointestinal Oncology, Peking University Cancer Hospital & Institute, Beijing 100142, China)
  • Online:2014-02-18 Published:2014-02-18

摘要: 目的:评价注射用紫杉醇(白蛋白结合型)治疗进展期胃癌的安全性和疗效。方法:选择2009年7月至2012年10月北京大学肿瘤医院 病理组织学或细胞学确诊的进展期胃腺癌患者,KPS评分≥60分,预计生存期> 12周。骨髓、肝、肾、心功能基本正常。应用注射用紫杉醇(白 蛋白结合型)单药或联合卡培他滨、替吉奥、曲妥珠单抗、西妥昔单抗治疗。每周期总剂量为200~400 mg(130~260 mg/m2),分为第1、8天或 第1、8、15天用药,静脉滴注30 min,每3周重复1次。不良反应按药物不良反应分级标准NCI-CTC3.0版进行评定,按照实体瘤疗效评定标准 (RECIST 1.0)评价疗效。结果:共25例患者入选本研究,中位年龄57岁(38~79岁)。大部分患者原发灶位于非胃食管结合部,转移部位为淋巴 结及腹膜。共完成了65个周期的治疗,中位周期数2(0.5~7)。初治患者11例,作为二线及以上治疗者14例。可评价疗效者16例,无完全缓解 (complete response CR)患者,部分缓解(partial response, PR) 5例,稳定(stable disease,SD) 5例,进展(progressed disease, PD) 6例 。其中初治患者中共8例可评价疗效,PR 3例,有效率37.5%,SD 1例,临床获益率50%。全组中位至治疗失败时间(time to treatment failure,TTF)为3.7个月(95% CI 2.32~5.08),中位至死亡时间(time to death,TTD)为7.9个月(95% CI 5.17~10.63)。初治患者与复治 患者、单药组与联合用药组的TTF及TTD差异无统计学意义。所有25例患者均可评价不良反应,大部分为1~2级,血液学毒性占多数,主要为白细 胞减少及中性粒细胞减少,在非血液学毒性中,常见的为恶心/呕吐、乏力、周围神经毒性,无过敏反应及治疗相关性死亡。结论:注射用紫杉 醇(白蛋白结合型)作为晚期胃癌患者的挽救治疗有一定疗效,但剂量水平低于乳腺癌患者,需要进行剂量探索性研究。

关键词: 白蛋白结合型紫杉醇, 胃肿瘤, 姑息疗法, 药物疗法

Abstract: Objective:To evaluate the safety and efficacy of albumin-bound paclitaxel in patients with advanced gastric cancer (AGC).Methods: The patients with histopathologic or cytopathologic diagnosed advanced gastric cancer (AGC), Karnofsky performance status≥60, and life expectancy>12 weeks, and with adequate organ functions of the bone marrow, liver, kidney and heart were recuited in our study. Albuminbound paclitaxel was administered alone or combined with capecitabine, TS1, trastuzumab or cetuxizumb. The total doses of albumin-bound paclitaxel were 200-400 mg (130-260 mg/m2), divided on days 1, 8 or days 1,8, and 15, given intravenously during 30 minutes of a 21-day cycle. Tumor response was evaluated according to the Response Evaluation Criteria in Solid Tumors (RECIST) 1.0. The adverse events (AE) were graded according to National Cancer Institute-Common Toxicity Criteria (NCI-CTC) 3.0 version. Results: From July 2009 to Octobor 2012, the total of 25 patients were treated and completed 65 cycles of chemotherapy (median: 2 cycles, and range: 0.5-7). The median age was 57 years (range: 38-79). The majority of the patients were with nongastroesophageal junction cancers and had metastasic disease with lymph nodes and peritoneum. Eleven patients were chemotherapy naive and the others had accepted previous systemic therapy for advanced disease. 16 patients were evaluable for clinical response. No complete response was observed and partial response (PR) was achieved in 5 patients. Five patients had stable disease and 6 patients progressed. Among the chemotherapy naive patients, 8 patients were evaluable for response, 3 patients had partial response (37.5%) and 1 patient had stable disease (tumor shrink). The clinical response rate was 50%. Time to treatment failure (TTF)was 3.7 months(95% CI 2.32-5.08) and time to death (TTD)was 7.9 months (95% CI 5.17-10.63). No statistical differences in TTF and TTD were observed between the untreated and the retreated patients or the monotherapy and the combination therapy groups. All the patients were suitable for safety assessment. Most toxicities were mild with grades 1/2. Hematologic AEs were more common with leucopenia and neutropenia. Meanwhile, nausea/vomiting, fatigue, peripheral neuropathy were the most common non hematologic AEs. No allergic reaction or treatment-related deaths were recorded.Conclusion:AGC patients could benefit from albumin-bound paclitaxel with lower dose level than breast cancer patients. Additional phase Ⅰ/Ⅱ studies of albumin-bound paclitaxel in gastric cancer are warranted.

Key words: Albumin-bound paclitaxel, Stomach neoplasms, Palliative care, Drug therapy

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