[Gemcitabine long-term maintenance chemotherapy benefits patients with survival: a multicenter, real-world study of advanced breast cancer treatment in China].

J Yue, G H Song, H P Li, T Sun, L H Song, Z S Tong, L L Zhang, Z C Song, Q C Ouyang, J Yang, Y Y Pan, P Yuan
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Abstract

Objective: This study collected a real-world data on survival and efficacy of gemcitabine-containing therapy in advanced breast cancer. Aimed to find the main reasons of affecting the duration of gemcitabine-base therapy in advanced breast cancer patients. Methods: Advanced breast cancer patients who received gemcitabine-base therapy from January 2017 to January 2019 were enrolled(10 hospitals). The clinicopathological data, the number of chemotherapy cycles and the reasons for treatment termination were collected and analyzed. To identify the reasons related with continuous treatment for advanced breast cancer and the factors which affect the survival and efficacy. Results: A total of 224 patients with advanced breast cancer were enrolled in this study, with a median age of 52 years (26-77 years), 55.4%(124/224) was postmenopausal. Luminal type were 83 cases, TNBC were 97 cases, and human epidermal growth factor receptor 2 (HER's-2) overexpression were 44. At the analysis, 224 patients who received the gemcitabine-based regimens were evaluated, included 5 complete reponse (CR), 77 partial response (PR), 112 stable disease (SD) and 27 progressive disease (PD). The objective response rate (ORR) was 36.6%(82/224). Seventy patients had serious adverse diseases, including leukopenia (9), neutrophilia (49), thrombocytopenia (15), and elevated transaminase (2). The median follow-up time was 41 months (26~61 months), and the median PFS was 5.6 months. The reasons of termination treatment were listed: disease progression were 90 patients; personal reasons were 51 patients; adverse drug reactions were 18 patients; completed treatment were 65 patients. It was found that progression-free survival (PFS) was significantly longer in patients receiving >6 cycles than that in patients with ≤6 cycles (8.2 months vs 5.4 months, HR=2.474, 95% CI: 1.730-3.538, P<0.001). Conclusions: Gemcitabine-based regimen is generally well tolerated in the Chinese population and has relatively ideal clinical efficacy in the real world. The median PFS is significantly prolonged when the number of treatment cycles are appropriately increased.

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[吉西他滨长期维持化疗可提高患者生存率:中国晚期乳腺癌治疗的多中心真实世界研究]。
研究目的本研究收集了晚期乳腺癌患者接受含吉西他滨治疗后的生存期和疗效的真实数据。旨在找出影响晚期乳腺癌患者吉西他滨基础治疗时间的主要原因。方法纳入2017年1月至2019年1月接受吉西他滨基础治疗的晚期乳腺癌患者(10家医院)。收集并分析临床病理数据、化疗周期数和治疗终止原因。找出晚期乳腺癌持续治疗的相关原因以及影响生存和疗效的因素。结果本研究共纳入了 224 例晚期乳腺癌患者,中位年龄为 52 岁(26-77 岁),55.4%(124/224)为绝经后患者。其中分叶型 83 例,TNBC 97 例,人表皮生长因子受体 2(HER's-2)过表达 44 例。分析评估了224例接受吉西他滨治疗方案的患者,其中包括5例完全应答(CR)、77例部分应答(PR)、112例疾病稳定(SD)和27例疾病进展(PD)。客观反应率(ORR)为36.6%(82/224)。70例患者出现严重不良反应,包括白细胞减少(9例)、中性粒细胞增多(49例)、血小板减少(15例)和转氨酶升高(2例)。中位随访时间为 41 个月(26~61 个月),中位 PFS 为 5.6 个月。终止治疗的原因如下:疾病进展 90 例;个人原因 51 例;药物不良反应 18 例;完成治疗 65 例。研究发现,接受6个周期以上治疗的患者的无进展生存期(PFS)明显长于接受6个周期以下治疗的患者(8.2个月 vs 5.4个月,HR=2.474,95% CI:1.730-3.538,P<0.001)。结论以吉西他滨为基础的治疗方案在中国人群中的耐受性普遍良好,在现实世界中的临床疗效也相对理想。适当增加治疗周期数可明显延长中位生存期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
中华肿瘤杂志
中华肿瘤杂志 Medicine-Medicine (all)
CiteScore
1.40
自引率
0.00%
发文量
10433
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