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卡培他滨联合或不联合奥沙利铂作为一线治疗转移性结直肠癌老年或虚弱患者的随机 II 期研究:韩国癌症研究组 CO06-01 的一项前瞻性、多中心试验。

Randomized phase II study of capecitabine with or without oxaliplatin as first-line treatment for elderly or fragile patients with metastatic colorectal cancer: a prospective, multicenter trial of the Korean Cancer Study Group CO06-01.

机构信息

*Center for Colorectal Cancer, Research Institute and Hospital, National Cancer Center, Goyang †Department of Clinical Epidemiology and Biostatistics ‡Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul §Department of Internal Medicine, St. Vincent's Hospital, Catholic University College of Medicine, Suwon ∥Department of Internal Medicine, Hallym University Medical Center, Hallym University College of Medicine, Anyang ¶Department of Internal Medicine, Division of Hematology and Medical Oncology, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam #Department of Internal Medicine, Cancer Metastasis Research Center, Yonsei Cancer Center, Yonsei University College of Medicine **Department of Internal Medicine, Samsung Medical Center, Division of Hematology-Oncology, Sungkyunkwan University School of Medicine, Seoul, Korea.

出版信息

Am J Clin Oncol. 2013 Dec;36(6):565-71. doi: 10.1097/COC.0b013e31825d52d5.

Abstract

BACKGROUND

To compare 2 different strategies of chemotherapy for elderly metastatic colorectal cancer patients.

METHODS

This randomized, multicenter phase II study involved 80 metastatic colorectal cancer patients aged 70 years and above (performance status [PS] 0-2) or 65 years and above (PS 2), randomly assigned to arm A (capecitabine 1250 mg/m twice daily on days 1-14) or arm B (capecitabine 1000 mg/m twice daily on days 1-14, oxaliplatin 100 mg/m on day 1 initially, 130 mg/m for subsequent cycles). Primary endpoint was response rate, and secondary endpoints were toxicity, progression-free survival, overall survival, and quality of life (QoL), which was assessed with the EORTC QLQ-C30 questionnaire.

RESULTS

Confirmed response rates were 22.5% and 35.0% (P=0.217), progression-free survival were 4.4 and 6.6 months (P=0.335), and overall survival were 14.2 and 11.0 months (P=0.106). Hematologic toxicities were frequently observed in arm B, but grade ≥3 toxicities were not different. Patients in arm A tended to present more favorable preservation of QoL in global health status, physical and role functioning, fatigue, and appetite loss.

CONCLUSIONS

Initial aggressive treatment strategy would not be recommended for this patient population because QoL appeared more preserved, treatments were better tolerated, and survivals did not differ in patients treated with initial capecitabine monotherapy.

摘要

背景

比较两种不同的化疗策略在老年转移性结直肠癌患者中的应用。

方法

这是一项随机、多中心的 II 期研究,共纳入 80 例年龄≥70 岁(体能状态 [PS] 0-2 分)或年龄≥65 岁(PS 2 分)、转移性结直肠癌患者,随机分为 A 组(卡培他滨 1250 mg/m 每日 2 次,第 1-14 天)或 B 组(卡培他滨 1000 mg/m 每日 2 次,第 1-14 天,奥沙利铂 100 mg/m 初始剂量,第 1 天,随后的周期为 130 mg/m)。主要终点为缓解率,次要终点为毒性、无进展生存期、总生存期和生活质量(QoL),采用 EORTC QLQ-C30 问卷进行评估。

结果

确认的缓解率分别为 22.5%和 35.0%(P=0.217),无进展生存期分别为 4.4 个月和 6.6 个月(P=0.335),总生存期分别为 14.2 个月和 11.0 个月(P=0.106)。B 组患者常出现血液学毒性,但≥3 级毒性无差异。A 组患者在总体健康状况、身体功能和角色功能、疲劳和食欲丧失方面的 QoL 保持更有利。

结论

对于这一患者群体,不建议采用初始强化治疗策略,因为初始卡培他滨单药治疗患者的 QoL 保持更有利、治疗耐受性更好、生存期无差异。

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