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奥沙利铂单药用于既往未接受治疗的结直肠癌患者:一项II期多中心研究。

Oxaliplatin as single agent in previously untreated colorectal carcinoma patients: a phase II multicentric study.

作者信息

Díaz-Rubio E, Sastre J, Zaniboni A, Labianca R, Cortés-Funes H, de Braud F, Boni C, Benavides M, Dallavalle G, Homerin M

机构信息

Hospital Clínico San Carlos, Madrid, Spain.

出版信息

Ann Oncol. 1998 Jan;9(1):105-8. doi: 10.1023/a:1008200825886.

DOI:10.1023/a:1008200825886
PMID:9541691
Abstract

BACKGROUND

Oxaliplatin is a new cytotoxic agent from the diaminocyclohexane family with proven antitumor activity against colon cancer cell lines. Activity in patients with colorectal carcinoma previously treated with 5-fluorouracil has been studied in three single-agent phase II trials, showing a reproducible response rate of 10%. Here we report a phase II trial with oxaliplatin as a first-line chemotherapy for metastatic colorectal cancer.

PATIENTS AND METHODS

Twenty-five patients were entered in the study. All of them had metastatic disease without previous chemotherapy, and at least one lesion had to be measurable by computed tomography (CT). Therapy consisted of a two-hour infusion of oxaliplatin at a dose of 130 mg/m2 every 21 days.

RESULTS

The overall response rate determined by investigators was 20% (95% CI, 6.8%-40.7%). Eight patients (32%) had stable disease. The median time to disease progression in responders was six months (range four to nine). The median progression-free survival was four months and median overall survival 14.5 months (95% CI, 10-20 months). The main toxic effects were peripheral neuropathy (92%) and laryngopharyngeal dysesthesia (75%). No severe grade 3-4 neurotoxicities (NCI-CTC) were found. Gastrointestinal and hematological toxicities were mild.

CONCLUSIONS

Oxaliplatin is an active agent in first-line chemotherapy for advanced colorectal cancer. It was well tolerated, caused no toxic deaths, had low hematotoxicity, well controlled gastrointestinal toxicity, and frequent but mild peripheral neurological symptoms. Therefore, it is of interest to associate oxaliplatin with other active compounds.

摘要

背景

奥沙利铂是一种来自二氨基环己烷家族的新型细胞毒性药物,已证实对结肠癌细胞系具有抗肿瘤活性。在三项单药II期试验中研究了其对先前接受过5-氟尿嘧啶治疗的结直肠癌患者的活性,显示可重复的缓解率为10%。在此我们报告一项以奥沙利铂作为转移性结直肠癌一线化疗的II期试验。

患者与方法

25名患者进入本研究。他们均有转移性疾病且未接受过先前化疗,并且至少有一个病灶必须可通过计算机断层扫描(CT)测量。治疗包括每21天一次剂量为130mg/m²的奥沙利铂两小时输注。

结果

研究者确定的总缓解率为20%(95%CI,6.8%-40.7%)。8名患者(32%)病情稳定。缓解者疾病进展的中位时间为6个月(范围4至9个月)。无进展生存期的中位时间为4个月,总生存期的中位时间为14.5个月(95%CI,10 - 20个月)。主要毒性作用为周围神经病变(92%)和咽喉感觉异常(75%)。未发现严重的3 - 4级神经毒性(NCI - CTC)。胃肠道和血液学毒性较轻。

结论

奥沙利铂是晚期结直肠癌一线化疗的活性药物。它耐受性良好,未导致毒性死亡,血液毒性低,胃肠道毒性得到良好控制,周围神经症状常见但较轻。因此,将奥沙利铂与其他活性化合物联合使用具有意义。

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