Ajani J A, Fairweather J, Dumas P, Patt Y Z, Pazdur R, Mansfield P F
Department of Gastrointestinal Oncology, University of Texas M. D. Anderson Cancer Center, Houston 77030, USA.
Cancer J Sci Am. 1998 Jul-Aug;4(4):269-74.
Taxol (paclitaxel) represents a new class of anticancer agent with activity against a wide variety of solid tumors. It has been found to be active in patients with adenocarcinoma and squamous cell carcinoma of the esophagus. To determine its activity against gastric adenocarcinoma, we conducted a phase II trial of Taxol in chemotherapy-naive patients with advanced disease.
Patients with measurable, unresectable, metastatic gastric carcinoma with performance status < or = 2 by Zubrod scale were eligible. Patients had to have normal liver, renal, and bone marrow functions. Written informed consent was obtained from all patients. The starting dose of Taxol was 200 mg/m2 infused over either 3 hours (in the first 15 patients) or 24 hours (in the subsequent 18 patients). Taxol was repeated every 21 days. Response was evaluated after two courses.
Thirty-three patients were registered. The median number of courses was two (range, 1 to 12; total, 112 courses). Thirty patients were evaluable for response and toxicity. Among the first 15 patients (two inevaluable) receiving Taxol over 3 hours, there were one partial response (PR) (one of 13 patients, or 8%; 95% confidence interval, 0% to 36%) and three minor responses (MRs). However, among the 18 patients (one inevaluable) receiving Taxol over 24 hours, there were four PRs (four of 17 patients or 23%; 95% confidence interval, 7% to 50%) and three MRs. The overall PR rate was 17% (five of 30 patients; 95% confidence interval, 6% to 35%). The median duration of PR was 6.5 months (range, 2.3 months to 11.3+ months. There were no treatment-related deaths. Myelosuppression was more severe with the 24-hour schedule than with the 3-hour schedule.
Taxol has a modest degree of activity against gastric carcinoma. It is well tolerated by the patients. Further studies of Taxol in combination with other active agents against gastric carcinoma should be considered.
紫杉醇是一类新型抗癌药物,对多种实体瘤具有活性。已发现其对食管腺癌和鳞状细胞癌患者有活性。为确定其对胃腺癌的活性,我们对初治的晚期胃腺癌患者进行了紫杉醇的II期试验。
符合条件的患者为可测量、不可切除、转移性胃癌患者,其Zubrod量表的体能状态评分为≤2分。患者的肝、肾和骨髓功能必须正常。所有患者均签署了书面知情同意书。紫杉醇的起始剂量为200mg/m²,静脉输注3小时(前15例患者)或24小时(随后18例患者)。每21天重复使用紫杉醇。两个疗程后评估疗效。
登记了33例患者。疗程中位数为2个(范围1至12个;共112个疗程)。30例患者可评估疗效和毒性。在前15例(2例不可评估)接受3小时紫杉醇输注的患者中,有1例部分缓解(PR)(13例患者中的1例,即8%;95%置信区间,0%至36%)和3例轻微缓解(MR)。然而,在18例(1例不可评估)接受24小时紫杉醇输注的患者中,有4例PR(17例患者中的4例,即23%;95%置信区间,7%至50%)和3例MR。总体PR率为17%(30例患者中的5例;95%置信区间,6%至35%)。PR的中位持续时间为6.5个月(范围,2.3个月至11.3+个月)。无治疗相关死亡。24小时给药方案的骨髓抑制比3小时给药方案更严重。
紫杉醇对胃癌有一定程度的活性。患者耐受性良好。应考虑进一步研究紫杉醇与其他抗胃癌活性药物联合应用。