Shepherd F A, Abratt R, Crino L, Green M, Sandler A, Steward W, Iglesias J, Anglin G
Princess Margaret Hospital, 610 University Avenue, Suite 5-104, Toronto, Ont, Canada M5G 2M9.
Lung Cancer. 2000 Nov;30(2):117-25. doi: 10.1016/s0169-5002(00)00135-5.
Gemcitabine-cisplatin combinations are among the most active for the treatment of non-small cell lung cancer. Previous reports have suggested that the day of cisplatin administration affects both toxicity and drug delivery. We undertook this retrospective analysis to determine whether it also affects response and survival.
This was a retrospective analysis of six studies of gemcitabine and cisplatin. Gemcitabine, 1000-1500 mg/m(2) was administered on days 1, 8, and 15 of a 28 day cycle. In four studies cisplatin 100 mg/m(2) was administered with mannitol diuresis every four weeks on either day 1, day 2 or day 15. In two studies cisplatin 25-30 mg/m(2) was administered on day 1, 8 and 15. Standard prognostic factors including age, gender, stage, performance status, and histologic subtype were analyzed along with day of cisplatin administration. Single variable Cox proportional hazards regressions were performed. This was followed by multiple variable Cox proportional hazards regression, beginning with a full model containing terms for gender, age, performance status and stage. The least statistically significant terms were subsequently dropped from the model to reach a final model with only statistically significant variables. A similar approach was followed to fit a multiple variable logistic regression model to overall response data.
Overall response rates were highest (36-46%) in the three studies that administered cisplatin on days 2 or 15, and these studies had the highest 1-year survival rates (52-58%). Survival was better for patients who received cisplatin on day 2 or 15 compared to those treated on either day 1 or weekly on days 1, 8, 15 (P=0.020). In the final model of the Cox regression analysis, survival was better for cisplatin on days 2 or 15 (hazard ratio=0.69, P=0.008) and female gender (hazard ratio=0.72, P=0.036). Only cisplatin delivery on day 2 or day 15 predicted for significantly better response (42 vs. 29%, P=0.036).
In a 28 day cycle in which gemcitabine is administered day 1, 8 and 15, the best therapeutic index is achieved with cisplatin administration on day 2 or 15.
吉西他滨 - 顺铂联合方案是治疗非小细胞肺癌最有效的方案之一。既往报道提示顺铂给药日期会影响毒性和药物递送。我们进行了这项回顾性分析,以确定其是否也会影响疗效和生存。
这是一项对六项吉西他滨与顺铂研究的回顾性分析。在28天周期的第1、8和15天给予吉西他滨,剂量为1000 - 1500mg/m²。在四项研究中,每四周在第1天、第2天或第15天给予顺铂100mg/m²并进行甘露醇利尿。在两项研究中,在第1、8和15天给予顺铂25 - 30mg/m²。分析了包括年龄、性别、分期、体能状态和组织学亚型在内的标准预后因素以及顺铂给药日期。进行了单变量Cox比例风险回归分析。随后进行多变量Cox比例风险回归分析,首先建立一个包含性别、年龄、体能状态和分期项的完整模型。随后从模型中剔除统计学意义最小的项,以得到仅包含统计学显著变量的最终模型。采用类似方法拟合多变量逻辑回归模型以分析总体缓解数据。
在第2天或第15天给予顺铂的三项研究中,总体缓解率最高(36 - 46%),且这些研究的1年生存率最高(52 - 58%)。与在第1天或在第1、8、15天每周给药的患者相比,在第2天或第15天接受顺铂治疗的患者生存情况更好(P = 0.020)。在Cox回归分析的最终模型中,在第2天或第15天给予顺铂的患者生存情况更好(风险比 = 0.69,P = 0.008),女性患者生存情况更好(风险比 = 0.72,P = 0.036)。仅在第2天或第15天给予顺铂预测缓解情况显著更好(42%对29%,P = 0.036)。
在28天周期中,于第1、8和15天给予吉西他滨,在第2天或第15天给予顺铂可获得最佳治疗指数。