Wieand S, Schroeder G, O'Fallon J R
Cancer Center Statistics, Mayo Clinic, Rochester, MN 55905.
Stat Med. 1994;13(13-14):1453-8. doi: 10.1002/sim.4780131321.
We discuss a procedure that offers the possibility of reducing the number of patients assigned to experimental regimens which are no more effective than a standard regimen. The procedure is useful in advanced cancer trials in which the length of the accrual period might be more than twice the median survival time for the standard regimen. The procedure is intuitively appealing and offers a 50 per cent chance of stopping accrual to ineffective therapies, yet is associated with a loss of power of less than 0.02.
我们讨论了一种程序,该程序有可能减少被分配到不比标准方案更有效的实验方案中的患者数量。该程序在晚期癌症试验中很有用,在这类试验中,入组期的长度可能超过标准方案中位生存期的两倍。该程序直观上很有吸引力,有50%的机会停止对无效疗法的入组,而且其效能损失小于0.02。