Falkson C I, Ibrahim J, Kirkwood J M, Coates A S, Atkins M B, Blum R H
University of Pretoria, South Africa.
J Clin Oncol. 1998 May;16(5):1743-51. doi: 10.1200/JCO.1998.16.5.1743.
To investigate the response rate, time to treatment failure (TTF), overall survival, and toxicity in patients with metastatic melanoma treated with dacarbazine alone, dacarbazine plus interferon (IFN), dacarbazine plus tamoxifen (TMX), or dacarbazine plus IFN plus TMX.
Two hundred seventy-one patients (258 were eligible) were randomized in a 2 x 2 factorial design to receive one of the above treatments. The trial was designed to detect a 50% improvement in survival with 83% power.
Nine complete (CRs) and 18 partial responses (PRs) were observed in the patients who received treatments that contained IFN compared with four CRs and 18 PRs in the patients who received treatments that did not contain IFN. Five CRs and 20 PRs occurred in patients treated with TMX compared with eight CRs and 16 PRs in those treated without TMX. Response differences were nonsignificant. The overall median TTF was 2.6 months, and the overall median survival was 8.9 months. There was no significant difference in TTF or survival among any of the different treatments. Poor performance status (PS), hepatic metastases, and weight loss were significant adverse prognostic factors. Twenty-three patients had a TTF greater than 20 months, and these durable responses were evenly distributed among the treatment arms. Significantly more severe and life-threatening toxic events occurred with treatments that contained IFN.
Neither IFN, TMX, nor the combination significantly improved the response rate, TTF, or survival when added to dacarbazine, but IFN significantly increased toxicity.
研究单独使用达卡巴嗪、达卡巴嗪加干扰素(IFN)、达卡巴嗪加他莫昔芬(TMX)或达卡巴嗪加IFN加TMX治疗转移性黑色素瘤患者的缓解率、治疗失败时间(TTF)、总生存期和毒性。
271例患者(258例符合条件)按2×2析因设计随机接受上述治疗之一。该试验旨在以83%的检验效能检测生存率提高50%的情况。
接受含IFN治疗的患者中观察到9例完全缓解(CR)和18例部分缓解(PR),而接受不含IFN治疗的患者中有4例CR和18例PR。接受TMX治疗的患者中有5例CR和20例PR,未接受TMX治疗的患者中有8例CR和16例PR。缓解差异无统计学意义。总体中位TTF为2.6个月,总体中位生存期为8.9个月。不同治疗组之间的TTF或生存期无显著差异。体能状态差(PS)、肝转移和体重减轻是显著的不良预后因素。23例患者的TTF大于20个月,这些持久缓解在各治疗组中分布均匀。含IFN的治疗出现的严重和危及生命的毒性事件明显更多。
IFN、TMX或两者联合添加到达卡巴嗪中时,均未显著提高缓解率、TTF或生存期,但IFN显著增加了毒性。