Clinical Trials Unit, Istituto Nazionale per lo Studio e la Cura dei Tumori, Fondazione G. Pascale-IRCCS, Napoli.
Clinical Trials Unit, Istituto Nazionale per lo Studio e la Cura dei Tumori, Fondazione G. Pascale-IRCCS, Napoli.
Ann Oncol. 2015 Apr;26(4):675-682. doi: 10.1093/annonc/mdu564. Epub 2014 Dec 8.
Evidence on adjuvant chemotherapy in older women with breast cancer is poor. We tested whether weekly docetaxel is more effective than standard chemotherapy.
We carried out a multicenter, randomized phase III study. Women aged 65-79, operated for breast cancer, with average to high risk of recurrence, were allocated 1 : 1 to CMF (cyclophosphamide 600 mg/m², methotrexate 40 mg/m², fluorouracil 600 mg/m², days 1, 8) or docetaxel (35 mg/m(2) days 1, 8, 15) every 4 weeks, for four or six cycles according to hormone receptor status. Primary end point was disease-free survival (DFS). A geriatric assessment was carried out. Quality of life (QoL) was assessed with EORTC C-30 and BR-23 questionnaires.
From July 2003 to April 2011, 302 patients were randomized and 299 (152 allocated CMF and 147 docetaxel) were eligible. After 70-month median follow-up, 109 DFS events were observed. Unadjusted hazard ratio (HR) of DFS for docetaxel versus CMF was 1.21 [95% confidence interval (CI) 0.83-1.76, P = 0.32]; DFS estimate at 5 years was 0.69 with CMF and 0.65 with docetaxel. HR of death was 1.34 (95% CI 0.80-2.22, P = 0.26). There was no interaction between treatment arms and geriatric scales measuring patients' ability or comorbidities. Hematological toxicity, mucositis and nausea were worse with CMF; allergy, fatigue, hair loss, onychopathy, dysgeusia, diarrhea, abdominal pain, neuropathy, cardiac and skin toxicity were worse with docetaxel. One death was attributed to CMF and two to docetaxel. Increasing age, impairment in instrumental daily living activities, number of comorbidities and docetaxel treatment were independently associated with severe nonhematological toxicity. QoL was worse with docetaxel for nausea-vomiting, appetite loss, diarrhea, body image, future perspective, treatment side-effects and hair loss items.
Weekly docetaxel is not more effective than standard CMF as adjuvant treatment of older women with breast cancer and worsens QoL and toxicity.
NCT00331097.
针对老年乳腺癌患者的辅助化疗证据有限。我们检测了每周多西紫杉醇是否比标准化疗更有效。
我们进行了一项多中心、随机的 III 期研究。年龄在 65-79 岁之间、接受过乳腺癌手术、具有中高危复发风险的女性,按 1:1 随机分配至 CMF(环磷酰胺 600mg/m²,甲氨蝶呤 40mg/m²,氟尿嘧啶 600mg/m²,第 1、8 天)或多西紫杉醇(35mg/m²,第 1、8、15 天),根据激素受体状态,每 4 周给药 4 或 6 个周期。主要终点为无病生存(DFS)。进行了老年评估。采用 EORTC C-30 和 BR-23 问卷评估生活质量(QoL)。
2003 年 7 月至 2011 年 4 月,共纳入 302 名患者,299 名(CMF 组 152 名,多西紫杉醇组 147 名)符合条件。中位随访 70 个月后,观察到 109 例 DFS 事件。未调整的多西紫杉醇与 CMF 相比的 DFS 风险比(HR)为 1.21(95%置信区间[CI]0.83-1.76,P=0.32);CMF 组和多西紫杉醇组的 5 年 DFS 估计值分别为 0.69 和 0.65。死亡风险 HR 为 1.34(95%CI 0.80-2.22,P=0.26)。治疗组之间没有交互作用,治疗组与测量患者能力或合并症的老年评估量表之间也没有交互作用。CMF 组的血液学毒性、黏膜炎和恶心更严重;过敏、疲劳、脱发、指甲病变、味觉障碍、腹泻、腹痛、神经病变、心脏毒性和皮肤毒性在多西紫杉醇组更严重。1 例死亡归因于 CMF,2 例归因于多西紫杉醇。年龄增长、日常生活活动能力受损、合并症数量和多西紫杉醇治疗与严重非血液学毒性独立相关。多西紫杉醇治疗的恶心-呕吐、食欲下降、腹泻、身体形象、未来展望、治疗副作用和脱发等方面的生活质量更差。
每周多西紫杉醇并不优于标准 CMF 作为老年乳腺癌患者的辅助治疗,且会降低生活质量并增加毒性。
临床试验.gov:NCT00331097。