Department of Medicine, Institut Gustave Roussy, Villejuif, France.
Department of Medical Social Sciences, Feinberg School of Medicine at Northwestern University, Chicago.
Ann Oncol. 2019 Apr 1;30(4):567-574. doi: 10.1093/annonc/mdz016.
We report longitudinal health-related quality-of-life (HRQoL) data from the international, randomized, double-blind, placebo-controlled phase III ExteNET study, which demonstrated an invasive disease-free survival benefit of extended adjuvant therapy with neratinib over placebo in human epidermal growth factor receptor-2-positive early-stage breast cancer.
Women (N = 2840) with early-stage HER2-positive breast cancer who had completed trastuzumab-based adjuvant therapy were randomly assigned to neratinib 240 mg/day or placebo for 12 months. HRQoL was an exploratory end point. Patients completed the Functional Assessment of Cancer Therapy-Breast (FACT-B) and EuroQol 5-Dimensions (EQ-5D) questionnaires at baseline and months 1, 3, 6, 9, and 12. Changes from baseline were compared using analysis of covariance with no imputation for missing values. Sensitivity analyses used alternative methods. Changes in HRQoL scores were regarded as clinically meaningful if they exceeded previously reported important differences (IDs).
Of the 2840 patients (intention-to-treat population), 2407 patients were evaluable for FACT-B (neratinib, N = 1171; placebo, N = 1236) and 2427 patients for EQ-5D (neratinib, N = 1186; placebo, N = 1241). Questionnaire completion rates exceeded 85%. Neratinib was associated with a decrease in global HRQoL scores at month 1 compared with placebo (adjusted mean differences: FACT-B total, -2.9 points; EQ-5D index, -0.02), after which between-group differences diminished at later time-points. Except for the FACT-B physical well-being (PWB) subscale at month 1; all between-group differences were less than reported IDs. The FACT-B breast cancer-specific subscale showed small improvements with neratinib at months 3-9, but all were less than IDs. Sensitivity analyses exploring missing data did not change the results.
Extended adjuvant neratinib was associated with a transient, reversible decrease in HRQoL during the first month of treatment, possibly linked to treatment-related diarrhea. With the exception of the PWB subscale at month 1, all neratinib-related HRQoL changes did not reach clinically meaningful thresholds. ClinicalTrials.gov: NCT00878709.
我们报告了国际、随机、双盲、安慰剂对照 III 期 ExteNET 研究的纵向与健康相关的生活质量(HRQoL)数据,该研究表明,与安慰剂相比,曲妥珠单抗辅助治疗后延长使用奈拉替尼可使人类表皮生长因子受体-2 阳性早期乳腺癌无侵袭性疾病生存获益。
完成曲妥珠单抗为基础的辅助治疗的早期 HER2 阳性乳腺癌女性(N=2840)被随机分配接受奈拉替尼 240mg/天或安慰剂治疗 12 个月。HRQoL 是探索性终点。患者在基线和第 1、3、6、9 和 12 个月时完成功能性评估癌症治疗-乳房(FACT-B)和欧洲五维健康量表(EQ-5D)问卷。缺失值无插补的协方差分析比较了从基线的变化。使用替代方法进行敏感性分析。如果 HRQoL 评分的变化超过之前报道的重要差异(IDs),则认为具有临床意义。
在 2840 名患者(意向治疗人群)中,2407 名患者可评估 FACT-B(奈拉替尼,N=1171;安慰剂,N=1236),2427 名患者可评估 EQ-5D(奈拉替尼,N=1186;安慰剂,N=1241)。问卷完成率超过 85%。与安慰剂相比,奈拉替尼在第 1 个月时与全球 HRQoL 评分下降相关(调整后的平均差异:FACT-B 总分,-2.9 分;EQ-5D 指数,-0.02),此后在后期时间点,组间差异缩小。除第 1 个月的 FACT-B 生理健康(PWB)亚量表外,所有组间差异均小于报道的 IDs。奈拉替尼在第 3-9 个月时与 FACT-B 乳腺癌特异性亚量表相关的小改善,但所有改善均小于 IDs。探索缺失数据的敏感性分析并未改变结果。
延长辅助使用奈拉替尼与治疗开始后第一个月的 HRQoL 短暂、可逆下降相关,可能与治疗相关腹泻有关。除第 1 个月的 PWB 亚量表外,奈拉替尼相关的所有 HRQoL 变化均未达到临床有意义的阈值。临床试验.gov:NCT00878709。