Breast Oncology Program, Dana-Farber Cancer Institute, Harvard Medical School, Boston, USA.
GZA Hospitals Sint-Augustinus, Wilrijk, Belgium.
ESMO Open. 2024 Sep;9(9):103691. doi: 10.1016/j.esmoop.2024.103691. Epub 2024 Sep 5.
Until recently, treatment options for patients with hormone receptor-positive/human epidermal growth factor 2-negative (HR+/HER2-) metastatic breast cancer (mBC) and resistance to endocrine therapy were limited to chemotherapy. This real-world study describes treatment patterns and outcomes in patients treated with chemotherapy in the United States before approval of antibody-drug conjugates.
This retrospective, observational study included adults with HR+/HER2- mBC from the ConcertAI Patient360™ Breast Cancer dataset who initiated their first chemotherapy in the metastatic setting between January 2011 and June 2021. Treatment patterns were described; real-world overall survival, time to next treatment or death, and real-world progression-free survival were evaluated for all eligible patients and patients treated with subsequent chemotherapy. Index dates were the start date of each chemotherapy treatment.
Among 1545 eligible patients, 76% were white, 12% had Eastern Cooperative Oncology Group performance status ≥2, 38% had de novo mBC, and median age was 61 years (range, 52-69 years). Within the index period, capecitabine was used the most as the first chemotherapy agent and decreased in later treatments, while the use of eribulin increased between first and fourth chemotherapies. Median (95% confidence interval) real-world overall survival was 23.3 months (21.3-25.4 months) from start of first chemotherapy, time to next treatment or death was 6.5 months (5.9-7.1 months), and real-world progression-free survival was 6.9 months (6.4-7.6 months); median times from second, third, and fourth chemotherapies decreased with each additional chemotherapy treatment.
This real-world study demonstrates that for patients with HR+/HER2- mBC, chemotherapy provides relatively limited survival benefit which decreases with each additional chemotherapy line, and highlights the need for improved treatment options.
直到最近,激素受体阳性/人表皮生长因子 2 阴性(HR+/HER2-)转移性乳腺癌(mBC)患者且对内分泌治疗耐药的治疗选择有限,仅限于化疗。本真实世界研究描述了在美国批准抗体药物偶联物之前,接受化疗治疗的患者的治疗模式和结局。
本回顾性观察性研究纳入了来自 ConcertAI Patient360™乳腺癌数据集的 HR+/HER2-mBC 成年患者,这些患者在 2011 年 1 月至 2021 年 6 月期间首次在转移性环境中接受化疗。描述了治疗模式;对所有符合条件的患者和接受后续化疗的患者评估了真实世界的总生存期、下一次治疗或死亡时间以及真实世界的无进展生存期。索引日期为每次化疗治疗的起始日期。
在 1545 名符合条件的患者中,76%为白人,12%的患者东部肿瘤协作组表现状态≥2,38%的患者为初诊 mBC,中位年龄为 61 岁(范围为 52-69 岁)。在索引期内,卡培他滨作为一线化疗药物的使用最多,而在后续治疗中则减少,而艾瑞布林的使用则在第一和第四次化疗之间增加。从首次化疗开始的中位(95%置信区间)真实世界总生存期为 23.3 个月(21.3-25.4 个月),下一次治疗或死亡的时间为 6.5 个月(5.9-7.1 个月),真实世界无进展生存期为 6.9 个月(6.4-7.6 个月);随着每次额外的化疗治疗,从中线时间从第二次、第三次和第四次化疗开始下降。
本真实世界研究表明,对于 HR+/HER2-mBC 患者,化疗提供的生存获益相对有限,且随着每次额外的化疗线增加而减少,这突显了需要改进治疗选择。