Cuyún Carter Gebra, Mohanty Maitreyee, Stenger Keri, Morato Guimaraes Claudia, Singuru Shivaprasad, Basa Pradeep, Singh Sheena, Tongbram Vanita, Kuemmel Sherko, Guarneri Valentina, Tolaney Sara M
Eli Lilly and Company, Indianapolis, IN, USA.
Global Health Economics and Outcomes Research, ICON Plc, New York, NY, USA.
Cancer Manag Res. 2021 Aug 20;13:6537-6566. doi: 10.2147/CMAR.S300869. eCollection 2021.
Advanced breast cancer is a heterogeneous disease with several well-defined subtypes, among which, hormone receptor-positive/human epidermal growth factor receptor 2-negative (HR+/HER2-) is most prevalent. Determination of HR and HER2 status influences prognosis and, thus, disease management. Although literature on these prognostic factors exist, especially in the early breast cancer setting, it remains unclear to what extent these factors can guide clinical decision-making in the advanced disease setting. Therefore, we sought to identify the strength and consistency of evidence for prognostic factors in patients with HR+/HER2- advanced breast cancer.
A systematic literature review (SLR) of the major electronic databases was conducted in November 2018 for primary research studies published since 2010. Endpoints of interest were tumor response, progression-free survival (PFS), overall survival (OS), and breast cancer-specific survival (BCSS).
Seventy-nine studies were included wherein all patients were diagnosed with advanced breast cancer and ≥50% of the population were HR+/HER2-. OS was the most commonly assessed endpoint (n=67) followed by PFS (n=33), BCSS (n=5) and tumor response (n=3). The prognostic factors with strongest evidence of association with worse OS were negative progesterone receptor status, higher tumor grade, higher circulating tumor cell (CTC) count and higher Ki67 level, number of metastatic sites (eg multiple vs single) and sites of metastases (eg presence of liver metastases vs absence), shorter time to recurrence or progression to advanced breast cancer, poor performance status, prior therapy attributes in the early or metastatic setting (type of therapy, treatment line, response of prior therapy), and race (black vs white). The prognostic factors that had strongest evidence of association with PFS included CTC count, number and sites of metastases, and absence of prior therapy or higher lines of therapy in the early or metastatic setting. The directionality of association was consistent for all prognostic factors except between lymph node and OS, and metastatic breast cancer and PFS.
Multiple disease, treatment, and patient-related prognostic factors impact survival, particularly OS, in patients with HR+/HER2- advanced breast cancer. Treatment outcomes can vary considerably due to these factors. Understanding poorer prognostic factors for patients can result in improved clinical decision-making.
晚期乳腺癌是一种具有多种明确亚型的异质性疾病,其中激素受体阳性/人表皮生长因子受体2阴性(HR+/HER2-)最为常见。HR和HER2状态的确定会影响预后,进而影响疾病管理。尽管存在关于这些预后因素的文献,尤其是在早期乳腺癌方面,但在晚期疾病情况下这些因素能在多大程度上指导临床决策仍不清楚。因此,我们试图确定HR+/HER2-晚期乳腺癌患者预后因素证据的强度和一致性。
2018年11月对主要电子数据库进行了系统文献综述(SLR),以查找自2010年以来发表的原发性研究。感兴趣的终点指标为肿瘤反应、无进展生存期(PFS)、总生存期(OS)和乳腺癌特异性生存期(BCSS)。
纳入了79项研究,其中所有患者均被诊断为晚期乳腺癌,且≥50%的人群为HR+/HER2-。OS是最常评估的终点指标(n = 67),其次是PFS(n = 33)、BCSS(n = 5)和肿瘤反应(n = 3)。与较差OS关联证据最充分的预后因素为孕激素受体阴性状态、更高的肿瘤分级、更高的循环肿瘤细胞(CTC)计数和更高的Ki67水平、转移部位数量(如多发与单发)和转移部位(如存在肝转移与不存在)、复发或进展为晚期乳腺癌的时间较短、体能状态差、早期或转移阶段的既往治疗属性(治疗类型、治疗线数、既往治疗反应)以及种族(黑人与白人)。与PFS关联证据最充分的预后因素包括CTC计数、转移的数量和部位,以及早期或转移阶段无既往治疗或更高的治疗线数。除淋巴结与OS、转移性乳腺癌与PFS之间外,所有预后因素的关联方向均一致。
多种疾病、治疗及患者相关的预后因素会影响HR+/HER2-晚期乳腺癌患者的生存,尤其是OS。由于这些因素治疗结果可能有很大差异。了解患者较差的预后因素可改善临床决策。