Division of Hematology and Medical Oncology, Icahn School of Medicine at Mount Sinai, 1 Gustave L Levy Place, New York, NY, 10029-6574, USA.
Sema4, Stamford, CT, USA.
Breast Cancer Res Treat. 2022 Apr;192(2):313-319. doi: 10.1007/s10549-021-06504-0. Epub 2022 Jan 10.
Higher levels of estrogen in obese patients may lead to incomplete inhibition by aromatase inhibitors (AIs). The aim of this study was to determine the impact of body mass index (BMI) on efficacy of AIs in patients with metastatic hormone receptor (HR)-positive breast cancer (BC).
We performed a retrospective chart review of all female patients with metastatic HR-positive BC on an AI in first- or second-line settings and seen at our academic institution between 2001 and 2020. The primary endpoint was progression-free survival (PFS), defined as the time from start of AI to disease progression or death from any cause.
We identified 219 patients who had received an AI in the first- or second-line settings for metastatic HR-positive BC and with documented information on BMI. Of the 219 patients, 56% (123) had a low BMI (defined as < 27 kg/m) and 44% (96) had a high BMI (≥ 27 kg/m). The median PFS was 21.9 months (95% CI 14.5 to 28.4) in the low BMI group versus 20.2 months (95% CI 14.3 to 27.5) in the high BMI group (p = 0.73).
While BMI influences efficacy of AIs in the adjuvant setting, our results suggest that in the metastatic setting, BMI may not impact the efficacy of AIs. This discrepancy could be due to other differences in disease characteristics that make complete aromatase inhibition more important in the adjuvant setting when disease burden is the lowest.
肥胖患者体内的雌激素水平较高,可能导致芳香化酶抑制剂(AIs)的抑制作用不完全。本研究旨在确定体重指数(BMI)对转移性激素受体(HR)阳性乳腺癌(BC)患者接受 AI 治疗效果的影响。
我们对 2001 年至 2020 年在我院接受 AI 一线或二线治疗的转移性 HR 阳性 BC 女性患者进行了回顾性病历审查。主要终点为无进展生存期(PFS),定义为从开始接受 AI 治疗到疾病进展或任何原因死亡的时间。
我们确定了 219 例在一线或二线接受 AI 治疗的转移性 HR 阳性 BC 患者,这些患者的 BMI 信息有记录。在 219 例患者中,56%(123 例)的 BMI 较低(定义为<27kg/m),44%(96 例)的 BMI 较高(≥27kg/m)。低 BMI 组的中位 PFS 为 21.9 个月(95%CI 14.5 至 28.4),高 BMI 组为 20.2 个月(95%CI 14.3 至 27.5)(p=0.73)。
虽然 BMI 影响辅助治疗中 AI 的疗效,但我们的结果表明,在转移性疾病环境下,BMI 可能不会影响 AI 的疗效。这种差异可能是由于疾病特征的其他差异所致,在疾病负担最低的辅助治疗中,完全抑制芳香化酶可能更为重要。