Siringo Marco, Gentile Gabriella, Caponnetto Salvatore, Sperduti Isabella, Santini Daniele, Cortesi Enrico, Gelibter Alain Jonathan
Medical Oncology Unit B, Department of Radiology, Oncology and Pathology, Policlinico Umberto I, Sapienza University of Rome, 00161 Rome, Italy.
Medical Oncology Department, Hospital Universitario 12 de Octubre, Instituto de Investigación i+12, 28041 Madrid, Spain.
Cancers (Basel). 2023 Jun 30;15(13):3422. doi: 10.3390/cancers15133422.
No evidence exists as to whether body mass index (BMI) impairs clinical outcomes from ALK inhibitors (ALKi) in patients with ALK-rearranged non-small cell lung cancer (NSCLC). Retrospective data of patients affected by metastatic ALK-rearranged NSCLC treated with ALKi were collected. We divided patients into "low- BMI" (≤25 kg/m) and "high- BMI" (>25 kg/m) categories and correlated them with overall survival (OS) and progression-free survival (PFS). We included 40 patients treated with ALKi. We observed a 3-year OS of 81.5% in high-BMI vs. 49.6% in low-BMI categories ( = 0.049); the 3-year first-line PFS was superior in high-BMI vs. low-BMI patients (47% vs. 19%, = 0.019). As expected, patients treated with Alectinib had a 55.6% 3-year PFS vs. 7.1% for others treated with ALKi ( = 0.025). High-BMI was associated with a 100% 3-year PFS rate vs. 25.4% in low-BMI Alectinib patients ( = 0.03). BMI was independently correlated with first-line PFS and OS at multivariate analysis with PS (HR 0.39, CI 95% 0.16-0.96, = 0.042; HR 0.18, CI 95% 0.05-0.61, = 0.006). High-BMI was associated with higher efficacy in ALK-rearranged patients. These results are particularly exciting for Alectinib and could be correlated to mechanisms that should be investigated in subsequent prospective studies.
关于体重指数(BMI)是否会影响间变性淋巴瘤激酶抑制剂(ALKi)治疗间变性淋巴瘤激酶(ALK)重排的非小细胞肺癌(NSCLC)患者的临床结局,目前尚无证据。收集了接受ALKi治疗的转移性ALK重排NSCLC患者的回顾性数据。我们将患者分为“低BMI”(≤25kg/m²)和“高BMI”(>25kg/m²)两类,并将其与总生存期(OS)和无进展生存期(PFS)进行关联分析。我们纳入了40例接受ALKi治疗的患者。我们观察到高BMI组的3年总生存率为81.5%,而低BMI组为49.6%(P = 0.049);高BMI组的3年一线无进展生存率高于低BMI组患者(47%对19%,P = 0.019)。正如预期的那样,接受阿来替尼治疗的患者3年无进展生存率为55.6%,而接受其他ALKi治疗的患者为7.1%(P = 0.025)。高BMI与阿来替尼治疗的患者3年无进展生存率100%相关,而低BMI患者为25.4%(P = 0.03)。在多变量分析中,BMI与一线无进展生存期和总生存期独立相关,校正了体能状态(PS)(风险比[HR]0.39,95%置信区间[CI]0.16 - 0.96,P = 0.042;HR 0.18,95%CI 0.05 - 0.61,P = 0.006)。高BMI与ALK重排患者的更高疗效相关。这些结果对阿来替尼来说尤其令人兴奋,并且可能与后续前瞻性研究中应研究的机制相关。