Nieder Carsten, Stanisavljevic Luka, Dalhaug Astrid, Haukland Ellinor Christin
Department of Oncology and Palliative Medicine, Nordland Hospital, Bodø, Norway.
Department of Clinical Medicine, Faculty of Health Sciences, University of Tromsø, Tromsø, Norway.
Cancer Diagn Progn. 2025 Mar 3;5(2):138-145. doi: 10.21873/cdp.10423. eCollection 2025 Mar-Apr.
BACKGROUND/AIM: Several recent studies, varying in design and the number of baseline parameters analyzed, suggest that a lower body mass index (BMI) is associated with shorter survival in men beginning treatment for metastatic castration-resistant prostate cancer (MCRPC), including treatments such as docetaxel. This study aimed to analyze the impact of BMI and numerous covariates on survival in a homogeneously treated cohort of Caucasian men who received first-line docetaxel for MCRPC.
This retrospective analysis included 112 consecutive patients managed between 2009 and 2023. Comorbidity, medications, and blood tests were included. Both, uni- and multivariate tests were performed.
The median age of the patients was 70 years with a median BMI of 26.8 kg/m. Most patients were free from serious comorbidities, had bone-only metastases, and experienced metachronous development of metastases. Hemoglobin values were significantly lower in patients with lower BMI (median 11.9 13.0 g/dl, =0.001). Lean patients had numerically shorter survival compared to overweight/obese patients (median 11.8 19.4 months, =0.15). In multivariate analysis of prognostic factors, only three baseline parameters retained statistical significance: serum lactate dehydrogenase (=0.03), hemoglobin (=0.007), and the presence of non-bone metastases (=0.004).
An interaction between BMI and hemoglobin was present in metastatic castration-resistant prostate cancer patients after docetaxel chemotherapy, explaining the observed survival difference between lean and overweight/obese patients. Comorbidities and medications had no significant impact on survival in this population with limited prognosis (median survival 16.1 months).
背景/目的:最近的几项研究,在设计和分析的基线参数数量上有所不同,表明较低的体重指数(BMI)与开始接受转移性去势抵抗性前列腺癌(MCRPC)治疗的男性患者生存期较短有关,包括多西他赛等治疗。本研究旨在分析BMI和众多协变量对接受一线多西他赛治疗MCRPC的同质白种人男性队列生存期的影响。
这项回顾性分析纳入了2009年至2023年间连续管理的112例患者。纳入了合并症、用药情况和血液检查结果。进行了单变量和多变量检验。
患者的中位年龄为70岁,中位BMI为26.8kg/m²。大多数患者没有严重合并症,仅有骨转移,且转移灶为异时性发生。BMI较低的患者血红蛋白值显著较低(中位数为11.9对13.0g/dl,P=0.001)。与超重/肥胖患者相比,消瘦患者的生存期在数值上较短(中位数为11.8对19.4个月,P=0.15)。在预后因素的多变量分析中,只有三个基线参数具有统计学意义:血清乳酸脱氢酶(P=0.03)、血红蛋白(P=0.007)和非骨转移的存在(P=0.004)。
多西他赛化疗后的转移性去势抵抗性前列腺癌患者中,BMI与血红蛋白之间存在相互作用,这解释了消瘦患者与超重/肥胖患者之间观察到的生存期差异。合并症和用药对这个预后有限(中位生存期16.1个月)的人群的生存期没有显著影响。