Department of Supportive Care, Institut Gustave Roussy, Villejuif, France.
Department of Oncology, University of Alberta, Edmonton, Canada.
Ann Oncol. 2010 Aug;21(8):1594-1598. doi: 10.1093/annonc/mdp605. Epub 2010 Jan 20.
Patients with severe depletion of skeletal muscle (sarcopenia) are prone to dose-limiting toxicity (DLT) during fluoropyrimidine therapy. We hypothesized that sarcopenia may also predict toxicity of targeted therapy drugs.
Metastatic renal cell cancer (RCC) patients (n = 55) received sorafenib 400 mg b.i.d. Weight, height and skeletal muscle cross-sectional area at the third lumbar vertebra were measured by computed tomography (CT). Toxicity was assessed.
DLT occurred in 22% of patients overall, of which three-quarters were dose reductions to 400 mg and the remainder entailed termination of treatment. DLT was most common (41%) in sarcopenic patients whose body mass index (BMI) was <25 kg/m(2) and least common (13%) in patients who were not sarcopenic and/or overweight or obese (P = 0.03). Toxicity was especially prevalent in sarcopenic male patients with BMI < 25, with 71% of men with these characteristics being unable to continue treatment at 800 mg/day. By contrast, only 5% of male patients whose muscle index was above the cut-off for sarcopenia and only 11% of male patients whose BMI was >25 experienced a DLT.
BMI < 25 kg/m(2) with diminished muscle mass is a significant predictor of toxicity in metastatic RCC patients treated with sorafenib.
严重消耗骨骼肌(肌少症)的患者在氟嘧啶治疗期间易发生剂量限制毒性(DLT)。我们假设肌少症也可能预测靶向治疗药物的毒性。
转移性肾细胞癌(RCC)患者(n = 55)接受索拉非尼 400 mg,每日两次。通过计算机断层扫描(CT)测量体重、身高和第三腰椎的骨骼肌横截面积。评估毒性。
总体而言,22%的患者发生 DLT,其中四分之三是将剂量减少至 400 mg,其余则需要停止治疗。在 BMI < 25 kg/m2 的肌少症患者中 DLT 最为常见(41%),而在非肌少症和/或超重或肥胖的患者中则最少见(13%)(P = 0.03)。在 BMI < 25 的肌少症男性患者中,毒性尤其常见,有 71%的男性患者无法继续以 800 mg/天的剂量治疗。相比之下,仅有 5%的男性患者的肌肉指数超过肌少症的截止值,仅有 11%的 BMI > 25 的男性患者发生 DLT。
BMI < 25 kg/m2 且肌肉量减少是接受索拉非尼治疗的转移性 RCC 患者发生毒性的重要预测因素。