Department of Hepato-Biliary-Pancreatic Medicine, Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Jpn J Clin Oncol. 2021 Apr 1;51(4):604-611. doi: 10.1093/jjco/hyaa247.
Although the efficacy of neoadjuvant chemotherapy with gemcitabine plus S-1 (NAC GS) has recently been reported in resectable pancreatic cancer, severe adverse events were frequently observed. Sarcopenia has been reported to be associated with reduced antitumor response and chemotherapy toxicity in several malignancies. The aim of this study is to evaluate the impact of body composition on short-term outcomes of NAC GS in resectable pancreatic cancer patients.
Clinicopathological data of consecutive patients treated with NAC GS at our institution from February 2019 to April 2020 were retrospectively reviewed. Anthropometric variables were calculated at the third lumbar vertebra using pretreatment computed tomography images. We investigated the association between body composition variables, and antitumor response and chemotherapy toxicity.
Among 62 patients included in this study, 25 patients (40%) were sarcopenic at diagnosis. Sixty-one patients received surgery at our institution and 57 patients received pancreatic resection (R0/R1 resection 56/1). Fifty-six patients completed two cycles of NAC GS and severe adverse events (≥grade 3) occurred in 42 patients (hematologic toxicity 41 patients [66%]; non-hematologic toxicity 3 patients). Body mass index and total adipose tissue index were significantly lower in sarcopenic patients compared to non-sarcopenic patients. Completion rate of NAC, rate of treatment delay/interruption, relative dose intensity of gemcitabine and S-1, radiological and pathological tumor response after NAC were not different between sarcopenic and non-sarcopenic patients. Furthermore, there was no significant association between body composition, and severe adverse events and intolerance.
In our experience, NAC GS was similarly tolerable and effective in resectable pancreatic cancer patients regardless of the presence of sarcopenia.
虽然吉西他滨加 S-1(NAC GS)新辅助化疗在可切除胰腺癌中的疗效最近已有报道,但严重不良事件经常发生。在几种恶性肿瘤中,肌肉减少症与抗肿瘤反应降低和化疗毒性相关。本研究旨在评估体成分对可切除胰腺癌患者 NAC GS 短期结局的影响。
回顾性分析 2019 年 2 月至 2020 年 4 月在我院接受 NAC GS 治疗的连续患者的临床病理资料。在治疗前的 CT 图像上,在第三腰椎处计算人体测量变量。我们研究了体成分变量与抗肿瘤反应和化疗毒性之间的关系。
本研究共纳入 62 例患者,其中 25 例(40%)在诊断时为肌肉减少症。61 例患者在我院接受手术,57 例患者接受胰腺切除术(R0/R1 切除 56/1)。56 例患者完成了两个周期的 NAC GS,42 例患者发生严重不良事件(≥3 级)(血液学毒性 41 例[66%];非血液学毒性 3 例)。与非肌肉减少症患者相比,肌肉减少症患者的 BMI 和总脂肪组织指数显著降低。NAC 完成率、治疗延迟/中断率、吉西他滨和 S-1 的相对剂量强度、NAC 后影像学和病理学肿瘤反应在肌肉减少症和非肌肉减少症患者之间无差异。此外,体成分与严重不良事件和不耐受之间也无显著相关性。
根据我们的经验,NAC GS 在可切除胰腺癌患者中耐受性和疗效相似,无论是否存在肌肉减少症。