Ding Ping'an, Yang Peigang, Yang Li, Sun Chenyu, Chen Shuya, Li Min, Lowe Scott, Guo Honghai, Tian Yuan, Liu Yang, Zhao Qun
The Third Department of Surgery, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China.
Hebei Key Laboratory of Precision Diagnosis and Comprehensive Treatment of Gastric Cancer, Shijiazhuang, China.
Front Oncol. 2022 Sep 23;12:949511. doi: 10.3389/fonc.2022.949511. eCollection 2022.
The relationship between sarcopenia and clinical outcomes during conversion therapy in patients with lavage cytology positive gastric cancer (GC-CY) remains unclear. This study aimed to investigate the impact of sarcopenia and skeletal muscle loss on the efficacy of conversion therapy, tumour response and survival in GC-CY patients.
Retrospective analysis of data from a prospective trial of conversion therapy conducted between April 2018 and August 2019 in patients with GC-CY (NCT03718624). Skeletal muscle index (SMI) was measured at the level of the third lumbar (L3) vertebra and the sarcopenia was defined using published cut-off points in all patients. We defined ΔSMI (%)/50 days above 9.53% for men and ΔSMI (%)/50 days above 8.81% for women as significant muscle loss (SML) and analysed the changes in skeletal muscle during conversion therapy in relation to treatment efficacy, survival and tumour response.
Of the 36 patients, 7 patients (19.44%) developed sarcopenia before conversion therapy, 6 (16.67%) developed new sarcopenia after conversion therapy, and 8 (22.22%) developed SML during treatment. Multivariate analysis showed that sarcopenia before treatment [Odds Ratio (OR) =8.923, 95%CI: 1.341-25.321, p=0.002] and SML during treatment (OR=7.803, 95%CI: 1.106-16.189, p=0.001) had a negative impact on the success rate of conversion therapy. Cox multifactorial analysis found that pre-treatment sarcopenia [overall survival (OS): Hazard Ratio (HR) =6.341, 95%CI: 1.269-18.943, p=0.001; progression-free survival (PFS): HR=8.212, 95%CI: 1.569-36.582, p=0.001], newly developed sarcopenia after conversion therapy (OS: HR=3.189, 95%CI: 1.023-9.811, p=0.012; PFS: HR=3.084, 95%CI: 1.042-14.236, p=0.013) and the presence of SML during treatment (OS: HR=10.234, 95%CI: 2.532-54.231, p=0.002; PFS: HR=9.562, 95%CI: 2.341-38.092, p=0.002) were independent risk factor for OS and PFS in GC-CY patients.
Pre-treatment sarcopenia and the presence of SML during treatment are strongly correlated with the immediate and long-term outcomes of GC-CY patients and can be used as imaging markers to predict the treatment efficacy and prognosis of patients in clinical practice.
灌洗细胞学阳性胃癌(GC-CY)患者转化治疗期间肌肉减少症与临床结局之间的关系尚不清楚。本研究旨在探讨肌肉减少症和骨骼肌丢失对GC-CY患者转化治疗疗效、肿瘤反应和生存的影响。
回顾性分析2018年4月至2019年8月对GC-CY患者进行的转化治疗前瞻性试验的数据(NCT03718624)。在第三腰椎(L3)水平测量骨骼肌指数(SMI),并根据已发表的切点对所有患者定义肌肉减少症。我们将男性ΔSMI(%)/50天高于9.53%和女性ΔSMI(%)/50天高于8.81%定义为显著肌肉丢失(SML),并分析转化治疗期间骨骼肌变化与治疗疗效、生存和肿瘤反应的关系。
36例患者中,7例(19.44%)在转化治疗前出现肌肉减少症,6例(16.67%)在转化治疗后出现新的肌肉减少症,8例(22.22%)在治疗期间出现SML。多因素分析显示,治疗前肌肉减少症[比值比(OR)=8.923,95%置信区间:1.341-25.321,p=0.002]和治疗期间SML(OR=7.803,95%置信区间:1.106-16.189,p=)对转化治疗成功率有负面影响。Cox多因素分析发现,治疗前肌肉减少症[总生存期(OS):风险比(HR)=6.341,95%置信区间:1.269-18.943,p=0.001;无进展生存期(PFS):HR=8.212,95%置信区间:1.569-36.582,p=0.001]、转化治疗后新出现的肌肉减少症(OS:HR=3.189,95%置信区间:1.023-9.811,p=0.012;PFS:HR=3.084,95%置信区间:1.042-14.236,p=0.013)以及治疗期间存在SML(OS:HR=10.234,95%置信区间:2.532-54.231,p=0.002;PFS:HR=9.562,95%置信区间:2.341-38.092,p=0.002)是GC-CY患者OS和PFS的独立危险因素。
治疗前肌肉减少症和治疗期间SML的存在与GC-CY患者的近期和长期结局密切相关,可作为影像学标志物在临床实践中预测患者的治疗疗效和预后。