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肌肉减少症与晚期胃癌患者严重化疗毒性和生存的关联。

Association of sarcopenia with severe chemotherapy toxicities and survival in patients with advanced gastric cancer.

机构信息

Department of Clinical Oncology, School of Clinical Medicine, LKS Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong.

Department of Surgery, School of Clinical Medicine, LKS Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong.

出版信息

Oncologist. 2024 Oct 3;29(10):e1272-e1279. doi: 10.1093/oncolo/oyae123.

Abstract

BACKGROUND

Sarcopenia or skeletal muscle depletion is a poor prognostic factor for gastric cancer (GC). However, existing cutoff values of skeletal muscle index (SMI) for defining sarcopenia have been found to have limitations when clinically applied. This study aimed to determine the optimal cutoff for SMI to predict severe toxicities of chemotherapy and overall survival (OS) in patients with advanced GC.

METHODS

Patients with metastatic gastric adenocarcinoma who received first-line palliative chemotherapy between January 2014 and December 2021 at Queen Mary Hospital, Hong Kong, were included in this study. The SMI was determined via a pre-chemotherapy computed tomography scan. Optimal cutoff points of SMI were identified by recursive partitioning analysis. Univariate and multivariate analyses evaluating risk factors of severe chemotherapy toxicities and OS were also performed.

RESULTS

A total of 158 patients (male: 108 (68.4%), median age: 65.3) were included. The SMI cutoff to define low SMI was ≤33 cm2/m2 for males and ≤28 cm2/m2 for females; 30 patients (19.0%) had low SMI. Patients with low SMI had a higher incidence of hematological toxicities (63.3% vs 32.0%, P = .001) and non-hematological toxicities (66.7% vs 36.7%, P = .003). Multivariable analysis indicated that low SMI and low serum albumin (≤28 g/L) were independent predictive factors of hematological toxicity, while low SMI and neutrophil-lymphocyte ratio ≥5 were predictive factors of non-hematological toxicity. Moreover, patients with low SMI had a significantly shorter OS (P = .011), lower response rate to chemotherapy (P = .045), and lower utilization of subsequent lines of treatment (P < .001).

CONCLUSIONS

Using pre-chemotherapy SMI cutoff (≤33 cm2/m2 for males and 28 cm2/m2 for females) one can identify individuals with a higher risk of severe chemotherapy toxicities and worse prognosis.

摘要

背景

骨骼肌减少症或骨骼肌耗竭是胃癌(GC)不良预后的一个因素。然而,目前用于定义骨骼肌减少症的骨骼肌指数(SMI)的临界值在临床应用中存在局限性。本研究旨在确定 SMI 的最佳临界值,以预测晚期 GC 患者化疗的严重毒性和总生存(OS)。

方法

本研究纳入了 2014 年 1 月至 2021 年 12 月期间在香港玛丽医院接受一线姑息性化疗的转移性胃腺癌患者。通过化疗前 CT 扫描确定 SMI。采用递归分割分析确定 SMI 的最佳临界值。还进行了单变量和多变量分析,以评估严重化疗毒性和 OS 的危险因素。

结果

共纳入 158 例患者(男性 108 例[68.4%],中位年龄 65.3 岁)。男性 SMI 临界值为≤33 cm2/m2,女性 SMI 临界值为≤28 cm2/m2;30 例(19.0%)患者存在低 SMI。低 SMI 患者的血液学毒性(63.3%比 32.0%,P=0.001)和非血液学毒性(66.7%比 36.7%,P=0.003)发生率更高。多变量分析表明,低 SMI 和低血清白蛋白(≤28 g/L)是血液学毒性的独立预测因素,而低 SMI 和中性粒细胞-淋巴细胞比值≥5 是非血液学毒性的预测因素。此外,低 SMI 患者的 OS 明显更短(P=0.011),化疗反应率更低(P=0.045),后续治疗线的使用率也更低(P<0.001)。

结论

使用化疗前 SMI 临界值(男性≤33 cm2/m2,女性≤28 cm2/m2),可以识别出化疗严重毒性和预后不良风险较高的个体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca19/11449055/a65011bb08ac/oyae123_fig1.jpg

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