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低骨骼肌量与血液系统恶性肿瘤成人患者的治疗结局:系统评价和荟萃分析。

Low skeletal muscle mass and treatment outcomes among adults with haematologic malignancies: A systematic review and meta-analysis.

机构信息

School of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.

Harvey Cushing/John Hay Whitney Medical Library, Yale University, New Haven, CT, USA.

出版信息

J Cachexia Sarcopenia Muscle. 2024 Jun;15(3):1084-1093. doi: 10.1002/jcsm.13446. Epub 2024 Apr 1.

Abstract

BACKGROUND

Low skeletal muscle mass (LSMM) and/or, function associated with an increased risk of treatment-related toxicities and inferior overall survival (OS) among adults with solid malignancies. However, the association between LSMM and treatment-related toxicities among adults with haematologic malignancies remains unclear.

METHODS

Using a pre-published protocol (CRD42020197814), we searched seven bibliographic databases from inception to 08/2021 for studies reporting the impact of LSMM among adults ≥18 years with a known haematologic malignancy. The primary outcome of interest was OS, and secondary outcomes included progression free survival (PFS) and non-relapse mortality (NRM). These effect sizes were quantified in terms of hazards ratio (HR) along with 95% confidence interval (CI) and pooled across studies using a DerSimonian-Laird random-effects model. Heterogeneity was assessed using the Cochran's Q and the I statistic. All hypothesis testing was two-sided with an alpha of 0.05.

RESULTS

Of 3791 studies screened, we identified 20 studies involving 3468 patients with a mean age of 60 years; 44% were female and the most common malignancy was diffuse large B-cell lymphoma (42%). Most studies measured muscle mass using single slice computed tomography imaging at the L3 level. The presence of LSMM was associated with worse OS (pooled HR = 1.81, 95% CI = 1.48-2.22, P < 0.001) with moderate heterogeneity (Cochran's Q, I = 60.4%), PFS (pooled HR = 1.61, 95% CI = 1.28-2.02, P < 0.001) with moderate heterogeneity (Cochran's Q, I = 66.0%). Similarly, LSMM was associated with worse NRM (HR = 1.72, 95% CI = 1.34-2.22, P < 0.001) with little evidence of heterogeneity (Cochran's Q, I = 0.0%).

CONCLUSIONS

LSMM is associated with worse survival outcomes among adults with haematologic malignancies. Further research into understanding the underlying mechanism of this association and mitigating the negative effects of LSMM among adults with haematologic malignancies is needed.

摘要

背景

低骨骼肌量(LSMM)和/或功能与患有实体恶性肿瘤的成年人的治疗相关毒性和总体生存(OS)降低相关。然而,LSMM 与血液恶性肿瘤成年人之间的治疗相关毒性之间的关联尚不清楚。

方法

使用预先发表的方案(CRD42020197814),我们从成立到 2021 年 8 月在七个文献数据库中搜索了报告已知血液恶性肿瘤的成年人中 LSMM 影响的研究。主要结局是 OS,次要结局包括无进展生存期(PFS)和非复发死亡率(NRM)。使用 DerSimonian-Laird 随机效应模型,使用风险比(HR)以及 95%置信区间(CI)对这些效应大小进行量化,并在研究中进行汇总。使用 Cochran's Q 和 I 统计量评估异质性。所有假设检验均为双侧检验,α 值为 0.05。

结果

在筛选的 3791 项研究中,我们确定了 20 项涉及 3468 名平均年龄为 60 岁的患者的研究;44%为女性,最常见的恶性肿瘤是弥漫性大 B 细胞淋巴瘤(42%)。大多数研究使用 L3 水平的单次切片计算机断层扫描成像来测量肌肉量。存在 LSMM 与较差的 OS(汇总 HR=1.81,95%CI=1.48-2.22,P<0.001)相关,存在中度异质性(Cochran's Q,I=60.4%),PFS(汇总 HR=1.61,95%CI=1.28-2.02,P<0.001)也存在中度异质性(Cochran's Q,I=66.0%)。同样,LSMM 与较差的 NRM(HR=1.72,95%CI=1.34-2.22,P<0.001)相关,异质性很小(Cochran's Q,I=0.0%)。

结论

LSMM 与血液恶性肿瘤成年人的生存结局较差相关。需要进一步研究以了解这种关联的潜在机制,并减轻血液恶性肿瘤成年人中 LSMM 的负面影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b160/11154774/2ec2486e2ac9/JCSM-15-1084-g003.jpg

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