Article Text
Abstract
Background Cancer cachexia is a complex metabolic syndrome characterised by a loss of muscle with or without loss of fat mass, and is associated with high morbidity and mortality. Despite its clinical importance, there is a lack of simple tools to screen patients for cancer cachexia. The aim of this study was to evaluate and validate the patient-generated subjective global assessment (PG-SGA) as a screening tool for cancer cachexia.
Methods This is a secondary analysis of a multicentre, cross-sectional, observational study. Cancer cachexia was diagnosed when there was weight loss ≥5% during the past 12 months and at least three of the five following conditions were present: decreased muscle strength, fatigue, anorexia, low Fat-Free Mass Index (FFMI) and abnormal laboratory findings. A quadratic discriminant analysis was conducted for the ability of PG-SGA to predict cachexia.
Results A total of 4231 patients with cancer were included in this analysis, and 351 patients (8.3%) were diagnosed as having cachexia. The highest incidence of cachexia was found among patients with pancreatic cancer (32.5%), oesophageal cancer (21.5%) and gastric cancer (17.9%). Compared with patients without cachexia, patients with cachexia had a lower body mass index, FFMI, hand grip strength, total protein, prealbumin, albumin, haemoglobin and Karnofsky performance status (p<0.05), while they had a higher C reactive protein level and PG-SGA Score (4.71±3.71 vs 10.87±4.84, p<0.05). The best cut-off value for PG-SGA was 6.5, with 79.8% of sensitivity and 72.3% specificity for cachexia, and the area under the receiver operating characteristic curve was 0.846 (95% CI 0.826 to 0.866, p<0.001).
Conclusions PG-SGA is a highly specific tool that can be used to screen patients for cancer cachexia.
Data availability statement
Data may be obtained from a third party and are not publicly available. The processed data required to reproduce these findings cannot be shared at this time as the data also form part of an ongoing study.
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Data availability statement
Data may be obtained from a third party and are not publicly available. The processed data required to reproduce these findings cannot be shared at this time as the data also form part of an ongoing study.
Footnotes
MC, CS and HX contributed equally.
Collaborators Ming-Hua Cong1, Chen-Xin Song1, Hong-Xia Xu2, Chun-Hua Song3, Chang Wang4, Zhen-Ming Fu5, Yi Ba6, Jing Wu7, Cong-Hua Xie8, Gong-Yan Chen9, Zi-Hua Chen10, Lan Zhou11, Tao Li12, Li Deng3, Xin Lin2, Liu-Qing Yang13, Jiu-Wei Cui4, Han-Ping Shi13; The Investigation on Nutrition Status and Clinical Outcome of Common Cancers (INSCOC) Group
Contributors All authors made contributions to data acquisition and interpretation. HS designed the INSCOC Study. HS and JC were involved in the development of study concept. MC, CXS, HX and CHS were major contributors in the data analysis, and MC drafted the manuscript. CS and HX revised the manuscript critically for important intellectual content. Authors MC, CXS, HX, CHS, CW, ZF, YB, JW, CX, GC, ZC, LZ, TL, LD, LX, LY, JC and HS read and approved the final manuscript.
Funding The present study was supported by grants from the National Key Research and Development Programme of China (No: 2017YFC1309200).
Competing interests None declared.
Provenance and peer review Not commissioned; externally peer reviewed.