Alternative lengthening of telomeres (ALT) influences survival in soft tissue sarcomas: a systematic review with meta-analysis

Lawlor, Rita T. and Veronese, Nicola and Pea, Antonio and Nottegar, Alessia and Smith, Lee and Pilati, Camilla and Demurtas, Jacopo and Fassan, Matteo and Cheng, Liang and Luchini, Claudio (2019) Alternative lengthening of telomeres (ALT) influences survival in soft tissue sarcomas: a systematic review with meta-analysis. BMC Cancer, 19. p. 232. ISSN 1471-2407

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Official URL: https://doi.org/10.1186/s12885-019-5424-8

Abstract

Background. Alternative lengthening of telomeres (ALT) is a telomerase-independent mechanism used by a broad range of neoplasms to maintain telomere length, permitting uncontrolled replication during their progression. ALT has been described in different types of sarcoma, but a comprehensive analysis of its clinical significance is still lacking. Therefore, we provide here the first meta-analysis on this topic. Methods. We searched SCOPUS and PubMed through July 2018 to identify all studies that investigated the prognostic role of ALT in sarcomas. We considered the risk of death (risk ratio, RR) calculated as the number of death vs. total participants during follow-up in ALT+ versus ALTpatients as the primary outcome. The secondary outcome was the hazard ratio (HR), adjusted for the maximum number of covariates available, using ALT- patients as reference. Results. Eight articles comprising a total of 551 patients with sarcomas (226 ALT+ and 325 ALT-) were selected. The ALT+ group showed a higher mitotic count and a higher tumor grade compared with the ALT- group (p<0.01). Furthermore, we demonstrate a strong impact of ALT on survival. In fact, ALT+ patients showed a statistically significant higher risk of death than ALTpatients, when also considering data from multivariate analyses (RR = 1.50; 95% CI: 1.15–1.96; p =0.003; HR = 2.02; 95% CI: 1.22–3.38; p = 0.007). Conclusions. Our results indicate that ALT is associated with an increased risk of death in patients with sarcoma. In these neoplasms, ALT should be taken into account for a precise prognostic stratification and design of potential therapeutic strategies.

Item Type: Journal Article
Keywords: ALT, Sarcoma, Survival, Mesenchymal, Prognosis, ATR, ATRX
Faculty: Faculty of Science & Engineering
Depositing User: Lee Smith
Date Deposited: 01 Mar 2019 14:57
Last Modified: 04 Dec 2019 12:10
URI: http://arro.anglia.ac.uk/id/eprint/704143

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