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

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...

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Main Authors: Rita T. Lawlor, Nicola Veronese, Antonio Pea, Alessia Nottegar, Lee Smith, Camilla Pilati, Jacopo Demurtas, Matteo Fassan, Liang Cheng, Claudio Luchini
Format: Article
Language:English
Published: BMC 2019-03-01
Series:BMC Cancer
Subjects:
ALT
ATR
Online Access:http://link.springer.com/article/10.1186/s12885-019-5424-8
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spelling doaj-ea2c4117ae884f8582e4344556ef20702020-11-25T02:31:43ZengBMCBMC Cancer1471-24072019-03-011911710.1186/s12885-019-5424-8Alternative lengthening of telomeres (ALT) influences survival in soft tissue sarcomas: a systematic review with meta-analysisRita T. Lawlor0Nicola Veronese1Antonio Pea2Alessia Nottegar3Lee Smith4Camilla Pilati5Jacopo Demurtas6Matteo Fassan7Liang Cheng8Claudio Luchini9ARC-Net Research Center, University and Hospital Trust of VeronaNational Institute of Gastroenterology-Research Hospital, IRCCS “S. de Bellis”, Castellana GrotteDepartment of General and Pancreatic Surgery, The Pancreas Institute, University and Hospital Trust of VeronaDepartment of Surgery, Section of Pathology, San Bortolo HospitalCambridge Centre for Sport and Exercise Sciences, Anglia Ruskin UniversityPersonalized Medicine, Pharmacogenomics, Therapeutic Optimization, Université Paris DescartesPrimary Care Department, Azienda USL Toscana Sud EstARC-Net Research Center, University and Hospital Trust of VeronaDepartment of Pathology and Laboratory Medicine, Indiana University School of MedicineDepartment of Diagnostics and Public Health, Section of Pathology, University and Hospital Trust of VeronaAbstract 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 ALT- patients 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 ALT- patients, 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.http://link.springer.com/article/10.1186/s12885-019-5424-8ALTSarcomaMesenchymalPrognosisSurvivalATR
collection DOAJ
language English
format Article
sources DOAJ
author Rita T. Lawlor
Nicola Veronese
Antonio Pea
Alessia Nottegar
Lee Smith
Camilla Pilati
Jacopo Demurtas
Matteo Fassan
Liang Cheng
Claudio Luchini
spellingShingle Rita T. Lawlor
Nicola Veronese
Antonio Pea
Alessia Nottegar
Lee Smith
Camilla Pilati
Jacopo Demurtas
Matteo Fassan
Liang Cheng
Claudio Luchini
Alternative lengthening of telomeres (ALT) influences survival in soft tissue sarcomas: a systematic review with meta-analysis
BMC Cancer
ALT
Sarcoma
Mesenchymal
Prognosis
Survival
ATR
author_facet Rita T. Lawlor
Nicola Veronese
Antonio Pea
Alessia Nottegar
Lee Smith
Camilla Pilati
Jacopo Demurtas
Matteo Fassan
Liang Cheng
Claudio Luchini
author_sort Rita T. Lawlor
title Alternative lengthening of telomeres (ALT) influences survival in soft tissue sarcomas: a systematic review with meta-analysis
title_short Alternative lengthening of telomeres (ALT) influences survival in soft tissue sarcomas: a systematic review with meta-analysis
title_full Alternative lengthening of telomeres (ALT) influences survival in soft tissue sarcomas: a systematic review with meta-analysis
title_fullStr Alternative lengthening of telomeres (ALT) influences survival in soft tissue sarcomas: a systematic review with meta-analysis
title_full_unstemmed Alternative lengthening of telomeres (ALT) influences survival in soft tissue sarcomas: a systematic review with meta-analysis
title_sort alternative lengthening of telomeres (alt) influences survival in soft tissue sarcomas: a systematic review with meta-analysis
publisher BMC
series BMC Cancer
issn 1471-2407
publishDate 2019-03-01
description 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 ALT- patients 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 ALT- patients, 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.
topic ALT
Sarcoma
Mesenchymal
Prognosis
Survival
ATR
url http://link.springer.com/article/10.1186/s12885-019-5424-8
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