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ISS-Ⅲ期伴1q扩增或17p缺失双重打击初诊多发性骨髓瘤患者的预后分析

OBJECTIVE: To evaluate the prognostic significance of combining ISS-Ⅲ and high risk cytogenetic abnormalities [HRCAs, including 1q gain/amplification and del (17p) ] in patients with newly-diagnosed multiple myeloma (NDMM) . METHODS: The clinical characteristics and relevant variables were retrospec...

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Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342365/
https://www.ncbi.nlm.nih.gov/pubmed/31856439
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.11.005
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description OBJECTIVE: To evaluate the prognostic significance of combining ISS-Ⅲ and high risk cytogenetic abnormalities [HRCAs, including 1q gain/amplification and del (17p) ] in patients with newly-diagnosed multiple myeloma (NDMM) . METHODS: The clinical characteristics and relevant variables were retrospectively analyzed in a total of 270 NDMM patients diagnosed between November 2009 and May 2018. ISS-Ⅲ stage and HRCAs [detected by FISH, including 1q gain/amplification and del (17p) ] were defined as risk factors (hit) . Based to the number of hit per case, these patients were divided into four groups carrying 0 to 3 risk factors, respectively. Progress-free survival (PFS) and overall survival (OS) were then analyzed using the Kaplan-Meier estimator. RESULTS: Patients who carried single hit (n=120, 44.4%) had shorter median PFS (23.0 vs 28.9 months; P>0.05) and OS (42.3 vs 53.7 months; P>0.05) than those with no risk factors (n=66, 24.4%) . Of note, the outcome of patients who had two or more risk factors (double/triple, n=84, 31.1%) was much worse than those with either no or one risk factor, indicated by significantly reduced median PFS (14.5 months; HR=1.584, 95%CI 1.082-2.319;P=0.003 for double/triple vs single hit) and OS (18.4 months, HR=2.299, 95%CI 1.485-3.560; P<0.001 for double/triple vs single hit) . Strikingly, patients who had three risk factor (triple hit, n=5, 1.9%) displayed the poorest survival with extraordinarily shorter PFS (0.9-15.1 months) and OS (0.9-18.9 months) compared to those carrying two risk factors (double hit) . Analogous results were obtained when different combinations of ISS stages and HRCAs were analyzed. CONCLUSION: These results suggest a potential but rather important role of combining multiple (e.g. double or triple) adverse factors determined via the routine ISS staging and FISH detection of cytogenetic abnormalities in risk stratification and prognostic prediction, which might be helpful to identify high risk patients more precisely at diagnosis. It also raised a possibility that a small group of ISS-Ⅲ patients carrying both 1q gain/amplification and del (17p) might represent an “extremely-high risk” subset of MM.
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spelling pubmed-73423652020-07-16 ISS-Ⅲ期伴1q扩增或17p缺失双重打击初诊多发性骨髓瘤患者的预后分析 Zhonghua Xue Ye Xue Za Zhi 论著 OBJECTIVE: To evaluate the prognostic significance of combining ISS-Ⅲ and high risk cytogenetic abnormalities [HRCAs, including 1q gain/amplification and del (17p) ] in patients with newly-diagnosed multiple myeloma (NDMM) . METHODS: The clinical characteristics and relevant variables were retrospectively analyzed in a total of 270 NDMM patients diagnosed between November 2009 and May 2018. ISS-Ⅲ stage and HRCAs [detected by FISH, including 1q gain/amplification and del (17p) ] were defined as risk factors (hit) . Based to the number of hit per case, these patients were divided into four groups carrying 0 to 3 risk factors, respectively. Progress-free survival (PFS) and overall survival (OS) were then analyzed using the Kaplan-Meier estimator. RESULTS: Patients who carried single hit (n=120, 44.4%) had shorter median PFS (23.0 vs 28.9 months; P>0.05) and OS (42.3 vs 53.7 months; P>0.05) than those with no risk factors (n=66, 24.4%) . Of note, the outcome of patients who had two or more risk factors (double/triple, n=84, 31.1%) was much worse than those with either no or one risk factor, indicated by significantly reduced median PFS (14.5 months; HR=1.584, 95%CI 1.082-2.319;P=0.003 for double/triple vs single hit) and OS (18.4 months, HR=2.299, 95%CI 1.485-3.560; P<0.001 for double/triple vs single hit) . Strikingly, patients who had three risk factor (triple hit, n=5, 1.9%) displayed the poorest survival with extraordinarily shorter PFS (0.9-15.1 months) and OS (0.9-18.9 months) compared to those carrying two risk factors (double hit) . Analogous results were obtained when different combinations of ISS stages and HRCAs were analyzed. CONCLUSION: These results suggest a potential but rather important role of combining multiple (e.g. double or triple) adverse factors determined via the routine ISS staging and FISH detection of cytogenetic abnormalities in risk stratification and prognostic prediction, which might be helpful to identify high risk patients more precisely at diagnosis. It also raised a possibility that a small group of ISS-Ⅲ patients carrying both 1q gain/amplification and del (17p) might represent an “extremely-high risk” subset of MM. Editorial office of Chinese Journal of Hematology 2019-11 /pmc/articles/PMC7342365/ /pubmed/31856439 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.11.005 Text en 2019年版权归中华医学会所有 http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution 3.0 License (CC-BY-NC). The Copyright own by Publisher. Without authorization, shall not reprint, except this publication article, shall not use this publication format design. Unless otherwise stated, all articles published in this journal do not represent the views of the Chinese Medical Association or the editorial board of this journal.
spellingShingle 论著
ISS-Ⅲ期伴1q扩增或17p缺失双重打击初诊多发性骨髓瘤患者的预后分析
title ISS-Ⅲ期伴1q扩增或17p缺失双重打击初诊多发性骨髓瘤患者的预后分析
title_full ISS-Ⅲ期伴1q扩增或17p缺失双重打击初诊多发性骨髓瘤患者的预后分析
title_fullStr ISS-Ⅲ期伴1q扩增或17p缺失双重打击初诊多发性骨髓瘤患者的预后分析
title_full_unstemmed ISS-Ⅲ期伴1q扩增或17p缺失双重打击初诊多发性骨髓瘤患者的预后分析
title_short ISS-Ⅲ期伴1q扩增或17p缺失双重打击初诊多发性骨髓瘤患者的预后分析
title_sort iss-ⅲ期伴1q扩增或17p缺失双重打击初诊多发性骨髓瘤患者的预后分析
topic 论著
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342365/
https://www.ncbi.nlm.nih.gov/pubmed/31856439
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.11.005
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