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182例初诊伴高危细胞遗传学异常多发性骨髓瘤患者的预后分析

OBJECTIVE: To evaluate the clinical characteristics and prognosis of high risk cytogenetic abnormalities (HRCA) and various combinations of cytogenetic abnormality in patients with newly-diagnosed multiple myeloma (NDMM). METHODS: This retrospective study collected 182 NDMM patients in the First Aff...

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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/PMC7342866/
https://www.ncbi.nlm.nih.gov/pubmed/31495130
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.08.004
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collection PubMed
description OBJECTIVE: To evaluate the clinical characteristics and prognosis of high risk cytogenetic abnormalities (HRCA) and various combinations of cytogenetic abnormality in patients with newly-diagnosed multiple myeloma (NDMM). METHODS: This retrospective study collected 182 NDMM patients in the First Affiliated Hospital of Jilin University between Nov. 2009 and May 2018. HRCA included 1q+, del (17p), t(4;14), and t(14;16) detected by FISH, and non-HRCA included del (13q), t(11;14) detected by FISH. The clinical characteristics among three groups, including cases who carrying a single HRCA, 1 HRCA in combination with non-HRCA and cases carrying two or more HRCAs (double/triple-hit) were observed. Kaplan-Meier curve was used to analyze both progression-free survival (PFS) and overall survival (OS) for the three groups. RESULTS: The survivals of patients with 1 HRCA in combination with non-HRCA were similar to those with two or more HRCAs (double/triple-hit), the median PFS (mPFS) was 19.1 m vs 12.1 m (P=0.248) and median OS (mOS) was 29.6 m vs 29.3 m (P=0.774). Furthermore, the prognosis of these two groups were both inferior to patients with a single HRCA, respectively. (mPFS: 32.2 m, P=0.040, P=0.001; mOS: 42.3 m, P=0.021, P=0.041). Strikingly, both the mPFS and the mOS of patients with 1 HRCA in combination with non-HRCA (regardless of high risk or not) were significantly shorter than that of cases with a single HRCA (mPFS: 15.1 m vs 32.2 m, HR=2.126, 95%CI 1.176–3.843, P=0.005; mOS: 29.3 m vs 42.3 m, HR=1.442, 95%CI 0.705–2.950, P=0.011). CONCLUSION: It is of prognostic significance value for detecting double/triple-hit based on FISH cytogenetics in NDMM.
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spelling pubmed-73428662020-07-16 182例初诊伴高危细胞遗传学异常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 clinical characteristics and prognosis of high risk cytogenetic abnormalities (HRCA) and various combinations of cytogenetic abnormality in patients with newly-diagnosed multiple myeloma (NDMM). METHODS: This retrospective study collected 182 NDMM patients in the First Affiliated Hospital of Jilin University between Nov. 2009 and May 2018. HRCA included 1q+, del (17p), t(4;14), and t(14;16) detected by FISH, and non-HRCA included del (13q), t(11;14) detected by FISH. The clinical characteristics among three groups, including cases who carrying a single HRCA, 1 HRCA in combination with non-HRCA and cases carrying two or more HRCAs (double/triple-hit) were observed. Kaplan-Meier curve was used to analyze both progression-free survival (PFS) and overall survival (OS) for the three groups. RESULTS: The survivals of patients with 1 HRCA in combination with non-HRCA were similar to those with two or more HRCAs (double/triple-hit), the median PFS (mPFS) was 19.1 m vs 12.1 m (P=0.248) and median OS (mOS) was 29.6 m vs 29.3 m (P=0.774). Furthermore, the prognosis of these two groups were both inferior to patients with a single HRCA, respectively. (mPFS: 32.2 m, P=0.040, P=0.001; mOS: 42.3 m, P=0.021, P=0.041). Strikingly, both the mPFS and the mOS of patients with 1 HRCA in combination with non-HRCA (regardless of high risk or not) were significantly shorter than that of cases with a single HRCA (mPFS: 15.1 m vs 32.2 m, HR=2.126, 95%CI 1.176–3.843, P=0.005; mOS: 29.3 m vs 42.3 m, HR=1.442, 95%CI 0.705–2.950, P=0.011). CONCLUSION: It is of prognostic significance value for detecting double/triple-hit based on FISH cytogenetics in NDMM. Editorial office of Chinese Journal of Hematology 2019-08 /pmc/articles/PMC7342866/ /pubmed/31495130 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.08.004 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
182例初诊伴高危细胞遗传学异常多发性骨髓瘤患者的预后分析
title 182例初诊伴高危细胞遗传学异常多发性骨髓瘤患者的预后分析
title_full 182例初诊伴高危细胞遗传学异常多发性骨髓瘤患者的预后分析
title_fullStr 182例初诊伴高危细胞遗传学异常多发性骨髓瘤患者的预后分析
title_full_unstemmed 182例初诊伴高危细胞遗传学异常多发性骨髓瘤患者的预后分析
title_short 182例初诊伴高危细胞遗传学异常多发性骨髓瘤患者的预后分析
title_sort 182例初诊伴高危细胞遗传学异常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/PMC7342866/
https://www.ncbi.nlm.nih.gov/pubmed/31495130
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.08.004
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