Cargando…

1q21 Gain Combined with High‐Risk Factors Is a Heterogeneous Prognostic Factor in Newly Diagnosed Multiple Myeloma: A Multicenter Study in China

BACKGROUND. The prognostic value of 1q21 gain in newly diagnosed multiple myeloma (NDMM) remains controversial. Our aim was to investigate the prognostic value of 1q21 gain in a Chinese population. MATERIALS AND METHODS. We retrospectively identified 565 patients with NDMM from multiple centers in C...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Xiaozhe, Chen, Wenming, Wu, Yin, Li, Jianyong, Chen, Lijuan, Fang, Baijun, Feng, Ying, Liu, Junru, Chen, Meilan, Gu, Jingli, Huang, Beihui, Li, Juan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6853115/
https://www.ncbi.nlm.nih.gov/pubmed/31455749
http://dx.doi.org/10.1634/theoncologist.2019-0132
_version_ 1783469982306271232
author Li, Xiaozhe
Chen, Wenming
Wu, Yin
Li, Jianyong
Chen, Lijuan
Fang, Baijun
Feng, Ying
Liu, Junru
Chen, Meilan
Gu, Jingli
Huang, Beihui
Li, Juan
author_facet Li, Xiaozhe
Chen, Wenming
Wu, Yin
Li, Jianyong
Chen, Lijuan
Fang, Baijun
Feng, Ying
Liu, Junru
Chen, Meilan
Gu, Jingli
Huang, Beihui
Li, Juan
author_sort Li, Xiaozhe
collection PubMed
description BACKGROUND. The prognostic value of 1q21 gain in newly diagnosed multiple myeloma (NDMM) remains controversial. Our aim was to investigate the prognostic value of 1q21 gain in a Chinese population. MATERIALS AND METHODS. We retrospectively identified 565 patients with NDMM from multiple centers in China. RESULTS. We detected 1q21 gain in 222 (39.3%) patients, among whom 144 had three copies of 1q21, 57 had four copies of 1q21, and 21 had at least five copies of 1q21. Copy number variation did not show any effect on the disease outcome. Multivariate analysis indicated that 1q21 gain was an independent factor for poor prognosis, but we found that 1q21 gain was strongly associated with other high‐risk factors, such as del(17p), t(4;14), t(14;16), lactate dehydrogenase (LDH) level >300 U/L and International Scoring System (ISS) stage II–III (p < .001). Further analysis revealed that in the absence of other high‐risk factors, isolated 1q21 gain resulted in similar progression‐free survival (PFS; 52.0 vs. 52.8 months, p = .810) and overall survival (OS; not reached vs. not reached, p = .833); additionally, when present with other high‐risk cytogenetic abnormalities or increased LDH levels, 1q21 gain lost its prognostic power. However, the presence of 1q21 gain increased the adverse impact of ISS stage. Furthermore, 1q21 gain predicted poor PFS and OS in patients who received bortezomib‐based regimens. Moreover, autologous stem cell transplantation reversed the poor prognosis in patients with 1q21 gain. CONCLUSION. Our results show that heterogeneity exists among patients with 1q21 gain and suggest that we should assess the impact of 1q21 gain on prognosis according to different treatment regimens and accompanying high‐risk factors. IMPLICATIONS FOR PRACTICE. 1q21 gain is one of the most common chromosomal aberrations in multiple myeloma (MM); however, the prognostic value of 1q21 gain remains controversial. This study investigated the prognostic value of 1q21 gain in a Chinese population with newly diagnosed MM. The results showed that heterogeneity exists among patients with 1q21 gain and suggested that the impact of 1q21 gain on prognosis should be assessed according to different treatment regimens and accompanying high‐risk factors. These results could help stratify risk in patients with MM and guide treatment decisions.
format Online
Article
Text
id pubmed-6853115
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher John Wiley & Sons, Inc.
record_format MEDLINE/PubMed
spelling pubmed-68531152019-11-24 1q21 Gain Combined with High‐Risk Factors Is a Heterogeneous Prognostic Factor in Newly Diagnosed Multiple Myeloma: A Multicenter Study in China Li, Xiaozhe Chen, Wenming Wu, Yin Li, Jianyong Chen, Lijuan Fang, Baijun Feng, Ying Liu, Junru Chen, Meilan Gu, Jingli Huang, Beihui Li, Juan Oncologist Hematologic Malignancies BACKGROUND. The prognostic value of 1q21 gain in newly diagnosed multiple myeloma (NDMM) remains controversial. Our aim was to investigate the prognostic value of 1q21 gain in a Chinese population. MATERIALS AND METHODS. We retrospectively identified 565 patients with NDMM from multiple centers in China. RESULTS. We detected 1q21 gain in 222 (39.3%) patients, among whom 144 had three copies of 1q21, 57 had four copies of 1q21, and 21 had at least five copies of 1q21. Copy number variation did not show any effect on the disease outcome. Multivariate analysis indicated that 1q21 gain was an independent factor for poor prognosis, but we found that 1q21 gain was strongly associated with other high‐risk factors, such as del(17p), t(4;14), t(14;16), lactate dehydrogenase (LDH) level >300 U/L and International Scoring System (ISS) stage II–III (p < .001). Further analysis revealed that in the absence of other high‐risk factors, isolated 1q21 gain resulted in similar progression‐free survival (PFS; 52.0 vs. 52.8 months, p = .810) and overall survival (OS; not reached vs. not reached, p = .833); additionally, when present with other high‐risk cytogenetic abnormalities or increased LDH levels, 1q21 gain lost its prognostic power. However, the presence of 1q21 gain increased the adverse impact of ISS stage. Furthermore, 1q21 gain predicted poor PFS and OS in patients who received bortezomib‐based regimens. Moreover, autologous stem cell transplantation reversed the poor prognosis in patients with 1q21 gain. CONCLUSION. Our results show that heterogeneity exists among patients with 1q21 gain and suggest that we should assess the impact of 1q21 gain on prognosis according to different treatment regimens and accompanying high‐risk factors. IMPLICATIONS FOR PRACTICE. 1q21 gain is one of the most common chromosomal aberrations in multiple myeloma (MM); however, the prognostic value of 1q21 gain remains controversial. This study investigated the prognostic value of 1q21 gain in a Chinese population with newly diagnosed MM. The results showed that heterogeneity exists among patients with 1q21 gain and suggested that the impact of 1q21 gain on prognosis should be assessed according to different treatment regimens and accompanying high‐risk factors. These results could help stratify risk in patients with MM and guide treatment decisions. John Wiley & Sons, Inc. 2019-08-27 2019-11 /pmc/articles/PMC6853115/ /pubmed/31455749 http://dx.doi.org/10.1634/theoncologist.2019-0132 Text en © 2019 The Authors. The Oncologist published by Wiley Periodicals, Inc. on behalf of AlphaMed Press. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Hematologic Malignancies
Li, Xiaozhe
Chen, Wenming
Wu, Yin
Li, Jianyong
Chen, Lijuan
Fang, Baijun
Feng, Ying
Liu, Junru
Chen, Meilan
Gu, Jingli
Huang, Beihui
Li, Juan
1q21 Gain Combined with High‐Risk Factors Is a Heterogeneous Prognostic Factor in Newly Diagnosed Multiple Myeloma: A Multicenter Study in China
title 1q21 Gain Combined with High‐Risk Factors Is a Heterogeneous Prognostic Factor in Newly Diagnosed Multiple Myeloma: A Multicenter Study in China
title_full 1q21 Gain Combined with High‐Risk Factors Is a Heterogeneous Prognostic Factor in Newly Diagnosed Multiple Myeloma: A Multicenter Study in China
title_fullStr 1q21 Gain Combined with High‐Risk Factors Is a Heterogeneous Prognostic Factor in Newly Diagnosed Multiple Myeloma: A Multicenter Study in China
title_full_unstemmed 1q21 Gain Combined with High‐Risk Factors Is a Heterogeneous Prognostic Factor in Newly Diagnosed Multiple Myeloma: A Multicenter Study in China
title_short 1q21 Gain Combined with High‐Risk Factors Is a Heterogeneous Prognostic Factor in Newly Diagnosed Multiple Myeloma: A Multicenter Study in China
title_sort 1q21 gain combined with high‐risk factors is a heterogeneous prognostic factor in newly diagnosed multiple myeloma: a multicenter study in china
topic Hematologic Malignancies
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6853115/
https://www.ncbi.nlm.nih.gov/pubmed/31455749
http://dx.doi.org/10.1634/theoncologist.2019-0132
work_keys_str_mv AT lixiaozhe 1q21gaincombinedwithhighriskfactorsisaheterogeneousprognosticfactorinnewlydiagnosedmultiplemyelomaamulticenterstudyinchina
AT chenwenming 1q21gaincombinedwithhighriskfactorsisaheterogeneousprognosticfactorinnewlydiagnosedmultiplemyelomaamulticenterstudyinchina
AT wuyin 1q21gaincombinedwithhighriskfactorsisaheterogeneousprognosticfactorinnewlydiagnosedmultiplemyelomaamulticenterstudyinchina
AT lijianyong 1q21gaincombinedwithhighriskfactorsisaheterogeneousprognosticfactorinnewlydiagnosedmultiplemyelomaamulticenterstudyinchina
AT chenlijuan 1q21gaincombinedwithhighriskfactorsisaheterogeneousprognosticfactorinnewlydiagnosedmultiplemyelomaamulticenterstudyinchina
AT fangbaijun 1q21gaincombinedwithhighriskfactorsisaheterogeneousprognosticfactorinnewlydiagnosedmultiplemyelomaamulticenterstudyinchina
AT fengying 1q21gaincombinedwithhighriskfactorsisaheterogeneousprognosticfactorinnewlydiagnosedmultiplemyelomaamulticenterstudyinchina
AT liujunru 1q21gaincombinedwithhighriskfactorsisaheterogeneousprognosticfactorinnewlydiagnosedmultiplemyelomaamulticenterstudyinchina
AT chenmeilan 1q21gaincombinedwithhighriskfactorsisaheterogeneousprognosticfactorinnewlydiagnosedmultiplemyelomaamulticenterstudyinchina
AT gujingli 1q21gaincombinedwithhighriskfactorsisaheterogeneousprognosticfactorinnewlydiagnosedmultiplemyelomaamulticenterstudyinchina
AT huangbeihui 1q21gaincombinedwithhighriskfactorsisaheterogeneousprognosticfactorinnewlydiagnosedmultiplemyelomaamulticenterstudyinchina
AT lijuan 1q21gaincombinedwithhighriskfactorsisaheterogeneousprognosticfactorinnewlydiagnosedmultiplemyelomaamulticenterstudyinchina