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Amp 1q21 is more predictable with dismal survival than gain 1q21 of newly diagnosed multiple myeloma in real‐world analysis

INTRODUCTION: The gain/amplification (amp) of 1q21 is one of the most common high‐risk chromosome abnormality (HRCA) in multiple myeloma (MM). The prognostic value of 1q21+ remains to be controversial on the status of gain or amp and the combination of other HRCAs. METHODS: In this retrospective stu...

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Autores principales: Wang, Yu‐tong, Bao, Li, Chu, Bin, Chen, Xiao‐huan, Lu, Min‐qiu, Shi, Lei, Gao, Shan, Fang, Li‐juan, Xiang, Qiu‐qing, Ding, Yue‐hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9280004/
https://www.ncbi.nlm.nih.gov/pubmed/35353920
http://dx.doi.org/10.1002/jcla.24375
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author Wang, Yu‐tong
Bao, Li
Chu, Bin
Chen, Xiao‐huan
Lu, Min‐qiu
Shi, Lei
Gao, Shan
Fang, Li‐juan
Xiang, Qiu‐qing
Ding, Yue‐hua
author_facet Wang, Yu‐tong
Bao, Li
Chu, Bin
Chen, Xiao‐huan
Lu, Min‐qiu
Shi, Lei
Gao, Shan
Fang, Li‐juan
Xiang, Qiu‐qing
Ding, Yue‐hua
author_sort Wang, Yu‐tong
collection PubMed
description INTRODUCTION: The gain/amplification (amp) of 1q21 is one of the most common high‐risk chromosome abnormality (HRCA) in multiple myeloma (MM). The prognostic value of 1q21+ remains to be controversial on the status of gain or amp and the combination of other HRCAs. METHODS: In this retrospective study, we included 318 newly diagnosed MM (NDMM) patients who had fluorescence in situ hybridization (FISH) data and treated with novel agents in our department. RESULTS: Our study noted MM patients with amp 1q21 were more likely accompanied with t(4;14), t(14;16), and t(14;20). Patients with amp 1q21 presented with elder age, advanced Revised International Staging System (R‐ISS) stages, anemia, and more plasma cells in bone marrow compared to patients with gain 1q21 alone and no 1q21+. Moreover, amp 1q21 alone correlated with shorter progression‐free survival (PFS) (22.8m vs. 40.5m vs. 39.6m) and overall survival (OS) (45.2m vs. NA vs. 83.5m) compared with gain 1q21 alone and no FISH abnormalities. Although the high ratio of proteasome inhibitor and immunomodulatory drugs used in patients with amp 1q21, the overall response (ORR) was the lowest compared with no 1q21+ and gain 1q21. Multivariate analysis defined amp 1q21 as an independent prognostic marker for NDMM patients, rather than gain 1q21. CONCLUSION: The amp 1q21 predict inferior treatment response and survival, especially coexisted with high‐risk IgH translocation.
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spelling pubmed-92800042022-07-15 Amp 1q21 is more predictable with dismal survival than gain 1q21 of newly diagnosed multiple myeloma in real‐world analysis Wang, Yu‐tong Bao, Li Chu, Bin Chen, Xiao‐huan Lu, Min‐qiu Shi, Lei Gao, Shan Fang, Li‐juan Xiang, Qiu‐qing Ding, Yue‐hua J Clin Lab Anal Research Articles INTRODUCTION: The gain/amplification (amp) of 1q21 is one of the most common high‐risk chromosome abnormality (HRCA) in multiple myeloma (MM). The prognostic value of 1q21+ remains to be controversial on the status of gain or amp and the combination of other HRCAs. METHODS: In this retrospective study, we included 318 newly diagnosed MM (NDMM) patients who had fluorescence in situ hybridization (FISH) data and treated with novel agents in our department. RESULTS: Our study noted MM patients with amp 1q21 were more likely accompanied with t(4;14), t(14;16), and t(14;20). Patients with amp 1q21 presented with elder age, advanced Revised International Staging System (R‐ISS) stages, anemia, and more plasma cells in bone marrow compared to patients with gain 1q21 alone and no 1q21+. Moreover, amp 1q21 alone correlated with shorter progression‐free survival (PFS) (22.8m vs. 40.5m vs. 39.6m) and overall survival (OS) (45.2m vs. NA vs. 83.5m) compared with gain 1q21 alone and no FISH abnormalities. Although the high ratio of proteasome inhibitor and immunomodulatory drugs used in patients with amp 1q21, the overall response (ORR) was the lowest compared with no 1q21+ and gain 1q21. Multivariate analysis defined amp 1q21 as an independent prognostic marker for NDMM patients, rather than gain 1q21. CONCLUSION: The amp 1q21 predict inferior treatment response and survival, especially coexisted with high‐risk IgH translocation. John Wiley and Sons Inc. 2022-03-30 /pmc/articles/PMC9280004/ /pubmed/35353920 http://dx.doi.org/10.1002/jcla.24375 Text en © 2022 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://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 Research Articles
Wang, Yu‐tong
Bao, Li
Chu, Bin
Chen, Xiao‐huan
Lu, Min‐qiu
Shi, Lei
Gao, Shan
Fang, Li‐juan
Xiang, Qiu‐qing
Ding, Yue‐hua
Amp 1q21 is more predictable with dismal survival than gain 1q21 of newly diagnosed multiple myeloma in real‐world analysis
title Amp 1q21 is more predictable with dismal survival than gain 1q21 of newly diagnosed multiple myeloma in real‐world analysis
title_full Amp 1q21 is more predictable with dismal survival than gain 1q21 of newly diagnosed multiple myeloma in real‐world analysis
title_fullStr Amp 1q21 is more predictable with dismal survival than gain 1q21 of newly diagnosed multiple myeloma in real‐world analysis
title_full_unstemmed Amp 1q21 is more predictable with dismal survival than gain 1q21 of newly diagnosed multiple myeloma in real‐world analysis
title_short Amp 1q21 is more predictable with dismal survival than gain 1q21 of newly diagnosed multiple myeloma in real‐world analysis
title_sort amp 1q21 is more predictable with dismal survival than gain 1q21 of newly diagnosed multiple myeloma in real‐world analysis
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9280004/
https://www.ncbi.nlm.nih.gov/pubmed/35353920
http://dx.doi.org/10.1002/jcla.24375
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