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Newly diagnosed multiple myeloma patients with CD56 expression benefit more from autologous stem cell transplantation

BACKGROUND: Several studies showed that lack of CD56 expression was a poor prognostic factor for patients with newly diagnosed multiple myeloma (NDMM). However, other studies were not able to confirm the prognostic value of CD56 in NDMM. This study aimed to evaluate the prognostic value of CD56 expr...

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Autores principales: Geng, Chuanying, Zhou, Huixing, Wang, Huijuan, Li, Yanchen, Leng, Yun, Zhang, Zhiyao, Jian, Yuan, Yang, Guangzhong, Chen, Wenming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9783713/
https://www.ncbi.nlm.nih.gov/pubmed/36564753
http://dx.doi.org/10.1186/s12885-022-10382-0
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author Geng, Chuanying
Zhou, Huixing
Wang, Huijuan
Li, Yanchen
Leng, Yun
Zhang, Zhiyao
Jian, Yuan
Yang, Guangzhong
Chen, Wenming
author_facet Geng, Chuanying
Zhou, Huixing
Wang, Huijuan
Li, Yanchen
Leng, Yun
Zhang, Zhiyao
Jian, Yuan
Yang, Guangzhong
Chen, Wenming
author_sort Geng, Chuanying
collection PubMed
description BACKGROUND: Several studies showed that lack of CD56 expression was a poor prognostic factor for patients with newly diagnosed multiple myeloma (NDMM). However, other studies were not able to confirm the prognostic value of CD56 in NDMM. This study aimed to evaluate the prognostic value of CD56 expression for patients with NDMM who received autologous stem cell transplantation (ASCT). METHODS: We retrospectively analyzed 370 patients with NDMM under 66 years old and the propensity score matching technique was used to reduce the bias between two groups. RESULTS: CD56 expression was observed in 250 (67.6%) patients, and only half of transplant-eligible patients received ASCT for financial and adverse effects concerns after induction therapy. 54.8% (137/250) CD56 positive patients received ASCT; and 47.5% (57/120) CD56 negative patients received ASCT. Univariate and multivariate analyses showed that ASCT was correlated with longer overall survival (OS) (p < 0.001) and progression-free survival (PFS) (p < 0.001) for CD56 positive patients. However, ASCT had no impact on OS and PFS in univariate and multivariate analysis (p > 0.05). In the propensity score matching analysis, 186 CD56 positive patients were identified, 93 patients had received ASCT and 93 patients had no ASCT. Among 120 CD56 negative patients, 80 patients, 40 in each group, were identified. Among 186 matched CD56 positive patients, patients with ASCT had longer OS (87.6 vs.56.1 months, p = 0.049) and PFS (36.7 vs.30.9 months, p = 0.040). However, ASCT had no impact on OS and PFS for matched CD56 negative patients (p > 0.05). CONCLUSIONS: These results demonstrated that ASCT may improve OS and PFS of CD56 positive patients and had no impact on survival of CD56 negative patients.
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spelling pubmed-97837132022-12-24 Newly diagnosed multiple myeloma patients with CD56 expression benefit more from autologous stem cell transplantation Geng, Chuanying Zhou, Huixing Wang, Huijuan Li, Yanchen Leng, Yun Zhang, Zhiyao Jian, Yuan Yang, Guangzhong Chen, Wenming BMC Cancer Research BACKGROUND: Several studies showed that lack of CD56 expression was a poor prognostic factor for patients with newly diagnosed multiple myeloma (NDMM). However, other studies were not able to confirm the prognostic value of CD56 in NDMM. This study aimed to evaluate the prognostic value of CD56 expression for patients with NDMM who received autologous stem cell transplantation (ASCT). METHODS: We retrospectively analyzed 370 patients with NDMM under 66 years old and the propensity score matching technique was used to reduce the bias between two groups. RESULTS: CD56 expression was observed in 250 (67.6%) patients, and only half of transplant-eligible patients received ASCT for financial and adverse effects concerns after induction therapy. 54.8% (137/250) CD56 positive patients received ASCT; and 47.5% (57/120) CD56 negative patients received ASCT. Univariate and multivariate analyses showed that ASCT was correlated with longer overall survival (OS) (p < 0.001) and progression-free survival (PFS) (p < 0.001) for CD56 positive patients. However, ASCT had no impact on OS and PFS in univariate and multivariate analysis (p > 0.05). In the propensity score matching analysis, 186 CD56 positive patients were identified, 93 patients had received ASCT and 93 patients had no ASCT. Among 120 CD56 negative patients, 80 patients, 40 in each group, were identified. Among 186 matched CD56 positive patients, patients with ASCT had longer OS (87.6 vs.56.1 months, p = 0.049) and PFS (36.7 vs.30.9 months, p = 0.040). However, ASCT had no impact on OS and PFS for matched CD56 negative patients (p > 0.05). CONCLUSIONS: These results demonstrated that ASCT may improve OS and PFS of CD56 positive patients and had no impact on survival of CD56 negative patients. BioMed Central 2022-12-23 /pmc/articles/PMC9783713/ /pubmed/36564753 http://dx.doi.org/10.1186/s12885-022-10382-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Geng, Chuanying
Zhou, Huixing
Wang, Huijuan
Li, Yanchen
Leng, Yun
Zhang, Zhiyao
Jian, Yuan
Yang, Guangzhong
Chen, Wenming
Newly diagnosed multiple myeloma patients with CD56 expression benefit more from autologous stem cell transplantation
title Newly diagnosed multiple myeloma patients with CD56 expression benefit more from autologous stem cell transplantation
title_full Newly diagnosed multiple myeloma patients with CD56 expression benefit more from autologous stem cell transplantation
title_fullStr Newly diagnosed multiple myeloma patients with CD56 expression benefit more from autologous stem cell transplantation
title_full_unstemmed Newly diagnosed multiple myeloma patients with CD56 expression benefit more from autologous stem cell transplantation
title_short Newly diagnosed multiple myeloma patients with CD56 expression benefit more from autologous stem cell transplantation
title_sort newly diagnosed multiple myeloma patients with cd56 expression benefit more from autologous stem cell transplantation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9783713/
https://www.ncbi.nlm.nih.gov/pubmed/36564753
http://dx.doi.org/10.1186/s12885-022-10382-0
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