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Incidence and risk factors for second malignancies among patients with myeloproliferative neoplasms

OBJECTIVE: The clinical characteristics and survival of patients with myeloproliferative neoplasms (MPNs) with secondary cancer were analyzed to explore the possible risk factors for secondary cancer in MPN patients. METHODS: The clinical characteristics of 1060 Chinese patients with MPN were retros...

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Autores principales: Zhang, Yuhui, Han, Yingdi, Teng, Guangshuai, Du, Chenxiao, Gao, Shan, Yuan, Weiping, Zhang, Lei, Bai, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10166886/
https://www.ncbi.nlm.nih.gov/pubmed/36727544
http://dx.doi.org/10.1002/cam4.5666
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author Zhang, Yuhui
Han, Yingdi
Teng, Guangshuai
Du, Chenxiao
Gao, Shan
Yuan, Weiping
Zhang, Lei
Bai, Jie
author_facet Zhang, Yuhui
Han, Yingdi
Teng, Guangshuai
Du, Chenxiao
Gao, Shan
Yuan, Weiping
Zhang, Lei
Bai, Jie
author_sort Zhang, Yuhui
collection PubMed
description OBJECTIVE: The clinical characteristics and survival of patients with myeloproliferative neoplasms (MPNs) with secondary cancer were analyzed to explore the possible risk factors for secondary cancer in MPN patients. METHODS: The clinical characteristics of 1060 Chinese patients with MPN were retrospectively analyzed. The Kaplan–Meier method was used to analyze the survival. The Cox multivariate regression model was used to analyze the risk factors for developing secondary cancer in patients with MPNs. RESULTS: The 1060 patients with MPN had a median follow‐up of 10 years (range 1–50) and a median age of 55 years (range 21–86), and 497 (45.2%) were male. The proportion of PV, ET, and PMF was 52.2%, 33.5%, and 14.3%, respectively. About 28.1% (298/1060) of 1060 MPN patients died. The median survival times of the PV, ET, and PMF groups were 20, 24, and 12 years, respectively (p < 0.0001). In age‐ and sex‐matched healthy Chinese patients, the standardized incidence ratio (SIR) value of developing secondary cancer in MPN patients was 6.41 (95% CI: 4.90–9.48). The median survival time was 14 years in the MPN with secondary cancer group. The Cox multivariate analysis showed that age ≥ 65 years (p < 0.0001, HR = 5.027, 95% CI [2.823, 8.952]), MF‐1 (p = 0.001, HR = 2.887, 95% CI [1.503, 5.545]) were risk factors for developing secondary cancer. CONCLUSIONS: The survival of MPN patients with secondary cancer was significantly worse than that of patients without secondary cancer. Compared with normal subjects, MPN patients had a 6.41‐fold increased risk of developing secondary cancer, and age ≥ 65 years and MF‐1 were risk factors for developing secondary cancer in MPN patients.
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spelling pubmed-101668862023-05-10 Incidence and risk factors for second malignancies among patients with myeloproliferative neoplasms Zhang, Yuhui Han, Yingdi Teng, Guangshuai Du, Chenxiao Gao, Shan Yuan, Weiping Zhang, Lei Bai, Jie Cancer Med RESEARCH ARTICLES OBJECTIVE: The clinical characteristics and survival of patients with myeloproliferative neoplasms (MPNs) with secondary cancer were analyzed to explore the possible risk factors for secondary cancer in MPN patients. METHODS: The clinical characteristics of 1060 Chinese patients with MPN were retrospectively analyzed. The Kaplan–Meier method was used to analyze the survival. The Cox multivariate regression model was used to analyze the risk factors for developing secondary cancer in patients with MPNs. RESULTS: The 1060 patients with MPN had a median follow‐up of 10 years (range 1–50) and a median age of 55 years (range 21–86), and 497 (45.2%) were male. The proportion of PV, ET, and PMF was 52.2%, 33.5%, and 14.3%, respectively. About 28.1% (298/1060) of 1060 MPN patients died. The median survival times of the PV, ET, and PMF groups were 20, 24, and 12 years, respectively (p < 0.0001). In age‐ and sex‐matched healthy Chinese patients, the standardized incidence ratio (SIR) value of developing secondary cancer in MPN patients was 6.41 (95% CI: 4.90–9.48). The median survival time was 14 years in the MPN with secondary cancer group. The Cox multivariate analysis showed that age ≥ 65 years (p < 0.0001, HR = 5.027, 95% CI [2.823, 8.952]), MF‐1 (p = 0.001, HR = 2.887, 95% CI [1.503, 5.545]) were risk factors for developing secondary cancer. CONCLUSIONS: The survival of MPN patients with secondary cancer was significantly worse than that of patients without secondary cancer. Compared with normal subjects, MPN patients had a 6.41‐fold increased risk of developing secondary cancer, and age ≥ 65 years and MF‐1 were risk factors for developing secondary cancer in MPN patients. John Wiley and Sons Inc. 2023-02-02 /pmc/articles/PMC10166886/ /pubmed/36727544 http://dx.doi.org/10.1002/cam4.5666 Text en © 2023 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle RESEARCH ARTICLES
Zhang, Yuhui
Han, Yingdi
Teng, Guangshuai
Du, Chenxiao
Gao, Shan
Yuan, Weiping
Zhang, Lei
Bai, Jie
Incidence and risk factors for second malignancies among patients with myeloproliferative neoplasms
title Incidence and risk factors for second malignancies among patients with myeloproliferative neoplasms
title_full Incidence and risk factors for second malignancies among patients with myeloproliferative neoplasms
title_fullStr Incidence and risk factors for second malignancies among patients with myeloproliferative neoplasms
title_full_unstemmed Incidence and risk factors for second malignancies among patients with myeloproliferative neoplasms
title_short Incidence and risk factors for second malignancies among patients with myeloproliferative neoplasms
title_sort incidence and risk factors for second malignancies among patients with myeloproliferative neoplasms
topic RESEARCH ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10166886/
https://www.ncbi.nlm.nih.gov/pubmed/36727544
http://dx.doi.org/10.1002/cam4.5666
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