Cargando…
获得性纯红细胞再生障碍67例临床分析
OBJECTIVE: To investigate secondary factors, laboratory features, treatment options, and prognosis of pure red cell aplastic anemia (PRCA). METHODS: This was a multicenter retrospective clinical study. Patients aged above 18 years newly diagnosed with PRCA between June 1, 2010, and June 1, 2019, wer...
Formato: | Online Artículo Texto |
---|---|
Lenguaje: | English |
Publicado: |
Editorial office of Chinese Journal of Hematology
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7378292/ https://www.ncbi.nlm.nih.gov/pubmed/32654466 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2020.06.013 |
_version_ | 1783562386379112448 |
---|---|
collection | PubMed |
description | OBJECTIVE: To investigate secondary factors, laboratory features, treatment options, and prognosis of pure red cell aplastic anemia (PRCA). METHODS: This was a multicenter retrospective clinical study. Patients aged above 18 years newly diagnosed with PRCA between June 1, 2010, and June 1, 2019, were recruited as the main study object. A comparative analysis of remission rate and overall survival rate was made according to different treatment schemes adopted by patients and different drug reduction rates. RESULTS: A total of 67 patients with PRCA were included in this study and the secondary PRCA group accounted for 44.8% (30/67). The most common secondary factors were thymoma (n=10) and T-cell large lymphocytic leukemia (T-LGLL) (n=6). The overall response rate of PRCA was 85.7% and the 3-year overall survival rate of PRCA was (74.3±7.5) %. The remission rate of cyclosporine A alone was slightly higher than that of oral glucocorticoid alone or combined with glucocorticoid[90.0% (36/40) vs 75.0% (12/16), P=0.147]. After patients applied with cyclosporine A treatment reached CR/PR and remained stable for 3–6 months, the dose of cyclosporine A was reduced by 25 mg each time. The cyclosporine A reduction interval of a 25 mg/d reduction in more than 1 month significantly prolonged the median disease-free survival compared with a 25 mg/d reduction in less than 1 month [not reached vs 15 (95% CI 7–23) months, P<0.001]. There were 62.5% (10/16) of patients who responded to the initial or incremental treatment regimen after relapse. CONCLUSION: PRCA has features of various secondary factors, high overall survival rate, and high remission rate. Treatment with cyclosporine A alone is preferred, and cyclosporine A should be slowly tapered to reduce the risk of later relapse after it takes effect and patients reach a steady state. |
format | Online Article Text |
id | pubmed-7378292 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Editorial office of Chinese Journal of Hematology |
record_format | MEDLINE/PubMed |
spelling | pubmed-73782922020-07-24 获得性纯红细胞再生障碍67例临床分析 Zhonghua Xue Ye Xue Za Zhi 论著 OBJECTIVE: To investigate secondary factors, laboratory features, treatment options, and prognosis of pure red cell aplastic anemia (PRCA). METHODS: This was a multicenter retrospective clinical study. Patients aged above 18 years newly diagnosed with PRCA between June 1, 2010, and June 1, 2019, were recruited as the main study object. A comparative analysis of remission rate and overall survival rate was made according to different treatment schemes adopted by patients and different drug reduction rates. RESULTS: A total of 67 patients with PRCA were included in this study and the secondary PRCA group accounted for 44.8% (30/67). The most common secondary factors were thymoma (n=10) and T-cell large lymphocytic leukemia (T-LGLL) (n=6). The overall response rate of PRCA was 85.7% and the 3-year overall survival rate of PRCA was (74.3±7.5) %. The remission rate of cyclosporine A alone was slightly higher than that of oral glucocorticoid alone or combined with glucocorticoid[90.0% (36/40) vs 75.0% (12/16), P=0.147]. After patients applied with cyclosporine A treatment reached CR/PR and remained stable for 3–6 months, the dose of cyclosporine A was reduced by 25 mg each time. The cyclosporine A reduction interval of a 25 mg/d reduction in more than 1 month significantly prolonged the median disease-free survival compared with a 25 mg/d reduction in less than 1 month [not reached vs 15 (95% CI 7–23) months, P<0.001]. There were 62.5% (10/16) of patients who responded to the initial or incremental treatment regimen after relapse. CONCLUSION: PRCA has features of various secondary factors, high overall survival rate, and high remission rate. Treatment with cyclosporine A alone is preferred, and cyclosporine A should be slowly tapered to reduce the risk of later relapse after it takes effect and patients reach a steady state. Editorial office of Chinese Journal of Hematology 2020-06 /pmc/articles/PMC7378292/ /pubmed/32654466 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2020.06.013 Text en 2020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 获得性纯红细胞再生障碍67例临床分析 |
title | 获得性纯红细胞再生障碍67例临床分析 |
title_full | 获得性纯红细胞再生障碍67例临床分析 |
title_fullStr | 获得性纯红细胞再生障碍67例临床分析 |
title_full_unstemmed | 获得性纯红细胞再生障碍67例临床分析 |
title_short | 获得性纯红细胞再生障碍67例临床分析 |
title_sort | 获得性纯红细胞再生障碍67例临床分析 |
topic | 论著 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7378292/ https://www.ncbi.nlm.nih.gov/pubmed/32654466 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2020.06.013 |
work_keys_str_mv | AT huòdéxìngchúnhóngxìbāozàishēngzhàngài67lìlínchuángfēnxī AT huòdéxìngchúnhóngxìbāozàishēngzhàngài67lìlínchuángfēnxī AT huòdéxìngchúnhóngxìbāozàishēngzhàngài67lìlínchuángfēnxī AT huòdéxìngchúnhóngxìbāozàishēngzhàngài67lìlínchuángfēnxī AT huòdéxìngchúnhóngxìbāozàishēngzhàngài67lìlínchuángfēnxī AT huòdéxìngchúnhóngxìbāozàishēngzhàngài67lìlínchuángfēnxī |