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伴单克隆免疫球蛋白边缘带淋巴瘤三例报告及文献复习

OBJECTIVE: To investigate the clinical features and treatment in patients of marginal zone lymphoma (MZL) with monoclonal immunoglobulin (McIg). METHODS: The clinical data of MZL patients with McIg, including 3 cases diagnosed and treated in Beijing Anzhen Hospital from Jan 2007 to Dec 2014 were ret...

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Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342304/
https://www.ncbi.nlm.nih.gov/pubmed/26876252
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2016.01.008
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description OBJECTIVE: To investigate the clinical features and treatment in patients of marginal zone lymphoma (MZL) with monoclonal immunoglobulin (McIg). METHODS: The clinical data of MZL patients with McIg, including 3 cases diagnosed and treated in Beijing Anzhen Hospital from Jan 2007 to Dec 2014 were retrospectively studied, meanwhile 36 patients searched from literatures were reviewed. RESULTS: Of a total of 39 patients, the ratio of male and female was 1.05∶1 with an average age of 65.1± 12.3 years old. 28 cases (71.8%) were with mucosa associated lymphoid tissue lymphomas (MALTL), 9 cases (23.1%) with nodal marginal zone lymphoma, and 2 cases (5.1%) with splenic marginal zone lymphoma. Nine cases (23.1%) were in the early stage, 30 cases (76.9%) in the advanced stage. The common initial symptom was non-mass lesions (65.5%), such as skin purpura, peripheral neuropathy; 13 patients (33.3%) were accompanied by autoimmune phenomenon, and most were with Sjogren's syndrome. Among MALTL patients, the common primary lesion was in non-gastrointestinal tract (17 cases, 60.7%). Most of patients with McIg were one with McIgM (82.0%); the others with McIgA, Mcκ-light chain, McIgG and double McIg. The level of plasma McIgM was (25.55±21.31)g/L, which was higher in advanced stage patients than in early stage ones [(29.85±20.60)g/L vs (3.23±2.95)g/L, P=0.008]. The complete remission (CR) rate was 56.0% and the overall response rate (ORR) 92.0%, respectively in 30 patients treated by chemotherapy. At a median follow-up of 10 months, the 3-year progression free survival and the 3-year overall survival were 44.7% and 76.5%, respectively. The rates of ORR and CR in the patients received rituximab-included regimen were seemly better than those without rituximab one (100.0% vs 78.6%, 63.6% vs 50.0%; P>0.05), but no statistic differences were found. The CR rate in patients with McIgM was significantly higher than that with non-McIgM (P=0.026). The plasma McIgM level decreased after chemotherapy (P=0.002). CONCLUSION: The MZL with McIg, perhaps a kind of unique subtype, usually occurred in 60 years or older patients. It was often diagnosed in patients of advanced stage and susceptible to autoimmune phenomenon. MALTL in non-gastrointestinal tract was more prone to find McIg. In MZL patients with McIg, McIgM was more common and other McIg rare. Rituximab-included regimen produced a better therapeutic response.
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spelling pubmed-73423042020-07-16 伴单克隆免疫球蛋白边缘带淋巴瘤三例报告及文献复习 Zhonghua Xue Ye Xue Za Zhi 论著 OBJECTIVE: To investigate the clinical features and treatment in patients of marginal zone lymphoma (MZL) with monoclonal immunoglobulin (McIg). METHODS: The clinical data of MZL patients with McIg, including 3 cases diagnosed and treated in Beijing Anzhen Hospital from Jan 2007 to Dec 2014 were retrospectively studied, meanwhile 36 patients searched from literatures were reviewed. RESULTS: Of a total of 39 patients, the ratio of male and female was 1.05∶1 with an average age of 65.1± 12.3 years old. 28 cases (71.8%) were with mucosa associated lymphoid tissue lymphomas (MALTL), 9 cases (23.1%) with nodal marginal zone lymphoma, and 2 cases (5.1%) with splenic marginal zone lymphoma. Nine cases (23.1%) were in the early stage, 30 cases (76.9%) in the advanced stage. The common initial symptom was non-mass lesions (65.5%), such as skin purpura, peripheral neuropathy; 13 patients (33.3%) were accompanied by autoimmune phenomenon, and most were with Sjogren's syndrome. Among MALTL patients, the common primary lesion was in non-gastrointestinal tract (17 cases, 60.7%). Most of patients with McIg were one with McIgM (82.0%); the others with McIgA, Mcκ-light chain, McIgG and double McIg. The level of plasma McIgM was (25.55±21.31)g/L, which was higher in advanced stage patients than in early stage ones [(29.85±20.60)g/L vs (3.23±2.95)g/L, P=0.008]. The complete remission (CR) rate was 56.0% and the overall response rate (ORR) 92.0%, respectively in 30 patients treated by chemotherapy. At a median follow-up of 10 months, the 3-year progression free survival and the 3-year overall survival were 44.7% and 76.5%, respectively. The rates of ORR and CR in the patients received rituximab-included regimen were seemly better than those without rituximab one (100.0% vs 78.6%, 63.6% vs 50.0%; P>0.05), but no statistic differences were found. The CR rate in patients with McIgM was significantly higher than that with non-McIgM (P=0.026). The plasma McIgM level decreased after chemotherapy (P=0.002). CONCLUSION: The MZL with McIg, perhaps a kind of unique subtype, usually occurred in 60 years or older patients. It was often diagnosed in patients of advanced stage and susceptible to autoimmune phenomenon. MALTL in non-gastrointestinal tract was more prone to find McIg. In MZL patients with McIg, McIgM was more common and other McIg rare. Rituximab-included regimen produced a better therapeutic response. Editorial office of Chinese Journal of Hematology 2016-01 /pmc/articles/PMC7342304/ /pubmed/26876252 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2016.01.008 Text en 2016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
伴单克隆免疫球蛋白边缘带淋巴瘤三例报告及文献复习
title 伴单克隆免疫球蛋白边缘带淋巴瘤三例报告及文献复习
title_full 伴单克隆免疫球蛋白边缘带淋巴瘤三例报告及文献复习
title_fullStr 伴单克隆免疫球蛋白边缘带淋巴瘤三例报告及文献复习
title_full_unstemmed 伴单克隆免疫球蛋白边缘带淋巴瘤三例报告及文献复习
title_short 伴单克隆免疫球蛋白边缘带淋巴瘤三例报告及文献复习
title_sort 伴单克隆免疫球蛋白边缘带淋巴瘤三例报告及文献复习
topic 论著
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342304/
https://www.ncbi.nlm.nih.gov/pubmed/26876252
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2016.01.008
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