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利妥昔单抗联合二线方案治疗七例复发难治性霍奇金淋巴瘤患者疗效观察

OBJECTIVE: To investigate the efficacy and safety of Rituximab combined with second line regimen for treatment of relapsed and refractory Hodgkin lymphoma. METHODS: Seven patients with relapsed and refractory Hodgkin lymphoma were treated with Rituximab combined with second line regimen. Among them,...

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Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342643/
https://www.ncbi.nlm.nih.gov/pubmed/26304082
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2015.07.011
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collection PubMed
description OBJECTIVE: To investigate the efficacy and safety of Rituximab combined with second line regimen for treatment of relapsed and refractory Hodgkin lymphoma. METHODS: Seven patients with relapsed and refractory Hodgkin lymphoma were treated with Rituximab combined with second line regimen. Among them, two patients were treated with R-GDP (E) [rituximab, gemcitabine, cisplatin, dexamethasone (etoposide)] regimen, another two patients with R-IGVP (rituximab, ifosfamide, gemcitabine, vinorelbine, prednisone) regimen, and the left three patients with R-BEACOPP (rituximab, bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, prednisone) regimen. The efficacy and safety were evaluated during and after chemotherapy. RESULTS: There're three male and four female patients, whose median age was 21 years (range 12–36 years) old. One patient was diagnosed as nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL), and the other six patients as classical HL (four nodular sclerosis HL, one lymphocyte-rich classical HL and one hmixed cellularity HL). The median cycles of salvage therapy were 4(1–4), and the median follow-up was 29 months (24–58 months). Among these 7 patients, the complete remission was observed in 4 patients, stable disease in 2 patients, but one patient died during salvage therapy. The two-year survival rates were 85.7% and the major toxic effects were bone marrow suppression. CONCLUSION: These results indicate that the Rituximab combined with second line regimen is an effective therapy for relapsed and refractory Hodgkin lymphoma.
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spelling pubmed-73426432020-07-16 利妥昔单抗联合二线方案治疗七例复发难治性霍奇金淋巴瘤患者疗效观察 Zhonghua Xue Ye Xue Za Zhi 论著 OBJECTIVE: To investigate the efficacy and safety of Rituximab combined with second line regimen for treatment of relapsed and refractory Hodgkin lymphoma. METHODS: Seven patients with relapsed and refractory Hodgkin lymphoma were treated with Rituximab combined with second line regimen. Among them, two patients were treated with R-GDP (E) [rituximab, gemcitabine, cisplatin, dexamethasone (etoposide)] regimen, another two patients with R-IGVP (rituximab, ifosfamide, gemcitabine, vinorelbine, prednisone) regimen, and the left three patients with R-BEACOPP (rituximab, bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, prednisone) regimen. The efficacy and safety were evaluated during and after chemotherapy. RESULTS: There're three male and four female patients, whose median age was 21 years (range 12–36 years) old. One patient was diagnosed as nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL), and the other six patients as classical HL (four nodular sclerosis HL, one lymphocyte-rich classical HL and one hmixed cellularity HL). The median cycles of salvage therapy were 4(1–4), and the median follow-up was 29 months (24–58 months). Among these 7 patients, the complete remission was observed in 4 patients, stable disease in 2 patients, but one patient died during salvage therapy. The two-year survival rates were 85.7% and the major toxic effects were bone marrow suppression. CONCLUSION: These results indicate that the Rituximab combined with second line regimen is an effective therapy for relapsed and refractory Hodgkin lymphoma. Editorial office of Chinese Journal of Hematology 2015-07 /pmc/articles/PMC7342643/ /pubmed/26304082 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2015.07.011 Text en 2015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
利妥昔单抗联合二线方案治疗七例复发难治性霍奇金淋巴瘤患者疗效观察
title 利妥昔单抗联合二线方案治疗七例复发难治性霍奇金淋巴瘤患者疗效观察
title_full 利妥昔单抗联合二线方案治疗七例复发难治性霍奇金淋巴瘤患者疗效观察
title_fullStr 利妥昔单抗联合二线方案治疗七例复发难治性霍奇金淋巴瘤患者疗效观察
title_full_unstemmed 利妥昔单抗联合二线方案治疗七例复发难治性霍奇金淋巴瘤患者疗效观察
title_short 利妥昔单抗联合二线方案治疗七例复发难治性霍奇金淋巴瘤患者疗效观察
title_sort 利妥昔单抗联合二线方案治疗七例复发难治性霍奇金淋巴瘤患者疗效观察
topic 论著
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342643/
https://www.ncbi.nlm.nih.gov/pubmed/26304082
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2015.07.011
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