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[经包括利妥昔单抗在内的挽救性治疗后通过表面抗体血清学转换而新发乙型肝炎的B细胞淋巴瘤]

[B-cell lymphoma developing de novo hepatitis B after salvage therapies including rituximab through seroconversion of surface antibody].

作者信息

Ishihara Toshimichi, Kanagawa Michiyo, Koyama Junichi, Hasegawa Kiminori, Suzuki Takashi, Hirayama Yasuo, Terui Takeshi

机构信息

Department of Internal Medicine, Kin-ikyo Chuo Hospital.

出版信息

Rinsho Ketsueki. 2014 Nov;55(11):2283-7.

PMID:25501408
Abstract

The patient was a 73-year-old woman. At 63 years of age, she had developed follicular lymphoma that showed a complete response to R-CHOP therapy. Over the subsequent 8 years, she experienced 4 relapses and was administered rituximab monotherapy once, combined rituximab-fludarabine therapy twice, and CHASE-R therapy once, achieving a complete response each time. Before her first therapy, hepatitis B virus (HBV) surface antigen was negative, while hepatitis B surface antibody (anti-HBs) and hepatitis B core antibody were not measured. Later, before her second salvage therapy, anti-HBs was negative, but then changed to positive before her third salvage therapy. HBV-DNA was negative before CHASE-R therapy. At 16 months after completing the CHASE-R therapy, she developed hepatitis and HBV-DNA had changed to positive. Hepatitis did not become fulminant and entecavir administration was effective. It was surmised that HBV had resolved, but she became negative for anti-HBs following the rituximab-containing chemotherapy. Therefore, this is a rare case in which de novo hepatitis developed after the final chemotherapy. The prognosis of patients with de novo hepatitis accompanying treatment of B-cell lymphoma is poor. In those who undergo lymphoma salvage therapy, the risk for and clinical course of HBV reactivation might differ from those of treatment-naïve patients.

摘要

该患者为一名73岁女性。63岁时,她被诊断出患有滤泡性淋巴瘤,对R-CHOP疗法显示出完全缓解。在随后的8年里,她经历了4次复发,接受过1次利妥昔单抗单药治疗、2次利妥昔单抗-氟达拉滨联合治疗以及1次CHASE-R治疗,每次均实现完全缓解。首次治疗前,乙肝病毒(HBV)表面抗原呈阴性,未检测乙肝表面抗体(抗-HBs)和乙肝核心抗体。后来,在第二次挽救治疗前,抗-HBs呈阴性,但在第三次挽救治疗前转为阳性。CHASE-R治疗前HBV-DNA呈阴性。在完成CHASE-R治疗16个月后,她患上肝炎,HBV-DNA转为阳性。肝炎未发展为暴发性,恩替卡韦治疗有效。据推测HBV已清除,但在接受含利妥昔单抗的化疗后,她的抗-HBs转为阴性。因此,这是一例在最后一次化疗后出现新发肝炎的罕见病例。B细胞淋巴瘤治疗后新发肝炎患者的预后较差。在接受淋巴瘤挽救治疗的患者中,HBV再激活的风险和临床过程可能与初治患者不同。

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1
[B-cell lymphoma developing de novo hepatitis B after salvage therapies including rituximab through seroconversion of surface antibody].[经包括利妥昔单抗在内的挽救性治疗后通过表面抗体血清学转换而新发乙型肝炎的B细胞淋巴瘤]
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2
Risk of hepatitis B virus (HBV) reactivation in hepatitis B surface antigen negative/hepatitis B core antibody positive patients receiving rituximab-containing combination chemotherapy without routine antiviral prophylaxis.乙肝表面抗原阴性/乙肝核心抗体阳性患者接受利妥昔单抗联合化疗而未常规进行抗病毒预防时乙型肝炎病毒(HBV)再激活的风险。
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4
Prospective analysis of hepatitis B virus reactivation in patients with diffuse large B-cell lymphoma after rituximab combination chemotherapy.利妥昔单抗联合化疗后弥漫大 B 细胞淋巴瘤患者乙型肝炎病毒再激活的前瞻性分析。
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Entecavir vs lamivudine for prevention of hepatitis B virus reactivation among patients with untreated diffuse large B-cell lymphoma receiving R-CHOP chemotherapy: a randomized clinical trial.恩替卡韦与拉米夫定预防未治疗弥漫性大 B 细胞淋巴瘤接受 R-CHOP 化疗患者乙型肝炎病毒再激活:一项随机临床试验。
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[Hepatitis B virus reactivation after cessation of prophylactic lamivudine therapy in B-cell lymphoma patients treated with rituximab combined CHOP therapy].[接受利妥昔单抗联合CHOP方案治疗的B细胞淋巴瘤患者预防性拉米夫定治疗停药后乙肝病毒再激活]
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Hepatitis B virus reactivation in lymphoma patients with prior resolved hepatitis B undergoing anticancer therapy with or without rituximab.既往乙肝已缓解的淋巴瘤患者在接受含或不含利妥昔单抗的抗癌治疗过程中发生的乙肝病毒再激活。
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