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包括血管内大B细胞淋巴瘤在内的播散性结外大B细胞淋巴瘤的前瞻性治疗研究。

Prospective therapeutic studies of disseminated extranodal large B-cell lymphoma including intravascular large B-cell lymphoma.

作者信息

Sakai Tomoyuki, Ueda Yusuke, Yanagisawa Hiroto, Arita Kotaro, Iwao Haruka, Yamada Kazunori, Mizuta Shuichi, Kawabata Hiroshi, Fukushima Toshihiro, Tai Katsunori, Kishi Shinji, Morinaga Koji, Murakami Jun, Takamatsu Hiroyuki, Terasaki Yasushi, Yoshio Nobuyuki, Kondo Yukio, Okumura Hirokazu, Matano Sadaya, Yamaguchi Masaki, Tsutani Hiroshi, Masaki Yasufumi

机构信息

Department of Hematology and Immunology, Kanazawa Medical University, Ishikawa, Japan.

Department of Medical Education, Kanazawa Medical University, Ishikawa, Japan.

出版信息

Glob Health Med. 2024 Aug 31;6(4):277-281. doi: 10.35772/ghm.2024.01021.

Abstract

This study aimed to establish a standard treatment for disseminated extranodal large B-cell lymphoma, including intravascular large B-cell lymphoma (DEN-LBCL/IVL), and to validate the clinical diagnostic criteria we proposed. Between 2006 and 2016, 22 patients were enrolled in a clinical trial conducted by the Hokuriku Hematology Oncology Study Group. The first cycle of chemotherapy consisted of dose-reduced cyclophosphamide, doxorubicin, vincristine, and prednisolone (CHOP) with delayed administration of rituximab. From the second to the sixth cycle, patients received conventional rituximab and CHOP therapy. The primary endpoint was overall survival (OS), while the secondary endpoints included the complete response (CR) rate and time to treatment failure (TTF). The results showed a CR rate of 73%, a median OS of 65 months, and a median TTF of 45 months. These findings indicate that patients with DEN-LBCL/IVL were effectively treated with our new chemoimmunotherapy regimen. Our clinical diagnostic criteria are useful for identifying patients who require early intervention.

摘要

本研究旨在建立一种针对播散性结外大B细胞淋巴瘤(包括血管内大B细胞淋巴瘤,DEN-LBCL/IVL)的标准治疗方法,并验证我们提出的临床诊断标准。2006年至2016年期间,22例患者参加了北陆血液肿瘤学研究组开展的一项临床试验。化疗的第一个周期包括剂量减少的环磷酰胺、阿霉素、长春新碱和泼尼松龙(CHOP),同时延迟使用利妥昔单抗。从第二个周期到第六个周期,患者接受常规的利妥昔单抗和CHOP治疗。主要终点是总生存期(OS),次要终点包括完全缓解(CR)率和治疗失败时间(TTF)。结果显示CR率为73%,中位OS为65个月,中位TTF为45个月。这些发现表明,DEN-LBCL/IVL患者通过我们新的化疗免疫治疗方案得到了有效治疗。我们的临床诊断标准有助于识别需要早期干预的患者。

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