Heavily Pretreated Refractory Diffuse Large B-Cell Lymphoma Successfully Treated with Epcoritamab: Case Report.

IF 0.7 Q4 ONCOLOGY
Case Reports in Oncology Pub Date : 2025-03-29 eCollection Date: 2025-01-01 DOI:10.1159/000545372
Jeremy Rosiecki, Natalie Wallace, Katelyn Kammers, Ann-Chee Cheng, Talia Wyckoff, Steven Liu
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引用次数: 0

Abstract

Introduction: Relapsed or refractory diffuse large B-cell lymphoma (DLBCL) poses considerable treatment challenges, with disheartening odds of long-term survival. Numerous strategies exist, including non-cross-resistant combination chemoimmunotherapy regimens, autologous stem cell transplantation, and chimeric antigen receptor (CAR) T-cell therapy, but some patients are not appropriate candidates or cannot sustain response to treatment. Epcoritamab, a bispecific CD20-directed CD3 T-cell engager, has been given accelerated approval by the US Food and Drug Administration for relapsed or refractory DLBCL.

Case presentation: We present the case of a 61-year-old male diagnosed with stage 4 "double-hit" DLBCL with MYC and BCL6 rearrangement, who initially received one cycle of rituximab HyperCVAD (initiated July 23, 2021). He then received dose-adjusted etoposide, prednisone, vincristine, cyclophosphamide, and doxorubicin (DA-EPOCH) followed by high-dose methotrexate and initially responded but relapsed several months later. As the patient was not a candidate for transplant, subsequent treatment rounds included rituximab, gemcitabine, dexamethasone, and cisplatin (R-GDP) and CD19 CAR T-cell therapy; tafasitamab-cxix and lenalidomide; and polatuzumab vedotin plus bendamustine and rituximab (pola-BR). Despite intermittent treatment response, his disease continued to progress. He began treatment with epcoritamab through the early access program but showed early signs of continued progression; his status deteriorated until further treatment had to be withheld. Within approximately 1 month, he could resume treatment, achieving a Deauville score of 1 approximately 3 months after beginning epcoritamab, and continues follow-up nearly 2 years later.

Conclusion: T-cell engager therapies, such as epcoritamab, can play a role in managing patients with refractory DLBCL, including those refractory to CAR T-cell therapy.

重度预处理的难治性弥漫性大b细胞淋巴瘤用依可他单抗成功治疗:病例报告。
复发或难治性弥漫性大b细胞淋巴瘤(DLBCL)带来了相当大的治疗挑战,其长期生存几率令人沮丧。存在许多策略,包括非交叉耐药联合化学免疫治疗方案,自体干细胞移植和嵌合抗原受体(CAR) t细胞治疗,但一些患者不适合或不能维持对治疗的反应。Epcoritamab是一种双特异性cd20定向CD3 t细胞结合剂,已被美国食品和药物管理局加速批准用于复发或难治性DLBCL。病例介绍:我们报告了一例61岁男性,被诊断为4期“双重打击”DLBCL,伴有MYC和BCL6重排,他最初接受了一个周期的利图昔单抗hypervad(于2021年7月23日开始)。然后他接受剂量调整依托泊苷、强的松、长春新碱、环磷酰胺和阿霉素(DA-EPOCH)治疗,随后接受大剂量甲氨蝶呤治疗,最初有反应,但几个月后复发。由于患者不是移植的候选者,随后的治疗包括利妥昔单抗、吉西他滨、地塞米松、顺铂(R-GDP)和顺铂(CD19 CAR - t细胞治疗);他法西他单抗和来那度胺;polatuzumab vedotin +苯达莫司汀和利妥昔单抗(pola-BR)。尽管间歇性治疗有效果,但他的病情仍在继续恶化。他通过早期进入项目开始使用epcoritamab治疗,但显示出持续进展的早期迹象;他的病情恶化,直到不得不停止进一步治疗。在大约1个月内,患者可以恢复治疗,在开始使用epcoritamab约3个月后达到1分的多维尔评分,并在近2年后继续随访。结论:t细胞参与疗法,如依霉素单抗,可以在治疗难治性DLBCL患者中发挥作用,包括那些对CAR - t细胞治疗难治性的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.40
自引率
12.50%
发文量
151
审稿时长
7 weeks
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