[Polatuzumab vedotin, bendamustine, and rituximab in patients with relapsed/refractory diffuse large B-cell lymphoma, including the outcome as a bridging treatment to CAR-T cell therapy or allogeneic hematopoietic stem cell transplant].

Yuka Morita, Yu Yagi, Yusuke Kanemasa, Yuki Sasaki, Kento Ishimine, Yudai Hayashi, Mano Mino, An Ohigashi, Taichi Tamura, Shohei Nakamura, Toshihiro Okuya, Takuya Shimizuguchi, Naoki Shingai, Takashi Toya, Hiroaki Shimizu, Yuho Najima, Takeshi Kobayashi, Kyoko Haraguchi, Noriko Doki, Yoshiki Okuyama, Kazuteru Ohashi, Tatsu Shimoyama
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Abstract

Pola-BR (polatuzumab vedotin, bendamustine, and rituximab) therapy received approval for relapsed/refractory diffuse large B-cell lymphoma (R/R DLBCL) in Japan in March 2021. There have been few reports on the efficacy and safety of Pola-BR therapy in Japanese clinical practice. A retrospective analysis was performed on twenty-nine patients with R/R DLBCL who received Pola-BR therapy at our institution (intent to cellular immunotherapy cohort: 20 patients, stand-alone treatment cohort: nine patients). The overall response rate was 69.0% (complete response 27.6%). The median progression-free survival was 5.1 months, with a 9.5-month median overall survival. In the intent to cellular immunotherapy cohort, 11 of 19 patients received chimeric antigen receptor T-cell (CAR-T) infusions, and one patient received allogeneic stem cell transplantation. Four patients received Pola-BR therapy, including bendamustine before leukapheresis, and all produced CAR-T products successfully. 3 of the 28 patients experienced grade3 or higher adverse events, and two required treatment discontinuation. Our single institution, a real-world cohort of R/R DLBCL patients showed high efficacy outcomes and a tolerable toxicity profile for Pola-BR therapy, which is comparable to previous studies. More cases are needed to determine its impact on CAR-T therapy and stem cell transplantation.

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[Polatuzumab vedotin,苯达莫司汀和利妥昔单抗在复发/难治性弥漫性大b细胞淋巴瘤患者中的应用,包括作为CAR-T细胞治疗或同种异体造血干细胞移植的桥接治疗的结果]。
Pola-BR (polatuzumab vedotin,苯达莫司汀和利妥昔单抗)治疗复发/难治性弥漫性大b细胞淋巴瘤(R/R DLBCL)于2021年3月在日本获得批准。在日本的临床实践中,关于Pola-BR治疗的有效性和安全性的报道很少。回顾性分析了29例在我院接受Pola-BR治疗的R/R DLBCL患者(细胞免疫治疗组:20例,独立治疗组:9例)。总有效率为69.0%(完全缓解率为27.6%)。中位无进展生存期为5.1个月,中位总生存期为9.5个月。在细胞免疫治疗队列中,19名患者中有11名接受了嵌合抗原受体t细胞(CAR-T)输注,1名患者接受了异体干细胞移植。4名患者接受了Pola-BR治疗,包括白血病采前的苯达莫司汀,所有患者都成功生产了CAR-T产品。28例患者中有3例出现3级或以上不良事件,2例需要停药。我们的单一机构,一个真实世界的R/R DLBCL患者队列显示了Pola-BR治疗的高疗效结果和可耐受的毒性特征,这与之前的研究相当。需要更多的病例来确定其对CAR-T治疗和干细胞移植的影响。
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