Risk factors for CAR‐T cell manufacturing failure among DLBCL patients: A nationwide survey in Japan

Summary For successful chimeric antigen receptor T (CAR‐T) cell therapy, CAR‐T cells must be manufactured without failure caused by suboptimal expansion. In order to determine risk factors for CAR‐T cell manufacturing failure, we performed a nationwide cohort study in Japan and analysed patients wit...

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Veröffentlicht in:British journal of haematology 2023-07, Vol.202 (2), p.256-266
Hauptverfasser: Jo, Tomoyasu, Yoshihara, Satoshi, Okuyama, Yoshiki, Fujii, Keiko, Henzan, Tomoko, Kahata, Kaoru, Yamazaki, Rie, Takeda, Wataru, Umezawa, Yoshihiro, Fukushima, Kentaro, Ashida, Takashi, Yamada‐Fujiwara, Minami, Hanajiri, Ryo, Yonetani, Noboru, Tada, Yuma, Shimura, Yuji, Nishikii, Hidekazu, Shiba, Norio, Mimura, Naoya, Ando, Jun, Sato, Takayuki, Nakashima, Yasuhiro, Ikemoto, Junko, Iwaki, Keita, Fujiwara, Shin‐ichiro, Ri, Masaki, Nagamura‐Inoue, Tokiko, Tanosaki, Ryuji, Arai, Yasuyuki
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Sprache:eng
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Zusammenfassung:Summary For successful chimeric antigen receptor T (CAR‐T) cell therapy, CAR‐T cells must be manufactured without failure caused by suboptimal expansion. In order to determine risk factors for CAR‐T cell manufacturing failure, we performed a nationwide cohort study in Japan and analysed patients with diffuse large B‐cell lymphoma (DLBCL) who underwent tisagenlecleucel production. We compared clinical factors between 30 cases that failed (7.4%) with those that succeeded (n = 378). Among the failures, the proportion of patients previously treated with bendamustine (43.3% vs. 14.8%; p 
ISSN:0007-1048
1365-2141
DOI:10.1111/bjh.18831