Efficacy and side effects of anti‐CD19 CAR T‐cell therapy in patients with relapsed/refractory gastrointestinal lymphoma

Abstract Introduction Although anti‐CD19 chimeric antigen receptor (CAR) T cell therapy was approved as a very effective salvage strategy in relapsed/refractory (R/R) B cell lymphoma, the experience in R/R gastrointestinal (GI) lymphoma is still insufficient. Methods We summarized the efficacy and s...

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Main Authors: Yi Li Jiang, Juan Mu, Rui Cui, Xin Li, Jia Wang, Qing Li, Jingyi Li, Nan Mou, Qi Deng
Format: Article
Language:English
Published: Wiley 2024-02-01
Series:Cancer Medicine
Subjects:
Online Access:https://doi.org/10.1002/cam4.7064
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author Yi Li Jiang
Juan Mu
Rui Cui
Xin Li
Jia Wang
Qing Li
Jingyi Li
Nan Mou
Qi Deng
author_facet Yi Li Jiang
Juan Mu
Rui Cui
Xin Li
Jia Wang
Qing Li
Jingyi Li
Nan Mou
Qi Deng
author_sort Yi Li Jiang
collection DOAJ
description Abstract Introduction Although anti‐CD19 chimeric antigen receptor (CAR) T cell therapy was approved as a very effective salvage strategy in relapsed/refractory (R/R) B cell lymphoma, the experience in R/R gastrointestinal (GI) lymphoma is still insufficient. Methods We summarized the efficacy and side effects of anti‐CD19 CAR T‐cell therapy in 12 patients with R/R GI lymphoma. Based on literature, the R/R GI lymphoma patients were divided into subgroups with different characteristics: Bulky/No bulky disease, Gastric/Gastrointestinal involvement, Gastrointestinal/Combined extra‐gastrointestinal lesions, Ulcer/Lumps or nodules type, With/without gastrointestinal bleeding. Results The objective response rate (ORR) was 66.67% in these 12 patients. The ORR was 83.33% in no bulky disease group, 80.00% in gastric involvement group, 100.00% in ulcer type group, and 80.00% in no gastrointestinal bleeding group. The CR rate was 33.33% in these 12 patients. The CR was 50.0% in no bulky disease group, 60.00% in gastric involvement group, and 80.00% in ulcer type group. The PFS and OS rate of the 12 patients at 6 months after infusion were 54.55% and 58.33%, respectively. The overall survival (OS) at 6 months was higher in no bulky disease group. There was no difference of the OS or the progression free survival (PFS) at 6 months between the other groups. The mean peak of CAR‐T cells and Cytokine Release Syndrome (CRS) grade were higher in gastrointestinal lesions group. The mean peak of IFN‐γ and CRS grade were higher in gastrointestinal bleeding group. Four out of six patients in group of gastrointestinal lesions group were patient with high tumor burden. Patients with gastrointestinal involvement only were at higher risk for gastrointestinal bleeding. Conclusions The ORR and CR of high tumor load, gastrointestinal involvement, lumps or nodules type and gastrointestinal bleeding group were lower. The CRS grade was higher in gastrointestinal lesions group and in gastrointestinal bleeding group. Patients with gastrointestinal involvement only were at higher risk for gastrointestinal bleeding.
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spelling doaj.art-9535177f35744ea48bd4af32d72041102024-03-12T04:52:34ZengWileyCancer Medicine2045-76342024-02-01134n/an/a10.1002/cam4.7064Efficacy and side effects of anti‐CD19 CAR T‐cell therapy in patients with relapsed/refractory gastrointestinal lymphomaYi Li Jiang0Juan Mu1Rui Cui2Xin Li3Jia Wang4Qing Li5Jingyi Li6Nan Mou7Qi Deng8Department of Hematology, Tianjin First Central Hospital, School of Medicine Nankai University Tianjin ChinaDepartment of Hematology, Tianjin First Central Hospital, School of Medicine Nankai University Tianjin ChinaDepartment of Hematology, Tianjin First Central Hospital, School of Medicine Nankai University Tianjin ChinaDepartment of Hematology, Tianjin First Central Hospital, School of Medicine Nankai University Tianjin ChinaDepartment of Hematology, Tianjin First Central Hospital, School of Medicine Nankai University Tianjin ChinaDepartment of Hematology, Tianjin First Central Hospital, School of Medicine Nankai University Tianjin ChinaDepartment of Hematology, Tianjin First Central Hospital, School of Medicine Nankai University Tianjin ChinaShanghai Genbase Biotechnology Co., Ltd Shanghai ChinaDepartment of Hematology, Tianjin First Central Hospital, School of Medicine Nankai University Tianjin ChinaAbstract Introduction Although anti‐CD19 chimeric antigen receptor (CAR) T cell therapy was approved as a very effective salvage strategy in relapsed/refractory (R/R) B cell lymphoma, the experience in R/R gastrointestinal (GI) lymphoma is still insufficient. Methods We summarized the efficacy and side effects of anti‐CD19 CAR T‐cell therapy in 12 patients with R/R GI lymphoma. Based on literature, the R/R GI lymphoma patients were divided into subgroups with different characteristics: Bulky/No bulky disease, Gastric/Gastrointestinal involvement, Gastrointestinal/Combined extra‐gastrointestinal lesions, Ulcer/Lumps or nodules type, With/without gastrointestinal bleeding. Results The objective response rate (ORR) was 66.67% in these 12 patients. The ORR was 83.33% in no bulky disease group, 80.00% in gastric involvement group, 100.00% in ulcer type group, and 80.00% in no gastrointestinal bleeding group. The CR rate was 33.33% in these 12 patients. The CR was 50.0% in no bulky disease group, 60.00% in gastric involvement group, and 80.00% in ulcer type group. The PFS and OS rate of the 12 patients at 6 months after infusion were 54.55% and 58.33%, respectively. The overall survival (OS) at 6 months was higher in no bulky disease group. There was no difference of the OS or the progression free survival (PFS) at 6 months between the other groups. The mean peak of CAR‐T cells and Cytokine Release Syndrome (CRS) grade were higher in gastrointestinal lesions group. The mean peak of IFN‐γ and CRS grade were higher in gastrointestinal bleeding group. Four out of six patients in group of gastrointestinal lesions group were patient with high tumor burden. Patients with gastrointestinal involvement only were at higher risk for gastrointestinal bleeding. Conclusions The ORR and CR of high tumor load, gastrointestinal involvement, lumps or nodules type and gastrointestinal bleeding group were lower. The CRS grade was higher in gastrointestinal lesions group and in gastrointestinal bleeding group. Patients with gastrointestinal involvement only were at higher risk for gastrointestinal bleeding.https://doi.org/10.1002/cam4.7064B‐cell lymphomachimeric antigen receptor (CAR)gastrointestinal lymphomarelapsed/refractory
spellingShingle Yi Li Jiang
Juan Mu
Rui Cui
Xin Li
Jia Wang
Qing Li
Jingyi Li
Nan Mou
Qi Deng
Efficacy and side effects of anti‐CD19 CAR T‐cell therapy in patients with relapsed/refractory gastrointestinal lymphoma
Cancer Medicine
B‐cell lymphoma
chimeric antigen receptor (CAR)
gastrointestinal lymphoma
relapsed/refractory
title Efficacy and side effects of anti‐CD19 CAR T‐cell therapy in patients with relapsed/refractory gastrointestinal lymphoma
title_full Efficacy and side effects of anti‐CD19 CAR T‐cell therapy in patients with relapsed/refractory gastrointestinal lymphoma
title_fullStr Efficacy and side effects of anti‐CD19 CAR T‐cell therapy in patients with relapsed/refractory gastrointestinal lymphoma
title_full_unstemmed Efficacy and side effects of anti‐CD19 CAR T‐cell therapy in patients with relapsed/refractory gastrointestinal lymphoma
title_short Efficacy and side effects of anti‐CD19 CAR T‐cell therapy in patients with relapsed/refractory gastrointestinal lymphoma
title_sort efficacy and side effects of anti cd19 car t cell therapy in patients with relapsed refractory gastrointestinal lymphoma
topic B‐cell lymphoma
chimeric antigen receptor (CAR)
gastrointestinal lymphoma
relapsed/refractory
url https://doi.org/10.1002/cam4.7064
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