Case Report: CD19 CAR T-cell therapy following autologous stem cell transplantation: a successful treatment for R/R CD20-negative transformed follicular lymphoma with TP53 mutation

被引:3
作者
Zhang, Jinjing [1 ]
Cai, Dali [1 ]
Gao, Ran [1 ]
Miao, Yuan [2 ]
Cui, Yan [3 ]
Liu, Zhenghua [1 ]
Zhang, Heyang [1 ]
Yan, Xiaojing [1 ]
Su, Nan [1 ]
机构
[1] China Med Univ, Affiliated Hosp 1, Dept Hematol, Shenyang, Liaoning, Peoples R China
[2] China Med Univ, Affiliated Hosp 1, Dept Pathol, Shenyang, Liaoning, Peoples R China
[3] China Med Univ, Affiliated Hosp 1, Dept Nucl Med, Shenyang, Liaoning, Peoples R China
来源
FRONTIERS IN IMMUNOLOGY | 2023年 / 14卷
关键词
transformed follicular lymphoma; diffuse large B-cell lymphoma; TP53; mutation; chimeric antigen receptor T-cell; autologous stem cell transplantation; HISTOLOGICAL TRANSFORMATION; RELAPSED DLBCL; ANTIGEN; IBRUTINIB; MULTICENTER; INHIBITION; EXPRESSION; EFFICACY; RISK;
D O I
10.3389/fimmu.2023.1307242
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Follicular lymphoma (FL), a common indolent B-cell lymphoma, has the potential to transform into an aggressive lymphoma, such as diffuse large B-cell lymphoma (DLBCL). The outcome of patients with transformed follicular lymphoma (tFL) is poor, especially in patients with transformed lymphoma after chemotherapy and patients with progression within 24 months (POD24). Chimeric antigen receptor (CAR) T-cell therapy combined with autologous stem cell transplantation (ASCT) has promising antitumor efficacy. Case presentation: Here, we described a 39-year-old male patient who was initially diagnosed with FL that transformed into DLBCL with POD24, CD20 negativity, TP53 mutation, and a bulky mass after 3 lines of therapy, all of which were adverse prognostic factors. We applied a combination approach: CD19 CAR T-cell infusion following ASCT. Ibrutinib was administered continuously to enhance efficacy, DHAP was administered as a salvage chemotherapy, and ICE was administered as a bridging regimen. The patient underwent BEAM conditioning on days -7 similar to -1, a total of 3.8 x 10(6)/kg CD34(+) stem cells were infused on days 01 similar to 02, and a total of 108 CAR T cells (relmacabtagene autoleucel, relma-cel, JWCAR029) were infused on day 03. The patient experienced grade 2 cytokine release syndrome (CRS), manifesting as fever and hypotension according to institutional standards. There was no immune effector cell-associated neurotoxicity syndrome (ICANS) after CAR T-cell infusion. Finally, the patient achieved CMR at +1 month, which has been maintained without any other adverse effects. Conclusion: This case highlights the amazing efficacy of CD19 CAR T-cell therapy following ASCT for R/R tFL, thus providing new insight on therapeutic strategies for the future.
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页数:8
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