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虚弱并非失败:合并症对接受CAR-T治疗的弥漫大B细胞淋巴瘤患者非复发死亡率及安全性的影响有限。

Frail is not fail: Limited impact of comorbidities on non-relapse mortality and safety in patients with LBCL treated with CAR-T.

作者信息

Galli Eugenio, Di Blasi Roberta, Pansini Ilaria, Cristinelli Caterina, Bommier Come, De Bernardis Ilenia, Corrente Alessandro, Viscovo Marcello, Montini Luca, Chiusolo Patrizia, Hohaus Stefan, Sorà Federica, Thieblemont Catherine, Sica Simona

机构信息

Department of Laboratory and Hematological Sciences, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.

Hemato-Oncology Department, Assistance Publique-Hôpitaux de Paris (AP-HP), Saint-Louis Hospital, Paris, France.

出版信息

Br J Haematol. 2025 Jun 23;207(2):642-7. doi: 10.1111/bjh.20222.


DOI:10.1111/bjh.20222
PMID:40551480
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12378911/
Abstract

We applied three major comorbidity scoring systems-CIRS, HCT-CI, and Severe4-to a cohort of 379 patients with LBCL treated with CAR-T therapy. A high comorbidity burden was identified in 7% to 34% of patients, depending on the score used. However, a high comorbidity burden did not negatively impact the tolerability of CAR-T treatment, including the incidence of CRS, or hematologic toxicity. The use of tocilizumab and corticosteroids was comparable between patients with low and high comorbidity burden, as was the cumulative incidence of non-relapse mortality.

摘要

我们将三种主要的合并症评分系统——累积疾病评分量表(CIRS)、造血细胞移植合并症指数(HCT-CI)和Severe4——应用于379例接受嵌合抗原受体T细胞(CAR-T)疗法治疗的大B细胞淋巴瘤(LBCL)患者队列。根据所使用的评分,7%至34%的患者被确定为合并症负担较高。然而,高合并症负担并未对CAR-T治疗的耐受性产生负面影响,包括细胞因子释放综合征(CRS)的发生率或血液学毒性。合并症负担低和高的患者之间,托珠单抗和皮质类固醇的使用情况以及非复发死亡率的累积发生率相当。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2204/12378911/eaeb621de95e/BJH-207-642-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2204/12378911/eaeb621de95e/BJH-207-642-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2204/12378911/eaeb621de95e/BJH-207-642-g001.jpg

相似文献

[1]
Frail is not fail: Limited impact of comorbidities on non-relapse mortality and safety in patients with LBCL treated with CAR-T.

Br J Haematol. 2025-6-23

[2]
Chimeric antigen receptor (CAR) T-cell therapy for people with relapsed or refractory diffuse large B-cell lymphoma.

Cochrane Database Syst Rev. 2021-9-13

[3]
Chimeric Antigen Receptor T-Cell Access in Patients with Relapsed/Refractory Large B-Cell Lymphoma: Association of Access with Social Determinants of Health and Travel Time to Treatment Centers.

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[4]
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[5]
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[6]
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2025-1

[7]
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[8]
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[9]
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[10]
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Transplant Cell Ther. 2024-6

本文引用的文献

[1]
Predicting therapy-related myeloid neoplasms after CAR-T with the Clonal Haematopoiesis Risk Score (CHRS).

Br J Haematol. 2025-1

[2]
A systematic review and meta-analysis of nonrelapse mortality after CAR T cell therapy.

Nat Med. 2024-9

[3]
Axicabtagene ciloleucel as second-line therapy in large B cell lymphoma ineligible for autologous stem cell transplantation: a phase 2 trial.

Nat Med. 2023-10

[4]
The CAR-HEMATOTOX score identifies patients at high risk for hematological toxicity, infectious complications, and poor treatment outcomes following brexucabtagene autoleucel for relapsed or refractory MCL.

Am J Hematol. 2023-11

[5]
Immune effector cell-associated hematotoxicity: EHA/EBMT consensus grading and best practice recommendations.

Blood. 2023-9-7

[6]
A validated composite comorbidity index predicts outcomes of CAR T-cell therapy in patients with diffuse large B-cell lymphoma.

Blood Adv. 2023-7-25

[7]
Endothelial activation predicts disseminated intravascular coagulopathy, cytokine release syndrome and prognosis in patients treated with anti-CD19 CAR-T cells.

Br J Haematol. 2023-4

[8]
Lisocabtagene maraleucel as second-line therapy in adults with relapsed or refractory large B-cell lymphoma who were not intended for haematopoietic stem cell transplantation (PILOT): an open-label, phase 2 study.

Lancet Oncol. 2022-8

[9]
CAR T-Cell Therapies in Italy: Patient Access Barriers and Recommendations for Health System Solutions.

Front Pharmacol. 2022-6-23

[10]
The CAR-HEMATOTOX risk-stratifies patients for severe infections and disease progression after CD19 CAR-T in R/R LBCL.

J Immunother Cancer. 2022-5

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