# Real-world clinical outcomes of CAR-T therapy from the Montefiore health system in the Bronx

**Authors:** Sonya Henry, Ahmed Abbasi, Aiman Hafeez, Aditi Vichare, R. Alejandro Sica, Tim Q. Duong

PMC · DOI: 10.1007/s00277-025-06727-x · 2025-11-13

## TL;DR

This study examines the real-world outcomes of CAR-T therapy for lymphoma in a diverse urban population in the Bronx, highlighting remission rates and complications.

## Contribution

The study provides real-world clinical data on CAR-T therapy outcomes in a diverse urban population, emphasizing remission and complication rates.

## Key findings

- CAR-T therapy achieved complete remission in 50.6% of DLBCL patients.
- Cumulative mortality was 34.2% by five years, with complete remission reducing 3-year mortality.
- CRS and ICANS were common complications, with ICANS correlating with ICU stay and sepsis.

## Abstract

Chimeric antigen receptor T-cell (CAR-T) therapy has transformed diffuse large B-cell lymphoma (DLBCL) treatment, but data in diverse urban populations remain limited. We report outcomes from a comprehensive cancer center in the Bronx. Montefiore Health System treated 79 DLBCL patients with CAR-T from March 2018 to July 2024. Demographics, comorbidities, socioeconomic factors, and acute complications, including immune effector cell neurotoxicity syndrome (ICANS), cytokine release syndrome (CRS), cardiotoxicity, and pulmonary events, were tabulated. Kaplan-Meier survival analysis was performed up to five years. Multivariate adjusted hazard ratios (aHR) were calculated for remission and 3-year mortality. CAR-T achieved complete remissions in 50.6%, partial remission in 16.5%, and progression in 22.8%. Cumulative mortality was 10.1% during treatment and 34.2% by five years. Complete remission reduced 3-year mortality (aHR 0.13; 95% CI 0.04–0.43). Complications included CRS (76.0%), ICANS (49.4%), neutropenic fever (58.2%), and sepsis (19.0%). ICANS correlated with CRS, ICU stay, and sepsis. Socioeconomic status was not linked to mortality, but comorbidities increased risk. CAR-T complete remission is an independent predictor of reduced mortality. High rates of complications, particularly CRS and ICAN, reinforce the need for vigilant monitoring and management strategies to enhance long-term outcomes.

The online version contains supplementary material available at 10.1007/s00277-025-06727-x.

## Linked entities

- **Diseases:** diffuse large B-cell lymphoma (MONDO:0018905), cytokine release syndrome (MONDO:0600008)

## Full-text entities

- **Diseases:** cardiotoxicity (MESH:D066126), immune effector cell (MESH:C000722498), sepsis (MESH:D018805), Complications (MESH:D008107), DLBCL (MESH:D016403), CRS (MESH:D000080424), cancer (MESH:D009369), neutropenic fever (MESH:D005334), neurotoxicity syndrome (MESH:D020258)
- **Chemicals:** CAR-T (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12764600/full.md

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Source: https://tomesphere.com/paper/PMC12764600