# Management of inpatient chimeric antigen receptor T-cell therapy for relapsed/refractory B-cell malignancies: an analysis using the Japanese Diagnosis Procedure Combination database

**Authors:** Keisuke Tanaka, Hiroaki Kikuchi, Yoshihiro Umezawa, Takehiko Mori, Kiyohide Fushimi, Masahide Yamamoto

PMC · DOI: 10.1007/s12185-025-04043-8 · International Journal of Hematology · 2025-08-06

## TL;DR

This study analyzes real-world data from Japan to understand how adverse events are managed in patients receiving CAR-T therapy for B-cell cancers.

## Contribution

The study provides new real-world evidence on perioperative management strategies for CAR-T therapy in Japan.

## Key findings

- Tocilizumab was used in over half of LBCL patients for cytokine release syndrome.
- Steroids were administered to a higher proportion of B-ALL patients compared to LBCL patients.
- Most patients received fungal infection prophylaxis during CAR-T infusion.

## Abstract

Chimeric antigen receptor T-cell (CAR-T) therapy has shown remarkable efficacy in treating relapsed/refractory B-cell malignancies, as supported by real-world evidence (RWE). However, limited RWE exists on the management of adverse events during the perioperative period following CAR-T infusion. This study was conducted to obtain RWE on perioperative management using the Japanese Diagnosis Procedure Combination database, a comprehensive repository of Japanese health and medical service data. Between November 2019 and March 2022, 388 patients received CAR-T therapy. Of these, 312 had large B-cell lymphoma (LBCL) and 76 had B-cell acute lymphoblastic leukemia (B-ALL). The number of CAR-T infusions increased every 6-month interval, correlating with the rise in LBCL cases. Tocilizumab was administered for cytokine release syndrome in 56.1% of LBCL and 42.1% of B-ALL patients. Steroids were used for 22.9% and 81.3%, respectively. Prophylaxis for fungal infections was administered during CAR-T infusion in most LBCL and B-ALL patients. Treatment intensity was escalated in 2.8% of LBCL and 7.0% of B-ALL patients, and treatment for cytomegalovirus infection was initiated in approximately 7% of patients. This analysis elucidated perioperative management strategies based on patients’ medication histories.

## Linked entities

- **Diseases:** large B-cell lymphoma (MONDO:0968974), B-cell acute lymphoblastic leukemia (MONDO:0004947), cytomegalovirus infection (MONDO:0005132)

## Full-text entities

- **Diseases:** B-ALL (MESH:D015456), fungal infections (MESH:D009181), B-cell malignancies (MESH:D016393), cytokine release syndrome (MESH:D000080424), cytomegalovirus infection (MESH:D003586)
- **Chemicals:** CAR-T (-), Steroids (MESH:D013256), Tocilizumab (MESH:C502936)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12638367