# Efficacy of chimeric antigen receptor T-cell therapy in testicular relapse of pediatric acute lymphoblastic leukemia: a multicenter retrospective study

**Authors:** Ning Wang, Yanjing Tang, Yong Zhuang, Jiaoyang Cai, Shaoyan Hu, Xue Yang, Yongjun Fang, Xiaoyan Wu, Ningling Wang, Lingzhen Wang, Xiaowen Zhai, Minghua Yang, Xin Tian, Yaqin Wang, Hong Li, Leifeng Zhao, Chi Kong Li, Xiaojuan Chen, Xiaofan Zhu

PMC · DOI: 10.3389/fimmu.2026.1766494 · Frontiers in Immunology · 2026-02-11

## TL;DR

This study evaluates the effectiveness of CAR-T therapy in treating testicular relapse in children with leukemia, finding it as effective as traditional treatments.

## Contribution

The study provides new evidence on CAR-T therapy's efficacy for testicular relapse in pediatric ALL.

## Key findings

- CAR-T therapy achieved a 2-year overall survival rate of 90.7% in treated patients.
- Survival rates with CAR-T therapy were comparable to conventional treatments like chemotherapy and orchiectomy.
- Testicular relapse typically occurred about 3 years after initial diagnosis.

## Abstract

Testicular relapse constitutes one of the most frequent extramedullary recurrences in pediatric acute lymphoblastic leukemia (ALL), yet its clinical management remains incompletely characterized.

This study assessed treatment outcomes and long-term survival in children with testicular relapse following initial therapy under the CCCG-ALL-2015 study (ChiCTR-IPR-14005706, http://www.chictr.org.cn). In total, 66 patients from 13 medical centers were retrospectively analyzed. Clinical characteristics and survival outcomes were compared across salvage treatment modalities.

The median interval from initial diagnosis to testicular relapse was 37 months. Among 59 patients who received post-relapse therapy, the 2-year overall survival (OS) rate was 86.1% after a median follow-up of 33 months. Patients treated with chimeric antigen receptor T-cell (CAR-T) therapy showed a 2-year OS of 90.7%, compared to 81.7% in those managed with conventional regimens, such as chemotherapy, orchiectomy, or hematopoietic stem-cell transplantation (P > 0.05). Among 37 children with isolated testicular relapse, 18 underwent CAR-T therapy and 10 underwent orchiectomy, achieving 2-year OS rates of 92.3% and 100%, respectively (P > 0.05).

Testicular relapse typically emerged approximately 3 years after initial diagnosis. CAR-T therapy proved to be both safe and effective, providing survival comparable to conventional regimens and offering potential advantages in preserving life quality among long-term survivors.

## Linked entities

- **Diseases:** acute lymphoblastic leukemia (MONDO:0004967)

## Full-text entities

- **Genes:** CD19 (CD19 molecule) [NCBI Gene 930] {aka B4, CVID3}, CD22 (CD22 molecule) [NCBI Gene 933] {aka SIGLEC-2, SIGLEC2}, KMT2A (lysine methyltransferase 2A) [NCBI Gene 4297] {aka ALL-1, ALL1, CXXC7, GAS7, HRX, HTRX}
- **Diseases:** seizure (MESH:D012640), B-cell aplasia (MESH:D015448), CTR (MESH:D009371), relapse (MESH:D012008), HL (MESH:C538324), ITR (MESH:D013733), testicular enlargement (OMIM:300888), Cancer (MESH:D009369), B-lineage (MESH:D006509), CRS (MESH:D000080424), CAR-T (MESH:C535887), death (MESH:D003643), extramedullary disease (MESH:D023981), leukemic (MESH:D007938), infection (MESH:D007239), fertility impairment (MESH:D007246), ALL (MESH:D054198), BM (MESH:D001855), toxicity (MESH:D064420)
- **Chemicals:** methotrexate (MESH:D008727), cyclophosphamide (MESH:D003520), T (MESH:D014316), CAR-T (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12932491/full.md

## References

18 references — full list in the complete paper: https://tomesphere.com/paper/PMC12932491/full.md

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Source: https://tomesphere.com/paper/PMC12932491