# Outcomes of point-of-care manufactured CAR T cell therapy for B cell acute lymphoblastic leukemia and non-Hodgkin lymphoma in Vietnam

**Authors:** Liem Thanh Nguyen, Duy D. Nguyen, Quoc Khanh Bach, Lan T.M. Dao, Trang Thi Kieu Phan, Hoang - Phuong Nguyen, Hong-Nhung Dao, Trang H. Pham, Phuong T. Pham, Hien T. Mai, Viet Huong T. Pham, Thanh Mai T. Nguyen, Van Binh Le, Nam Lam Phung, Ngoc Quang Nguyen, Michelle L. Hermiston, Quynh Lan Phan, Do Quang Trung Nguyen, Lan Mai, Quoc Nhat Nguyen, Van T. Hoang

PMC · DOI: 10.1016/j.omton.2026.201156 · Molecular Therapy Oncology · 2026-02-13

## TL;DR

A clinical trial in Vietnam shows that on-site CAR T cell therapy is safe and effective for treating certain blood cancers, offering hope for low-resource regions.

## Contribution

Demonstrates the safety and feasibility of point-of-care CAR T cell therapy in a resource-limited setting for the first time.

## Key findings

- 100% complete remission in ALL patients at day 30, with 62.5% at day 180.
- 87.5% complete remission in NHL patients at both day 90 and day 180.
- Toxicity was manageable, with most cytokine release syndrome cases being grade 1–2.

## Abstract

Chimeric antigen receptor (CAR) T cell therapy has transformed the treatment of relapsed/refractory (R/R) B cell acute lymphoblastic leukemia (ALL) and non-Hodgkin lymphoma (NHL), but access remains limited in resource-constrained settings. This phase I study evaluated the safety and feasibility of point-of-care (PoC) manufactured CD19-targeted CAR T cell therapy in Vietnamese patients. Between August 2023 and June 2025, 16 patients, eight with R/R ALL and eight with R/R NHL, were enrolled. All received fresh CAR T cells produced on-site using the CliniMACS Prodigy system, with a median dose of 1.9 × 106 CAR T cells/kg (range, 0.83–2.17 × 106). Cytokine release syndrome (CRS) occurred in 13 patients (12 with grade 1–2, one with grade 3), and grade 1 neurotoxicity was observed in two patients. In ALL, the complete remission (CR) rates were 100% on day 30, 75% on day 90, and 62.5% on day 180. Patients with NHL showed CR rates of 87.5% on both day 90 and day 180. The estimated 1-year progression-free survival rates were 62.5% (95% confidence interval [CI]: 36.5%–100%) for ALL and 87.5% (95% CI: 67.3%–100%) for NHL. PoC manufactured CD19 CAR T cells demonstrated manageable toxicity and encouraging early efficacy in Vietnamese patients with R/R ALL and NHL. This model offers a cost-effective strategy for delivering advanced therapy in resource-limited settings.

This phase 1 clinical trial in Vietnam demonstrates that point-of-care CD19-targeted CAR T cell therapies are safe and effective for relapsed/refractory ALL and NHL. The findings highlight the feasibility of delivering advanced cellular therapies in resource-limited settings, offering a promising strategy to expand access to life-saving treatments for B cell malignancies.

## Linked entities

- **Proteins:** CD19 (CD19 molecule)
- **Diseases:** B cell acute lymphoblastic leukemia (MONDO:0004947), non-Hodgkin lymphoma (MONDO:0018908), cytokine release syndrome (MONDO:0600008), neurotoxicity (MONDO:0005527)

## Full-text entities

- **Genes:** CD247 (CD247 molecule) [NCBI Gene 919] {aka CD3-ZETA, CD3H, CD3Q, CD3Z, CD3ZETA, IMD25}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CSF2 (colony stimulating factor 2) [NCBI Gene 1437] {aka CSF, GMCSF}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, CD22 (CD22 molecule) [NCBI Gene 933] {aka SIGLEC-2, SIGLEC2}, CD27 (CD27 molecule) [NCBI Gene 939] {aka S152, S152. LPFS2, T14, TNFRSF7, Tp55}, CD19 (CD19 molecule) [NCBI Gene 930] {aka B4, CVID3}, TNFRSF19 (TNF receptor superfamily member 19) [NCBI Gene 55504] {aka TAJ, TAJ-alpha, TRADE, TROY}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, KRT20 (keratin 20) [NCBI Gene 54474] {aka CD20, CK-20, CK20, K20, KRT21}, CD38 (CD38 molecule) [NCBI Gene 952] {aka ADPRC 1, ADPRC1, cADPR1}, CXADRP1 (CXADR pseudogene 1) [NCBI Gene 653108] {aka CAR, CXADRP}, SDC1 (syndecan 1) [NCBI Gene 6382] {aka CD138, SDC, SYND1, syndecan}
- **Diseases:** death (MESH:D003643), PoC (MESH:D003428), follicular lymphoma (MESH:D008224), B cell ALL (MESH:D015456), SAEs (MESH:D064420), ALL (MESH:D054198), BM (MESH:D001855), ICANS (MESH:C000722498), infection (MESH:D007239), HDDD (OMIM:607485), NHL (MESH:D008228), B cell NHL (MESH:D016393), CRS (MESH:D000080424), release (MESH:C566759), cell (MESH:D002292), CR (MESH:D012075), DLBCL (MESH:D016403), mantle cell lymphoma (MESH:D020522), disease (MESH:D004194), Cancer (MESH:D009369), neurotoxicity (MESH:D020258), Hypogammaglobulinemia (MESH:D000361), febrile (MESH:D000071072), Fever (MESH:D005334), hematologic malignancies (MESH:D019337), B cell aplasia (MESH:D015448), Acute Leukemia (MESH:D015470)
- **Chemicals:** BN03 (-), Dexamethasone (MESH:D003907), Tocilizumab (MESH:C502936), fludarabine (MESH:C024352), cyclophosphamide (MESH:D003520)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mycoplasma (genus) [taxon 2093]
- **Cell lines:** BN10 — Homo sapiens (Human), Plasma cell myeloma, Cancer cell line (CVCL_Y432), NALM6 — Homo sapiens (Human), Adult B acute lymphoblastic leukemia, Cancer cell line (CVCL_0092)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12969028/full.md

## References

46 references — full list in the complete paper: https://tomesphere.com/paper/PMC12969028/full.md

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Source: https://tomesphere.com/paper/PMC12969028