# Successful treatment of an elderly patient with relapsed/refractory angioimmunoblastic T-cell lymphoma with the PI3Kδ inhibitor linperlisib: a Case Report

**Authors:** Ming-Qiang Chu, Ting-Juan Zhang, Qian Yang, Yuan Feng, Chao Lu, Yong-Hui Ji, Jun Qian, Jing-Dong Zhou

PMC · DOI: 10.3389/fphar.2025.1554501 · Frontiers in Pharmacology · 2025-05-15

## TL;DR

An elderly patient with aggressive T-cell lymphoma achieved partial remission using linperlisib, a drug that targets a specific pathway and is well-tolerated.

## Contribution

This case report demonstrates linperlisib's effectiveness and safety in treating elderly patients with relapsed/refractory AITL.

## Key findings

- Linperlisib combined with gemcitabine/oxaliplatin induced sustained partial remission in an 80-year-old patient.
- The treatment was exceptionally safe with no grade ≥2 toxicities observed.
- Linperlisib maintenance therapy was well-tolerated in a frail elderly population.

## Abstract

Angioimmunoblastic T-cell lymphoma (AITL), a highly aggressive peripheral T-cell lymphoma (PTCL), carries a poor prognosis in elderly patients due to frequent relapse and limited salvage options after multiline therapy. We present the case of an 80-year-old woman with relapsed/refractory (R/R) AITL who relapsed after CHOP and exhibited resistance to the following sequential therapies: second-line chidamide plus COP and third-line chidamide with mitoxantrone hydrochloride liposome. Molecular analysis revealed DNMT3A and IDH2 mutations, reflecting disease complexity. Salvage therapy with linperlisib, a selective PI3Kδ inhibitor, combined with gemcitabine/oxaliplatin induced sustained partial remission, followed by linperlisib maintenance. The regimen demonstrated exceptional safety, with no grade ≥2 toxicities, even in this frail population. This case highlights the dual role of linperlisib as an effective and well-tolerated therapy for elderly R/R AITL patients who have exhausted prior lines. By precisely targeting PI3Kδ, our findings offer critical real-world evidence to address the unmet need for safe salvage strategies in this vulnerable population.

## Linked entities

- **Genes:** DNMT3A (DNA methyltransferase 3 alpha) [NCBI Gene 1788], IDH2 (isocitrate dehydrogenase (NADP(+)) 2) [NCBI Gene 3418]
- **Chemicals:** chidamide (PubChem CID 9800555), gemcitabine (PubChem CID 60750), oxaliplatin (PubChem CID 9887053), linperlisib (PubChem CID 91754520)
- **Diseases:** angioimmunoblastic T-cell lymphoma (MONDO:0004977), peripheral T-cell lymphoma (MONDO:0000430)

## Full-text entities

- **Genes:** DNMT3A (DNA methyltransferase 3 alpha) [NCBI Gene 1788] {aka DNMT3A2, HESJAS, M.HsaIIIA, TBRS}, IDH2 (isocitrate dehydrogenase (NADP(+)) 2) [NCBI Gene 3418] {aka D2HGA2, ICD-M, IDH, IDH-2, IDHM, IDP}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}
- **Diseases:** AITL (MESH:D016399), PTCL (MESH:D016411), toxicities (MESH:D064420)
- **Chemicals:** CHOP (-), mitoxantrone hydrochloride (MESH:D008942), chidamide (MESH:C547816), gemcitabine/oxaliplatin (MESH:C508870)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12119530/full.md

## References

26 references — full list in the complete paper: https://tomesphere.com/paper/PMC12119530/full.md

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Source: https://tomesphere.com/paper/PMC12119530