# Re-treatment of relapse in elderly AML with time-limited venetoclax-based regimen: a case report and literature review

**Authors:** Jun Yen Ng, Veena Gullapalli, Jad Othman, Dipti Talaulikar

PMC · DOI: 10.1007/s00277-026-06781-z · 2026-02-17

## TL;DR

An elderly AML patient with NPM1 mutation responded well to re-treatment with venetoclax and low-dose cytarabine after relapse, suggesting potential for this approach in similar cases.

## Contribution

This case report adds to the limited evidence on re-treating relapsed AML with a time-limited venetoclax-based regimen.

## Key findings

- The patient achieved a sustained response after re-treatment with venetoclax and low-dose cytarabine.
- The case highlights the potential of re-treatment with venetoclax-based therapy in relapsed AML.
- Prospective studies are needed to confirm the efficacy and safety of this strategy.

## Abstract

Venetoclax and hypomethylating agent combination therapy is now the standard of care in acute myeloid leukemia (AML) for patients ineligible for intensive therapy, including the elderly; however, venetoclax and low-dose cytarabine remain a viable option for select patients. Relapse in this cohort remains a significant challenge, with a poor prognosis and an unmet need for further treatment options. This case discusses an elderly patient with NPM1-mutated AML successfully retreated with time-limited venetoclax and low-dose cytarabine at relapse. The sustained response observed contributes to the limited literature on the efficacy of re-treatment with venetoclax-based therapy in this setting. However, prospective data are required to assess the efficacy and safety of this strategy as well as to establish the role of molecular monitoring. The role of time-limited venetoclax therapy for preventing treatment resistance and limiting treatment-related adverse effects remains an important question in the cohort ineligible for intensive therapies, given the poor prognosis and limited options of relapsed/refractory AML post-venetoclax and hypomethylating agent therapy.

## Linked entities

- **Genes:** NPM1 (nucleophosmin 1) [NCBI Gene 4869]
- **Chemicals:** venetoclax (PubChem CID 49846579), cytarabine (PubChem CID 6253)
- **Diseases:** acute myeloid leukemia (MONDO:0015667), AML (MONDO:0018874)

## Full-text entities

- **Genes:** RUNX1 (RUNX family transcription factor 1) [NCBI Gene 861] {aka AML1, AML1-EVI-1, AMLCR1, CBF2alpha, CBFA2, EVI-1}, IDH2 (isocitrate dehydrogenase (NADP(+)) 2) [NCBI Gene 3418] {aka D2HGA2, ICD-M, IDH, IDH-2, IDHM, IDP}, NPM1 (nucleophosmin 1) [NCBI Gene 4869] {aka B23, NPM}, SRSF2 (serine and arginine rich splicing factor 2) [NCBI Gene 6427] {aka PR264, SC-35, SC35, SFRS2, SFRS2A, SRp30b}, FLT3 (fms related receptor tyrosine kinase 3) [NCBI Gene 2322] {aka CD135, FLK-2, FLK2, STK1}, MCL1 (MCL1 apoptosis regulator, BCL2 family member) [NCBI Gene 4170] {aka BCL2L3, EAT, MCL1-ES, MCL1L, MCL1S, Mcl-1}, ELN (elastin) [NCBI Gene 2006] {aka ADCL1, SVAS, WBS, WS}, TET2 (tet methylcytosine dioxygenase 2) [NCBI Gene 54790] {aka IMD75, KIAA1546, MDS}, BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596] {aka Bcl-2, PPP1R50}, DDX41 (DEAD-box helicase 41) [NCBI Gene 51428] {aka ABS, MPLPF}
- **Diseases:** neuropathy (MESH:D009422), febrile neutropenia (MESH:D064147), AML (MESH:D015470), MDS (MESH:D009190), RCMD (MESH:D000069279), PD (MESH:D018450), ocular toxicity (MESH:D000081028), VIALE-Cs (MESH:C566879), macrocytosis (MESH:C564004), cardiac failure (MESH:D006333), Campylobacter gastroenteritis (MESH:D002169), MLD (MESH:D015456), cytotoxic (MESH:D064420), ND (MESH:C537849), idiopathic dilated cardiomyopathy (MESH:D002311), demyelinating polyneuropathy (MESH:D003711), cytopenia (MESH:D006402), neutropenia (MESH:D009503), multilineage dysplasia (MESH:D015792), Leukemia (MESH:D007938), CIDP (MESH:D020277), disease (MESH:D004194), dental abscesses (MESH:D000038), inflammatory (MESH:D007249)
- **Chemicals:** Azacitidine (MESH:D001374), decitabine (MESH:D000077209), cytarabine (MESH:D003561), Venetoclax (MESH:C579720), anthracycline (MESH:D018943), HMA (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12909330/full.md

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Source: https://tomesphere.com/paper/PMC12909330