# Treatment of Acute Myeloid Leukemia in Elderly Patients With Azacitidine–Venetoclax Combination in Developing Countries: A Single-Center Experience

**Authors:** Rim Chakara, Aznag Mohamed Amine, Abderrahim Raissi

PMC · DOI: 10.7759/cureus.102308 · Cureus · 2026-01-26

## TL;DR

This study shows that azacitidine-venetoclax is effective for elderly AML patients in Morocco, with a 25-month median survival, but highlights challenges with toxicity and drug cost.

## Contribution

Provides real-world evidence of AZA-VEN effectiveness and safety in elderly AML patients from a North African setting.

## Key findings

- Four out of eight patients achieved complete remission after the first AZA-VEN cycle.
- Median survival was 25 months, with four patients alive at two years.
- Grade 3-4 hematologic toxicities and infectious complications were common.

## Abstract

Background and objectives: Acute myeloid leukemia (AML) predominantly affects elderly patients and is associated with a poor prognosis. Therapeutic options remain limited for patients who are ineligible for intensive chemotherapy. Real-world data on the use of azacitidine-venetoclax (AZA-VEN) in North African populations are scarce. This study aimed to assess the effectiveness, composite complete remission rates, and safety profile of AZA-VEN in elderly AML patients treated at a Moroccan center.

Materials and methods: We conducted a retrospective study including patients aged ≥60 years who received AZA-VEN between July 2021 and August 2024 at the Military Hospital Ibn Sina in Marrakech. VEN was administered with a ramp-up protocol, combined with AZA and prophylactic voriconazole. Treatment response was assessed after the first cycle using bone marrow aspiration and blood counts. Overall survival (OS) was estimated using Kaplan-Meier curves.

Results: Eight patients were included, with a median age of 67 years and a male predominance. Seven patients had comorbidities. Four patients achieved complete remission (CR) after the first cycle, while two showed no response. Four patients experienced relapse or disease progression during follow-up. Grade 3-4 hematologic toxicities were frequent: neutropenia in all eight patients, anemia in seven patients, and thrombocytopenia in seven patients. All patients developed infectious complications. Median follow-up was 17 months, with a median survival of 25 months. Four out of eight patients were alive at two years.

Conclusions: Our single-center experience confirms that AZA-VEN is an effective and feasible therapeutic option for elderly AML patients, with a median survival of 25 months. Hematologic and infectious toxicities remain major challenges. In a North African context, limited access to VEN due to its cost can be partially mitigated through dose adjustments with azole antifungals. Further prospective multicenter studies are warranted.

## Linked entities

- **Chemicals:** azacitidine (PubChem CID 9444), venetoclax (PubChem CID 49846579), voriconazole (PubChem CID 71616)
- **Diseases:** acute myeloid leukemia (MONDO:0015667)

## Full-text entities

- **Genes:** IDH2 (isocitrate dehydrogenase (NADP(+)) 2) [NCBI Gene 3418] {aka D2HGA2, ICD-M, IDH, IDH-2, IDHM, IDP}, ASXL1 (ASXL transcriptional regulator 1) [NCBI Gene 171023] {aka BOPS, MDS}, BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596] {aka Bcl-2, PPP1R50}, ELN (elastin) [NCBI Gene 2006] {aka ADCL1, SVAS, WBS, WS}
- **Diseases:** pneumonia (MESH:D011014), myelofibrosis (MESH:D055728), diarrhea (MESH:D003967), leukopenia (MESH:D007970), hemorrhagic (MESH:D006470), frailty (MESH:D000073496), vomiting (MESH:D014839), AML (MESH:D015470), hematologic malignancy (MESH:D019337), fever (MESH:D005334), myelodysplastic syndrome (MESH:D009190), myeloproliferative neoplasm (MESH:D009369), hypokalemia (MESH:D007008), bacterial and (MESH:D001424), Infectious complications (MESH:D003141), febrile neutropenia (MESH:D064147), fungal infections (MESH:D009181), tumor lysis (MESH:D015275), Neutropenia (MESH:D009503), death (MESH:D003643), Hematologic toxicity (MESH:D006402), leukemia (MESH:D007938), anemia (MESH:D000740), phlebitis (MESH:D010689), Toxicities (MESH:D064420), leukocytosis (MESH:D007964), oral mucositis (MESH:D013280), infections (MESH:D007239), bacteremia (MESH:D016470), thrombocytopenia (MESH:D013921)
- **Chemicals:** Voriconazole (MESH:D065819), methicillin (MESH:D008712), VEN (MESH:C579720), AZA (MESH:D001379), azole (MESH:D001393), AZA (MESH:D001374), AZA-VEN (-)
- **Species:** Klebsiella pneumoniae (species) [taxon 573], Homo sapiens (human, species) [taxon 9606], Staphylococcus epidermidis (species) [taxon 1282], Staphylococcus aureus (species) [taxon 1280]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12934194/full.md

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12934194/full.md

## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC12934194/full.md

---
Source: https://tomesphere.com/paper/PMC12934194