Venetoclax combined with ATRA shows promising therapeutic potential for TFG:: RARA variant APL: a case report

Most cases of acute promyelocytic leukemia (APL) are driven by the PML::RARA fusion gene, which is sensitive to differentiation induction therapy comprising of all-trans retinoic acid (ATRA) and arsenic trioxide (ATO). Treatment with ATRA plus ATO has achieved remarkable clinical outcome in patients with typical APL. However, 5% of patients still died from relapsed/refractory disease, predominantly high-risk APL and variant APL. The diagnosis and treatment of variant APL remain challenging. Here, we report a case of TFG::RARA variant APL recognized by targeted RNA sequencing. The patient achieved a sustained complete response following treatment with venetoclax combined with ATRA. Currently, the overall survival (OS) of the patient has exceeded 30 months, and the progression-free survival (PFS) has reached 29 months. Our results suggest that venetoclax combined with ATRA may be an ideal treatment option for patients with TFG::RARA variant APL.

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Publication Details

Journal
Frontiers in Oncology
Published
2025-05-02
DOI
https://doi.org/10.3389/fonc.2025.1529640
Citations
1
Primary Topic
Retinoids in leukemia and cellular processes
Type
article
Field-Weighted Citation Impact
0.81
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article

Venetoclax combined with ATRA shows promising therapeutic potential for TFG:: RARA variant APL: a case report

Wenfeng Zhu, Jianguo Yan, Xianfeng Ouyang, Qian Zhou et al.
1 citations
Frontiers in Oncology
Retinoids in leukemia and cellular processes
0.81
article

Venetoclax combined with ATRA shows promising therapeutic potential for TFG:: RARA variant APL: a case report

Wenfeng Zhu, Jianguo Yan, Xianfeng Ouyang, Qian Zhou, Fei Hu, Su Hu
article en
1 citations

Abstract

Most cases of acute promyelocytic leukemia (APL) are driven by the PML::RARA fusion gene, which is sensitive to differentiation induction therapy comprising of all-trans retinoic acid (ATRA) and arsenic trioxide (ATO). Treatment with ATRA plus ATO has achieved remarkable clinical outcome in patients with typical APL. However, 5% of patients still died from relapsed/refractory disease, predominantly high-risk APL and variant APL. The diagnosis and treatment of variant APL remain challenging. Here, we report a case of TFG::RARA variant APL recognized by targeted RNA sequencing. The patient achieved a sustained complete response following treatment with venetoclax combined with ATRA. Currently, the overall survival (OS) of the patient has exceeded 30 months, and the progression-free survival (PFS) has reached 29 months. Our results suggest that venetoclax combined with ATRA may be an ideal treatment option for patients with TFG::RARA variant APL.

Frontiers in OncologyVol. 15
Jiujiang First People's Hospital (CN)
Good health and well-being
Openalex Percentile: Top 28%
Retinoids in leukemia and cellular processes
0.81
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Venetoclax combined with ATRA shows promising therapeutic potential for TFG:: RARA variant APL: a case report — Wenfeng Zhu, Jianguo Yan, et al. · Frontiers in Oncology (2025) | TGRS Research Map | TGRS