Impact of <i>TP53</i> mutation on survival outcomes in acute lymphoblastic leukemia at a tertiary center

Mutations in <i>TP53</i> in acute lymphoblastic leukemia (ALL) predict poor outcomes, however, the literature in adults remains limited. In a retrospective study at Cleveland Clinic, we investigated the outcomes of 72 patients with next-generation sequencing (NGS) at baseline out of 161 patients from January 2017 to August 2023. Eleven patients had TP53 mutations (muTP53-ALL) (15.3%). Patients with muTP53-ALL were older (65 vs 56 years), had more high-risk cytogenetics (45% vs 16%), and no BCR-ABL1 rearrangements (34% vs 0) compared to wild-type TP53 (wt<i>TP53</i>). The muTP53-ALL group had lower flow-cytometry measurable residual disease (MRD)-negative responses (odds ratio: 0.1, 95%CI 0.01-0.47.8, <i>p</i> = .003) and worse 12-month overall survival (OS) compared to wtTP53 ALL (62% vs 90%, <i>p</i> = 0.023). The muTP53-ALL patients are less likely to achieve deep responses to first-line therapy and have worse long-term OS. Future studies should explore early transplants or the use of front-line immunotherapies to improve outcomes.

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Publication Details

Journal
Leukemia & lymphoma/Leukemia and lymphoma
Published
2025-04-09
DOI
https://doi.org/10.1080/10428194.2025.2482131
Citations
4
Primary Topic
Acute Lymphoblastic Leukemia research
Type
article
Field-Weighted Citation Impact
7.51
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article

Impact of TP53 mutation on survival outcomes in acute lymphoblastic leukemia at a tertiary center

Jinan Chen, John C. Molina, Hetty E. Carraway, Moaath K. Mustafa Ali et al.
4 citations
Leukemia & lymphoma/Leukemia and lymphoma
Acute Lymphoblastic Leukemia research
7.51
article

Impact of TP53 mutation on survival outcomes in acute lymphoblastic leukemia at a tertiary center

Jinan Chen, John C. Molina, Hetty E. Carraway, Moaath K. Mustafa Ali, Aaron T. Gerds, Joy Nakitandwe, Akriti Gupta Jain, Abhay Singh, Sophia Balderman, Emily Craig Zabor, Ahmed Allam Mohamed, Hadil Zureigat, Anjali S. Advani, Meera Patel, Sudipto Mukherjee, Zheng Jin Tu
article en
4 citations

Abstract

Mutations in <i>TP53</i> in acute lymphoblastic leukemia (ALL) predict poor outcomes, however, the literature in adults remains limited. In a retrospective study at Cleveland Clinic, we investigated the outcomes of 72 patients with next-generation sequencing (NGS) at baseline out of 161 patients from January 2017 to August 2023. Eleven patients had TP53 mutations (muTP53-ALL) (15.3%). Patients with muTP53-ALL were older (65 vs 56 years), had more high-risk cytogenetics (45% vs 16%), and no BCR-ABL1 rearrangements (34% vs 0) compared to wild-type TP53 (wt<i>TP53</i>). The muTP53-ALL group had lower flow-cytometry measurable residual disease (MRD)-negative responses (odds ratio: 0.1, 95%CI 0.01-0.47.8, <i>p</i> = .003) and worse 12-month overall survival (OS) compared to wtTP53 ALL (62% vs 90%, <i>p</i> = 0.023). The muTP53-ALL patients are less likely to achieve deep responses to first-line therapy and have worse long-term OS. Future studies should explore early transplants or the use of front-line immunotherapies to improve outcomes.

Leukemia & lymphoma/Leukemia and lymphomaVol. 66(8)
Cleveland Clinic (US), Cancer Institute (WIA) (IN)
Openalex Percentile: Top 3%
Acute Lymphoblastic Leukemia research
7.51
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