TY - JOUR
T1 - Survival of TP53-mutated acute myeloid leukemia patients receiving allogeneic stem cell transplantation after first induction or salvage therapy
T2 - results from the Consortium on Myeloid Malignancies and Neoplastic Diseases (COMMAND)
AU - Badar, Talha
AU - Atallah, Ehab
AU - Shallis, Rory
AU - Saliba, Antoine N.
AU - Patel, Anand
AU - Bewersdorf, Jan P.
AU - Grenet, Justin
AU - Stahl, Maximilian
AU - Duvall, Adam
AU - Burkart, Madelyn
AU - Palmisiano, Neil
AU - Bradshaw, Danielle
AU - Kubiak, Michal
AU - Dinner, Shira
AU - Goldberg, Aaron D.
AU - Abaza, Yasmin
AU - Murthy, Guru Subramanian Guru
AU - Kota, Vamsi
AU - Litzow, Mark R.
N1 - Funding Information:
TB: Received Mayo Clinic Cancer Center Support Grant (P30 CA015083), serve in advisory board for Pfizer and Takeda AP: Consulting for Abbvie, research funding from Kronos Bio, Pfizer, Celgene/BMS, Servier, VK: Advisory board for Novartis and Pfizer, MS: Consulting for Curis Oncology, advisory board for Novartis, Kymera, Sierra Oncology, participated in GME activities for Novartis, Curis Oncology, Haymarket and Clinical Care Options.
Publisher Copyright:
© 2023, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2023
Y1 - 2023
N2 - We conducted a multi-center study to analyze factors predicting survival among patients with TP53-mutated (m) AML receiving allogeneic hematopoietic stem cell transplant (allo-HSCT) in the recent era. Out of 370 TP53m AML patients, 68 (18%) patients were bridged to allo-HSCT. The median age of the patients was 63 years (range, 33–75), 82% of patients had complex cytogenetics and 66% of patients had multi-hit TP53m. Forty three percent received myeloablative conditioning and 57% received reduced intensity conditioning. The incidence of acute graft versus host disease (GVHD) was 37% and chronic GVHD was 44%. The median event-free survival (EFS) from the time of allo-HSCT was 12.4 months (95% CI: 6.24–18.55) and median overall survival (OS) was 24.5 months (95% CI: 21.80–27.25). In multivariate analysis utilizing variables that showed significance in univariate analysis, complete remission at day 100 post allo-HSCT retained significance for EFS (HR: 0.24, 95% CI: 0.10–0.57, p = 0.001) and OS (HR: 0.22, 95% CI: 0.10–0.50, p ≤ 0.001). Similarly, occurrence of chronic GVHD retained significance for EFS (HR: 0.21, 95% CI: 0.09–0.46, p ≤ 0.001) and OS (HR: 0.34, 95% CI: 0.15–0.75, p = 0.007). Our report suggests that allo-HSCT offers the best opportunity to improve long-term outcome among patients with TP53m AML.
AB - We conducted a multi-center study to analyze factors predicting survival among patients with TP53-mutated (m) AML receiving allogeneic hematopoietic stem cell transplant (allo-HSCT) in the recent era. Out of 370 TP53m AML patients, 68 (18%) patients were bridged to allo-HSCT. The median age of the patients was 63 years (range, 33–75), 82% of patients had complex cytogenetics and 66% of patients had multi-hit TP53m. Forty three percent received myeloablative conditioning and 57% received reduced intensity conditioning. The incidence of acute graft versus host disease (GVHD) was 37% and chronic GVHD was 44%. The median event-free survival (EFS) from the time of allo-HSCT was 12.4 months (95% CI: 6.24–18.55) and median overall survival (OS) was 24.5 months (95% CI: 21.80–27.25). In multivariate analysis utilizing variables that showed significance in univariate analysis, complete remission at day 100 post allo-HSCT retained significance for EFS (HR: 0.24, 95% CI: 0.10–0.57, p = 0.001) and OS (HR: 0.22, 95% CI: 0.10–0.50, p ≤ 0.001). Similarly, occurrence of chronic GVHD retained significance for EFS (HR: 0.21, 95% CI: 0.09–0.46, p ≤ 0.001) and OS (HR: 0.34, 95% CI: 0.15–0.75, p = 0.007). Our report suggests that allo-HSCT offers the best opportunity to improve long-term outcome among patients with TP53m AML.
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U2 - 10.1038/s41375-023-01847-7
DO - 10.1038/s41375-023-01847-7
M3 - Article
AN - SCOPUS:85148365155
SN - 0887-6924
JO - Leukemia
JF - Leukemia
ER -