Eprenetapopt Plus Azacitidine in <i>TP53</i>-Mutated Myelodysplastic Syndromes and Acute Myeloid Leukemia: A Phase II Study by the Groupe Francophone des Myélodysplasies (GFM)

Thomas Cluzeau(Inserm), Marie Sébert(Assistance Publique – Hôpitaux de Paris), Ramy Rahmé(Assistance Publique – Hôpitaux de Paris), Stefania Cuzzubbo(Assistance Publique – Hôpitaux de Paris), Jacqueline Lehmann‐Che(Assistance Publique – Hôpitaux de Paris), Isabelle Madelaine(Assistance Publique – Hôpitaux de Paris), Pierre Péterlin(Laboratoire de Thermique et Energie de Nantes), Blandine Bève, Habiba Attalah, Fatiha Chermat, Elsa Miekoutima(Assistance Publique – Hôpitaux de Paris), Odile Beyne Rauzy(Institut universitaire du cancer de Toulouse Oncopole), Christian Récher(Institut universitaire du cancer de Toulouse Oncopole), Aspasia Stamatoullas(Centre Virchow-Villermé), Lise Willems(Hôpital Cochin), Emmanuel Raffoux(Assistance Publique – Hôpitaux de Paris), Céline Berthon(Lille’s Cardiology Hospital), Bruno Quesnel(Lille’s Cardiology Hospital), Michaël Loschi(Inserm), Alain Carpentier(Assistance Publique – Hôpitaux de Paris), David A. Sallman(Moffitt Cancer Center), Rami S. Komrokji(Moffitt Cancer Center), Anouk Walter‐Petrich(Assistance Publique – Hôpitaux de Paris), Sylvie Chevret(Assistance Publique – Hôpitaux de Paris), Lionel Adès(Assistance Publique – Hôpitaux de Paris), Pierre Fenaux(Assistance Publique – Hôpitaux de Paris)
Journal of Clinical Oncology
February 18, 2021
Cited by 266Open Access
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Abstract

PURPOSE TP53-mutated ( TP53m) myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML) have very poor outcome irrespective of the treatment received, including 40% responses (20% complete remission [CR]) with azacitidine (AZA) alone, short response duration, and a median overall survival (OS) of approximately 6 months. Eprenetapopt (APR-246), a novel first-in-class drug, leads to p53 protein reconformation and reactivates its proapoptotic and cell-cycle arrest functions. PATIENTS AND METHODS This phase II study assessed the safety and efficacy of eprenetapopt in combination with AZA in untreated high or very high International Prognostic Scoring System-R TP53m MDS and AML patients. RESULTS Fifty-two TP53m patients (34 MDS, 18 AML [including seven with more than 30% blasts]) were enrolled. In MDS, we observed an overall response rate (ORR) of 62%, including 47% CR, with a median duration of response at 10.4 months. In AML, the ORR was 33% including 17% CR (27% and 0% CR in AML with less than and more than 30% marrow blasts, respectively). Seventy-three percent of responders achieved TP53 next-generation sequencing negativity (ie, variant allele frequency &lt; 5%). The main treatment-related adverse events were febrile neutropenia (36%) and neurologic adverse events (40%), the latter correlating with a lower glomerular filtration rate at treatment onset ( P &lt; .01) and higher age ( P = .05), and resolving with temporary drug interruption without recurrence after adequate eprenetapopt dose reduction. With a median follow-up of 9.7 months, median OS was 12.1 months in MDS, and 13.9 and 3.0 months in AML with less than and more than 30% marrow blasts, respectively. CONCLUSION In this very high-risk population of TP53m MDS and AML patients, eprenetapopt combined with AZA was safe and showed potentially higher ORR and CR rate, and longer OS than reported with AZA alone.


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