Evidence Level:Sensitive: B - Late Trials
Title:
Aprea Therapeutics Receives FDA Fast Track Designation and Orphan Drug Designation for APR-246 for the Treatment of Myelodysplastic Syndromes (MDS)
Excerpt:Aprea Therapeutics...today announced that the U.S. Food and Drug Administration (FDA) has granted Fast Track designation to APR-246 for the treatment of patients with MDS having a TP53 mutation.
Evidence Level:Sensitive: C2 – Inclusion Criteria
New
Title:
APR-246 in Combination With Azacitidine for TP53 Mutated AML (Acute Myeloid Leukemia) or MDS (Myelodysplastic Syndromes) Following Allogeneic Stem Cell Transplant
Excerpt:...To Assess Relapse-free Survival (RFS) in Patients With TP53 Mutated AML or MDS After Undergoing Allogeneic Hematopoietic Stem Cell Transplant (HSCT)....
Evidence Level:Sensitive: C2 – Inclusion Criteria
New
Title:
Study of systemic Azacitidine chemotherapy in combination with or without APR-246 in patients with a type of Myelodysplastic Syndrome
Excerpt:...Having at least one TP53 mutation which is not benign or likely benign 6. ...
More C2 evidence
Evidence Level:Sensitive: C2 – Inclusion Criteria
New
Title:
Study of the Safety and Efficacy of APR-246 in Combination With Azacitidine
Excerpt:...Documentation of a TP53 gene mutation by next-generation sequencing (NGS) based on central or local evaluation....
Evidence Level:Sensitive: C2 – Inclusion Criteria
New
Title:
Phase 1b/2 Safety and Efficacy of APR-246 w/Azacitidine for tx of TP53 Mutant Myeloid Neoplasms
Excerpt:...- Documentation of a TP53 gene mutation by NGS based on central or local evaluation....
Evidence Level:Sensitive: C2 – Inclusion Criteria
New
Title:
APR-246 & Azacitidine for the Treatment of TP53 Mutant Myelodysplastic Syndromes (MDS)
Excerpt:...- Having at least one TP53 mutation which is...
Less C2 evidence
Evidence Level:Sensitive: C3 – Early Trials
Title:
39 - Phase II Trial of Eprenetapopt (APR-246) in Combination with Azacitidine (AZA) As Maintenance Therapy for TP53 Mutated Acute Myeloid Leukemia (AML) or Myelodysplastic Syndromes (MDS) Following Allogeneic Hematopoietic Cell Transplantation (HCT)
Excerpt:...maintenance therapy with eprenetapopt in combination with AZA was safe and tolerable with favorable results in patients with TP53 mutant MDS and AML.
Evidence Level:Sensitive: C3 – Early Trials
Title:
Phase II Trial of Eprenetapopt (APR-246) in Combination with Azacitidine (AZA) As Maintenance Therapy for TP53 Mutated AML or MDS Following Allogeneic Stem Cell Transplantation (SCT)
Excerpt:...eprenetapopt in combination with AZA was safe and tolerable with favorable results in patients with TP53 mutant MDS and AML…
DOI:10.1182/blood-2021-147962
Evidence Level:Sensitive: C3 – Early Trials
Title:
Aprea Therapeutics Announces Positive Results from Phase 2 Trial of Eprenetapopt + Azacitidine for Post-Transplant Maintenance Therapy in TP53 Mutant MDS and AML
Excerpt:Aprea Therapeutics, Inc....today announced positive results from its Phase 2 trial evaluating eprenetapopt with azacitidine for post-transplant maintenance therapy in patients with TP53 mutant MDS and AML....In 33 patients enrolled in the trial, the relapse free survival (RFS) at 1 year post-transplant was 58% and the median RFS was 12.1 months. The overall survival (OS) at 1 year post-transplant was 79%, with a median OS of 19.3 months.
Evidence Level:Sensitive: C3 – Early Trials
Title:
Eprenetapopt Plus Azacitidine in TP53-Mutated Myelodysplastic Syndromes and Acute Myeloid Leukemia: A Phase II Study by the Groupe Francophone des Myélodysplasies (GFM)
Excerpt: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….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.
Evidence Level:Sensitive: C3 – Early Trials
New
Title:
Eprenetapopt (APR-246) and Azacitidine in TP53-Mutant Myelodysplastic Syndromes
Excerpt:...Fifty-five patients (40 MDS, 11 AML, and four MDS/myeloproliferative neoplasms) with at least one TP53 mutation were treated. The overall response rate was 71% with 44% achieving CR. Of patients with MDS, 73% (n = 29) responded with 50% (n = 20) achieving CR and 58% (23/40) a cytogenetic response....Combination treatment with eprenetapopt and azacitidine is well-tolerated yielding high rates of clinical response and molecular remissions in patients with TP53-mutant MDS and oligoblastic AML.