Eprenetapopt with azacitidine for TP53-mutant MDS/AML: Results from two ongoing clinical trials

Patients with TP53-mutant myelodysplastic syndromes (MDS) or acute myeloid leukemia (AML) experience suboptimal responses to currently available treatments. Although remission rates with hypomethylating agents are comparable between patients with TP53-mutant and wildtype MDS, TP53 mutations are associated with significantly reduced complete remission (CR) duration.¹

Herein lies an unmet clinical requirement for targeted therapies in the TP53-mutant MDS/AML setting. The small molecule TP53 activator, eprenetapopt (APR-246), has exhibited synergy with azacitidine both in vitro and in vivo,² and is currently being evaluated in several clinical trials for the treatment of patients with AML/MDS and mutated TP53. Promising early clinical data resulted in the Fast Track designation of eprenetapopt by the U.S. Food and Drug Administration (FDA) for the treatment of TP53-mutant AML.

In July of 2020, a decision was made to expand a phase I trial (NCT04214860) to include an additional cohort of patients with TP53 mutations who will be treated with eprenetapopt plus azacitidine as a frontline treatment. This decision came following promising results from two independent phase Ib/II clinical trials, NCT03072043¹ and NCT03588078,³ and updated results from these studies have recently been published by David A. Sallman et al. and Thomas Cluzeau et al., respectively. The AML Hub is happy to provide a summary.

Study designs^1,3

The two studies followed a similar study design; evaluating the safety and efficacy of eprenetapopt in combination with azacitidine in patients aged ≥ 18 years with TP53-mutant MDS or AML. Patients had an Eastern Cooperative Oncology Group performance status of 0–2, were classified as having intermediate-, high-, or very high-risk disease, and had ≥ one TP53 mutation as determined by next-generation sequencing.

The key distinguishing features are that NCT03072043 enrolled patients with AML and 20–30% blasts, while the NCT03588078 trial included patients with AML with > 30% blasts, as well as allowing continued maintenance with eprenetapopt + azacitidine for up to 1 year following allogeneic stem cell transplant (allo-SCT).

NCT03072043¹

• Phase Ib/II open-label, multicenter, dose-escalation/-expansion study.
• 3 × 3 dose escalation and identification of dose-limiting toxicities were used to determine the recommended phase II dose.
• Primary endpoint: CR as defined by 2006 International Working Group criteria.

• Secondary endpoints: Overall response rate (ORR), duration of response (DoR), and overall survival (OS).

Results

• The intention to treat (ITT) and response evaluable populations comprised 55 and 45 patients, respectively.
• Patient characteristics are shown in Table 1.

Table 1. Baseline characteristics of patients enrolled in the NCT03072043 trial.¹

Efficacy

• In the ITT population, ORR and CR rates were 71% and 44%, respectively. The hematological responses by disease type in the ITT population are shown in Table 2.

Table 2. Responses to eprenetapopt in combination with azacitidine in the ITT population of the NCT03072043 trial.¹

Safety

• No dose-limiting toxicities were observed in any of the 12 patients involved in the dose-escalation stage.
• Recommended phase II dose of eprenetapopt + azacitidine: 100 mg/kg/d lean body mass (LBM).
• The most common Grade ≥ 3 treatment-emergent adverse events (TEAEs) are shown in Table 3.
  • < 5% were believed to be related to eprenetapopt.

Table 3. Grade ≥ 3 TEAEs observed in ≥ 5% of patients and in the intention to treat group.¹

Biomarker analysis

Patients who harbored mutations in TP53 alone demonstrated superior CR rates compared with patients who had concomitant mutations.

NCT03588078³

• Phase II open-label, multicenter study.
• Primary endpoint: Response in the ITT and evaluable population groups determined by the International Working Group (IWG) 2006 and 2003 criteria for MDS and AML, respectively.
• Secondary endpoints:
  • Safety
  • OS
  • DoR
  • AML progression rate
  • Association between TP53 variant allele frequency (VAF) and response

Results

• Patient characteristics are shown in Table 4.

Table 4. Baseline characteristics of patients enrolled in the NCT03588078 trial.³

Efficacy

• Patient OS rates at the median follow up (9.7 months) are shown in Table 5.
• Patient responses to therapy by disease classification are shown in Table 6.

Table 5. OS in the ITT population of the NCT03588078 trial who received eprenetapopt in combination with azacitidine.³

Table 6. Responses to eprenetapopt in combination with azacitidine in the ITT population of the NCT03588078 trial.³

Safety

• The most commonly observed adverse events (AEs) were febrile neutropenia (37%) and neurologic events (40%). Grade > 3 AEs were observed in three patients (one acute confusion and two ataxia) and were reversible by drug discontinuation.
• Incidence of neurologic AEs was associated with reduced glomerular filtration (p = 0.01) and increased age (p = 0.05).
• One patient with renal failure experienced early treatment discontinuation due to an eprenetapopt-related neurologic AE.

TP53 status

• Of the patients who responded to treatment, 73% and 30% achieved TP53 VAF levels lower than the 5% and 0.1% thresholds, respectively.
• TP53 VAF decrease was significantly coupled with response (p < 0.0001), CR (p = 0.002), and DoR (p < 0.0001).
• Patients who achieved TP53 VAF levels lower than the 5% threshold demonstrated significantly improved DoR (p = 0.001) and OS (p < 0.0001).
• Patients who achieved TP53 VAF levels lower than the 0.1% threshold demonstrated significantly improved OS (p < 0.05).

Conclusions^1,3

Both clinical trials report the feasibility of combining eprenetapopt with azacitidine for the treatment of patients with TP53-mutant MDS or AML, a high-risk patient population with limited treatment options. Eprenetapopt plus azacitidine demonstrated an encouraging safety profile and promising remission rates. Results from these studies endorse the phase III trial (NCT03745716) comparing eprenetapopt plus azacitidine versus azacitidine alone for the treatment of patients with TP53-mutant MDS.  Unfortunately, this trial did not meet its primary endpoint in improving CR rates in the latest interim analysis. 

Additional resources

Read a summary of the results from the GFM-APR trial (NCT03931291), investigating the safety and efficacy of eprenetapopt plus azacitidine as maintenance therapy for patients with TP53 mutant AML or MDS following allo-SCT, here.