Treatment of minimal residual disease in myeloid malignancies after allo-HSCT with venetoclax-based regimens in patients ineligible for or failed in the immunotherapy

Hematology. 2024 Dec;29(1):2418653. doi: 10.1080/16078454.2024.2418653. Epub 2024 Nov 12.

Abstract

Background: Relapse was the major cause of treatment failure in patients with myeloid malignancies after allogeneic hematopoietic stem cell transplantation (allo-HSCT). Patients who still suffer from the disease while cannot be detected by morphological analysis can be identified by the minimal residual disease (MRD) monitoring. The most used first-line regimens for MRD are immunotherapies. However, for patients who were ineligible for or failed in first-line immunotherapies, options were limited.

Methods: A total of 20 patients with myeloid malignancies with recurrent MRD after allo-HSCT were included in this study. The safety and efficacy of venetoclax-based regimens were analyzed.

Results: There were 13 patients (65%) treated with venetoclax combined with hypomethylating agents concomitantly and seven patients (35%) treated with venetoclax monotherapy. After venetoclax-based regimens, MRD was eliminated in 11 patients (55%) with 6 subsequently developing recurrent MRD and 5 remaining in molecular remission. MRD declined in two patients (10%), and no responses in seven patients (35%). Among the two patients with declined MRD, one patient finally eliminated MRD after two cycles of the venetoclax-based regimen, and the other patient's MRD further declined after the second regimen. The objective response rate (ORR) was 65%. The median duration of response was 103 (12-313) days. The incidences of grades 3-4 neutropenia, anemia, and thrombocytopenia independently of pretreatment status were 30%, 20% and 20%, respectively.

Conclusion: Venetoclax-based regimens are efficient and safe for MRD in patients with myeloid malignancies ineligible for or failed in the first-line immunotherapies after allo-HSCT.

Keywords: Minimal residual disease; allogeneic hematopoietic stem cell transplantation; myeloid malignancies; venetoclax.

Plain language summary

What is the context?: Relapse was the major cause of treatment failure in patients with myeloid malignancies after allogeneic hematopoietic stem cell transplantation (allo-HSCT).Patients who still suffer from the disease while cannot be detected by morphological analysis can be identified by the minimal residual disease (MRD) monitoring.The most used first-line regimens for MRD are immunotherapies.For patients who were ineligible for or failed in first-line immunotherapies, options were limited.What is new?: A total of 20 patients with myeloid malignancies with recurrent MRD after allo-HSCT were included in this study. The safety and efficacy of venetoclax-based regimens were analyzed. ⮚ Venetoclax-based regimens are efficient for MRD in patients with myeloid malignancies ineligible for or failed in the first-line immunotherapies after allo-HSCT.⮚ After venetoclax-based regimens, MRD was eliminated in 11 patients (55%), and five patients were still MRD eliminated at the time of this writing or until death.⮚ MRD declined in two patients (10%), and no responses in seven patients (35%). Among the two patients with declined MRD, one patient finally eliminated MRD after two cycles of the venetoclax-based regimen, and the other patient’s MRD further declined after the second regimen.⮚ The objective response rate (ORR) was 65%.⮚ The median duration of response was 103 (12-313) days.Venetoclax-based regimens are safe for MRD in patients with myeloid malignancies ineligible for or failed in the first-line immunotherapies after allo-HSCT. ⮚ The incidences of grades 3–4 neutropenia, anemia, and thrombocytopenia independently of pretreatment status were 30%, 20% and 20%, respectively.What is the impact? This study provides evidence that in the context of preemptive treatment for post-transplant MRD, venetoclax-based regimens may be a choice in patients who were ineligible for or failed in the first-line immunotherapies.

MeSH terms

  • Adult
  • Aged
  • Bridged Bicyclo Compounds, Heterocyclic* / therapeutic use
  • Female
  • Hematopoietic Stem Cell Transplantation* / adverse effects
  • Humans
  • Immunotherapy*
  • Male
  • Middle Aged
  • Neoplasm, Residual*
  • Sulfonamides* / administration & dosage
  • Sulfonamides* / therapeutic use
  • Transplantation, Homologous

Substances

  • Sulfonamides
  • venetoclax
  • Bridged Bicyclo Compounds, Heterocyclic