drugset / Trial / NCT02751255

Daratumumab in Combination With ATRA

NCT02751255

NaSingle-groupOpen-labelTreatment

Summary

Multiple myeloma (MM) patients who develop bortezomib and lenalidomide-resistant disease have a very poor survival of only a median of 9 months, indicating that new agents are urgently needed. Recent studies have shown that daratumumab as a single agent is effective and well tolerated in these heavily pretreated MM patients. However, approximately 60% of patients do not achieve a partial response, and ultimately all patients will develop progressive disease during daratumumab therapy. The investigators have demonstrated that levels of the target antigen CD38, and expression levels of the complement inhibitory proteins CD55 and CD59 determine the susceptibility of the MM cells towards daratumumab. In addition, MM cells have lower CD38 expression levels and higher levels of CD55/CD59 at the time of progression. Importantly, all-trans retinoic acid (ATRA) upregulates CD38 levels and downregulates CD55/CD59 levels on MM cells, both in daratumumab naïve cells and in cells that are resistant to daratumumab because of previous exposure to this drug. These alterations in expression explain the strong synergy between ATRA and daratumumab, both in MM cells derived from daratumumab naïve patients and from patients with daratumumab-refractory disease. These data form the preclinical rationale for clinical evaluation of ATRA and daratumumab in MM patients.

Timeline

Start
2016-07-06
Primary completion
2022-10-18
Completion
2022-10-18

Drugs

EvaluationDrugModalityDoseRoute
Subject Tretinoin Small molecule 15 mg/m2 Oral
Subject Tretinoin Small molecule 30 mg/m2 Oral
Subject Tretinoin Small molecule 45 mg/m2 Oral

Indications