Daratumumab/Pomalidomide Combo Approved for Relapsed, Refractory Myeloma

Article

The FDA has approved daratumumab in combination with pomalidomide and dexamethasone for the treatment of relapsed or refractory multiple myeloma.

Approval was based on results of the EQUULEUS study

The US Food and Drug Administration (FDA) approved the combination of daratumumab (Darzalex, Genmab) with pomalidomide and dexamethasone for the treatment of relapsed or refractory multiple myeloma, according to a press release from the drug’s manufacturer.

Patients with relapsed or refractory myeloma who have had at least two prior therapies including lenalidomide and a proteasome inhibitor are now eligible to receive daratumumab, the first monoclonal antibody to receive approval for the treatment of multiple myeloma.

The FDA based its approval on the results of the phase I EQUULEUS study. The open-label study included 103 patients with multiple myeloma who received 16 mg/kg daratumumab combined with pomalidomide and dexamethasone.

The overall response rate for the drug combination was 59% (95% CI, 49.1%–68.8%). Eight percent of patients achieved stringent complete response, 6% of patients achieved a complete response, and more than one-quarter (28%) of patients achieved a very good partial response. The median time to response to treatment was 1 month, and the median duration of response was longer than 1 year (13.6 months).

Patients treated with the daratumumab combination reported infusion reactions (50%), diarrhea (38%), nausea (30%), vomiting (21%), fatigue (50%), pyrexia (25%), upper respiratory tract infection (50%), muscle spasms (26%), cough (43%) and dyspnea (33%).

About one-half of patients experienced a serious adverse reaction to the drug combination. The most common grade 3/4 treatment-related hematologic events were lymphopenia, neutropenia, thrombocytopenia, and anemia.

“We are very pleased to receive the FDA’s decision to approve Darzalex in combination with pomalidomide and dexamethasone. This offers another alternative to patients with multiple myeloma who haven’t seen lasting effects from other types of treatment,” said Jan van de Winkel, PhD, chief executive officer of Genmab, in a press release.

Daratumumab is also approved in combination with lenalidomide and dexamethasone or bortezomib and dexamethasone for patients with relapsed multiple myeloma who have failed on at least one prior therapy. Both of those approvals were based on phase III data.

Recent Videos
Elucidating nonresponses to bispecific T-cell engagers may be an important research consideration in the multiple myeloma field.
Fixed treatment durations with bispecific antibodies followed by observation may help in mitigating infection-related AEs, according to Shebli Atrash, MD.
Shebli Atrash, MD, stated that MRD should be considered carefully as an end point, given potential recurrence despite MRD negativity.
The National ICE-T Conference may inspire future collaboration between community and academic oncologists in the management of different cancers.
Long-term toxicities like infections and secondary primary malignancies remain a concern when sequencing novel agents for those with multiple myeloma.
Management of adverse effects and access to cellular therapies among community oncologists represented key points of discussion in multiple myeloma.
“If you have a [patient in the] fourth or fifth line, [JNJ-5322] could be a valid drug of choice,” said Rakesh Popat, BSc, MBBS, MRCP, FRCPath, PhD.
Earlier treatment with daratumumab may be better tolerated for patients with pretreated MRD-negative multiple myeloma.
The trispecific antibody JNJ-5322 demonstrated superior efficacy vs approved agents in multiple myeloma in results shared at the 2025 EHA Congress.
More follow-up data will better elucidate the impact of frontline use of hypomethylating agents in patients with myelodysplastic syndromes.
Related Content