NOTE
🌱 created from: treatment of multiple myeloma (MM)
cassiopeia
卡西歐佩亞是希臘神話裡的一個人物,她是衣索比亞國王克甫斯的王后。她因為驕傲自大和虛榮被懲罰。 Title
Daratumumab Plus VRd in Transplantation-Eligible Patients with Newly Diagnosed Multiple Myeloma
Information
- Design: Phase 3, randomized, controlled, multi-center
- Number of patients: 709
- Patients characteristics: Transplantation-eligible patients with newly diagnosed multiple myeloma
- Agent: Subcutaneous daratumumab combined with bortezomib, lenalidomide, and dexamethasone (D-VRd) vs VRd alone
- Treatment line: First-line therapy
- Trial Name or NCT Number: PERSEUS (NCT03710603, EudraCT 2018-002992-16)
Comparison of two groups
Endpoint | D-VRd | VRd |
---|---|---|
Progression-Free Survival at 48 months | 84.3% | 67.7% |
Hazard Ratio for Disease Progression or Death | 0.42 (95% CI, 0.30 to 0.59); P<0.001 | - |
Complete Response or Better | 87.9% | 70.1%; P<0.001 |
Minimal Residual Disease (MRD)–Negative Status | 75.2% | 47.5%; P<0.001 |
Other findings
- Death occurred in 34 patients in the D-VRd group and 44 patients in the VRd group
- Grade 3 or 4 adverse events occurred in most patients in both groups, with neutropenia and thrombocytopenia being the most common
- Serious adverse events occurred in 57.0% of patients in the D-VRd group and 49.3% of those in the VRd group
Summary In this phase 3 trial, the addition of subcutaneous daratumumab to VRd induction and consolidation therapy and to lenalidomide maintenance therapy significantly improved progression-free survival among transplantation-eligible patients with newly diagnosed multiple myeloma. The D-VRd group also had higher rates of complete response or better and MRD-negative status compared to the VRd group.