Among patients who were newly diagnosed with multiple myeloma, Kyprolis (carfilzomib) plus Revlimid (lenalidomide) and dexamethasone (KRd) was associated with improvements in progression-free survival (PFS) compared with Velcade (bortezomib) plus Revlimid and dexamethasone (VRd), according to interim results from the phase 3 COBRA trial.
The findings, presented during the 2025 ASH Annual Meeting, demonstrated that KRd (126 patients) reduced the risk of progression or death by 43% versus VRd (124 patients) in the intent-to-treat population at a median follow-up of 53 months. The median PFS was not reached (NR) in the KRd group versus 48.8 months in the VRd arm.
The data demonstrated consistent directional benefits across cytogenetic subgroups. Among patients with standard-risk disease, KRd (97 patients) achieved a statistically significant improvement in PFS versus VRd (96 patients); the median PFS was NR in the KRd group compared with 48.8 months for VRd. In this subgroup, 27% of patients treated with KRd experienced progression or death versus 40% with VRd. In the high-risk cohort, KRd (29 patients) again demonstrated favorable outcomes versus VRd (28 patients), with 31% versus 48% of patients experiencing progression or death. The median PFS was NR versus 34.9 months, respectively.
“COBRA showed superior efficacy of KRd versus VRd in newly diagnosed multiple myeloma, achieving both co-primary endpoints of MRD-negative CR at 12 months andPFS,” noted presenting author Dr. Dominik Dytfeld. “The PFS benefit of KRd was observed regardless of cytogenetic risk, and KRd produced deeper responses, with higher rates of complete response [CR] and minimal residual disease [MRD]–negativity. KRd [also] demonstrated anticipated toxicity profiles with higher rates of neutropenia and cardiac [side effects], but less neuropathy. COBRA results support further evaluation of KRd-based induction regimens in newly diagnosed multiple myeloma.”
Dytfeld is an associate professor of medicine at the Poznan University of Medical Sciences in Poland and founder/chief executive officer of the Polish Myeloma Consortium.
What was the design of the COBRA trial?
The COBRA trial was a multicenter, randomized, open-label phase 3 study designed to compare KRd with VRd in patients with newly diagnosed multiple myeloma who had an International Myeloma Working Group (IMWG) Frailty Score of less than 2. A total of 250 patients were randomly assigned to the KRd or VRd treatment arms.
Patients in the KRd arm received up to 24, 28-day cycles of therapy consisting of Kyprolis at 56 mg/m² administered on days 1, 8 and 15 (with twice-weekly dosing during cycles 1 and 2), Revlimid at 25 mg on days 1 through 21, and dexamethasone at 40 mg weekly (or 20 mg for patients 75 years of age or older). Stem-cell collection occurred after cycle 4 in this transplant-deferred design. Following completion of induction, patients continued on Revlimid 5 mg daily as maintenance until disease progression.
Patients in the VRd arm received eight 28-day cycles of Velcade at 1.3 mg/m² on days 1, 4, 8 and 11; Revlimid at 25 mg on days 1 through 14; and dexamethasone at 20 mg on days 1, 2, 4, 5, 8, 9, 11 and 12. After completion of the VRd induction phase, patients transitioned to consolidation with Revlimid and dexamethasone for 18 28-day cycles, followed by Revlimid 5 mg maintenance until progression.
How did KRd and VRd compare in transplant-eligible versus transplant-ineligible patients?
The subgroup analysis by transplant eligibility showed distinct patterns in PFS favoring KRd among patients considered eligible for autologous stem cell transplant. In the transplant-eligible cohort, KRd reduced the risk of progression or death by 60% relative to VRd. Only 23% of patients treated with KRd experienced progression or death compared with 45% in the VRd arm. Median PFS was NR with KRd, whereas VRd demonstrated a median PFS of 40.1 months.
In contrast, outcomes were comparable between the two regimens in the transplant-ineligible population. In this subgroup, both KRd and VRd produced identical progression or death rates of 30%. Median PFS remained NR with KRd versus 52.9 months for VRd, resulting in no statistically significant difference between the arms.
What were the safety outcomes of the COBRA trial?
The safety profile of KRd and VRd in the COBRA trial demonstrated that both regimens were associated with high rates of side effects, although specific toxicity patterns differed between the treatment arms. Grade 3 (severe) or higher side effects occurred in 73% of patients receiving KRd and 62% of those receiving VRd, while any-grade side effects were nearly universal across both cohorts (96% with KRd and 94% with VRd). Treatment discontinuation due to side effects occurred in 11% of KRd-treated patients and 8% of VRd-treated patients.
Grade 5 (fatal) side effects were infrequent but observed in both arms, occurring in five patients (4%) in the KRd arm and seven patients (6%) in the VRd arm. Reported fatal side effects in the KRd cohort included COVID-19, stroke, pneumonia, sepsis and acute kidney failure, whereas the VRd arm included deaths from COVID-19, pneumonia, respiratory failure and two side effects of unknown cause. Neutropenia of any grade occurred in 29% of KRd-treated patients and 17% of VRd-treated patients, with grade 3 or higher neutropenia reported in 21% and 11%, respectively.
Neuropathy, a known Velcade-associated toxicity, was more common with VRd: 56% of patients experienced neuropathy of any grade compared with 17% in the KRd arm, although grade 3 or higher neuropathy remained low in both groups (2% in each arm). Cardiac side effects occurred more frequently with KRd (18% any grade; 6% grade 3 or higher) than with VRd (10% any grade; 2% grade 3 or higher), consistent with the known cardiovascular risk profile of Kyprolis. Infection rates were high in both groups but were more common in the KRd arm, where 75% experienced infections of any grade and 25% developed grade 3 or higher infections, compared with 60% and 23% in the VRd arm, respectively.
References
- “Carfilzomib, lenalidomide, and dexamethasone (KRd) versus bortezomib, lenalidomide, and dexamethasone (VRd) in patients with newly diagnosed multiple myeloma: results of the randomized phase III COBRA trial,” by Dr. Dominik Dytfeld et al., Blood.
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