Francesca Gay, MD, PhD, discusses the FORTE trial comparing carfilzomib plus lenalidomide and dexamethasone versus carfilzomib plus cyclophosphamide and dexamethasone in newly diagnosed patients with multiple myeloma.
Francesca Gay, MD, PhD
The combination of carfilzomib (Kyprolis), lenalidomide (Revlimid), and dexamethasone (KRd) may represent a new standard of care for patients with newly diagnosed multiple myeloma, including those with high-risk disease, said Francesca Gay, MD, PhD.
Gay, a hematologist in the Myeloma Unit, Division of Hematology, Azienda Ospedaliero Universitaria Città della Salute e della Scienza, presented updated efficacy results from the FORTE trial at the 2018 European Hematology Association Congress. If validated by survival results, KRd could represent a new standard of care for these patients, she explained.
FORTE compared KRd (n = 315) versus carfilzomib plus cyclophosphamide/dexamethasone (KCd; n = 159). One percent of patients in each group was refractory to treatment.
Patients assigned to KRd had superior outcomes for stringent complete response/complete response (sCR/CR; 14% vs 4%), at least near CR (32% vs 21%), and at least very good partial response (VGPR; 73% vs 57%; P <.001). Similarly, the rate of partial response (PR) or better also favored the KRd group (94% vs 86%). Gay added that KRd was associated with better results across all subgroups.
Minimal residual disease (MRD) status was available for 144 patients assigned to KRd and 56 assigned to KCd. The rate of MRD negativity was 53% versus 29% (P = .002) in favor of KRd. Results in high-risk patients were similar to those found in the overall population.
KRd is approved by the FDA for the treatment of patients with relapsed/refractory multiple myeloma following 1 to 3 lines of therapy.
In an interview with OncLive®, Gay reviewed the results of the FORTE trial and discussed how including MRD assessment and risk status can make clinical trials more valuable for patients.Gay: We saw that, by an intent-to-treat analysis, the rate of PR after induction was very high in both arms at around 90%. However, the objective response was higher in patients treated with KRd; they achieved a significantly higher rate of VGPR, near CR, at least VGPR, at least near CR, and CR/stringent CR. This was true not only in the overall population of patients, but also in the high-risk subgroup, defined as those with high-risk fluorescence in situ hybridization or International Staging System (ISS) stage II/III disease or with revised ISS stage II/III disease. The rate of response was also comparable with the overall population.
We also evaluated MRD by second-generation flow cytometry with a sensitivity of 10-5. We saw that in the subset of patients for whom the data were available, 50% of the patients on KRd achieved MRD negativity versus 30% with KCd. This difference was significant. The rate of MRD negativity was similar in high-risk patients and comparable with the overall population.These results demonstrate that this regimen is highly effective, so we need to probably wait for the survival data before deciding on the next step. However, these results are promising for our patients including those who are at high risk—a group that currently represents an unmet medical need.We have again demonstrated the efficacy of combining proteasome inhibitors and immunomodulatory agents. The second-generation proteasome inhibitor carfilzomib works very well and may be safer because we did not have an unexpected rate of toxicity. If the survival data confirm these results, I hope we have a new standard of treatment; however, it is not currently available everywhere.The current standard of care varies in different countries based on regulatory approval. The current standard of care, however, is the combination of the proteasome inhibitors and immunomodulatory agents. In Europe, what is approved is bortezomib/thalidomide/dexamethasone. We hope soon to add the combination of bendamustine/lenalidomide/dexamethasone, which is available in the United States. This is the induction, then the current standard is to move to autologous stem cell transplant.We should start to prospectively evaluate the role of MRD within clinical trials and design studies that adopt a treatment strategy according to MRD response achieved and the patient's baseline risk. That is something we are working on, but we still do not have trials that provide us with these answers.
Gay F, Scalabrini DR, Belotti A, et al. Updated efficacy and MRD data according to risk-status in newly diagnosed myeloma patients treated with carfilzomib plus lenalidomide or cyclophosphamide: results from the FORTE trial. In: Proceedings from the 2018 EHA Congress; June 14-17, 2018; Stockholm, Sweden. Abstract S109.