https://doi.org/10.55788/afdd4a47
A head-to-head comparison between bortezomib-melphalan-prednisone (VMP) and lenalidomide-dexamethasone (Rd) did not show a progression-free survival (PFS) difference between both treatment regimens in transplant-ineligible patients with multiple myeloma (MM). However, a trend was observed that VMP seems to be the better option in high-risk patients.
“VMP and Rd are both standard therapies for patients with untreated MM who cannot receive transplant,” explained Dr Sara Bringhen (Università degli Studi di Torino, Italy). “It has not yet been established whether one of the treatment regimens leads to better health outcomes than the other.” To investigate this matter, the phase 4 REAL-MM trial (NCT03829371) randomised 231 patients with newly diagnosed MM who were ineligible for transplant 1:1 to VMP or Rd [1]. The primary outcome was PFS.
After a median follow-up of 18.9 months, there was no difference in PFS between participants in the VMP arm and those in the Rd arm (HR 0.82; 95% CI 0.51–1.31; P=0.41), with 2-year PFS rates of 56% and 55%. Although the association was not significant, the data showed that in participants with high cytogenetic risk (n=35), VMP may be preferred over Rd (HR 0.22; 95% CI 0.05–1.07; P=0.06). Dr Bringhen added that there was no PFS difference according to frailty status. Finally, the 2-year overall survival (OS) rates appeared to favour participants who were treated with VMP (89% vs 75%; HR 0.53; 95% CI 0.26–1.07; P=0.076). However, longer follow-up is needed to evaluate whether this trend will lead to a significant OS benefit.
- Bringhen S, et al. Bortezomib-Melphalan-Prednisone (VMP) Vs. Lenalidomide-Dexamethasone (Rd) in Transplant-Ineligible Real-Life Multiple Myeloma Patients: Updated Results of the Randomized Phase IV Real MM Trial. Abstract 751, ASH 64th Annual Meeting, 10–13 December 2022, New Orleans, LA, USA.
Copyright ©2023 Medicom Medical Publishers
Posted on
« Zanubrutinib wins battle of BTK inhibitors in relapsed or refractory CLL/SLL Next Article
CAR-Hematotox score proves useful in relapsed/refractory MM »
Table of Contents: ASH 2022
Featured articles
Acute Lymphoblastic Leukaemia
Blinatumomab candidate for standard-of-care in newly diagnosed B-ALL
High-dose methotrexate or standard interim maintenance in young patients with ALL?
Acute Myeloid Leukaemia
Excellent results for triplet regimen in FLT3-mutated AML
MRD by qPCR prognostic of outcomes in venetoclax-treated NPM1-mutated AML
Promising results for triplet therapy with magrolimab in AML
Should we use intensive chemotherapy prior to allo-HCT in relapsed/refractory AML?
Chronic Leukaemia
Zanubrutinib wins battle of BTK inhibitors in relapsed or refractory CLL/SLL
Ibrutinib plus venetoclax displays long-term benefits in CLL
Multiple Myeloma
Talquetamab further investigated in heavily pre-treated MM after promising phase 2 data
Promising results of elranatamab for MM in phase 2 MagnetisMM-3 trial
Deep and durable responses for quadruple therapy in smouldering MM
Ultra-sensitive MRD assessment in MM with BloodFlow
CAR-Hematotox score proves useful in relapsed/refractory MM
Head-to-head: VMP versus Rd in transplant-ineligible MM
Lymphoma
Ibrutinib added to ASCT improves clinical outcomes in mantle cell lymphoma
High-dose chemotherapy plus ASCT superior to standard immuno-chemotherapy in primary CNS lymphoma
Odronextamab has considerable anti-tumour effects in relapsed/refractory diffuse large B-cell lymphoma and follicular lymphoma
Excellent results for AFM13-complexed NK cells in CD30-positive lymphoma
CAR-Hematotox score predicts toxicity, infections, and clinical outcomes in MCL
Myeloproliferative Neoplasms
Efgartigimod successful in immune thrombocytopenia
INCA033989: novel investigational agent for CALR-mutated MPN
Ruxolitinib mediates clonal evolution of RAS pathway mutations in MPN
Immune Thrombocytopenia
Long-term risk for haematologic disease in persistent, isolated mild thrombocytopenia
Various Topics
C1 inhibitor deficiency linked to thrombosis
Durable responses to gene therapy in haemophilia A
Long-term benefits from beti-cel in transfusion-dependent β-thalassaemia
Neutrodiet: non-restricted diet is the preferred option after SCT
Iptacopan offers solution for patients with PNH and residual anaemia after standard-of-care
Novel therapy may replace standard-of-care prophylaxis for GVHD
LMWH does not result in higher live birth rates in women with inherited thrombophilia
Related Articles
C1 inhibitor deficiency linked to thrombosis
Durable responses to gene therapy in haemophilia A
© 2023 Medicom Medical Publishers. All rights reserved. Terms and Conditions | Privacy Policy