Response and progression-free survival according to planned treatment duration in patients with relapsed multiple myeloma treated with carfilzomib, lenalidomide, and dexamethasone (KRd) versus lenalidomide and dexamethasone (Rd) in the phase III ASPIRE study

Επιστημονική δημοσίευση - Άρθρο Περιοδικού uoadl:3086008 12 Αναγνώσεις

Μονάδα:
Ερευνητικό υλικό ΕΚΠΑ
Τίτλος:
Response and progression-free survival according to planned treatment duration in patients with relapsed multiple myeloma treated with carfilzomib, lenalidomide, and dexamethasone (KRd) versus lenalidomide and dexamethasone (Rd) in the phase III ASPIRE study
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
Background: In ASPIRE, carfilzomib, lenalidomide, and dexamethasone (KRd) significantly improved progression-free survival (PFS) and response rates versus lenalidomide and dexamethasone (Rd) in patients with relapsed multiple myeloma. Per protocol, patients received KRd for a maximum of 18 cycles followed by Rd to progression, so the benefit/risk profile of KRd to progression was not established. Methods: This post hoc analysis evaluated the efficacy and safety of KRd versus Rd at 18 months from randomization. Cumulative rates of complete response (CR) or better over time and PFS hazard ratio (HR) at 18 months were evaluated for KRd versus Rd. PFS HRs were also assessed according to cytogenetic risk, prior lines of therapy, and prior bortezomib treatment. Cox regression analysis was used to evaluate PFS HRs. Results: The hazard ratio (HR) for PFS at 18 months was 0.58 versus 0.69 for the overall ASPIRE study. Patients with high-risk cytogenetics, ≥ 1 prior lines of therapy, and prior bortezomib exposure benefited from KRd up to 18 months versus Rd. The HRs for PFS at 18 months in the pre-defined subgroups were lower than those in the overall study. The difference in the proportion of KRd and Rd patients achieving at least a complete response (CR) increased dramatically over the first 18 months and then remained relatively constant. The safety profile at 18 months was consistent with previous findings. Conclusions: The improved PFS HR at 18 months and the continued increase in CR rates for KRd through 18 cycles suggest that there may be a benefit of continued carfilzomib treatment. Trial registration: Clinical trials.gov NCT01080391. Registered 2 March 2010. © 2018 The Author(s).
Έτος δημοσίευσης:
2018
Συγγραφείς:
Dimopoulos, M.
Wang, M.
Maisnar, V.
Minarik, J.
Bensinger, W.
Mateos, M.-V.
Obreja, M.
Blaedel, J.
Moreau, P.
Περιοδικό:
Journal of Hematology and Oncology
Εκδότης:
BioMed Central Ltd.
Τόμος:
11
Αριθμός / τεύχος:
1
Λέξεις-κλειδιά:
bortezomib; carfilzomib; dexamethasone; lenalidomide; antineoplastic agent; carfilzomib; dexamethasone; lenalidomide; oligopeptide, acute kidney failure; anemia; Article; cancer recurrence; controlled study; cytogenetics; drug efficacy; drug exposure; drug fatality; drug response; drug safety; drug withdrawal; dyspnea; hazard ratio; heart failure; high risk patient; human; hypertension; major clinical study; multiple myeloma; neutropenia; peripheral neuropathy; phase 3 clinical trial; post hoc analysis; progression free survival; randomized controlled trial; thrombocytopenia; treatment duration; clinical trial; female; male; mortality; multiple myeloma; pathology; recurrent disease, Antineoplastic Combined Chemotherapy Protocols; Dexamethasone; Female; Humans; Lenalidomide; Male; Multiple Myeloma; Oligopeptides; Progression-Free Survival; Recurrence
Επίσημο URL (Εκδότης):
DOI:
10.1186/s13045-018-0583-7
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