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Lancet Haematol ; 3(11): e506-e515, 2016 Nov.
Article in English | MEDLINE | ID: mdl-27751707

ABSTRACT

BACKGROUND: Panobinostat plus bortezomib and dexamethasone significantly increased median progression-free survival compared with placebo plus bortezomib and dexamethasone in the phase 3 PANORAMA 1 trial. Here, we present the final overall survival analysis for this trial. METHODS: PANORAMA 1 is a randomised, placebo-controlled, double-blind, phase 3 trial of patients with relapsed or relapsed and refractory multiple myeloma with one to three previous treatments. Patients were randomly assigned (1:1) to receive panobinostat (20 mg orally) or placebo, with bortezomib (1·3 mg/m2 intravenously) and dexamethasone (20 mg orally), over two distinct treatment phases. In treatment phase 1 (eight 3-week cycles), patients received: panobinostat or placebo on days 1, 3, 5, 8, 10, and 12; bortezomib on days 1, 4, 8, and 11; and dexamethasone on days 1, 2, 4, 5, 8, 9, 11, and 12. During treatment phase 2 (four 6-week cycles with a 2 weeks on, 1 week off schedule), panobinostat or placebo was given three times a week, bortezomib was administered once a week, and dexamethasone was given on the days of and following bortezomib administration. The primary endpoint was progression-free survival; overall survival was a key secondary endpoint. This study is registered at ClinicalTrials.gov, NCT01023308. FINDINGS: Between Jan 21, 2010, and Feb 29, 2012, 768 patients were enrolled into the study and randomly assigned to receive either panobinostat (n=387) or placebo (n=381), plus bortezomib and dexamethasone. At data cutoff (June 29, 2015), 415 patients had died. Median overall survival was 40·3 months (95% CI 35·0-44·8) in those who received panobinostat, bortezomib, and dexamethasone versus 35·8 months (29·0-40·6) in those who received placebo, bortezomib, and dexamethasone (hazard ratio [HR] 0·94, 95% CI 0·78-1·14; p=0·54). Of patients who had received at least two previous regimens including bortezomib and an immunomodulatory drug, median overall survival was 25·5 months (95% CI 19·6-34·3) in 73 patients who received panobinostat, bortezomib, and dexamethasone versus 19·5 months (14·1-32·5) in 74 who received placebo (HR 1·01, 95% CI 0·68-1·50). INTERPRETATION: The overall survival benefit with panobinostat over placebo with bortezomib and dexamethasone was modest. However, optimisation of the regimen could potentially prolong treatment duration and improve patients' outcomes, although further trials will be required to confirm this. FUNDING: Novartis Pharmaceuticals.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/adverse effects , Antineoplastic Combined Chemotherapy Protocols/pharmacology , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Bortezomib/adverse effects , Bortezomib/pharmacology , Bortezomib/therapeutic use , Dexamethasone/adverse effects , Dexamethasone/pharmacology , Dexamethasone/therapeutic use , Drug Resistance, Neoplasm/drug effects , Hydroxamic Acids/adverse effects , Hydroxamic Acids/pharmacology , Hydroxamic Acids/therapeutic use , Indoles/adverse effects , Indoles/pharmacology , Indoles/therapeutic use , Multiple Myeloma/drug therapy , Multiple Myeloma/mortality , Neoplasm Recurrence, Local/drug therapy , Neoplasm Recurrence, Local/mortality , Patient Dropouts/statistics & numerical data , Activities of Daily Living/classification , Adult , Age Factors , Aged , Antineoplastic Agents, Alkylating/therapeutic use , Asian People/ethnology , Asthenia/chemically induced , Blood Cell Count/statistics & numerical data , Bortezomib/pharmacokinetics , Chromosome Aberrations/drug effects , Chromosome Aberrations/statistics & numerical data , Creatinine/blood , Diarrhea/chemically induced , Disease Progression , Disease-Free Survival , Double-Blind Method , Fatigue/chemically induced , Female , Geography/statistics & numerical data , Hematopoietic Stem Cell Transplantation/statistics & numerical data , Humans , Hydroxamic Acids/pharmacokinetics , Immunologic Factors/therapeutic use , Indoles/pharmacokinetics , Male , Middle Aged , Multiple Myeloma/complications , Multiple Myeloma/ethnology , Neoplasm Staging , Panobinostat , Peripheral Nervous System Diseases/chemically induced , Quality of Life , Renal Insufficiency/complications , Sex Factors , Steroids/therapeutic use , Survival Analysis , Thrombocytopenia/chemically induced , Time Factors , Treatment Outcome
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