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Clinical Trial
. 2015 Sep;16(9):1025-1036.
doi: 10.1016/S1470-2045(15)00201-6. Epub 2015 Jul 30.

Vosaroxin plus cytarabine versus placebo plus cytarabine in patients with first relapsed or refractory acute myeloid leukaemia (VALOR): a randomised, controlled, double-blind, multinational, phase 3 study

Farhad Ravandi  1 , Ellen K Ritchie  2 , Hamid Sayar  3 , Jeffrey E Lancet  4 , Michael D Craig  5 , Norbert Vey  6 , Stephen A Strickland  7 , Gary J Schiller  8 , Elias Jabbour  9 , Harry P Erba  10 , Arnaud Pigneux  11 , Heinz-August Horst  12 , Christian Recher  13 , Virginia M Klimek  14 , Jorge Cortes  9 , Gail J Roboz  2 , Olatoyosi Odenike  15 , Xavier Thomas  16 , Violaine Havelange  17 , Johan Maertens  18 , Hans-Günter Derigs  19 , Michael Heuser  20 , Lloyd Damon  21 , Bayard L Powell  22 , Gianluca Gaidano  23 , Angelo-Michele Carella  24 , Andrew Wei  25 , Donna Hogge  26 , Adam R Craig  27 , Judith A Fox  27 , Renee Ward  27 , Jennifer A Smith  27 , Gary Acton  27 , Cyrus Mehta  28 , Robert K Stuart  29 , Hagop M Kantarjian  9
Affiliations
Free PMC article
Clinical Trial

Vosaroxin plus cytarabine versus placebo plus cytarabine in patients with first relapsed or refractory acute myeloid leukaemia (VALOR): a randomised, controlled, double-blind, multinational, phase 3 study

Farhad Ravandi et al. Lancet Oncol. 2015 Sep.
Free PMC article

Abstract

Background: Safe and effective treatments are urgently needed for patients with relapsed or refractory acute myeloid leukaemia. We investigated the efficacy and safety of vosaroxin, a first-in-class anticancer quinolone derivative, plus cytarabine in patients with relapsed or refractory acute myeloid leukaemia.

Methods: This phase 3, double-blind, placebo-controlled trial was undertaken at 101 international sites. Eligible patients with acute myeloid leukaemia were aged 18 years of age or older and had refractory disease or were in first relapse after one or two cycles of previous induction chemotherapy, including at least one cycle of anthracycline (or anthracenedione) plus cytarabine. Patients were randomly assigned 1:1 to vosaroxin (90 mg/m(2) intravenously on days 1 and 4 in a first cycle; 70 mg/m(2) in subsequent cycles) plus cytarabine (1 g/m(2) intravenously on days 1-5) or placebo plus cytarabine through a central interactive voice system with a permuted block procedure stratified by disease status, age, and geographical location. All participants were masked to treatment assignment. The primary efficacy endpoint was overall survival and the primary safety endpoint was 30-day and 60-day all-cause mortality. Efficacy analyses were done by intention to treat; safety analyses included all treated patients. This study is registered with ClinicalTrials.gov, number NCT01191801.

Findings: Between Dec 17, 2010, and Sept 25, 2013, 711 patients were randomly assigned to vosaroxin plus cytarabine (n=356) or placebo plus cytarabine (n=355). At the final analysis, median overall survival was 7·5 months (95% CI 6·4-8·5) in the vosaroxin plus cytarabine group and 6·1 months (5·2-7·1) in the placebo plus cytarabine group (hazard ratio 0·87, 95% CI 0·73-1·02; unstratified log-rank p=0·061; stratified p=0·024). A higher proportion of patients achieved complete remission in the vosaroxin plus cytarabine group than in the placebo plus cytarabine group (107 [30%] of 356 patients vs 58 [16%] of 355 patients, p<0·0001). Early mortality was similar between treatment groups (30-day: 28 [8%] of 355 patients in the vosaroxin plus cytarabine group vs 23 [7%] of 350 in the placebo plus cytarabine group; 60-day: 70 [20%] vs 68 [19%]). Treatment-related deaths occurred at any time in 20 (6%) of 355 patients given vosaroxin plus cytarabine and in eight (2%) of 350 patients given placebo plus cytarabine. Treatment-related serious adverse events occurred in 116 (33%) and 58 (17%) patients in each group, respectively. Grade 3 or worse adverse events that were more frequent in the vosaroxin plus cytarabine group than in the placebo plus cytarabine group included febrile neutropenia (167 [47%] vs 117 [33%]), neutropenia (66 [19%] vs 49 [14%]), stomatitis (54 [15%] vs 10 [3%]), hypokalaemia (52 [15%] vs 21 [6%]), bacteraemia (43 [12%] vs 16 [5%]), sepsis (42 [12%] vs 18 [5%]), and pneumonia (39 [11%] vs 26 [7%]).

Interpretation: Although there was no significant difference in the primary endpoint between groups, the prespecified secondary analysis stratified by randomisation factors suggests that the addition of vosaroxin to cytarabine might be of clinical benefit to some patients with relapsed or refractory acute myeloid leukaemia.

Funding: Sunesis Pharmaceuticals.

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Conflict of interest statement

Declaration of interests

FR reports grants and advisory fees from Sunesis during the conduct of the study, and grants from Sunesis outside the submitted work. NV reports advisory fees from Sunesis during the conduct of the study. SAS and AW report advisory fees from Sunesis outside the submitted work. HPE reports grants and consulting fees from Sunesis during the conduct of the study, and reports fees from Novartis, Incyte, Celgene, Ariad, and Seattle Genetics and grants from Millennium, Seattle Genetics, Celator, Amgen, and Astellas, outside the submitted work. CR reports advisory fees from Sunesis during the conduct of the study, and reports grants from Amgen, Chugai, and Celgene and advisory fees from Celgene outside the submitted work. VMK and GJR report clinical trial support from Sunesis during the conduct of the study and advisory fees from Sunesis outside the submitted work. JC reports grants from Ambit, Arog, Astellas, Celator, Novartis and consulting fees from Novartis and Astellas, outside the submitted work. OO reports grants from Sunesis during the conduct of the study, and reports fees from Sunesis, Algeta, and Spectrum Pharmaceuticals and grants from Astex, MEI-Pharma, Topotarget, Lilly, and Celgene outside the submitted work. MH reports grants and consulting fees from Sunesis during the conduct of the study. LD reports research funds from Sunesis during the conduct of the study, and reports consulting fees from Maxygen and research funds from Celator outside the submitted work. GG reports fees from Amgen, Celgene, GlaxoSmithKline, Janssen, Novartis, and Roche, outside the submitted work. RKS reports grants and advisory fees from Sunesis during the conduct of the study. CM is an employee of Cytel Inc. and receives no remuneration other than his Cytel salary; he has nothing to disclose. ARC, JAF, RW, JAS, and GA were employed by Sunesis Pharmaceuticals during the conduct of the study. EKR, HS, JEL, MEC, GJS, EJ, AP, H-AH, XT, VH, JM, H-GD, BLP, A-MC, and DH have nothing to disclose.

Figures

Figure 1
Figure 1
Overall survival (OS) in patients with relapsed and refractory acute myeloid leukaemia treated with vosaroxin or placebo in combination with cytarabine, for all patients (A), censored for allogeneic stem cell transplant (alloSCT) (B), patients aged ≥60 years vs <60 years (C, D); and early relapsed vs late relapsed vs refractory patients (E, F, G). CI= confidence interval; HR=hazard ratio; Pla/Cyt=placebo+cytarabine; Vos/Cyt=vosaroxin+cytarabine.
Figure 1
Figure 1
Overall survival (OS) in patients with relapsed and refractory acute myeloid leukaemia treated with vosaroxin or placebo in combination with cytarabine, for all patients (A), censored for allogeneic stem cell transplant (alloSCT) (B), patients aged ≥60 years vs <60 years (C, D); and early relapsed vs late relapsed vs refractory patients (E, F, G). CI= confidence interval; HR=hazard ratio; Pla/Cyt=placebo+cytarabine; Vos/Cyt=vosaroxin+cytarabine.
Figure 1
Figure 1
Overall survival (OS) in patients with relapsed and refractory acute myeloid leukaemia treated with vosaroxin or placebo in combination with cytarabine, for all patients (A), censored for allogeneic stem cell transplant (alloSCT) (B), patients aged ≥60 years vs <60 years (C, D); and early relapsed vs late relapsed vs refractory patients (E, F, G). CI= confidence interval; HR=hazard ratio; Pla/Cyt=placebo+cytarabine; Vos/Cyt=vosaroxin+cytarabine.
Figure 1
Figure 1
Overall survival (OS) in patients with relapsed and refractory acute myeloid leukaemia treated with vosaroxin or placebo in combination with cytarabine, for all patients (A), censored for allogeneic stem cell transplant (alloSCT) (B), patients aged ≥60 years vs <60 years (C, D); and early relapsed vs late relapsed vs refractory patients (E, F, G). CI= confidence interval; HR=hazard ratio; Pla/Cyt=placebo+cytarabine; Vos/Cyt=vosaroxin+cytarabine.
Figure 2
Figure 2
Forest plot of overall survival in subgroups of patients treated with vosaroxin or placebo in combination with cytarabine. The vertical dashed line indicates the hazard ratio in the overall population. CI= confidence interval; ITT=intention-to-treat.
Figure 2
Figure 2
Forest plot of overall survival in subgroups of patients treated with vosaroxin or placebo in combination with cytarabine. The vertical dashed line indicates the hazard ratio in the overall population. CI= confidence interval; ITT=intention-to-treat.
See this image and copyright information in PMC

Comment in

  • Vosaroxin in acute myeloid leukaemia.
    Bornhäuser M. Bornhäuser M. Lancet Oncol. 2015 Sep;16(9):1000-1001. doi: 10.1016/S1470-2045(15)00165-5. Epub 2015 Jul 30. Lancet Oncol. 2015. PMID: 26234173 No abstract available.

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