Merck announced today that a Phase III study of Zolinza (vorinostat), for investigational use in combination with bortezomib in patients with progressive multiple myeloma, met its primary endpoint, demonstrating a 23 percent reduction in the risk of progression compared to the standard therapy of bortezomib (p=0.01).
The Phase III results from VANTAGE 088 (Vorinostat in Combination with Bortezomib in Patients with Relapsed/Refractory Multiple Myeloma: A Global, Randomized Phase III Trial) were presented at the 53rd Annual Meeting of the American Society of Hematology (ASH).
Also presented were full results from VANTAGE 095 (Vorinostat in Combination with Bortezomib in Salvage Multiple Myeloma Patients: A Global Phase IIb Trial). Additionally, investigational clinical and pre-clinical vorinostat data across a variety of hematologic cancers were presented in more than 10 oral and poster presentations at the meeting.
"Most patients with multiple myeloma eventually relapse or become resistant to treatment ," said Meletios Dimopoulos, M.D., professor and chairman, Department of Clinical Therapeutics, University of Athens School of Medicine, Athens, Greece. "We are encouraged by the results of the investigational use of Zolinza in combination therapy in this difficult-to-treat patient population."
Vorinostat (marketed as Zolinza) is a histone deacetylase (HDAC) inhibitor indicated for use in the United States for the treatment of cutaneous manifestations in patients with cutaneous T-cell lymphoma (CTCL) who have progressive, persistent, or recurrent disease on or following two systemic therapies. Zolinza inhibits the enzymatic activity of histone deacetylases HDAC1, HDAC2, and HDAC3 (Class I), and HDAC6 (Class II) at nanomolar concentrations (IC50<86 nM).
VANTAGE 088, a Phase III randomized, double-blinded, placebo-controlled study in patients with progressive multiple myeloma who received between one and three prior treatment regimens, was designed to demonstrate an improvement in progression-free survival (PFS) in patients treated with the combination of the investigational use of Zolinza and bortezomib compared to bortezomib alone. The PFS endpoint was assessed by an Independent Adjudication Committee.
Based on the full analysis of 417 PFS events in 637 patients, patients treated with Zolinza (n= 317) and bortezomib (n= 320) had a 23 percent reduction in the risk of progression compared to bortezomib alone with a hazard ratio of 0.774 (p=0.01). The observed median PFS was 7.6 months in the Zolinza and bortezomib arm, and 6.8 months in the bortezomib arm.
In addition to the improvement in PFS, significant improvement in overall response rate (ORR) was also observed in the combination arm (Zolinza and bortezomib, 56 percent; bortezomib and placebo, 41 percent; p<0.0001). The duration of response was 8.5 months in the combination arm and 8.4 months in the control arm. A trend in favor of overall survival (OS) was observed in the Zolinza and bortezomib arm, but the difference was not statistically significant (hazard ratio = 0.86; Zolinza and bortezomib vs. bortezomib and placebo; p=0.35).
In the Phase III study, significantly more patients treated with the combination of Zolinza and bortezomib versus bortezomib alone experienced thrombocytopenia (55 percent vs. 33 percent), diarrhea (62 percent vs. 43 percent), nausea (61 percent vs. 39 percent), vomiting (45 percent vs. 26 percent) and fatigue (40 percent vs. 31 percent) (p<0.05 for all grades). No difference was observed between the discontinuation rates due to an adverse event for vorinostat compared to the placebo arm (21 percent vs. 22 percent).
Selected Important Safety Information for Zolinza
Zolinza is contraindicated in patients with severe hepatic impairment. Z olinza should be used with caution in patients with mild to moderate hepatic impairment.
As pulmonary embolism and deep vein thrombosis have been reported as adverse reactions, physicians should monitor patients for the signs and symptoms of these events, particularly patients with a prior history of thromboembolic events. Treatment with Zolinza can cause dose-related thrombocytopenia and anemia. If platelet counts and/or hemoglobin are reduced during treatment with Zolinza, the dose should be modified or therapy discontinued.
Gastrointestinal (GI) disturbances, including nausea, vomiting and diarrhea, have been reported and may require the use of antiemetic, antidiarrheal medications and fluid and electrolytes replacement to prevent dehydration. Pre-existing GI disturbances should be adequately controlled before beginning therapy with Zolinza. Based on reports of dehydration as a serious drug-related adverse event in clinical trials, patients should be instructed to drink at least 2 L/day of fluids for adequate hydration.
Hyperglycemia has been observed in patients receiving Zolinza. Serum glucose should be monitored, especially in diabetic or potentially diabetic patients receiving Zolinza. Adjustment of diet therapy for increased glucose, or both may be necessary to prevent hyperglycemia. Electrolytes should be monitored at baseline and periodically during treatment. Hypokalemia or hypomagnesemia should be corrected prior to administration with Zolinza.
Severe thrombocytopenia and GI bleeding have been reported with concomitant use of Zolinza and other HDAC inhibitors (e.g., valproic acid). Platelet count should be monitored every 2 weeks for the first 2 months.
Patients who are concurrently administered Zolinza and coumarin derivatives should be carefully monitored for prolongation of prothrombin time and international normalized ratio.
The most common adverse events observed in clinical trials with Zolinza, regardless of causality, were fatigue (52 percent), diarrhea (52 percent), nausea (41 percent), dysgeusia (28 percent), thrombocytopenia (26 percent), anorexia (24 percent), decreased weight (21 percent), and muscle spasms (20 percent).
The most common serious adverse events, regardless of causality, were pulmonary embolism (4.7 percent), squamous cell carcinoma (3.5 percent), and anemia (2.3 percent).
Zolinza can cause fetal harm when administered to a pregnant woman. It is not known whether Zolinza is excreted in human milk. Because of the potential for serious adverse reactions in nursing infants, a decision should be made whether to discontinue nursing or the drug.