Addition of Vorinostat to Azacitidine in Higher Risk MDS a Phase II add-on Study in Patients With Azacitidine Failure

Phase 2

Terminated

Conditions: Myelodysplastic Syndrome

Interventions: Drug: Azacitidine and oral vorinostat

Registration Number: NCT01748240

Lead Sponsor: Groupe Francophone des Myelodysplasies

Brief Summary: Azacytidine (AZA) is the current standard of care for frontline patient treated with high-risk MDS and is clinically active in all type of MDS, however, 50% of the patients will never respond. Vorinostat is an orally available HDAC inhibitor with clinical activity in MDS and proven in vitro synergy with AZA. Patient treated upfront with a combination of this agents have shown more responses based on phase I/II data. In the present study, we will use the combination of these two drugs to try to create a synergetic effect and generate a response for patients who experienced treatment failure after AZA.

All eligible patients will be treated with Azacitidine and oral vorinostat for 6 cycles of 28 days. Study Design

Detailed Description: Patients who meet eligibility criteria will be administered vorinostat orally at 300mg two times daily for 7 days as outlined in table 1.1. AZA will be administered SC at 75 mg/m2/day x 7 consecutive days or at maximum tolerated dose if a dose reduction of AZA was needed before entering the trial with a minimum dose of 50mg/m2/d for 7 consecutive days.

Each cycle will last 28 days with AZA starting on day 1 of each cycle and vorinostat starting on day 3.

Patients will receive 6 cycles unless progression is documented. Patients with a complete remission (CR), partial remission (PR), or hematological improvement (HI), will be treated until progression.

Recruitment & Eligibility

Status: TERMINATED

Sex: All

Target Recruitment: 21

Inclusion Criteria

Myelodysplastic syndrome (WHO and FAB classified) including: RA, RARS, RCMD, RCMD-RS RAEB , RAEB-t and CMML with WBC < 13000/mm3)
IPSS score 1.5 or higher (IPSS intermediate-2 and high risk categories) at the beginning of azacitidine,
Absence of response (CR, PR, marrow CR or HI according to IWG 2006) after a minimum of 6 cycles of azacitidine single agent at 75 mg/m²/d for 7 days per cycle. Patients with a previous dose reduction of AZA may be eligible if the maximum tolerated dose was equal to or above 350mg/m2/cycle (i.e. 50 mg/m²/d for 7 days or 75mg/m2/d for 5 days).
Age more or egal to 18 years
ECOG performance status ≤ 2 (cf. appendix 2);
Patient must have adequate organ function as indicated by the following laboratory values

Renal Serum creatinine or calculated creatinine clearancea < 2 mg/dl OR ≥ 60 mL/min for patients with creatinine levels > 1.5 X institutional ULN Hepatic

Serum total bilirubin ≤ 2.5 X ULN OR direct bilirubin ≤ ULN for patients with total bilirubin levels ≥ 2 mg/dL.

AST (SGOT) and ALT (SGPT) ≤ 2.5 times ULN Alkaline Phosphatase ≤ 5 X ULN If > 2.5 X ULN, then liver fraction should be ≤ 2.5 X ULN a Creatinine clearance should be calculated per institutional standard.

Patient is known to not be refractory to platelet transfusions.
Patient ineligible for allogeneic hematopoietic stem cell transplantation at the time of inclusion in the study
Adherence to the study visit schedule;
Women of childbearing potential must:

Agree to use effective contraception without interruption throughout the study and for a further 3 months after the end of treatment;

Men must: Agree to not conceive during the treatment and to use effective contraception during the treatment period (including periods of dose reduction or temporary suspension) and for a further 3 months after the end of treatment if their partner is of childbearing potential.

Agree to learn about the procedures for preservation of sperm.

Exclusion Criteria

Patient had prior treatment with an HDAC inhibitor (e.g., depsipeptide or NSC-630176, MS 275, LAQ-824, PXD-101, LBH589, MGCD0103, CRA024781, etc). Patients who have received compounds with HDAC inhibitor-like activity, such as valproic acid, as anti-tumor therapy should not enroll in this study. Patients who have received such compounds for other indications, e.g. valproic acid for epilepsy, may enroll after a 30-day washout period.
Severe infection or any other uncontrolled severe condition.
Last dose of AZA was given more than 3 months before entering the trial.
Patient already enrolled in another therapeutic trial of an investigational drug
HIV infection or active hepatitis B or C.
Patient has a known allergy or hypersensitivity to any component of vorinostat or azacitidine.
Active cancer, or cancer during the year prior to trial entry other than basal cell carcinoma or carcinoma in situ of the cervix or breast.
Less than 30 days since prior treatment with growth factors (EPO, G-CSF) or non-cytotoxic agents (including low-dose oral chemotherapy); in the event of prior treatment with cytotoxic or demethylating agents, an interval of 3 months is required;
Patient is on any systemic steroids that have not been stabilized to the equivalent of ≤ 10 mg/day prednisone during the 4 weeks prior to the start of the study drugs.
Patients with clinical evidence of CNS leukemia.
Patient has a history of GI surgery or other procedures that might interfere with the absorption or swallowing of the study drugs.
Women who are or could become pregnant, or who are currently breastfeeding
Patient eligible for allotransplantation at the time of inclusion.

Study & Design

Study Type: INTERVENTIONAL

Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Azacitidine and oral vorinostat	Azacitidine and oral vorinostat	Patients who meet eligibility criteria will be administered vorinostat orally at 300mg two times daily for 7 days. AZA will be administered SC at 75 mg/m2/day x 7 consecutive days or at maximum tolerated dose if a dose reduction of AZA was needed before entering the trial with a minimum dose of 50mg/m2/d for 7 consecutive days. Each cycle will last 28 days with AZA starting on day 1 of each cycle and vorinostat starting on day 3.

Primary Outcome Measures

Name	Time	Method
Response Rate	6 month	All eligible patients will be treated with Azacitidine and oral vorinostat for 6 cycles of 28 days. The response rate (CR, PR, HI or marrow CR) will be evaluated after six cycles, according to IWG 2006. In patients still responding after six cycles, the drugs will continue to be supplied, and follow up until death or unacceptable tolerance will be continued in all patients. Complete Response (CR): Bone marrow: less than 5% myeloblasts with Peripheral blood: HI responses). Partial remission (RP): Bone marrow blasts decreased by at least 50% but still more than 5% with Peripheral blood: HI responses). Marrow CR:Bone marrow: maximum of 5% myeloblasts and decrease by at least 50% over pretreatment HI (hematologic improvement) * Erythroid response: Hgb increase at least by 1.5 g/dL * Platelet response: Increase from less than 20x109/L to more than 20x109/L and by at least 100% * Neutrophil response: At least 100% increase and an absolute increase of at least 0.5x109/L

Secondary Outcome Measures

Name	Time	Method

Trial Locations

Locations (24): CHU de Grenoble
🇫🇷
Grenoble, France
CHU d'Angers
🇫🇷
Angers, France
CH Annecy
🇫🇷
Annecy, France
Hôpital Avignon
🇫🇷
Avignon, France
Centre hospitalier de la côte Basque
🇫🇷
Bayonne, France
Hôpital Avicenne
🇫🇷
Bobigny, France
CH Le mans
🇫🇷
Le mans, France
IPC-Unité d'Hématologie 3
🇫🇷
Marseille, France
CH Lyon Sud
🇫🇷
Lyon, France
CHU Nantes
🇫🇷
Nantes, France
Hôpital Archet1
🇫🇷
Nice, France
GHU Caremeau
🇫🇷
Nimes, France
Hopital Saint Louis - AP-HP, Hematology Dpt
🇫🇷
Paris, France
Hôpital Saint Louis
🇫🇷
Paris, France
Hopital Cochin-Hematology
🇫🇷
Paris, France
Hôpital Saint-Louis
🇫🇷
Paris, France
Centre Hospitalier Joffre
🇫🇷
Perpignan, France
CHU de Haut-Lévèque
🇫🇷
Pessac, France
Centre Henri Becquerel
🇫🇷
Rouen, France
Hopital Purpan-Medecine interne
🇫🇷
Toulouse, France
Hôpital PURPAN, Service d'Hématologie Clinique
🇫🇷
Toulouse, France
CHU Bretonneau
🇫🇷
Tours, France
CHU Brabois
🇫🇷
Vandœuvre-lès-Nancy, France
CH de Valence
🇫🇷
Valence, France