Study of Decitabine Induction Prior to Allogeneic Hematopoietic Cell Transplant in Newly Diagnosed MDS Patients

Phase 2

Terminated

• Conditions: Myelodysplastic Syndrome
• Interventions: Drug: Decitabine

• Registration Number: NCT01333449
• Lead Sponsor: Singapore General Hospital

Brief Summary

Allogeneic blood stem cell transplant remains the only potential curative treatment for myelodysplastic syndromes (MDS) to date. Pre-transplant induction chemotherapy with leukemia-type regimens is associated with significant toxicity and even death. The hypomethylating agents decitabine and 5-azacytidine have been shown in studies to cause improved hematologic parameters and partial or complete responses in patients with high risk MDS compared to standard therapy. In contrast to leukemia-type chemotherapy, decitabine is associated with a relatively low risk of toxicity. We therefore propose to treat transplant-eligible MDS patients with Decitabine as induction therapy and a bridge to transplant.

Hypothesis:

1. Decitabine is able to reduce disease burden as measured by blood and marrow blast counts prior to allogeneic hematopoietic stem cell transplant to below 5%.

2. Decitabine is well-tolerated by patients with high-risk MDS and will be a safe induction agent and bridge prior to allogeneic transplant in transplant-eligible patients.

Detailed Description

Primary endpoint:

1. safety and tolerability of Decitabine prior to transplant (assessed by occurence of non-hematologic toxicities of grade 3 or more as defined by CTC grading)

2. reduction in pre-transplant disease burden ability to achieve blast \<5% in the bone marrow and peripheral blood

Secondary endpoints:

1. Proportion of patients with suitable donor able to proceed to an allogeneic hematopoietic cell transplant.

2. Non-relapse mortality

3. time to neutrophil engraftment

4. Overall survival and disease-free survival.

Patients will receive Decitabine until blast \<5% is achieved, suitable HLA-matched donor or umbilical cord blood is available up to a maximum of 6 cycles. Patient who progress on therapy or are unable to find a donor by 6 cycles will be removed from protocol. The method, conditioning regimen and choice of donor will be determined based on patient's age and functional status, and transplant physician's discretion. The available regimens are standardized within the center

Study Timeline

• Study Start: 2010-07
• Study First Submitted: 2010-11-30
• Study First Submitted QC: 2011-04-10
• Study First Posted: 2011-04-12
• Primary Completion: 2013-08
• Study Completion: 2013-08
• Status Verified: 2014-06
• Last Update Submitted: 2014-06-16
• Last Update Posted: 2014-06-17

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 6

Inclusion Criteria

1. Newly diagnosed MDS patients aged 21 to 65 years belonging to any of the following categories: refractory cytopenia with multilineage dysplasia (RCMD) with or without ringed sideroblasts (i.e. RCMD and RCMD-RS), refractory anemia with excess blasts-1 (RAEB-1) or RAEB-2 if the prognostic scores are IPSS (international prognostic scoring system) Int-2 or IPSS-high or with WPSS (WHO prognostic scoring system) 3 and above
2. Therapy-related MDS with IPSS Int-2 and above or WPSS 3
3. Acceptable cardiac function MUGA or Echocardiography left ventricular ejection fraction of 40% and above
4. Acceptable lung function: FEV1>70% predicted, DLCO>60% predicted
5. Acceptable renal function: CCT > 50ml/min
6. Acceptable liver function: abnormalities in bilirubin or transaminases not > 2times upper limit of normal
7. Performance status of ECOG 2 or HCT-specific Comorbidity Index < 3

Exclusion Criteria

1. Any co-morbidity other than MDS which limits life-expectancy to <3mth
2. Diagnosis of other active cancer other than squamous cell carcinoma, basal cell carcinoma or carcinoma-in-situ 1 or 2 of the cervix
3. Presence of active infections not under control
4. Receipt of 5-azacytidine or other induction chemotherapy for MDS/AML
5. Patients not keen to explore allogeneic HCT as part of curative treatment plan
6. Pregnancy

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Single Arm	Decitabine	Decitabine 20mg/m\^2 infusion one hour per day, for 5days,every 28days,total 2-6cycles.

Primary Outcome Measures

Name	Time	Method
Reduction in pre-transplant disease burden	2 years

Secondary Outcome Measures

Name	Time	Method
Overall survival survival	3 years
Disease free survival	3 years
Proportion of patients with suitable donor able to proceed to an allogeneic HCT	2 years
Non-relapse mortality	3 years
Time to neutrophil engraftment	2 years

Trial Locations

Locations (1)

Singapore General Hospital; 🇸🇬 Singapore, Singapore