Exploratory Study of IMATINIB High Dose in Intermediate Risk Chronic Myeloid Leukemia in Chronic Phase

Myeloid Leukemia, Chronic, Chronic-Phase Clinical Trial

Official title:

CML/021 "A Phase II Exploratory Study of IMATINIB High Dose (800mg/gg) in the Treatment of Newly Diagnosed Intermediate Risk Chronic Myeloid Leukemia in Chronic Phase"

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00510926
• Other study ID #: CML/021
• Status: Completed
• Phase: Phase 2
• First received: August 2, 2007
• Last updated: August 2, 2007
• Start date: January 2004
• Est. completion date: November 2006

Study information

• Verified date: August 2007
• Source: University of Bologna
• Contact: n/a
• Is FDA regulated: No
• Health authority: Italy: The Italian Medicines AgencyItaly: Ethics Committee
• Study type: Interventional

Clinical Trial Summary

Results in CP are better in patients treated early after the onset of the disease with respect to late CP . To date, the early McR rate to imatinib is clearly higher in low and intermediate risk versus high risk (88 and 84% versus 65%). High dose of imatinib, as shown in phase I-III trials may offer the possibility to increase the response rate of patients belonging to this risk category.

Description:

This is a phase II multicenter, open-label study designed to investigate the efficacy (hematological response, cytogenetic response and molecular response) and feasibility (tolerance, compliance and safety) of the tyrosine kinase inhibitor imatinib mesylate (formerly STI 571, GLIVECÔ, Novartis Pharma) at high dose (800 mg/daily) (serial number protocol ICSG/CML/021) in patients with Ph+ chronic myeloid leukemia (CML) in chronic phase (CP) previously untreated, at intermediate Sokal risk.

With aIFN, responses (HR and CgR) are significantly influenced by the disease phase and, in CP patients, by risk. aIFN induces rare and short lived HR and CgR (any degree) in late CP and particularly in accelerated and blastic phase.

Moreover, in CP patients Sokal's risk influences significantly the probability of obtaining a MCgR after aIfaIFN . As far as survival, after aIFN even in CCgR patients, the long term survival is signifcantly influenced by risk. The European investigators on Interferon in CML (EICML) collected informations on response and survival on 317 complete cytogenetic responders to IFN. The 10 years survival of the whole patients population was 75% but, after stratification by risk, a significant difference in 10 years survival rates was found in favour of low risk patients (89%) if compared with intermediate risk (70%) and high risk patients (54%) (low vs high risk p 0.0001; intermediate vs high p 0.003, log-rank test).

Long term survival data still lacks after imatinib. However, it has been already shown that the disease phase influences the efficacy of imatinib in CML: responses (HR and particularly CgR) are better in CP versus accelerated and blastic phase. Results in CP are better in patients treated early after the onset of the disease with respect to late CP . To date, the early McR rate to imatinib is clearly higher in low and intermediate risk versus high risk (88 and 84% versus 65%).

Two scoring systems are available for disease risk evaluation, Sokal and Euro. Sokal risk is based on chemotherapy treated patients and Euro risk is based on aIFN trated patients: it is not known to date if one or both of the scoring systems will apply to imatinib treated patients. Moreover, the Sokal system has been applied to stratify the patients by risk in all the large clinical trials of imatinib in CML in the last 3 years and consequently, Sokal score will be employed in the present trial.

Study objectives

Primary:

To determine the rate of complete cytogenetic response at 12 months in adult patients with previously untreated intermediate Sokal risk CML treated with imatinib 800 mg/daily

Secondary:

To determine:

1. The rate of major cytogenetic response at 6 and 12 months.

2. The kinetic of cytogenetic response at 6 and 12 months

3. The duration of complete cytogenetic response.

4. The rate and duration of hematologic response.

5. The degree and the timing of molecular response

6. The time to accelerated and blast crisis and overall survival

7. The safety and tolerability of the treatment.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 80
• Est. completion date: November 2006
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age >/=18 years

• First chronic phase, less than 6 months of duration

• Intermediate Sokal's risk

• Ph positive

• No previous treatment or hydroxiurea only.

• Performance status (ECOG/WHO) < or = 2

• Written informed consent

Exclusion Criteria:

• Age <18

• Low or high Sokal risk score.

• More than 6 months from diagnosis.

• Second chronic, accelerated or blastic phase

• Scheduled allogeneic stem cell transplantation within 1 year from diagnosis.

• Performance status (ECOG/WHO) > 2 (see Appendix 2)

• Inability to provide written informed consent

• Pregnancy

• Formal refusal of any recommendation of a safe contraception

• Alcohol or drug addiction

• Altered hepatic or renal function as defined by AST/ALT or bilirubine > 3 times upper normal limits (UNL) and by creatinine ³ 20mg/L Any other disease or condition that by the advise of the responsible physician would make the treatment dangerous for the patient or would make the patient ineligible for the study, including physical, psychiatric, social and behavioural problems.

Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Leukemia
• Leukemia, Myelogenous, Chronic, BCR-ABL Positive
• Leukemia, Myeloid
• Leukemia, Myeloid, Chronic-Phase
• Myeloid Leukemia, Chronic, Chronic-Phase

Intervention

Drug:
• Imatinib Mesilate (Glivec)

Locations

Country	Name	City	State
Italy	Policlinico S.Orsola-Malpighi, Istituto di Ematologia e Oncologia Medica "L. e A. Seràgnoli"	Bologna

Sponsors (1)

Lead Sponsor	Collaborator
University of Bologna

Country where clinical trial is conducted

Italy, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Rate of complete cytogenetic response at 12 months
Secondary	The rate of major cytogenetic response at 6 and 12 months.
Secondary	The kinetic of cytogenetic response at 6 and 12 months
Secondary	The duration of complete cytogenetic response.
Secondary	The rate and duration of hematologic response.
Secondary	The degree and the timing of molecular response (see section 13 and 14.5).
Secondary	The time to accelerated and blast crisis and overall survival (see section 14.2)
Secondary	The safety and tolerability of the treatment.