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Phase II Study for Safety and Efficacy Evaluation of Imatinib Mesylate in Children With Chronic Myeloid Leukemia (CML) Philadelphia Chromosome-positive (Ph+)


Phase 2
N/A
18 Years
Open (Enrolling)
Both
Chronic Myeloid Leukemia (CML) With Philadelphia Chromosome-positive (Ph+)

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Trial Information

Phase II Study for Safety and Efficacy Evaluation of Imatinib Mesylate in Children With Chronic Myeloid Leukemia (CML) Philadelphia Chromosome-positive (Ph+)


Inclusion Criteria:



1. Diagnose: suspected CML (hematology and/or myelogram and/or immunophenotyping and/or
Leukocyte alkaline phosphatase [LAP]) to be confirmed, after, by cytogenetic and/or
molecular biology. OBS: only CML Ph+ newly-diagnose in chronic or accelerate phase;
resistant CML Ph+ to Interferon α (INF-α), Hydroxyurea and/or low-dose ARA-C in
chronic or accelerate phase; CML Ph+ with cytogenetic relapse after BMT, that didn't
use Imatinib previously, in chronic or accelerate phase.

2. Female patients of childbearing age, should have pregnancy test (blood βhCG)
performed before treatment initiation. Effective contraception must be used. Pregnant
women won't be included.

3. Karnofsky and Lansky scale: ≥40.

4. Life expectation > 8 weeks.

5. Laboratory: renal function (serum creatinine ≤ 1,5 x ULN and/or Clearance ≥70
ml/min/1,73m2), hepatic function (total bilirubin ≤ 1,5 x ULN, TGP < 3 x ULN and
albumin > 2 g/dl.

6. CNS toxicity ≤ II

7. Cardiac function: normal ejection fraction.

8. Signed ICF by child legal responsible.

Exclusion Criteria:

1. Patient receiving any other tyrosine kinase inhibitor (TKI).

2. Pregnant patient or breastfeeding.

3. Patient considered incapable to follow purposed treatment.

4. Patients with molecular relapsed.

5. Medications:

- Colony stimulating: it cannot be administered at least 1 week before treatment.

- Anticonvulsants: Imatinib is metabolized by P-450 enzyme, thereby subject cannot
receive drug that activates the P-450 system. The anticonvulsants allowed are
valproic acid and benzodiazepines.

- Anticoagulants: The use of warfarin (Marevan) is not allowed. If anticoagulant
is needed, low-molecular-weight heparin (LMWH) can be used. Avoid anticoagulants
with platelets < 50000.

- INF-Α 48h before D1.

- Hydroxyurea 24h before D1.

- ARA-C doses >100 mg/m2 for 5-7 days, 14 days before D1.

- Anthracyclines, Mitoxantrone or Etoposide 21 days before D1.

- Any other chemotherapeutic agent 28 days before D1.

- Hematopoietic Cell Transplantation (HCT) 6 weeks before D1.

Type of Study:

Interventional

Study Design:

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

Evaluate the complete cytogenetic response with continuous-use of Imatinib.

Outcome Time Frame:

Up to 12 months

Safety Issue:

No

Principal Investigator

Alejandro M Arancibia, MD

Investigator Role:

Study Chair

Investigator Affiliation:

Casa de Saúde Santa Marcelina

Authority:

Brazil: Ethics Committee

Study ID:

CSTI571ABR23T

NCT ID:

NCT01221376

Start Date:

February 2011

Completion Date:

December 2013

Related Keywords:

  • Chronic Myeloid Leukemia (CML) With Philadelphia Chromosome-positive (Ph+)
  • Leukemia
  • Leukemia, Myeloid
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive
  • Philadelphia Chromosome

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