CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 300 target
Drug / intervention
ATRA +3 moredrug
Likely dose
ATRA 45 mg/m2from record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00408278
NCT00408278Phase 4Completed

Treatment of Newly Diagnosed Patients With Acute Promyelocytic Leukemia (PETHEMA LPA 2005): Remission Induction With ATRA + Idarubicin. Risk-adapted Consolidation With ATRA and Anthracycline-based Chemotherapy (Idarubicin/Mitoxantrone) With Addition of Ara-C for High-risk Patients. Maintenance Therapy With ATRA + Low Dose Chemotherapy (Methotrexate + Mercaptopurine).

PETHEMA Foundation·interventional·Posted Dec 6, 2006·Updated Oct 28, 2014

In Brief

A Phase 4 clinical trial evaluating ATRA, Idarubicina, and 2 other interventions for Acute Promyelocytic Leukemia. Completed, enrolled 300 participants across 42 sites in 3 countries.

Detailed Summary

Primary objectives * To evaluate the efficacy and toxicity of a risk-adapted protocol that use idarubicin for induction and consolidation therapy in patients with APL. * To evaluate the impact of mitoxantrone reduction on the event-free, disease-free, and overall survival, as well as on the duration of remission and cumulative incidence of relapse in low- and intermediate-risk patients with APL. * To evaluate the impact of the addition of ara-C to idarubicin courses of consolidation for high-risk patients (administered as in the original GIMEMA protocols) on the event-free, disease-free, and overall survival, as well as on the duration of remission and cumulative incidence of relapse. * To evaluate the toxicity of the induction, consolidation, and maintenance chemotherapy in the whole series and in each treatment group in patients with APL. Secondary objectives • To compare all outcomes with those achieved with the PETHEMA LPA99 protocol.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesPoland, Spain, Uruguay
Collaborators--

Timeline

Phase 4CompletedFinished
20052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedDec 6, 2006
Enrollment StartJul 1, 2005
Primary CompletionApr 1, 2012
Study CompletionDec 1, 2013
TodayJul 2, 2026
Enrollment to primary: 6.8 yearsPosted 19.6 years ago

Interventions

ATRAdrug

45 mg/m2 day until CR Consolidation: 3 cycles (45 mg/m2 days 1-15) Maintenance:15 days every 3 months

Idarubicinadrug

Induction: 12 mg/m2 days 2, 4, 6 and 8 Consolidation: 5 mg/m2 days 1-4 in cycle 1 and 12 mg/m2 day 1 in cycle 3.

Mitoxantronedrug

Consolidation: Mitoxantrone 10 mg/m2 days 1-3 in cycle 2

ARA-Cdrug

In high risk patients, consolidation with ara-C in cycles 1 and 3.