CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 176 enrolled
Drug / intervention
ATO +7 moredrug
Likely dose
Not stated in 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/NCT02200978
NCT02200978Phase 4Completed

A Multicenter and Randomized Prospective Study for Improving the Outcome of Childhood Acute Promyeloid Leukemia

South China Children's Leukemia Group·interventional·Posted Jul 25, 2014·Updated May 10, 2022

In Brief

A Phase 4 clinical trial evaluating ATO, RIF, and 6 other interventions for Childhood Acute Promyelocytic Leukemia. Completed, enrolled 176 participants across 1 site.

Detailed Summary

Outcome of acute promyelocytic leukemia (APL) has greatly improved since the introduction of all-trans-retinoic acid (ATRA). Treatment with ATRA and anthracycline-based chemotherapy (ATRA + chemotherapy) decreases relapses of the disease as well as early hemorrhagic deaths. Nowadays patients with APL have an event-free survival (EFS) of up to 80%. However, there remains a subset of the patients in whom the disease relapses. Recently, a randomized prospective study showed that the addition of ATO to "ATRA + chemotherapy" treatment protocol had a significantly higher EFS in patients with APL than those treated with "ATRA + chemotherapy" protocol. The patients treated with "ATO + ATRA + chemotherapy" had a five years EFS of 89.2%. Moreover, a recent study showed that Indigo naturalis formula (RIF), a traditional Chinese medicine with tetraarsenic tetrasulfide (As4S4), indirubin, and tanshinone IIA as major active ingredients, yielded synergy in the treatment of a murine APL model in vivo and in the induction of APL cell differentiation in vitro . It is about 20 years since RIF was used to treat ALP in China. Clinical studies showed that this agent was effective against APL. Compared to ATO, RIF is relatively inexpensive and can be taken orally, resulting in reducing the number of hospital days and the treatment cost. However, there is no report comparing treatment outcomes of "ATO + ATRA + chemotherapy" and "RIF + ATRA + chemotherapy" protocols in children with APL so far. For this purpose, therefore, investigators are going to conduct a multicenter and randomized prospective study in children with APL.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina
Collaborators--

Timeline

Phase 4CompletedFinished
201220132014201520162017201820192020202120222023202420252026
First PostedJul 25, 2014
Enrollment StartSep 1, 2011
Primary CompletionOct 1, 2021
TodayJul 2, 2026
Enrollment to primary: 10.1 yearsPosted 11.9 years ago

Interventions

ATOdrug

Given IV

RIFdrug

Given orally

ATRAdrug

Given orally

mitoxantronedrug

Given IV

Ara-Cdrug

Given IV

MTXdrug

Given orally

6MPdrug

Given orally

intrathecal injectionother

Ara-C and dexamethasone