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NCT02938858Completed

French Registry of First-line Treatment of Acute Promyelocytic Leukemia

The French Registry on the First-line Treatment of Non High-risk Acute Promyelocytic Leukemia (APL) in Patients Aged ≤ 70 Years

Source: ClinicalTrials.gov · Last updated 11 Sept 2026

Brief summary (registry, in English)

The registry aims to compare the two first-line available treatment approaches in non-high-risk APL patients aged ≤ 70 years - ATRA plus chemotherapy and ATRA plus ATO - in terms of practitioner's choice between the two options, clinical effectiveness and cost-effectiveness, long-term outcome, and short- and long-term toxic effects.

Status (registry)
Completed
Study type
Observational
Enrollment
400 (actual)
First submitted
22 Sept 2016
Start date
Oct 2015
Primary completion date
Jul 2026
Lead sponsor
Groupe Francophone des Myelodysplasies
NCT number
NCT02938858

What you commit to

  • Study type: Observational
  • Participants enrolled: 400
  • From Oct 2015 to the primary completion date, Jul 2026
  • 27 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Lab values

  • Newly-diagnosed High-risk APL (White Blood Count \> 10000/μl at presentation)

Age

  • Age \> 70 years

Other

  • Relapsed APL

Who the study is looking for

  • Newly-diagnosed APL (either de novo or therapy-related) based on cytologic criteria and confirmed by the presence of the t(15;17) translocation and/or by the detection of the fusion transcript PML/RARα.
  • Non-high-risk APL (White Blood Count \< 10000/μl at presentation)
  • Age ≤ 70 years

Age in the registry: - to 70 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (27)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Centre Hospitalier d'Aix en Provence
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Aix-en-ProvenceFranceUnknown status
Groupe Hospitalier SUD
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AmiensFranceUnknown status
Centre Hospitalier V. Dupouy
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ArgenteuilFranceUnknown status
Hopital Jean Minjoz
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BesançonFranceUnknown status
CHU Bordeaux Pellegrin enfant
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BordeauxFranceUnknown status
CHRU de Brest - Pédiatrie Spécialisée
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BrestFranceUnknown status
CHU Estaing
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Clermont-FerrandFranceUnknown status
Hopital Henri Mondor
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CréteilFranceUnknown status
CHU de Grenoble
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GrenobleFranceUnknown status
Hôpital André Mignot
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Le ChesnayFranceUnknown status
CH Dr Schaffner
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LensFranceUnknown status
CHRU, Hôpital Claude Huriez
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LilleFranceUnknown status
Hôpital Universitaire Dupuytren
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LimogesFranceUnknown status
Institut Paoli-Calmettes
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MarseilleFranceUnknown status
Chu Timone
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MarseilleFranceUnknown status
CHR Metz-Thionville - Hôpital de Marcy
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MetzFranceUnknown status
CHU Saint-Eloi
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MontpellierFranceUnknown status
CHU Hôtel Dieu
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NantesFranceUnknown status
Hôpital de la Source
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OrléansFranceUnknown status
Hopital Robert Debre
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ParisFranceUnknown status
Hôpital Necker
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ParisFranceUnknown status
Hôpital Trousseau
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ParisFranceUnknown status
CHU Hôpital Sud - service Hémato-oncologie Pédiatrique
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RennesFranceUnknown status
Hôpital V. Provo
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RoubaixFranceUnknown status
Centre Henri Becquerel
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RouenFranceUnknown status
Institut de Cancerologie de La Loire
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Saint-Priest-en-JarezFranceUnknown status
IUCT Oncopôle
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ToulouseFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.