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Long-term QoL in Acute Promyelocytic Leukemia Treated With ATO or Standard Chemotherapy

G

Gruppo Italiano Malattie EMatologiche dell'Adulto

Status

Unknown

Conditions

Acute Promyelocytic Leukemia

Treatments

Other: QoL questionnaires

Study type

Observational

Funder types

Other

Identifiers

NCT03096496
QoL-APL0816

Details and patient eligibility

About

This is a prospective and international observational study run by the GIMEMA. All data will be centrally collected and analyzed at the GIMEMA Data Center in Rome (Italy). Patients reported outcomes will be collected using internationally validated questionnaires.

Enrollment

161 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • APL survivors enrolled in GIMEMA APL0406 clinical trial and in first molecular CR after third consolidation treatment
  • Written informed consent.

Exclusion criteria

  • APL patients previously enrolled in GIMEMA APL0406 trial who cannot be reached or who are lost to follow-up.

Trial design

161 participants in 1 patient group

GIMEMA APL0406 patients
Description:
APL survivors previously enrolled in GIMEMA APL0406 clinical trial and in 1st molecular CR after third consolidation treatment.
Treatment:
Other: QoL questionnaires

Trial contacts and locations

16

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Data sourced from clinicaltrials.gov

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