QOL-APL0512: Long-Term Quality of Life in Patients With Acute Promyelocytic Leukemia

Sponsor
Gruppo Italiano Malattie EMatologiche dell'Adulto (Other)
Overall Status
Completed
CT.gov ID
NCT01910623
Collaborator
(none)
38
16.9

Study Details

Study Description

Brief Summary

This study will focus on acute promyelocytic leukemia patients who have been diagnosed more than 5 years ago and their present quality of life.

The possible late effects of cancer treatment can include several issues and, thus, there has been an increasing interest worldwide in studying the long-term impact of these in patients' life.

Condition or Disease Intervention/Treatment Phase
  • Other: Health Related Quality of Life (HRQOL) measures

Detailed Description

This study will focus on long-term survivors as defined by the America Cancer Society, that is surviving the initial diagnosis for more than 5 years. Previous research has investigated long-term Health Related Quality of Life (HRQOL) in patients with acute myeloid leukemia, however, this will be the first research conducted to investigate long-term HRQOL outcomes in patients with acute promyelocytic leukemia (APL).

The potential late effects of cancer treatment can include second malignancies or other chronic conditions affecting physical and emotional well-being. Therefore, there has been an increasing interest worldwide in evaluating the longer-term impact of cancer and its treatment. Currently large cohort of patients enjoys disease-free survival of 5 years or longer. However, a disease-free status is not synonymous with a life free of physical and psychological health related to the cancer and/or its treatment. Research shows that cancer related health concerns persist long after initial treatment and this has been shown in several cancer populations including prostate, testicular, breast cancer and lymphoma patients. Long-term cancer survivors can experience treatment-induced morbidity (e.g. cardiovascular damage due to chemotherapy or radiotherapy; infertility and second tumors), chronic disease and treatment-related symptoms, functional impairment, psychosocial problems, and practical problems.

Since the introduction of the vitamin A derivative all-trans retinoic acid (ATRA) as front-line therapy for APL, the outcome of this acute leukemia subtype has changed from the state of a most frequently fatal leukemia to the condition of a highly curable disease. The Italian cooperative group GIMEMA designed in 1993 the AIDA (Atra plus IDArubicin) trial for newly diagnosed APL. Results on over 800 patients showed a complete remission (CR) rate > 90% and an overall survival of 76% and confirmed that the concomitant administration of ATRA and chemotherapy is more effective than the sequential administration. Following the identification of distinct prognostic categories among APL patients, the GIMEMA group designed a new trial (AIDA2000) in which the intensity of post-remission treatment was adapted to the relapse risk and 498 patients were enrolled since January 2000. The results recently published showed a CR rate >90% with molecular remission rate after third consolidation of 98%. The new schedule allowed a Disease Free Survival (DFS) of 86% and showed that a risk-adapted strategy including ATRA for consolidation provides an outcome improvement in newly diagnosed patients. As reported by an international panel of experts, simultaneous ATRA and anthracycline chemotherapy schedules such as those used in the AIDA protocols represent the state of the art therapy for newly diagnosed APL.

Study Design

Study Type:
Observational
Observational Model:
Case-Control
Time Perspective:
Cross-Sectional
Official Title:
Long-Term Quality of Life in Patients With Acute Promyelocytic Leukemia: a Follow-up Observational Study of Patients Enrolled in the GIMEMA AIDA 0493 and AIDA 200
Study Start Date :
Feb 1, 2013
Actual Primary Completion Date :
Jul 1, 2014
Actual Study Completion Date :
Jul 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Patients being studied

APL patients previously enrolled in GIMEMA AIDA 0493 and AIDA 2000 studies.

Other: Health Related Quality of Life (HRQOL) measures
Other Names:
  • SF-36 health survey.
  • EORTC QOL-C30 questionnaire.
  • FACIT-Fatigue questionnaire.
  • Self-administered Comorbidity Questionnaire (SCQ).
  • Multidimensional Scale of Perceived Social Support (MSPSS).
  • MD Anderson Symptom Inventory (MDASI).
  • Outcome Measures

    Primary Outcome Measures

    1. Clinical significance on each of the SF-36 questionnaire scales. [One month from study entry.]

      This will be performed by using HRQOL scores available for the Italian population. This will help identify which specific areas are mostly impaired and to what extent these patients recover in terms of HRQOL over the long run. This kind of comparison, which is only possible when HRQOL cultural-based norms are available, is largely used when investigating long-term HRQOL in cancer survivors and it is widely recognized as one of the most valuable approach in this kind of research setting.

    Secondary Outcome Measures

    1. Association of EORTC-QLQC30 scales with social-demographic and clinical treatment related variables. [One month from study entry.]

    2. Association of MDASI scales (i.e., symptom severity and symptom interference) with different treatment strategies tested in the two GIMEMA trials. [One month from study entry.]

    3. Association of EORTC-QLQC30 scales with different treatment strategies tested in the two GIMEMA trials. [One month from study entry.]

    4. Association of rate of secondary malignancies with different treatment strategies tested in the two GIMEMA trials. [One month from study entry]

    5. Possible differences in EORTC-QLQC30, MDASI and SF-36 scales between patients who were less than eighteen years old at the time of diagnosis and patients who were at least eighteen years old at the time of diagnosis. [One month from study entry]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • APL patients previously enrolled in the studies GIMEMA AIDA0493 and AIDA2000 surviving the initial diagnosis for more than 5 years and are in CR.

    • Written informed consent provided.

    • Adult patients at the time of registration onto this study.

    Exclusion Criteria:
    • Concomitant major psychiatric disorders or cognitive dysfunctions that would interfere with a self-reported evaluation.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 S.O.C. di Ematologia - Azienda Ospedaliera - SS. Antonio e Biagio e Cesare Arrigo Alessandria Italy
    2 Azienda Ospedaliera - Nuovo Ospedale "Torrette" Ancona Italy
    3 Az.Ospedaliera S.G.Moscati Avellino Italy
    4 UO Ematologia con trapianto-Università degli Studi di Bari Aldo Moro Bari Italy
    5 Divisione di Ematologia - Ospedali Riuniti Bergamo Italy
    6 Istituto di Ematologia "Lorenzo e A. Seragnoli" - Università degli Studi di Bologna - Policlinico S. Orsola - Malpighi Bologna Italy
    7 Azienda Sanitaria di Bolzano - Ospedale Centrale - Ematologia e Centro TMO Bolzano Italy
    8 Spedali Civili - Brescia - Azienda Ospedaliera - U.O. Ematologia Brescia Italy
    9 ASL N.8 - Ospedale "A. Businco" - Struttura Complessa di Ematologia e CTMO Cagliari Italy
    10 Università di Catania - Cattedra di Ematologia - Ospedale "Ferrarotto" Catania Italy
    11 Azienda Ospedaliera Pugliese Ciaccio - Presidio Ospedaliero A.Pugliese - Unità Operativa di Ematologia Catanzaro Italy
    12 Policlinico di Careggi Firenze Italy
    13 Clinica Ematologica - DiMI - Università degli Studi di Genova Genova Italy
    14 IRCCS_AOU San Martino-IST-Ematologia 1-Monoblocco 11°piano- lato ponente Genova Italy
    15 Divisione di Ematologia Ospedale "Santa Maria Goretti" Latina Italy
    16 Ospedale Niguarda " Ca Granda" Milano Italy
    17 Centro Oncologico Modenese - Dipartimento di Oncoematologia Modena Italy
    18 N. Osp. divisione di Ematologia "S.Gerardo dei Tintori!" Monza Italy
    19 Azienda Ospedaliera di Rilievo Nazionale "A. Cardarelli" Napoli Italy
    20 Azienda Ospedaliera Universitaria - Università degli Studi di Napoli "Federico II" - Facoltà di Medicina e Chirurgia Napoli Italy
    21 Servizio Sanitario Nazionale - Azienda Ospedaliera di Rilievo Nazionale "A. Cardarelli" - Struttura Complessa di Ematologia - Div. TERE- 4° piano - Padiglione Palermo Napoli Italy
    22 Sez. di Ematologia Clinica Ospedale San Francesco Nuoro Italy
    23 Divisione di Ematologia con trapianto di midollo - A.U. Policlinico "Paolo Giaccone" Palermo Italy
    24 Ospedali Riuniti "Villa Sofia-Cervello" Palermo Italy
    25 Cattedra di Ematologia CTMO Università degli Studi di Parma Parma Italy
    26 S.C. Ematologia - Fondazione IRCCS Policlinico S. Matteo Pavia Italy
    27 Sezione di Ematologia ed Immunologia Clinica - Ospedale S.Maria della Misericordia Perugia Italy
    28 U.O. Ematologia Clinica - Azienda USL di Pescara Pescara Italy
    29 Calabria Dipartimento Emato-Oncologia A.O."Bianchi-Melacrino-Morelli" Reggio Calabria Italy
    30 Unità Operativa Complessa di Ematologia - Arcispedale S. Maria Nuova Reggio Emilia Italy
    31 U.O.C. Ematologia - Ospedale S.Eugenio Roma Italy
    32 Università Cattolica del Sacro Cuore - Policlinico A. Gemelli Roma Italy
    33 UOC Pronto Soccorso e Accettazione Ematologica - Dipartimento Biotecnologie Cellulari ed Ematologia - Università degli Studi di Roma "Sapienza" Roma Italy
    34 Istituto di Ematologia - IRCCS Ospedale Casa Sollievo della Sofferenza S. G. Rotondo Italy
    35 SCDO Ematologia 2 AOU S.Giovanni Battista Torino Italy
    36 Clinica Ematologica - Policlinico Universitario Udine Italy
    37 Università degli Studi di Verona - A. O. - Istituti Ospitalieri di Verona- Div. di Ematologia - Policlinico G.B. Rossi Verona Italy
    38 ULSS N.6 Osp. S. Bortolo Vicenza Italy

    Sponsors and Collaborators

    • Gruppo Italiano Malattie EMatologiche dell'Adulto

    Investigators

    • Principal Investigator: Fabio Efficace, PhD, GIMEMA Foundation

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Gruppo Italiano Malattie EMatologiche dell'Adulto
    ClinicalTrials.gov Identifier:
    NCT01910623
    Other Study ID Numbers:
    • QOL-APL0512
    First Posted:
    Jul 29, 2013
    Last Update Posted:
    Oct 2, 2014
    Last Verified:
    Oct 1, 2014
    Keywords provided by Gruppo Italiano Malattie EMatologiche dell'Adulto
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 2, 2014