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Brief Title: Italian Observational Study of Patients With Acute Myeloid Leukemia Treated With Small Molecule Inhibiting BCL-2
Official Title: Italian Observational Study of Patients With Acute Myeloid Leukemia Treated With Small Molecule Inhibiting B-cell Lymphoma 2 (BCL-2)
Study ID: NCT04070807
Brief Summary: This is a multi-center retrospective observational study. Every patient with Acute Myeloid Leukemia (AML) treated with anti-B-cell lymphoma 2 (BCL2) treatment outside clinical trial from 1st January 2015 up to 01 April 2019 may be included in this study. No additional drug/procedures/patient visits in comparison with the usual clinical practice are planned for the study. The decision to treat patient with ant-BCL2 inhibitors is made by the physician based on his clinical judgment, independently from the decision to include the patient in this study.
Detailed Description: In phase 1-2 studies, anti BCL-2 treatment has shown evidence of anti-leukemic activity as single agent and in combination and proved to be particularly effective in providing a deep response, with an acceptable safety profile. Since 2015 anti-BCL2 treatment has been available in other indications and in off-label use in Italy. In this non-interventional retrospective study, toxicity, effectiveness and costs assessment data will be collected from patients with AML, to improve the knowledge about anti-BCL2 treatment in clinical practice. Collecting and analyzing data from a large unbiased patient-set receiving anti-BCL2, would enlarge our knowledge on therapies inhibiting BCL2. This is a multi-center retrospective observational study. Every patient with AML treated with anti-BCL2 treatment outside clinical trial from 1st January 2015 up to 01 April 2019 may be included in this study. No additional drug/procedures/patient visits in comparison with the usual clinical practice are planned for the study. The decision to treat patient with ant-BCL2 inhibitors is made by the physician based on his clinical judgment, independently from the decision to include the patient in this study. As this study is intended to be purely observational (not interventional), the patient's medical records will be the source of all data to be recorded. No additional procedures/patient visits should be planned in the study with respect to clinical practice. Clinical data (treatment, survival, adverse events) will be collected for patients enrolled.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
ASST Cremona, Cremona, CR, Italy
A.O. Pugliese Ciaccio, Catanzaro, CZ, Italy
Irst Irccs, Meldola, FC, Italy
AOU Careggi, Firenze, FI, Italy
IRCCS Casa Sollievo sofferenza, San Giovanni Rotondo, Foggia, Italy
Ospedale F. Spaziani, Frosinone, FR, Italy
P.O. Vito Fazzi, Lecce, LE, Italy
Ospedale Santa Maria Goretti, Latina, LT, Italy
Asst Monza, Monza, MB, Italy
ASST Grande Ospedale Metropolitano Niguarda, Milano, MI, Italy
Ospedale S.Spirito - ASL Pescara, Pescara, PE, Italy
Ospedale Santa Maria della Misericordia, Perugia, PG, Italy
AOU San Giovanni di Dio e Ruggi D'Aragona, Salerno, SA, Italy
Policlinico Santa Maria alle Scotte, Siena, SI, Italy
AOU Città della Salute e della Scienza di Torino, Torino, TO, Italy
A.O. Ordine Mauriziano, Torino, TO, Italy
Ospedale Ca' Foncello, Treviso, TV, Italy
European Institute of Oncology, Milano, , Italy
Fondazione IRCCS Ca' Granda OSPEDALE MAGGIORE POLICLINICO, Milano, , Italy
Ospedale Roma S.Eugenio, Roma, , Italy
Name: Giovanni Martinelli, MD
Affiliation: IRST IRCCS
Role: PRINCIPAL_INVESTIGATOR