- ICH GCP
- Yhdysvaltain kliinisten tutkimusten rekisteri
- Kliininen tutkimus NCT01310010
Study of Dasatinib to Treat Philadelphia Positive Acute Lymphoblastic Leukemia (DASA-TRAS)
Multicenter, Non-randomized Phase II Pilot Study to Assess the Efficacy and Safety of Dasatinib After Allogeneic Stem Cell Transplantation in Patients With de Novo Philadelphia Positive (Bcr-abl +) Acute Lymphoblastic Leukemia
Study hypothesis:
Treatment with dasatinib 100 mg QD is safe and efficacious when given to patients with Ph+ ALL in the post SCT setting.
Tutkimuksen yleiskatsaus
Tila
Interventio / Hoito
Yksityiskohtainen kuvaus
Participants - inclusion criteria
- Adult patients ≥ 18 years.
- Diagnostic confirmation of de novo Ph+ ALL.
- Patients in first/second CR (assessed by cytology, karyotyping and/or FISH) at transplantation.
- Patients with sustained hematologic and cytogenetic CR at the time of study entry.
- Any modality of allogeneic SCT.
- Patients are in days between 120 until 180 after allogeneic SCT with stable graft.
- Ability to understand and voluntarily sign the informed consent form.
- Women of childbearing potential (WOCBP) must be using an adequate method of contraception to avoid pregnancy and have a negative pregnancy test, a maximum of 48 hours prior to study drug start.
Participants - exclusion criteria:
- Patients with ECOG 3-4 at study entry
Any of the following laboratory abnormalities:
- Absolute neutrophil count < 1.5 x 109/l or platelets < 75 x 109/l
- Serum creatinine > 2.0 mg/dl (177 mmol/l).
- Serum glutamic oxalacetic transaminase (SGOT) or serum glutamate pyruvate transaminase (SGPT) > 5,0 x upper limit of normal (ULN).
- Total bilirubin > 3 mg/dl.
- Known HIV infection or any other uncontrolled infection at study entry
- Known pleural effusion of any grade at study entry.
- Morphologic or cytogenetic or molecular relapse at study entry
- Evidence of digestive dysfunction that could prevent administration of study therapy
- Prior therapy with dasatinib during >21 days
- Other concurrent malignancy at study entry
- Uncontrolled or significant cardiovascular disease, including myocardial infarction within 6 months, uncontrolled angina within 3 months, prolonged QT interval, congestive heart failure within 3 months and clinically significant ventricular arrhythmias
- Any psychiatric condition that could prevent patient from signing the informed consent o could put the patient at an unacceptable risk in case of participating in the trial
- Subjects enrolled in another clinical trial at study entry. If patients have received other investigational agent, a minimum of 30 days wash-out period must have elapsed.
Primary Outcome measures
The primary objective of this study is to assess the efficacy of dasatinib maintenance in terms of Disease Free Survival at 2 years in patients with Ph+ ALL who receive maintenance with dasatinib after allogeneic SCT.
Secondary Outcome measures
.To assess the efficacy of maintenance with dasatinib in terms of duration of hematologic, cytogenetic and molecular remission, Relapse rate at 2 years, survival at 2 years, overall DFS, and Overall Survival (OS).
·To assess the safety and tolerability of dasatinib maintenance regimen after allogeneic SCT
Regarding the secondary objective "To assess the safety and tolerability of dasatinib maintenance regimen after allogeneic SCT", such safety analysis includes the frequency of all adverse events and laboratory abnormalities as well as frequency of dose interruptions, dose reductions and treatment discontinuation for drug-related toxicity. Frequency tables will be reported using the "All treated subjects" dataset. Safety will be reported for all treated patients and assessed by baseline findings, AEs and SAEs (definition, pattern, seriousness and intensity according to NCI CTCAE v3.0, relationship with dasatinib and outcome). Hematologic toxicity will be analyzed separately.
Opintotyyppi
Ilmoittautuminen (Odotettu)
Vaihe
- Vaihe 2
Yhteystiedot ja paikat
Opiskelupaikat
-
-
-
Valencia, Espanja, 46009
- Hospital La Fe
-
-
Osallistumiskriteerit
Kelpoisuusvaatimukset
Opintokelpoiset iät
Hyväksyy terveitä vapaaehtoisia
Sukupuolet, jotka voivat opiskella
Kuvaus
Inclusion Criteria:
- Adult patients ≥ 18 years
- Diagnostic confirmation of de novo Ph+ ALL
- Patients in first/second CR (assessed by cytology, karyotyping and/or FISH) at transplantation
- Patients with sustained hematologic and cytogenetic CR at the time of study entry
- Any modality of allogeneic SCT
- Patients are in days between 120 until 180 after allogeneic SCT with stable graft.
- Ability to understand and voluntarily sign the informed consent form
- Women of childbearing potential (WOCBP) must be using an adequate method of contraception to avoid pregnancy and have a negative pregnancy test, a maximum of 48 hours prior to study drug start
Exclusion Criteria:
- Patients with ECOG 3-4 at study entry
Any of the following laboratory abnormalities:
- Absolute neutrophil count < 1.5 x 109/l or platelets < 75 x 109/l
- Serum creatinine > 2.0 mg/dl (177 mmol/l).
- Serum glutamic oxalacetic transaminase (SGOT) or serum glutamate pyruvate transaminase (SGPT) > 5,0 x upper limit of normal (ULN).
- Total bilirubin > 3 mg/dl.
- Known HIV infection or any other uncontrolled infection at study entry
- Known pleural effusion of any grade at study entry.
- Morphologic or cytogenetic or molecular relapse at study entry
- Evidence of digestive dysfunction that could prevent administration of study therapy
- Prior therapy with dasatinib during >21 days
- Other concurrent malignancy at study entry
- Uncontrolled or significant cardiovascular disease, including myocardial infarction within 6 months, uncontrolled angina within 3 months, prolonged QT interval, congestive heart failure within 3 months and clinically significant ventricular arrhythmias
- Any psychiatric condition that could prevent patient from signing the informed consent o could put the patient at an unacceptable risk in case of participating in the trial
- Subjects enrolled in another clinical trial at study entry. If patients have received other investigational agent, a minimum of 30 days wash-out period must have elapsed.
Opintosuunnitelma
Miten tutkimus on suunniteltu?
Suunnittelun yksityiskohdat
- Ensisijainen käyttötarkoitus: Hoito
- Jako: Ei käytössä
- Inventiomalli: Yksittäinen ryhmätehtävä
- Naamiointi: Ei mitään (avoin tarra)
Aseet ja interventiot
Osallistujaryhmä / Arm |
Interventio / Hoito |
|---|---|
|
Kokeellinen: Dasatinibi
|
Treatment with 100 mg QD of dasatinib (Sprycel®) administered orally as continuous daily dosing (CDD).
Muut nimet:
|
Mitä tutkimuksessa mitataan?
Ensisijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
|
The efficacy of dasatinib
Aikaikkuna: at 2 years
|
The primary objective of this study is to assess the efficacy of dasatinib maintenance in terms of Disease Free Survival at 2 years in patients with Ph+ ALL who receive maintenance with dasatinib after allogeneic SCT.
|
at 2 years
|
Toissijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
|
To assess the efficacy of maintenance with dasatinib in terms of duration of hematologic, cytogenetic and molecular remission
Aikaikkuna: at 2 years
|
To assess the efficacy of maintenance with dasatinib in terms of duration of hematologic, cytogenetic and molecular remission, Relapse rate at 2 years, survival at 2 years, overall DFS, and Overall Survival (OS).
|
at 2 years
|
|
To assess the safety and tolerability of dasatinib maintenance regimen after allogeneic SCT
Aikaikkuna: at 2 years
|
To assess the safety and tolerability of dasatinib maintenance regimen after allogeneic SCT
|
at 2 years
|
Yhteistyökumppanit ja tutkijat
Tutkijat
- Päätutkija: Guillermo Sanz, Doctor, Hospital La Fe de Valencia
Opintojen ennätyspäivät
Opi tärkeimmät päivämäärät
Opiskelun aloitus
Ensisijainen valmistuminen (Todellinen)
Opintojen valmistuminen (Todellinen)
Opintoihin ilmoittautumispäivät
Ensimmäinen lähetetty
Ensimmäinen toimitettu, joka täytti QC-kriteerit
Ensimmäinen Lähetetty (Arvio)
Tutkimustietojen päivitykset
Viimeisin päivitys julkaistu (Todellinen)
Viimeisin lähetetty päivitys, joka täytti QC-kriteerit
Viimeksi vahvistettu
Lisää tietoa
Tähän tutkimukseen liittyvät termit
Muita asiaankuuluvia MeSH-ehtoja
- Immuunijärjestelmän sairaudet
- Neoplasmat histologisen tyypin mukaan
- Neoplasmat
- Lymfoproliferatiiviset häiriöt
- Lymfaattiset sairaudet
- Immunoproliferatiiviset häiriöt
- Leukemia
- Prekursorisolulymfoblastinen leukemia-lymfooma
- Leukemia, imusolmukkeet
- Farmakologisen vaikutuksen molekyylimekanismit
- Entsyymin estäjät
- Antineoplastiset aineet
- Proteiinikinaasin estäjät
- Dasatinibi
Muut tutkimustunnusnumerot
- DASA-TRAS
Nämä tiedot haettiin suoraan verkkosivustolta clinicaltrials.gov ilman muutoksia. Jos sinulla on pyyntöjä muuttaa, poistaa tai päivittää tutkimustietojasi, ota yhteyttä register@clinicaltrials.gov. Heti kun muutos on otettu käyttöön osoitteessa clinicaltrials.gov, se päivitetään automaattisesti myös verkkosivustollemme .