Acute Myeloid Leukemia Clinical Trial
— ICAML2015Official title:
Feasibility Study of the Use of Intermediate Doses of Cytarabine Associated With Autologous Hematopoietic Stem Cells as Consolidation Treatment of Young Adults With Low- or Intermediate-risk de Novo Acute Myeloid Leukemia
Create a network of institutions in developing countries that will perform AML diagnosis, risk classification, treatment, supportive care and follow-up evaluation according to a common protocol and will register data using common clinical research forms (CRFs) in a single database and available on the internet.
Status | Recruiting |
Enrollment | 547 |
Est. completion date | January 2022 |
Est. primary completion date | January 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: 1. Acute myeloid leukemia (AML) diagnosis according to WHO criteria; 2. AML not treated previously, including: de novo AML or secondary to myelodysplastic syndromes; 3. Absence of t(15;17), or PML-RARA rearrangement and its variants (acute promyelocytic leukemia diagnosis); 4. Age greater than or equal to 18 years old or lower than or equal to 65 years old; 5. Functional status ECOG from 0 to 2; 6. Signed informed consent; 7. Ability to follow the protocol procedures; 8. Willingness to use birth control methods during the treatment until its conclusion; 9. Adequate renal and liver function: - Bilirubin = 1.5x the upper limit of normality; - AST and ALT = 2.5x the upper limit of normality; - Creatinine = 2.5 mg/dL. 10. Suitable cardiac function: left ventricular ejection fraction = 50%. Exclusion Criteria: 1. Acute promyelocytic leukemia (APL) diagnosis according to WHO criteria; 2. Diagnosis of acute leukemia of ambiguous lineage, biphenotypic acute leukemia or undifferentiated acute leukemia, according to WHO criteria; 3. AML previously treated, except with hydroxyurea administration for cytoreduction; 4. Age greater than 65 years old or lower than 18 years old; 5. Functional status ECOG greater than 2; 6. Do not sign the informed consent; 7. Inability to follow the protocol procedures; 8. Be fertile female who are unwilling to take any birth control method during the treatment; 9. Hypersensitivity to any drug of the treatment protocol; 10. Positive serology for HIV; 11. Altered liver and renal function not related to the primary disease (AML): - Bilirubin > 1.5x the upper limit of normality - AST and ALT > the 2.5x upper limit of normality - Creatinine > 2.5 mg/dL n) Altered cardiac function, with LVEF <50% |
Country | Name | City | State |
---|---|---|---|
Brazil | Hospital das Clínicas da Unicamp | Campinas | São Paulo |
Brazil | Hospital das Clinicas de Porto Alegre | Porto Alegre | Rio Grande do Sul |
Brazil | Hospital das Clinicas de Ribeirão Preto | Ribeirao Preto | São Paulo |
Brazil | Hospital Mario Covas | Santo Andre | São Paulo |
Brazil | Hospital de Base de São José do Rio Preto | Sao Jose do Rio Preto | São Paulo |
Brazil | Hospital São Paulo | Sao Paulo | São Paulo |
Lead Sponsor | Collaborator |
---|---|
International Consortium on Acute Leukemias |
Brazil,
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* Note: There are 49 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
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Primary | Disease free survival | Time from diagnosis until relapse | 2 years | |
Secondary | Overall survival | Time from diagnosis until death from any cause | 2 years |
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