Status:
RECRUITING
Oral Arsenic With ATRA for Newly Diagnosed Patients With Acute Promyelocytic Leukemia
Lead Sponsor:
Instituto do Cancer do Estado de São Paulo
Collaborating Sponsors:
American Society of Hematology
Conditions:
Acute Promyelocytic Leukemia (APL)
Eligibility:
All Genders
18-75 years
Phase:
PHASE2
Brief Summary
It is a non-randomized, multicenter, prospective study, aiming to treat patients with newly diagnosed acute promyelocytic leukemia with a combination of oral arsenic and atra, with low dose chemothera...
Detailed Description
This is a non-randomized, multicenter, prospective study aimed at treating patients with newly diagnosed acute promyelocytic leukemia (APL) using a combination of oral arsenic and ATRA. For patients c...
Eligibility Criteria
Inclusion
- Informed consent
- New diagnosis of APL by cytomorphology, confirmed for molecular analysis
- Age ≥18 and ≤75 years
- Serum total bilirubin ≤ 3.0 mg/dl (≤ 51 μmol/l)
- Serum creatinine ≤ 3.0 mg/dl (≤ 260 μmol/l)
- Women must meet at least one of the following criteria to be eligible for inclusion in the study: Postmenopausal (12 months of amenorrhea or 6 months of amenorrhea with serum FSH \> 40 U/ml); After undergoing hysterectomy or bilateral oophorectomy; Continuous and correct use of a contraceptive method with a Pearl Index \<1% (e.g., implants, oral contraceptives, intrauterine devices); Sexual abstinence; Vasectomy of sexual partner.
Exclusion
- High-risk patients who are not eligible for chemotherapy according to the judgment of the treating physician;
- Age \<18 or \>75 years
- Other active malignancy at the time of study entry
- Lack of diagnostic confirmation at the genetic level
- Significant arrhythmias, ECG abnormalities, or neuropathy: Congenital long QT syndrome; History or presence of significant ventricular or atrial tachyarrhythmia; Clinically significant resting bradycardia (\<50 beats per minute); QTc \> 500 ms on ECG screening for both sexes; Right bundle branch block with left anterior hemiblock or bifascicular block
- High-risk patients with other cardiac contraindications for intensive chemotherapy (LVEF \< 50%)
- Uncontrolled and potentially fatal infections
- Severe uncontrolled pulmonary or cardiac disease
- Severe hepatic or renal dysfunction
- Known HIV and/or hepatitis C infection
- Pregnant or breastfeeding women
- Allergy to the study drug or excipients in the study medication
- Substance abuse, medical, psychological, or social conditions that may interfere with the patient's participation in the study or the assessment of study outcomes
- Use of other investigational drugs at the time of enrollment or within 30 days before study entry.
Key Trial Info
Start Date :
October 20 2023
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
November 1 2029
Estimated Enrollment :
115 Patients enrolled
Trial Details
Trial ID
NCT06982274
Start Date
October 20 2023
End Date
November 1 2029
Last Update
May 30 2025
Active Locations (1)
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1
Instituto do Cancer do Estado de Sao Paulo
São Paulo, São Paulo, Brazil, 01246000