To Evaluate Efficacy of Belinostat or Pralatrexate in Combination Against CHOP Alone in PTCL

Launched by ACROTECH BIOPHARMA INC. · Oct 2, 2023

Keywords

ClinConnect Summary

This clinical trial is studying two new treatment combinations for patients with a type of cancer called Peripheral T Cell Lymphoma (PTCL) that has just been diagnosed. The researchers want to find out if adding either Belinostat or Pralatrexate to the standard treatment known as CHOP can help patients live longer without their cancer getting worse. The trial is divided into two parts: the first part will determine the best dose of the new medications, while the second part will compare how well these new combinations work against the standard treatment alone.

To participate in this trial, patients must be adults aged 18 or older with newly diagnosed PTCL, and they must not have received any prior treatment for this condition. They will need to meet certain health criteria to ensure their bodies can handle the treatments. If they join the study, patients can expect to receive treatment for up to six cycles, which usually involves regular visits to the clinic for monitoring. It's important to note that participants will be closely watched for any side effects, and the study is currently open for enrollment.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• 1. Patient with newly diagnosed, untreated histology-proven PTCL based on local pathology review who is eligible for receiving, Belinostat, Pralatrexate, and CHOP. Pathology material must be available at the site for each patient before enrollment so that it can be sent to the Sponsor (or designee) for later confirmation. The following subtypes, as defined by the updated World Health Organization (WHO) classification, may be included. This information should be available for eligibility:
• 1. Pathology subtype:
• • Peripheral T-cell lymphoma, not otherwise specified
• • Angioimmunoblastic T-cell lymphoma
• • Anaplastic lymphoma kinase (ALK)-negative anaplastic large-cell lymphoma (ALCL) patients are eligible only if Brentuximab Vedotin (BV) is not commercially approved for use, not available in the country or patient is contraindicated to receive BV.
• • Follicular T-cell lymphoma
• • Others: Extra-nodal natural killer/T-cell lymphoma, nasal type; enteropathy-associated T-cell lymphoma; hepatosplenic T-cell lymphoma; and subcutaneous panniculitis-like T-cell lymphoma
• • 2. CD30 expression and T-cell Follicular Helper (TFH) phenotype status must be available for documentation.
• • 2. Patient has at least 1 site of measurable disease according to Response Evaluation Criteria in Lymphoma (RECIL) 2017 criteria as assessed by the local Investigator (Appendix 3)
• • 3. Patient has an Eastern Cooperative Oncology Group performance (ECOG) status ≤2
• 4. For Part 1 (Dose Finding) - Patient has adequate hematological, hepatic, and renal function as defined by:
• • 1. Absolute neutrophil count ≥ 1.5 × 10⁹/L or ≥ 1.0 × 10⁹/L if evidence of bone marrow involvement
• • 2. Platelet count ≥100×10⁹/L or ≥ 75×10⁹/L if evidence of bone marrow involvement
• • 3. Total bilirubin ≤1.5 mg/dL
• • 4. Aspartate aminotransferase (AST)/serum glutamic-oxaloacetic transaminase (SGOT), alanine aminotransferase (ALT)/serum glutamic-pyruvic transaminase (SGPT) ≤ 3×upper limit of normal (ULN; AST/ALT ≤5×ULN if documented hepatic involvement with lymphoma)
• • 5. Calculated creatinine clearance of ≥ 60 mL/min
• 5. Part 2 (Efficacy and Safety) - disease related hypoplasia, hepatological or renal dysfunction can be included if any of the treatment groups can be administered based on package insert recommendation with the following restrictions:
• • 1. Absolute neutrophil count ≥ 1.5 × 10⁹/L or ≥ 1.0 × 10⁹/L if evidence of bone marrow involvement
• • 2. Platelet count ≥100×10⁹/L or ≥ 75×10⁹/L if evidence of bone marrow involvement
• • 3. Total bilirubin ≤1.5 mg/dL
• • 4. Aspartate aminotransferase (AST)/serum glutamic-oxaloacetic transaminase (SGOT), alanine aminotransferase (ALT)/serum glutamic-pyruvic transaminase (SGPT) ≤ 3 x the upper limit of normal (ULN; AST/ALT ≤5×ULN if documented hepatic involvement with lymphoma)
• • 5. Calculated creatinine clearance of ≥ 60 mL/min
• • 6. UGT1A1 genotype has been characterized (see Belinostat dose modifications if abnormal) and must be available for documentation.
• • 7. Patient must be willing and capable of giving written informed consent and must be able to adhere to dosing and visit schedules and meet all study requirements
• • 8. Patient (male or female) is at least 18 years of age at the time of informed consent
• • 9. Patient is willing to practice 2 forms of contraception, one of which must be a barrier method, from study entry until at least 6 months after the last dose of study treatment.
• • 10. Females of childbearing potential must have a negative urine pregnancy test within 4 weeks prior to the first day of study treatment. Females who are postmenopausal for at least 1 year (defined as more than 12 months since last menses) or are surgically sterilized do not require this test.
• Exclusion Criteria:
• A patient will not be eligible for inclusion if ANY of the criteria listed below apply:
• 1. Patients with a diagnosis of:
• • 1. Precursor T-cell lymphoma or leukemia
• • 2. Adult T-cell lymphoma/leukemia
• • 3. T-cell prolymphocytic leukemia
• • 4. T-cell large granular lymphocytic leukemia
• • 5. Primary cutaneous type ALCL
• • 6. Cutaneous T-cell lymphoma (mycosis fungoides/Sezary syndrome)
• • 7. ALCL if they can be treated with Brentuximab Vedotin (BV)
• • 2. Patients taking drugs which are potent UGT1A1 inhibitors must discontinue one week before randomization; drug can be resumed if the treatment doesn't include belinostat
• • 3. Patient with an active concurrent malignancy/life-threatening disease with the exception of non melanoma skin tumors and in situ cervical cancer if they have received treatment resulting in complete resolution of the cancer and currently have no clinical, radiologic, or laboratory evidence of active or recurrent disease. If there is a history of prior malignancies/life-threatening diseases, the patient must be disease free for at least 5 years
• • 4. Prior histone deacetylase (HDAC) inhibitor or pralatrexate therapy
• • 5. Any known cardiac abnormalities such as baseline prolongation of QT/corrected QT (QTc) interval (i.e. demonstration of a QTc interval \>450 msec); long QT syndrome; myocardial infarction within 6 months prior to starting study; history of significant cardiovascular disease; the required use of a concomitant medication that may cause Torsades de Pointes
• • 6. Patient with uncontrolled hypertension
• 7. Patients status on the following:
• • 1. Has a known HIV-positive diagnosis with uncontrolled and detectable viral load
• • 2. Has Hepatitis B or Hepatitis C virus diagnosis with uncontrolled and detectable viral load or immunological evidence of chronic active disease
• • 8. Patient with central nervous system metastasis
• • 9. Patient with an active uncontrolled infection, underlying medical condition, laboratory abnormality, or other serious illness that would impair the ability of the patient to receive protocol treatment
• • 10. Patient who has used any investigational drugs, biologics, or devices within 28 days prior to study treatment or plans to use any of these during the course of the study
• • 11. Patient with a known history of drug or alcohol abuse
• • 12. Pregnant or breastfeeding women