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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06040320
Other study ID # 202308116
Secondary ID
Status Recruiting
Phase Phase 1/Phase 2
First received
Last updated
Start date October 4, 2023
Est. completion date May 31, 2031

Study information

Verified date January 2024
Source Washington University School of Medicine
Contact Neha Mehta-Shah, M.D.
Phone 314-747-7510
Email mehta-n@wustl.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will test polatuzumab vedotin in combination with rituximab in patients with treatment-naïve CD20-positive post-transplant lymphoproliferative disorder (PTLD) based on the established efficacy of polatuzumab vedotin in B-cell lymphomas and the inadequate response rate of PTLD to single-agent rituximab. The hypothesis is that this combination therapy will be safe, well-tolerated, and effective. If so, patients with PTLD will be able to be spared the toxicity of anthracycline-based chemotherapy. Additionally, the role of the tumor microenvironment and the role of anellovirus, a non-human pathogen virus, will be explored as prognostic markers in PTLD.


Recruitment information / eligibility

Status Recruiting
Enrollment 12
Est. completion date May 31, 2031
Est. primary completion date May 31, 2026
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Previously untreated biopsy-confirmed CD20-positive monomorphic post-transplant lymphoproliferative disorder (or CD20-positive lymphoma associated with immune deficiency) arising after solid organ or hematopoietic stem cell transplant. This may be defined by either the 2016 World Health Organization classification of lymphoid neoplasms or the 2022 International consensus Classification of Mature Lymphoid Neoplasms or the 2022 World Health Organization classification. - At least 18 years of age. - ECOG performance status = 3. - Adequate hematologic and organ function (unless due to underlying lymphoma per the investigator) as defined below: - Absolute neutrophil count = 1.0 K/cumm - Platelets = 75 K/cumm - Hemoglobin = 8.0 g/dL - Total bilirubin < 1.5 x IULN - AST(SGOT)/ALT(SGPT) < 2.5 x IULN - Creatinine clearance > 30 mL/min measured or by Cockcroft-Gault - Note: Patients with extensive bone marrow involvement by lymphoma and/or disease-related cytopenias may be enrolled if the following criteria are met: - ANC = 0.5 K/cumm - Platelets = 50 K/cumm - Hemoglobin = 7.0 g/dL - The effects of polatuzumab vedotin and rituximab on the developing human fetus are unknown. For this reason, women of childbearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control, abstinence) prior to study entry and for the duration of study participation. Should a participant become pregnant or suspect pregnancy while participating in this study, the participant must inform the treating physician immediately. - Ability to understand and willingness to sign an IRB approved written informed consent document. Exclusion Criteria: - Active central nervous system involvement with lymphoma / PTLD. - Current grade = 2 peripheral neuropathy. - Current ejection fraction < 40% on transthoracic echocardiogram or multigated acquisition (MUGA) scan - Subjects with history of concurrent second cancers requiring active, ongoing systemic treatment with the following exceptions: - Patients with non-melanoma skin cancer or carcinoma in situ of the cervix will not be excluded. - Patients with previous malignancies are eligible if disease-free for > 2 years. - Patients on long term hormonal therapy to prevent recurrence of a prior cancer (e.g., hormonal therapy for breast cancer) will not be excluded. - Currently receiving any other investigational agents or received any investigational agents during the 4 weeks prior to the first dose of polatuzumab vedotin. - A history of allergic reactions attributed to compounds of similar chemical or biologic composition to polatuzumab vedotin, rituximab, or other agents used in the study. - Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection (bacterial, fungal, viral, parasitic, or mycobacterial), interstitial lung disease, active non-infectious pneumonitis, congestive heart failure NYHA grade = 3, unstable angina pectoris, or cardiac arrhythmia. - Pregnant and/or breastfeeding. Women of childbearing potential must have a negative serum or urine pregnancy test within 7 days prior to C1D1 - Patients with HIV are eligible provided the meet the following criteria: - On antiretroviral regimen and stable on that regimen - Healthy from an HIV perspective - CD4 count > 250 cells/mcL - Minimal anticipated interactions or overlapping toxicity with polatuzumab vedotin or rituximab - HIV viral load < 200 copies/mm3 by standard clinical assays - Active hepatitis B infection. - Patients who are hepatitis B surface antigen (HBsAg) negative and hepatitis B core antibody (HBcAb) positive must be negative for hepatitis B virus (HBV) polymerase chain reaction (PCR) to be eligible for study participation. - Active hepatitis C infection. - Patients who are positive for hepatitis C virus (HCV) antibody must be negative for HCV by PCR to be eligible for study participation. - Any serious medical condition or abnormality in clinical laboratory tests that, in the investigator's judgment, precludes the patient's safe participation in and completion of the study, or which could affect compliance with the protocol or interpretation of results.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Polatuzumab vedotin
Given at 1.8 mg/kg
Rituximab
Given at 375 mg/m^2
CHP
Cyclophosphamide (750 mg/m^2) + doxorubicin (50 mg/m^2) + prednisone (100 mg days 2-6)

Locations

Country Name City State
United States Washington University School of Medicine Saint Louis Missouri

Sponsors (1)

Lead Sponsor Collaborator
Washington University School of Medicine

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Frequency and severity of treatment-related adverse events (AEs) From start of treatment through 30 days after completion of treatment (estimated to be 5-7 months)
Primary Number of dose-limiting toxicities (DLTs) (Safety Lead-In Cohort only) A dose-limiting toxicity (DLT) is defined as an occurrence of an adverse event delineated by the protocol that is at least possibly related to polatuzumab vedotin, rituximab, or the combination within Cycle 1 or Cycle 2. From start of treatment through cycle 2 (estimated to be 42 days, each cycle is 21 days)
Primary Rate of completion of the regimen Through completion of treatment (estimated to be 4-6 months)
Secondary Complete metabolic response (CR) rate by PET/CT -Per Lugano Response Criteria After cycle 2 (estimated to be day 42, each cycle is 21 days)
Secondary Complete metabolic response (CR) rate by PET/CT -Per Lugano Response Criteria End of treatment (estimated to be between 4-6 months)
Secondary Overall response rate (ORR) Per Lugano Response Criteria
Overall Response Rate: The proportion of patients who have a complete or partial response to therapy.
End of treatment (estimated to be between 4-6 months)
Secondary Best overall response Per Lugano Response Criteria
Best Overall Response: Best response recorded from start of treatment until disease progression/recurrence (taking as reference for PD the smallest measurements recorded since the treatment started).
Through completion of treatment (estimated to be between 4-6 months)
Secondary Duration of response Per Lugano Response Criteria
Duration of Response: The time from onset of response to disease progression or death in patients who achieve complete or partial response.
Through 5 years from completion of treatment (estimated to be between 64 and 66 months)
Secondary Progression-free survival (PFS) Per Lugano Response Criteria
Progression-Free Survival: The time from initiation of treatment to the occurrence of disease progression or death.
Through 5 years from completion of treatment (estimated to be between 64 and 66 months)
Secondary Overall survival (OS) -Overall Survival: The time from initiation of treatment to death. Through 5 years from completion of treatment (estimated to be between 64 and 66 months)
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