RecruitingPhase 2NCT05404945

Fitness-adapted, Pembrolizumab-based Therapy for Untreated Classical Hodgkin Lymphoma Patients 60 Years of Age and Above

Fitness-adapted, Pembrolizumab-based Therapy for Untreated Classical Hodgkin Lymphoma Patients 60 Years of Age and Above (cHL 001)


Sponsor

University of Virginia

Enrollment

44 participants

Start Date

Jul 26, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

This is a multi-center, open-label phase II study to assess the efficacy of a novel fitness-adapted regimen in previously untreated older patients with classical Hodgkin lymphoma. All participants will receive up to a total of 8 cycles of pembrolizumab (Q6 week dosing). The first cycle of pembrolizumab will be administered in combination with brentuximab vedotin (BV) ("lead-in treatment"). Following lead-in treatment, all participants will undergo interim PET/CT (iPET) as well as fitness testing to help inform participant level of fitness for subsequent lymphoma-directed therapies. Participants deemed "Frail" by this assessment will continue 3 additional 6 week cycles of concurrent pembrolizumab and BV ("induction therapy", each cycle is 42 days), then continue single-agent pembrolizumab to complete up to 4 additional cycles (i.e., 8 total) of therapy ("consolidation and maintenance therapy", Frail cohort). Two additional BV doses will be given as consolidation, at days 1 and 22 of pembrolizumab cycle 5. Those deemed "fit" after lead-in therapy (Fit cohort) will continue pembrolizumab and switch from BV to concurrently-administered combination chemotherapy using doxorubicin (A), vinblastine (V), and dacarbazine (D) for a total of 4 planned AVD cycles (3, 6-week pembrolizumab cycles, "induction therapy"). Chemotherapy drugs will be given at standard doses as in ABVD (no bleomycin will be given in this study) on days 1 and 15 of each 28-day cycle (C1AVD), and pembrolizumab dosing will remain every 42 days. Following end-induction PET/CT, pembrolizumab will continue every 42 days for up to 4 cycles in the consolidation/maintenance phase. Two additional BV doses will be given as consolidation, at days 1 and 22 of pembrolizumab cycle 5. Participants deemed "unfit" after lead-in therapy and by fitness assessment will continue pembrolizumab and switch from BV to concurrently administered combination chemotherapy termed "mini-avd" as induction therapy. Mini-avd consists of lower doses of conventional AVD chemotherapy (doxorubicin, vinblastine and dacarbazine) and will be administered for on days 1 and 15 of a 28 day cycle for 4 planned cycles. Pembrolizumab will continue every 42 days. Following end-induction PET/CT, pembrolizumab will continue every 42 days for up to 4 cycles in the consolidation/maintenance phase. Two additional BV doses will be given as consolidation, at days 1 and 22 of pembrolizumab cycle 5.


Eligibility

Min Age: 60 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a fitness-tailored treatment approach using pembrolizumab (an immunotherapy drug) for older adults aged 60 and above with classical Hodgkin lymphoma — a type of blood cancer — who may not tolerate standard intensive chemotherapy. **You may be eligible if...** - You are 60 years old or older - You have been newly diagnosed with classical Hodgkin lymphoma confirmed by biopsy - Your cancer is visible on a PET scan with at least one measurable tumor site - Your overall health is good enough to receive treatment (assessed by a geriatric fitness evaluation) **You may NOT be eligible if...** - You have previously received treatment for Hodgkin lymphoma - You have active autoimmune disease requiring systemic treatment - You have HIV, active hepatitis B, or hepatitis C - You are on systemic corticosteroids or other immunosuppressants Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGPembrolizumab

Pembrolizumab 400 mg IV

DRUGDoxorubicin

Doxorubicin 25mg/m2 IV

DRUGVinblastine

Vinblastine 6mg/m2 IV

DRUGDacarbazine

Dacarbazine 375mg/m2 IV

DRUGBrentuximab vedotin

Brentuximab vedotin 1.8 mg/kg IV


Locations(3)

Rutgers Cancer Institute of New Jersey

New Brunswick, New Jersey, United States

University of Pennsylvania

Philadelphia, Pennsylvania, United States

University of Virginia

Charlottesville, Virginia, United States

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NCT05404945


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