RecruitingPhase 2NCT04745949

PACIFIC: Primary Mediastinal Large B-cell Lymphoma Treated With Antibody Therapy, Checkpoint Inhibitor in Frontline With ImmunoChemotherapy

A Phase II Study to Determine the Response Kinetics, Safety, and Efficacy of Brentuximab Vedotin and Nivolumab Alone and Then Combined With Rituximab, Cyclophosphamide, Doxorubicin, and Prednisone for Patients With Untreated Primary Mediastinal Large B-Cell Lymphoma


Sponsor

M.D. Anderson Cancer Center

Enrollment

31 participants

Start Date

May 10, 2021

Study Type

INTERVENTIONAL

Conditions

Summary

This phase II trial studies the effect of brentuximab vedotin and nivolumab alone and in combination with rituximab, cyclophosphamide, doxorubicin, and prednisone in treating patients with untreated, stage I-IV primary mediastinal large B-cell lymphoma. Brentuximab vedotin is a monoclonal antibody, called brentuximab, linked to a toxic agent, called vedotin. Brentuximab is a form of targeted therapy because it attaches to specific molecules (receptors) on the surface of cancer cells, known as CD30 receptors, and delivers vedotin to kill them. Immunotherapy with monoclonal antibodies, such as nivolumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Rituximab is a type of antibody therapy, which targets and attaches to the CD20 protein found on the surface of blood cells with cancer and some healthy blood cells. Chemotherapy drugs, such as cyclophosphamide, and doxorubicin, work in different ways to stop the growth of cancer cells, either by killing the cells, or by stopping them from dividing. Prednisone is a steroid, a hormone (chemical messengers) with multiple roles, notably in the immune system and inflammation reduction. Steroids are poisonous to lymphocytes (white blood cells from which lymphomas develop). Giving brentuximab vedotin and nivolumab in combination with rituximab, cyclophosphamide, doxorubicin, and prednisone may help to control the disease and be a less harmful regimen than standard chemotherapy in patients with primary mediastinal large B-cell lymphoma.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests a new combination treatment — adding a checkpoint inhibitor (pembrolizumab) and a targeted antibody (brentuximab vedotin) to standard chemotherapy — for people newly diagnosed with primary mediastinal large B-cell lymphoma (PMBL), an aggressive lymphoma that forms in the chest. **You may be eligible if...** - You have a confirmed new diagnosis of PMBL - Your tumor expresses CD30 (a protein found on the cancer cells) - You have not received prior chemotherapy (limited prior radiation or short steroid courses are allowed) - Your disease is stage II or higher (or stage I with tumor ≥5 cm) - You are 18 or older with adequate organ function **You may NOT be eligible if...** - You have been previously treated with chemotherapy for this lymphoma - You are CD30-negative on tumor testing - You have active serious infections or autoimmune conditions requiring treatment - You are pregnant or breastfeeding 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

DRUGBrentuximab Vedotin

Given IV

DRUGCyclophosphamide

Given IV

DRUGDoxorubicin

Given IV

BIOLOGICALNivolumab

Given IV

DRUGPrednisone

Given PO

OTHERQuality-of-Life Assessment

Ancillary studies

BIOLOGICALRituximab

Given IV


Locations(1)

M D Anderson Cancer Center

Houston, Texas, United States

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NCT04745949