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Spots Global Cancer Trial Database for Brentuximab Vedotin Plus AVD in Limited-stage Hodgkin Lymphoma

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Trial Identification

Brief Title: Brentuximab Vedotin Plus AVD in Limited-stage Hodgkin Lymphoma

Official Title: Brentuximab Vedotin Plus AVD in Non-bulky Limited Stage Hodgkin Lymphoma

Study ID: NCT01534078

Study Description

Brief Summary: Brentuximab is an antibody-drug conjugate (ADC), which is the combination of an antibody (a protein that binds to cells) and a chemotherapy molecule. Brentuximab works by using the antibody portion to enter into the Hodgkin lymphoma cells and then releasing the chemotherapy portion, which attempts to destroy the cell. The intravenous chemotherapy drugs Adriamycin, Vinblastine and Dacarbazine (AVD) which you will receive in this research study are approved for use in people with Hodgkin Lymphoma. A drug called bleomycin is usually included with AVD, but since it appears to be a less effective drug with significant potential risks, it is being replaced in this study with the drug brentuximab. In this research study, the investigators are looking to see whether brentuximab in combination with AVD is effective in treating limited-stage Hodgkin Lymphoma.

Detailed Description: Each treatment cycle is 28 days. You will receive brentuximab alone on Day 1 and 15 of the first cycle (lead-in cycle). After cycle 1, you will receive brentuximab combined with AVD on Day 1 and 15 for 4-6 cycles, depending on your response to therapy. Brentuximab and AVD will be given to you by intravenous infusion (IV). The following test and procedures will be performed on Days 1 and 15 of each cycle: * Review of any side effects you have experienced and all medications you are taking * Performance Status * Physical exam and vital signs * Routine blood tests * Questionnaire to evaluate symptoms of neuropathy * Research blood sample to look at markers to see how your body is responding to study medication * PET-CT scan prior to completing cycle 2 of combination brentuximab/AVD After the final dose of the study drug: The following assessments will be performed within one month of your last dose of study medication: * Review of any side effects you have experienced and all medications you are taking * Performance Status * Physical exam and vital signs * Routine blood tests * Questionnaire to evaluate symptoms of neuropathy * Research blood sample to look at markers to see how your body is responding to study medication * PET-CT scan Follow up will include the following * Review of any side effects you have experienced and all medications you are taking * Performance Status * Review and Physical exam * Routine blood tests * Questionnaire to evaluate symptoms of neuropathy * CT scans

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Moffitt Cancer Center, Tampa, Florida, United States

Massachusetts General Hosptial, Boston, Massachusetts, United States

Dana-Farber Cancer Institute, Boston, Massachusetts, United States

Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States

Contact Details

Name: Jeremy Abramson, M.D.

Affiliation: Massachusetts General Hospital

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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