Overview

This trial is active, not recruiting.

Conditions adult lymphocyte depletion hodgkin lymphoma, adult lymphocyte predominant hodgkin lymphoma, adult mixed cellularity hodgkin lymphoma, adult nodular sclerosis hodgkin lymphoma, stage ii adult hodgkin lymphoma, stage iii adult hodgkin lymphoma, stage iv adult hodgkin lymphoma
Treatments brentuximab vedotin, doxorubicin hydrochloride, vinblastine, dacarbazine, quality-of-life assessment, dna analysis, rna analysis, fludeoxyglucose f 18, positron emission tomography, laboratory biomarker analysis, immunohistochemistry staining method, polymorphism analysis
Phase phase 2
Sponsor Northwestern University
Collaborator Robert H. Lurie Cancer Center
Start date November 2011
End date May 2017
Trial size 48 participants
Trial identifier NCT01476410, NCI-2011-00684, NU 11H01, STU00046908

Summary

This phase II trial studies how well giving brentuximab vedotin together with combination chemotherapy works in treating older patients with previously untreated stage II-IV Hodgkin lymphoma (HL). Monoclonal antibody-drug conjugates, such as brentuximab vedotin, can block cancer growth in different ways by targeting certain cells. Drugs used in chemotherapy, such as doxorubicin hydrochloride, vinblastine, and dacarbazine (AVD), work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Giving brentuximab vedotin, doxorubicin hydrochloride, vinblastine, and dacarbazine together may kill more cancer cells.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Endpoint classification efficacy study
Intervention model single group assignment
Masking open label
Primary purpose treatment
Arm
(Experimental)
LEAD-IN: Patients receive brentuximab vedotin IV over 30 minutes on day 1. Treatment repeats every 21 days for 2 courses in the absence of disease progression or unacceptable toxicity. AVD CHEMOTHERAPY: Patients then receive doxorubicin hydrochloride IV, vinblastine IV, and dacarbazine IV over 30 minutes on days 1 and 15. Treatment repeats every 28 days for 6 courses in the absence of disease progression or unacceptable toxicity. CONSOLIDATION: Patients achieving CR receive brentuximab vedotin IV over 30 minutes on day 1. Treatment repeats every 21 days for 4 courses in the absence of disease progression or unacceptable toxicity.
brentuximab vedotin anti-CD30 ADC SGN-35
Given IV
doxorubicin hydrochloride ADM
Given IV
vinblastine Velban
Given IV
dacarbazine DIC
Given IV
quality-of-life assessment quality of life assessment
Ancillary studies
dna analysis
Optional correlative studies
rna analysis
Optional correlative studies
fludeoxyglucose f 18 18FDG
Correlative studies
positron emission tomography FDG-PET
Correlative studies
laboratory biomarker analysis
Optional correlative studies
immunohistochemistry staining method immunohistochemistry
Optional correlative studies
polymorphism analysis
Optional correlative studies

Primary Outcomes

Measure
Overall response rate after chemotherapy
time frame: 2 years

Secondary Outcomes

Measure
Overall response rate
time frame: Baseline, every 3 weeks during the first 2 cycles, every 2 weeks during next 6 cycles, every 4 weeks furing the last 4 cycles, and then every 3 months for up to 3 years from entering the study
Overall response rate based on best response (CR and PR) and the tumor local control rate (CR, PR, and stable disease [SD])
time frame: Baseline, every 3 weeks during the first 2 cycles, every 2 weeks during next 6 cycles, every 4 weeks furing the last 4 cycles, and then every 3 months for up to 3 years from entering the study

Eligibility Criteria

Male or female participants at least 60 years old.

Inclusion Criteria: - Voluntary written informed consent before performance of any study-related procedure not part of normal medical care, with the understanding that consent may be withdrawn by the subject at any time without prejudice to future medical care - Previously untreated classical Hodgkin lymphoma (i.e., nodular sclerosis, mixed cellularity, lymphocyte depleted, lymphocyte-rich, and not otherwise specified [NOS]); nodular lymphocyte predominant Hodgkin lymphoma is not eligible - Stage II, III, and IV disease by Ann Arbor classification - Eastern Cooperative Oncology Group (ECOG) performance status score of 0, 1, or 2 - Patients must have bi-dimensional measurable disease documented in the lymphoma baseline tumor assessment form within 30 days prior to registration (at least 1.5 cm); patients with non-measurable disease in addition to measurable disease must have been assessed within 60 days prior to registration - Patients must have a bone marrow biopsy (bilateral preferred, unilateral acceptable) within 60 days prior to registration - Patients must have a multi gated acquisition scan (MUGA) or echocardiogram within 60 days prior to study registration and the ejection fraction must be >= 45% - Absolute neutrophil count (ANC) > 1000/mm^3 - Platelet count > 75,000/mm^3 - Creatinine < 2.5 mg/dl - Bilirubin < 3.0 mg/dl - Patients with documented marrow involvement by lymphoma at the time of registration are not required to meet the above hematologic parameters - Patients must not have received prior chemotherapy or radiation therapy for the treatment of Hodgkin lymphoma - Both females and males who have partners of childbearing potential must agree to use an effective contraceptive method during the study and for 30 days following the last dose of study drug - Patients must sign the informed consent form before registration Exclusion Criteria: - Previous treatment with brentuximab vedotin or any other prior anti-CD30-based antibody therapy - History of another primary malignancy that has not been in remission for at least 3 years; (the following are exempt from the 3-year limit: early stage [stage I or II] breast cancer treated with surgery and radiation +/- hormones [without adjuvant chemotherapy], non-melanoma skin cancer, fully excised melanoma in situ [stage 0], curatively treated localized prostate cancer, and cervical carcinoma in situ on biopsy or a squamous intraepithelial lesion on Papanicolaou test [PAP smear]) - Known cerebral/meningeal disease - Any active systemic viral, bacterial, or fungal infection requiring treatment with antimicrobial therapy within 1 week prior to first dose - Patients with hepatitis B surface antigen (HBsAg) positive hepatitis B virus (HBV) infection; patients with prior history of hepatitis B infection, but immune, with only Immunoglobulin G (IgG) hepatitis core antibody + (HBcAb +) must receive anti-viral prophylaxis (e.g., lamivudine 100mg orally [po] daily) for at least 1 week prior to cycle 1 and throughout induction and continuation therapy and for at least 6 months after the last brentuximab vedotin dose; in addition, consultation with a hepatologist is recommended - Patients with a known hypersensitivity to any excipient contained in the drug formulation - Patients with dementia or an altered mental state that would preclude the understanding and rendering of informed consent

Additional Information

Official title A Phase II Trial of Sequential SGN-35 Therapy With Adriamycin, Vinblastine, and Dacarbazine (S-AVD) for Older Patients With Untreated Hodgkin Lymphoma
Principal investigator Leo Gordon, MD
Description LEAD IN: Patients receive brentuximab vedotin intravenously (IV) over 30 minutes on day 1. Treatment repeats every 21 days for 2 courses in the absence of disease progression or unacceptable toxicity. AVD CHEMOTHERAPY: Patients then receive doxorubicin hydrochloride IV, vinblastine IV, and dacarbazine IV over 30 minutes on days 1 and 15. Treatment repeats every 28 days for 6 courses in the absence of disease progression or unacceptable toxicity. CONSOLIDATION: Patients achieving CR receive brentuximab vedotin IV over 30 minutes on day 1. Treatment repeats every 21 days for 4 courses in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed up at 30 days.
Trial information was received from ClinicalTrials.gov and was last updated in September 2016.
Information provided to ClinicalTrials.gov by Northwestern University.
Location data was received from the National Cancer Institute and was last updated in October 2016.