Brentuximab Vedotin and Combination Chemotherapy in Treating Older Patients With Previously Untreated Stage II-IV Hodgkin Lymphoma

Stage IV Adult Hodgkin Lymphoma Clinical Trial

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

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT01476410
• Other study ID #: NU 11H01
• Secondary ID: NCI-2011-00684ST
• Status: Active, not recruiting
• Phase: Phase 2
• Start date: November 2011
• Est. completion date: May 2021

Study information

• Verified date: February 2020
• Source: Northwestern University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 48
• Est. completion date: May 2021
• Est. primary completion date: May 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 60 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Adult Lymphocyte Depletion Hodgkin Lymphoma
• Adult Lymphocyte Predominant Hodgkin Lymphoma
• Adult Mixed Cellularity Hodgkin Lymphoma
• Adult Nodular Sclerosis Hodgkin Lymphoma
• Hodgkin Disease
• Lymphoma
• Stage II Adult Hodgkin Lymphoma
• Stage III Adult Hodgkin Lymphoma
• Stage IV Adult Hodgkin Lymphoma

Intervention

Drug:
• brentuximab vedotin
Given IV
• doxorubicin hydrochloride
Given IV
• vinblastine
Given IV
• dacarbazine
Given IV

Procedure:
• quality-of-life assessment
Ancillary studies

Genetic:
• DNA analysis
Optional correlative studies
• RNA analysis
Optional correlative studies

Radiation:
• fludeoxyglucose F 18
Correlative studies

Procedure:
• positron emission tomography
Correlative studies

Other:
• laboratory biomarker analysis
Optional correlative studies
• immunohistochemistry staining method
Optional correlative studies

Genetic:
• polymorphism analysis
Optional correlative studies

Locations

Country	Name	City	State
United States	Tufts Medical Center	Boston	Massachusetts
United States	NorthwesternU	Chicago	Illinois
United States	University of Chicago	Chicago	Illinois
United States	MD Anderson Cancer Center	Houston	Texas
United States	Memorial Sloan- Kettering Cancer Center	New York	New York
United States	University of Nebraska Medical Center	Omaha	Nebraska
United States	Stanford University Medical Center	Stanford	California

Sponsors (3)

Lead Sponsor	Collaborator
Northwestern University	Robert H. Lurie Cancer Center, Seattle Genetics, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Overall response rate after chemotherapy	The primary objective of this study is to assess the overall response rate among older patients with HL receiving sequential brentuximab vedotin therapy with AVD chemotherapy	2 years
Secondary	Overall response rate	Overall response rate progression-free survival (PFS), time to treatment failure (TTF), freedom from progression (FFP), and overall survival (OS) rates following SGN-35/AVD sequential therapy.	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
Secondary	Overall response rate based on best response (CR and PR) and the tumor local control rate (CR, PR, and stable disease [SD])	Estimates of response rate based on best response (CR and PR) and the tumor local control rate (CR, PR, and stable disease [SD])	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