Publication
Nivolumab for Newly Diagnosed Advanced-Stage Classic Hodgkin Lymphoma: Safety and Efficacy in the Phase II CheckMate 205 Study
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- Persistent URL
- Last modified
- 05/15/2025
- Type of Material
- Authors
- Language
- English
- Date
- 2019-08-10
- Publisher
- American Society of Clinical Oncology
- Publication Version
- Copyright Statement
- © 2019 by American Society of Clinical Oncology
- Final Published Version (URL)
- Title of Journal or Parent Work
- Volume
- 37
- Issue
- 23
- Start Page
- 1997
- End Page
- 2007
- Grant/Funding Information
- Supported by Bristol-Myers Squibb, which also funded medical writing support. Also supported by the Center for Immuno-Oncology of the Dana-Farber Cancer Institute (S.J.R.), National Cancer Institute Grant No. R01 CA161026 (M.A.S.), and the Miller Family Fund (M.A.S.).
- Medical writing and editorial support, under the direction of the authors, were provided by Adam Gill at Caudex and were funded by Bristol-Myers Squibb. The views expressed in this article are the authors’ own and not an official position of Bristol-Myers Squibb or the authors’ respective institutions.
- Abstract
- Nivolumab, an anti–programmed death-1 monoclonal antibody, has demonstrated frequent and durable responses in relapsed/refractory classic Hodgkin lymphoma (cHL). We report results from Cohort D of the CheckMate 205 trial, which assessed nivolumab monotherapy followed by nivolumab plus doxorubicin, vinblastine, and dacarbazine (N-AVD) for newly diagnosed cHL.
- Author Notes
- Research Categories
- Health Sciences, Immunology
- Health Sciences, Oncology
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Publication File - vsdgm.pdf | Primary Content | 2025-05-05 | Public | Download |