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Atkins, Michael B.

0000-0003-3901-9924

Mayo Clinic

Georgetown University Medical Center

Citations 22

Meta-Analysis of Phase II Cooperative Group Trials in Metastatic Stage IV Melanoma to Determine Progression-Free and Overall Survival Benchmarks for Future Phase II Trials
Liu, Ping-Yu, Chapman, J. W. , Niedzwiecki, Donna , Sondak, Vernon K. , Eisenhauer, Elizabeth A. , Parulekar, Wendy R. , Saxman, Scott, Korn, Edward L. , Lee, Sandra J. , Chapman, Judith‐Anne W. , Suman, Vera J. , Moon, James , Atkins, Michael B. , Markovic, Svetomir N. , Kirkwood, John M. , Niedzwiecki, Donna

Journal of Clinical Oncology | January 30, 2008 | Volume: 26 | Issue: 4 | Pages: 527-534

10.1200/jco.2007.12.7837 Get It

Purpose Objective tumor response rates observed in phase II trials for metastatic melanoma have historically not provided a reliable indicator of meaningful survival benefits. To facilitate using overall survival (OS) or progression-free survival (PFS) as an endpoint for future phase II trials, we evaluated historical data from cooperative group phase II trials to attempt to develop benchmarks for OS and PFS as reference points for future phase II trials. Patients and Methods Individual-level and trial-level data were obtained for patients enrolled onto 42 phase II trials (70 trial arms) that completed accrual in the years 1975 through 2005 and conducted by Southwest Oncology Group, Eastern Cooperative Oncology Group, Cancer and Leukemia Group B, North Central Cancer Treatment Group, and the Clinical Trials Group of the National Cancer Institute of Canada. Univariate and multivariate analyses were performed to identify prognostic variables, and between-trial(-arm) variability in 1-year OS rates and 6-month PFS rates were examined. Results Statistically significant individual-level and trial-level prognostic factors found in a multivariate survival analysis for OS were performance status, presence of visceral disease, sex, and whether the trial excluded patients with brain metastases. Performance status, sex, and age were statistically significant prognostic factors for PFS. Controlling for these prognostic variables essentially eliminated between-trial variability in 1-year OS rates but not in 6-month PFS rates. Conclusion Benchmarks are provided for 1-year OS or OS curves that make use of the distribution of prognostic factors of the patients in the phase II trial. A similar benchmark for 6-month PFS is provided, but its use is more problematic because of residual between-trial variation in this endpoint.
Innovations and Challenges in Renal Cell Carcinoma: Summary Statement from the Second Cambridge Conference
Figlin, Robert A. , George, Daniel J. , Kaelin, William G. , Kwon, Eugene D., Libermann, Towia A. , Pantuck, Allan J., Rosen, Mark, Sosman, Jeffrey A. , Sukhatme, Vikas P. , Vieweg, Johannes, Wood, Christopher G. , Atkins, Michael B. , Ernstoff, Marc S. , Flaherty, Keith T. , Linehan, William Marston , McDermott, David F. , Ochoa, Augusto C. , Rini, Brian I. , King, Laura

Clinical Cancer Research | January 25, 2007 | Volume: 13 | Issue: 2 | Pages: 667s-670s

10.1158/1078-0432.ccr-06-2231 Get It

Abstract Innovations and Challenges in Renal Cancer, chaired by Michael B. Atkins, was held April 28 to 29, 2006 in Cambridge, Massachusetts. The conference brought together leading experts in the fields of cancer research, medical oncology, urology, immunology, radiology, and immunotherapy, with the goal of advancing the field of renal cancer treatment by critiquing new data from ongoing clinical trials and stimulating communication among those involved in basic and clinical research. The conference proceedings published in this educational supplement to Clinical Cancer Research are intended to provide timely information and recommendations on important aspects of renal cancer genetics and biology and advances in prognostic classification and treatment.