|
|
|
|
|
|
||
|
|
||||
|
|
||||
|
||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Clinical Investigations |
Division of Biostatistics (K.V.B., B.R.L.), Division of Medical Oncology (J.C.B.), Department of Radiation Oncology (P.D.B.), and Department of Pathology (C.G.), Mayo Clinic College of Medicine, Rochester, MN; Metro-Minnesota Community Clinical Oncology Program (P.J.F.), St. Louis Park, MN; and Department of Neurology (K.A.J.), Mayo Clinic, Jacksonville, FL; USA
1 Address correspondence to Karla Ballman, Ph.D., Mayo Clinic, Division of Biostatistics, 200 First Street SW, Rochester, MN 55905, USA (ballman{at}mayo.edu).
Common end points for phase II trials in patients with glioblastoma multiforme (GBM) are six-month progression-free survival (PFS6) and 12-month overall survival (OS12). OS12 can be accurately measured but may be confounded with subsequent therapies upon progression, whereas the converse is true for PFS6. Our goal was to assess the relationship between these end points separately for phase II trials in patients with newly diagnosed GBM and patients with recurrent GBM. Data were pooled from 11 North Central Cancer Treatment Group trials for patients with newly diagnosed GBM (n = 1348). All patients received radiotherapy and pharmaceutical therapy (before, during, or after radiotherapy). Data were pooled from 16 trials that used various pharmaceuticals in treating patients for recurrent GBM (n = 345). All trial regimens were declared nonefficacious by predefined criteria. Overall per-patient concordance was estimated with a kappa statistic. The relationship between OS12 and PFS6 across study arms was assessed by weighted linear regression and Pearson's correlation. Simulation was used to determine the agreement of study outcomes when using PFS6 versus OS12 end points. Cox models with progression status as a time-dependent variable and Kaplan-Meier estimators were used to ascertain the association between progression-free survival status and overall survival. At present, 97% of the patients with newly diagnosed GBM and 95% of those with recurrent GBM have died. The PFS6 and OS12 were 43% and 41%, respectively, for patients with newly diagnosed disease and 9% and 14% for patients with recurrent disease. There was only moderate concordance between the end points on both the patient level and the study level. For the simulation studies, we established phase II efficacy criteria for each end point by using the pooled estimates of OS12 (PFS6) as historical controls. The study decisions made using PFS6 and OS12 were in agreement 88% and 90% of the time for the trials of newly diagnosed and recurrent disease, respectively. Finally, there was a strong association between progression-free survival status and overall survival. PFS6 seems to be a reasonable end point for phase II trials in patients with recurrent glioblastoma.
Key Words: end points • glioblastoma multiforme • phase II clinical trials
This article has been cited by other articles:
|
|
 |
|
  R. I. Jakacki, A. Yates, S. M. Blaney, T. Zhou, R. Timmerman, A. M. Ingle, L. Flom, M. D. Prados, P. C. Adamson, and I. F. Pollack A phase I trial of temozolomide and lomustine in newly diagnosed high-grade gliomas of childhood Neuro-oncol, August 1, 2008; 10(4): 569 - 576. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
K. R. Lamborn, W. K. A. Yung, S. M. Chang, P. Y. Wen, T. F. Cloughesy, L. M. DeAngelis, H. I. Robins, F. S. Lieberman, H. A. Fine, K. L. Fink, et al. Progression-free survival: An important end point in evaluating therapy for recurrent high-grade gliomas Neuro-oncol, April 1, 2008; 10(2): 162 - 170. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 J.W. Henson, S. Ulmer, and G.J. Harris Brain Tumor Imaging in Clinical Trials AJNR Am. J. Neuroradiol., March 1, 2008; 29(3): 419 - 424. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 P. A. Gimotty, D. Guerry, and K. Flaherty Using Benchmarks Based on Historical Survival Rates for Screening New Therapies for Stage IV Melanoma Patients J. Clin. Oncol., February 1, 2008; 26(4): 517 - 518. [Full Text] [PDF]
|
|
|
|
 |
|
 M. Hutterer, P. Knyazev, A. Abate, M. Reschke, H. Maier, N. Stefanova, T. Knyazeva, V. Barbieri, M. Reindl, A. Muigg, et al. Axl and Growth Arrest Specific Gene 6 Are Frequently Overexpressed in Human Gliomas and Predict Poor Prognosis in Patients with Glioblastoma Multiforme Clin. Cancer Res., January 1, 2008; 14(1): 130 - 138. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
H. A. Fine, L. Kim, P. S. Albert, J. P. Duic, H. Ma, W. Zhang, T. Tohnya, W. D. Figg, and C. Royce A Phase I Trial of Lenalidomide in Patients with Recurrent Primary Central Nervous System Tumors Clin. Cancer Res., December 1, 2007; 13(23): 7101 - 7106. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 F. B. Furnari, T. Fenton, R. M. Bachoo, A. Mukasa, J. M. Stommel, A. Stegh, W. C. Hahn, K. L. Ligon, D. N. Louis, C. Brennan, et al. Malignant astrocytic glioma: genetics, biology, and paths to treatment Genes & Dev., November 1, 2007; 21(21): 2683 - 2710. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
J. J. Vredenburgh, A. Desjardins, J. E. Herndon II, J. Marcello, D. A. Reardon, J. A. Quinn, J. N. Rich, S. Sathornsumetee, S. Gururangan, J. Sampson, et al. Bevacizumab Plus Irinotecan in Recurrent Glioblastoma Multiforme J. Clin. Oncol., October 20, 2007; 25(30): 4722 - 4729. [Abstract] [Full Text] [PDF]
|
|
|
|
