Is surgery at progression a prognostic marker for improved 6-month progression-free survival or overall survival for patients with recurrent glioblastoma?

被引:89
|
作者
Clarke, Jennifer L. [1 ]
Ennis, Michele M.
Yung, W. K. Alfred [3 ]
Chang, Susan M. [1 ]
Wen, Patrick Y. [6 ]
Cloughesy, Timothy F. [2 ]
DeAngelis, Lisa M. [7 ]
Robins, H. Ian [8 ]
Lieberman, Frank S. [9 ]
Fine, Howard A. [10 ]
Abrey, Lauren [7 ]
Gilbert, Mark R. [3 ]
Mehta, Minesh [11 ]
Kuhn, John G. [4 ,5 ]
Aldape, Kenneth D. [3 ]
Lamborn, Kathleen R. [1 ]
Prados, Michael D. [1 ]
机构
[1] Univ Calif San Francisco, Dept Neurol Surg, San Francisco, CA 94143 USA
[2] Univ Calif Los Angeles, Dept Neurol, Los Angeles, CA 90024 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Neurooncol, Houston, TX 77030 USA
[4] Univ Texas Hlth Sci Ctr San Antonio, Dept Neurol, San Antonio, TX 78229 USA
[5] Univ Texas Hlth Sci Ctr San Antonio, Pharmacotherapy Educ & Res Ctr, San Antonio, TX 78229 USA
[6] Dana Farber Canc Inst, Boston, MA 02115 USA
[7] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[8] Univ Wisconsin Hosp, Madison, WI USA
[9] Univ Pittsburgh, Med Ctr Canc Pavil, Div Neurooncol, Pittsburgh, PA USA
[10] NCI, Neurooncol Branch, NIH, Bethesda, MD 20892 USA
[11] Northwestern Univ, Dept Radiat Oncol, Chicago, IL 60611 USA
关键词
glioblastoma; PFS6; prognosis; recurrence; surgery; II CLINICAL-TRIALS; PHASE-II; GLIOMA; THERAPY;
D O I
10.1093/neuonc/nor110
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Historically, the North American Brain Tumor Consortium used 6-month progression-free survival (PFS6) as the primary outcome for recurrent glioma phase II clinical trials. In some trials, a subset of patients received the trial treatment before surgery to assess tumor uptake and biological activity. We compared PFS6 and overall survival (OS) for patients with glioblastoma undergoing surgery at progression to results for those without surgery to evaluate the impact of surgical intervention on these outcomes. Two data sets were analyzed. The first included 511 patients enrolled during the period 1998-2005, 105 of whom had surgery (excluding biopsies) during the study or <= 30 days prior to registration. Analysis was stratified on the basis of whether temozolomide was part of the protocol treatment regimen. The second data set included 247 patients enrolled during 2005-2008, 103 of whom underwent surgery during the clinical trial or immediately prior to study registration. A combined data set consisting of all patients who did not receive temozolomide was also compiled. No statistically significant difference in PFS6 or OS was found between the surgery and nonsurgery groups in either data set alone or in the combined data set (P > .45). We conclude that PFS6 and OS results for patients with and without surgical intervention at the time of progression are similar, allowing data from these patients to be combined in assessing the benefit of new treatments without the need for stratification or other statistical adjustment.
引用
收藏
页码:1118 / 1124
页数:7
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