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

被引:88
|
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
相关论文
共 50 条
  • [31] KLK15 is a prognostic marker for progression-free survival in patients with radical prostatectomy
    Rabien, Anja
    Fritzsche, Florian R.
    Jung, Monika
    Toelle, Angelika
    Diamandis, Eleftherios P.
    Miller, Kurt
    Jung, Klaus
    Kristiansen, Glen
    Stephan, Carsten
    INTERNATIONAL JOURNAL OF CANCER, 2010, 127 (10) : 2386 - 2394
  • [32] The relationship between six-month progression-free survival and 12-month overall survival end points for phase II trials in patients with glioblastoma multiforme
    Ballman, Karla V.
    Buckner, Jan C.
    Brown, Paul D.
    Giannini, Caterina
    Flynn, Patrick J.
    LaPlant, Betsy R.
    Jaeckle, Kurt A.
    NEURO-ONCOLOGY, 2007, 9 (01) : 29 - 38
  • [33] SIX-MONTH PROGRESSION-FREE SURVIVAL AS AN ALTERNATIVE PRIMARY EFFICACY END POINT TO OVERALL SURVIVAL IN NEWLY DIAGNOSED GLIOBLASTOMA PATIENTS RECEIVING TEMOZOLOMIDE
    Polley, Mei-Yin C.
    Lamborn, Kathleen L.
    Chang, Susan
    Butowski, Nicholas A.
    Clarke, Jennifer L.
    Prados, Michael
    NEURO-ONCOLOGY, 2009, 11 (05) : 621 - 621
  • [34] IS PROGRESSION-FREE SURVIVAL A GOOD INDICATOR OF OVERALL SURVIVAL FOR PAZOPANIB IN PATIENTS WITH SYNOVIAL SARCOMA?
    Han, J.
    Lee, S.
    Cho, E.
    VALUE IN HEALTH, 2022, 25 (12) : S489 - S490
  • [35] Association of Morbid Progression With Overall Survival Among Patients With Multiple Myeloma: Validation of the Progression-free Survival Endpoint
    Rosenberg, Aaron S.
    Facon, Thierry
    Parikh, Kejal
    Chung, Weiyuan
    Srinivasan, Shankar
    Kotey, Stanley
    Tuscano, Joseph
    CLINICAL LYMPHOMA MYELOMA & LEUKEMIA, 2021, 21 (05): : 345 - +
  • [36] Interpretation of meta-analysis evaluating progression-free survival as a surrogate endpoint for overall survival in glioblastoma
    Han, Kelong
    Ren, Melanie
    Wick, Wolfgang
    Abrey, Lauren
    Das, Asha
    Jin, Jin
    Reardon, David A.
    NEURO-ONCOLOGY, 2015, 17 (05) : 764 - 765
  • [37] Overall Survival and Progression-Free Survival of Patients Following Luspatercept Treatment in the MEDALIST Trial
    Santini, Valeria
    Fenaux, Pierre
    Zeidan, Amer M.
    Komrokji, Rami S.
    Buckstein, Rena
    Oliva, Esther Natalie
    Ha, Xianwei
    Miteva, Dimana
    Yucel, Aylin
    Nadal, Jose Alberto
    Platzbecker, Uwe
    BLOOD, 2022, 140 : 4079 - 4081
  • [38] Progression-free survival as a surrogate endpoint of overall survival in patients with metastatic colorectal cancer
    Cicero, Giuseppe
    De Luca, Rossella
    Dieli, Francesco
    ONCOTARGETS AND THERAPY, 2018, 11 : 3059 - 3063
  • [39] Prognostic factors for progression-free and overall survival in advanced biliary tract cancer
    Bridgewater, J.
    Lopes, A.
    Wasan, H.
    Malka, D.
    Jensen, L.
    Okusaka, T.
    Knox, J.
    Wagner, D.
    Cunningham, D.
    Shannon, J.
    Goldstein, D.
    Moehler, M.
    Bekaii-Saab, T.
    McNamara, M. G.
    Valle, J. W.
    ANNALS OF ONCOLOGY, 2016, 27 (01) : 134 - 140
  • [40] Correlation of treatment effects on progression-free survival at 6 months (PFS-6) and overall survival (OS) in patients with newly diagnosed glioblastoma (GBM).
    Ye, X.
    Grossman, S. A.
    Desideri, S.
    Piantadosi, S.
    JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (15)