When Progressive Disease Does Not Mean Treatment Failure: Reconsidering the Criteria for Progression

被引:102
作者
Oxnard, Geoffrey R. [1 ,2 ]
Morris, Michael J. [3 ,4 ]
Hodi, F. Stephen [1 ,2 ]
Baker, Laurence H. [5 ,6 ]
Kris, Mark G. [3 ,4 ]
Venook, Alan P. [7 ]
Schwartz, Lawrence H. [8 ]
机构
[1] Harvard Univ, Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Boston, MA 02215 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Med, New York, NY 10021 USA
[4] Weill Cornell Med Coll, New York, NY USA
[5] Univ Michigan, Dept Pharmacol, Ann Arbor, MI 48109 USA
[6] Univ Michigan, Dept Internal Med, Ann Arbor, MI 48109 USA
[7] Univ Calif San Francisco, San Francisco, CA 94143 USA
[8] Columbia Univ, Med Ctr, Dept Radiol, New York, NY USA
来源
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE | 2012年 / 104卷 / 20期
关键词
CELL-LUNG-CANCER; PHASE-II; CLINICAL-TRIALS; END-POINTS; ACQUIRED-RESISTANCE; PROSTATE-CANCER; RESPONSE EVALUATION; FREE SURVIVAL; SOLID TUMORS; ERLOTINIB;
D O I
10.1093/jnci/djs353
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although progression-based endpoints, such as progression-free survival, are often key clinical trial endpoints for anticancer agents, the clinical meaning of objective progression is much less certain. As scrutiny of progression-based endpoints in clinical trials increases, it should be remembered that the Response Evaluation Criteria In Solid Tumors (RECIST) progression criteria were not developed as a surrogate for survival. Now that progression-free survival has come to be an increasingly important trial endpoint, the criteria that define progression deserve critical evaluation to determine whether alternate definitions of progression might facilitate the development of stronger surrogate endpoints and more meaningful trial results. In this commentary, we review the genesis of the criteria for progression, highlight recent data that question their value as a marker of treatment failure, and advocate for several research strategies that could lay the groundwork for a clinically validated definition of disease progression in solid tumor oncology.
引用
收藏
页码:1534 / 1541
页数:8
相关论文
共 58 条
[11]  
D'Agostino RB, 2011, NEW ENGL J MED, V365, DOI [10.1056/NEJMp1106984, 10.1056/nejmp1106984]
[12]   KRAS wild-type state predicts survival and is associated to early radiological response in metastatic colorectal cancer treated with cetuximab [J].
De Roock, W. ;
Piessevaux, H. ;
De Schutter, J. ;
Janssens, M. ;
De Hertogh, G. ;
Personeni, N. ;
Biesmans, B. ;
Van Laethem, J. -L. ;
Peeters, M. ;
Humblet, Y. ;
Van Cutsem, E. ;
Tejpar, S. .
ANNALS OF ONCOLOGY, 2008, 19 (03) :508-515
[13]   Bone Scan Index: A Quantitative Treatment Response Biomarker for Castration-Resistant Metastatic Prostate Cancer [J].
Dennis, Elizabeth R. ;
Jia, Xiaoyu ;
Mezheritskiy, Irina S. ;
Stephenson, Ryan D. ;
Schoder, Heiko ;
Fox, Josef J. ;
Heller, Glenn ;
Scher, Howard I. ;
Larson, Steven M. ;
Morris, Michael J. .
JOURNAL OF CLINICAL ONCOLOGY, 2012, 30 (05) :519-524
[14]   New response evaluation criteria in solid tumours: Revised RECIST guideline (version 1.1) [J].
Eisenhauer, E. A. ;
Therasse, P. ;
Bogaerts, J. ;
Schwartz, L. H. ;
Sargent, D. ;
Ford, R. ;
Dancey, J. ;
Arbuck, S. ;
Gwyther, S. ;
Mooney, M. ;
Rubinstein, L. ;
Shankar, L. ;
Dodd, L. ;
Kaplan, R. ;
Lacombe, D. ;
Verweij, J. .
EUROPEAN JOURNAL OF CANCER, 2009, 45 (02) :228-247
[15]   SOUTHWEST-ONCOLOGY-GROUP STANDARD RESPONSE CRITERIA, END-POINT DEFINITIONS AND TOXICITY CRITERIA [J].
GREEN, S ;
WEISS, GR .
INVESTIGATIONAL NEW DRUGS, 1992, 10 (04) :239-253
[16]   "Pulsatile" high-dose weekly erlotinib for CNS metastases from EGFR mutant non-small cell lung cancer [J].
Grommes, Christian ;
Oxnard, Geoffrey R. ;
Kris, Mark G. ;
Miller, Vincent A. ;
Pao, William ;
Holodny, Andrei I. ;
Clarke, Jennifer L. ;
Lassman, Andrew B. .
NEURO-ONCOLOGY, 2011, 13 (12) :1364-1369
[17]   Assessing oncologic benefit in clinical trials of immunotherapy agents [J].
Hales, R. K. ;
Banchereau, J. ;
Ribas, A. ;
Tarhini, A. A. ;
Weber, J. S. ;
Fox, B. A. ;
Drake, C. G. .
ANNALS OF ONCOLOGY, 2010, 21 (10) :1944-1951
[18]   Immunologic and clinical effects of antibody blockade of cytotoxic T lymphocyte-associated antigen 4 in previously vaccinated cancer patients [J].
Hodi, F. Stephen ;
Butler, Marcus ;
Oble, Darryl A. ;
Seiden, Michael V. ;
Haluska, Frank G. ;
Kruse, Andrea ;
MacRae, Suzanne ;
Nelson, Marybeth ;
Canning, Christine ;
Lowy, Israel ;
Korman, Alan ;
Lautz, David ;
Russell, Sara ;
Jaklitsch, Michael T. ;
Ramaiya, Nikhil ;
Chen, Teresa C. ;
Neuberg, Donna ;
Allison, James P. ;
Mihm, Martin C. ;
Dranoff, Glenn .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (08) :3005-3010
[19]   Improved Survival with Ipilimumab in Patients with Metastatic Melanoma [J].
Hodi, F. Stephen ;
O'Day, Steven J. ;
McDermott, David F. ;
Weber, Robert W. ;
Sosman, Jeffrey A. ;
Haanen, John B. ;
Gonzalez, Rene ;
Robert, Caroline ;
Schadendorf, Dirk ;
Hassel, Jessica C. ;
Akerley, Wallace ;
van den Eertwegh, Alfons J. M. ;
Lutzky, Jose ;
Lorigan, Paul ;
Vaubel, Julia M. ;
Linette, Gerald P. ;
Hogg, David ;
Ottensmeier, Christian H. ;
Lebbe, Celeste ;
Peschel, Christian ;
Quirt, Ian ;
Clark, Joseph I. ;
Wolchok, Jedd D. ;
Weber, Jeffrey S. ;
Tian, Jason ;
Yellin, Michael J. ;
Nichol, Geoffrey M. ;
Hoos, Axel ;
Urba, Walter J. .
NEW ENGLAND JOURNAL OF MEDICINE, 2010, 363 (08) :711-723
[20]   Improved Endpoints for Cancer Immunotherapy Trials [J].
Hoos, Axel ;
Eggermont, Alexander M. M. ;
Janetzki, Sylvia ;
Hodi, F. Stephen ;
Ibrahim, Ramy ;
Anderson, Aparna ;
Humphrey, Rachel ;
Blumenstein, Brent ;
Old, Lloyd ;
Wolchok, Jedd .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2010, 102 (18) :1388-1397