Delay of treatment change after objective progression on first-line erlotinib in epidermal growth factor receptor-mutant lung cancer

被引:43
作者
Lo, Peter C. [1 ]
Dahlberg, Suzanne E. [2 ,3 ]
Nishino, Mizuki [4 ,5 ]
Johnson, Bruce E. [1 ,5 ,6 ]
Sequist, Lecia V. [5 ,7 ]
Jackman, David M. [1 ,5 ,6 ]
Jaenne, Pasi A. [1 ,5 ,6 ,8 ]
Oxnard, Geoffrey R. [1 ,5 ,6 ]
机构
[1] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02114 USA
[2] Dana Farber Canc Inst, Dept Biostat, Boston, MA 02114 USA
[3] Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USA
[4] Dana Farber Canc Inst, Dept Radiol, Boston, MA 02114 USA
[5] Harvard Univ, Sch Med, Boston, MA USA
[6] Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
[7] Massachusetts Gen Hosp, Dept Med, Boston, MA 02114 USA
[8] Dana Farber Canc Inst, Belfer Inst Appl Canc Sci, Boston, MA 02114 USA
基金
美国国家卫生研究院;
关键词
disease progression; epidermal growth factor receptor mutation; erlotinib; non-small cell lung cancer; time until treatment change; TYROSINE KINASE INHIBITOR; DISEASE-CONTROL; CHEMOTHERAPY; STRATEGY; EVALUATE; THERAPY; FAILURE; TRIAL;
D O I
10.1002/cncr.29397
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUNDErlotinib is a highly active epidermal growth factor receptor (EGFR) kinase inhibitor that is approved for first-line use in lung cancers harboring EGFR mutations. Anecdotal experience suggests that this drug may provide continued disease control after patients develop objective progression of disease (PD), although this has not been systematically studied to date. METHODSPatients who had Response Evaluation Criteria In Solid Tumors-defined PD who were participating in 3 prospective trials of first-line erlotinib in advanced lung cancer were studied retrospectively, and the progression characteristics were compared between patients with and without EGFR-sensitizing mutations. Factors were studied that influenced the time until treatment change (TTC), defined as the time from PD to the start of a new systemic therapy or death. The rate of tumor progression was assessed by comparing tumor measurements between the computed tomography scan obtained at the time of PD and the preceding scan. RESULTSIn total, 92 eligible patients were studied, including 42 with and 50 without an EGFR-sensitizing mutation. The EGFR-mutant cohort had a slower rate of progression (P=.003) and a longer TTC (P<.001). Among the patients with EGFR-mutant cancers, 28 (66%) continued single-agent erlotinib after PD, and 21 (50%) were able to delay a change in systemic therapy for >3 months; only 2 patients received local debulking therapy during that period. Multivariate analysis of the patients with EGFR-mutant tumors demonstrated that a longer time to progression, a slower rate of progression, and a lack of new extrathoracic metastases were associated with a longer TTC. CONCLUSIONSA change in systemic therapy commonly can be delayed in patients with EGFR-mutant lung cancer who objectively progress on first-line erlotinib, particularly in those with a longer time to progression, a slow rate of progression, and a lack of new extrathoracic metastases. Cancer 2015;121:2570-2577. (c) 2015 American Cancer Society. Anecdotal experience suggests that some patients with non-small cell lung cancer who progress on erlotinib can have continued disease control without a change in treatment. In this analysis, investigators study 92 patients with non-small cell lung cancer who develop objective disease progression while receiving first-line erlotinib on 3 clinical trials and demonstrate the potential benefits of delaying a change in treatment for patients who have epidermal growth factor receptor-mutant lung cancer and favorable progression characteristics.
引用
收藏
页码:2570 / 2577
页数:8
相关论文
共 17 条
[1]  
[Anonymous], J CLIN ONCOL
[2]   Alternative End Points to Evaluate a Therapeutic Strategy in Advanced Colorectal Cancer: Evaluation of Progression-Free Survival, Duration of Disease Control, and Time to Failure of Strategy-An Aide et Recherche en Cancerologie Digestive Group Study [J].
Chibaudel, Benoist ;
Bonnetain, Franck ;
Shi, Qian ;
Buyse, Marc ;
Tournigand, Christophe ;
Sargent, Daniel J. ;
Allegra, Carmen J. ;
Goldberg, Richard M. ;
de Gramont, Aimery .
JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (31) :4199-4204
[3]   Optimization of Dosing for EGFR-Mutant Non-Small Cell Lung Cancer with Evolutionary Cancer Modeling [J].
Chmielecki, Juliann ;
Foo, Jasmine ;
Oxnard, Geoffrey R. ;
Hutchinson, Katherine ;
Ohashi, Kadoaki ;
Somwar, Romel ;
Wang, Lu ;
Amato, Katherine R. ;
Arcila, Maria ;
Sos, Martin L. ;
Socci, Nicholas D. ;
Viale, Agnes ;
de Stanchina, Elisa ;
Ginsberg, Michelle S. ;
Thomas, Roman K. ;
Kris, Mark G. ;
Inoue, Akira ;
Ladanyi, Marc ;
Miller, Vincent A. ;
Michor, Franziska ;
Pao, William .
SCIENCE TRANSLATIONAL MEDICINE, 2011, 3 (90)
[4]  
Jackman DM, 2009, J CLIN ONCOL, V27
[5]   Phase II clinical trial of chemotherapy-naive patients ≥ 70 years of age treated with erlotinib for advanced non-small-cell lung cancer [J].
Jackman, David M. ;
Yeap, Beow Y. ;
Lindeman, Neal I. ;
Fidias, Panos ;
Rabin, Michael S. ;
Temel, Jennifer ;
Skarin, Arthur T. ;
Meyerson, Matthew ;
Holmes, Alison J. ;
Borras, Ana M. ;
Freidlin, Boris ;
Ostler, Patricia A. ;
Lucca, Joan ;
Lynch, Thomas J. ;
Johnson, Bruce E. ;
Jaenne, Pasi A. .
JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (07) :760-766
[6]   Randomized Phase II Trial of Erlotinib Alone or With Carboplatin and Paclitaxel in Patients Who Were Never or Light Former Smokers With Advanced Lung Adenocarcinoma: CALGB 30406 Trial [J].
Jaenne, Pasi A. ;
Wang, Xiaofei ;
Socinski, Mark A. ;
Crawford, Jeffrey ;
Stinchcombe, Thomas E. ;
Gu, Lin ;
Capelletti, Marzia ;
Edelman, Martin J. ;
Villalona-Calero, Miguel A. ;
Kratzke, Robert ;
Vokes, Everett E. ;
Miller, Vincent A. .
JOURNAL OF CLINICAL ONCOLOGY, 2012, 30 (17) :2063-2069
[7]   A rapid and sensitive enzymatic method for epidermal growth factor receptor mutation screening [J].
Jänne, PA ;
Borras, AM ;
Kuang, YN ;
Rogers, AM ;
Joshi, VA ;
Liyanage, H ;
Lindeman, N ;
Lee, JC ;
Halmos, B ;
Maher, EA ;
Distel, RJ ;
Meyerson, M ;
Johnson, BE .
CLINICAL CANCER RESEARCH, 2006, 12 (03) :751-758
[8]   Randomized phase II study of two intercalated combinations of eribulin mesylate and erlotinib in patients with previously treated advanced non-small-cell lung cancer [J].
Mok, T. S. ;
Geater, S. L. ;
Iannotti, N. ;
Thongprasert, S. ;
Spira, A. ;
Smith, D. ;
Lee, V. ;
Lim, W. T. ;
Reyderman, L. ;
Wang, B. ;
Gopalakrishna, P. ;
Garzon, F. ;
Xu, L. ;
Reynolds, C. .
ANNALS OF ONCOLOGY, 2014, 25 (08) :1578-1584
[9]   Clinical benefit of continuing ALK inhibition with crizotinib beyond initial disease progression in patients with advanced ALK-positive NSCLC [J].
Ou, S. -H. I. ;
Jaenne, P. A. ;
Bartlett, C. H. ;
Tang, Y. ;
Kim, D. -W. ;
Otterson, G. A. ;
Crino, L. ;
Selaru, P. ;
Cohen, D. P. ;
Clark, J. W. ;
Riely, G. J. .
ANNALS OF ONCOLOGY, 2014, 25 (02) :415-422
[10]   When Progressive Disease Does Not Mean Treatment Failure: Reconsidering the Criteria for Progression [J].
Oxnard, Geoffrey R. ;
Morris, Michael J. ;
Hodi, F. Stephen ;
Baker, Laurence H. ;
Kris, Mark G. ;
Venook, Alan P. ;
Schwartz, Lawrence H. .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2012, 104 (20) :1534-1541