Tumor Volume Decrease at 8 Weeks Is Associated with Longer Survival in EGFR-Mutant Advanced Non-Small-Cell Lung Cancer Patients Treated with EGFR TKI

被引:44
作者
Nishino, Mizuki [1 ,5 ]
Dahlberg, Suzanne E. [2 ]
Cardarella, Stephanie [3 ,4 ]
Jackman, David M. [3 ,4 ]
Rabin, Michael S. [3 ,4 ]
Hatabu, Hiroto [5 ]
Jaenne, Pasi A. [3 ,4 ]
Johnson, Bruce E. [3 ,4 ]
机构
[1] Dana Farber Canc Inst, Dept Imaging, Boston, MA 02215 USA
[2] Dana Farber Canc Inst, Dept Biostat & Computat Biol, Boston, MA 02215 USA
[3] Dana Farber Canc Inst, Dept Med Oncol & Med, Boston, MA 02215 USA
[4] Brigham & Womens Hosp, Boston, MA 02215 USA
[5] Brigham & Womens Hosp, Dept Radiol, Boston, MA 02215 USA
基金
美国国家卫生研究院;
关键词
Lung cancer; Computed tomography scans; Tumor volume; Epidermal growth factor receptor mutations; Epidermal growth factor receptor tyrosine kinase inhibitors; GROWTH-FACTOR RECEPTOR; RESPONSE EVALUATION CRITERIA; TYROSINE KINASE INHIBITORS; ACQUIRED-RESISTANCE; 1ST-LINE TREATMENT; PROGNOSTIC-FACTOR; OPEN-LABEL; GEFITINIB; CHEMOTHERAPY; CT;
D O I
10.1097/JTO.0b013e318294c909
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The study investigated whether tumor volume changes at 8 weeks of therapy is associated with outcomes in advanced non-small-cell lung cancer (NSCLC) patients harboring sensitizing epidermal growth factor receptor (EGFR) mutations treated with EGFR tyrosine kinase inhibitors (TKIs). Methods: In 56 advanced NSCLC patients with sensitizing EGFR mutations treated with first-line erlotinib or gefitinib, tumor volumes of dominant lung lesions were measured on baseline and follow-up computed tomography, and were analyzed for association with survival. Results: Among 56 eligible patients, the median tumor volume was 17.8cm(3) (range, 1.3-172.7cm(3)) on the baseline scans. Forty-nine patients had follow-up computed tomography at approximately 8 weeks; the median tumor volume at 8 weeks was 7.1cm(3) (range, 0.4-62.3cm(3)), with the median proportional volume change of -59% (range, -90% to +91%) from baseline. The proportional volume change at 8 weeks was associated with survival (p = 0.02). Using the cutoff value of 38% volume decrease (75th percentile) at 8 weeks, patients with volume decrease more than 38% (n = 37) had a median overall survival of 43.5 months compared with 16.3 months among those with volume decrease of 38% or less (n = 12; p = 0.01). The median progression-free survival for patients with more than 38% volume decrease was 12.6 months, compared with 5.5 months for those with 38% or lesser volume decrease (p = 0.2). Conclusion: The proportional volume change at 8 weeks is associated with overall survival in EGFR-mutant advanced NSCLC patients treated with first-line EGFR-TKIs. The observation of the study, if confirmed in larger study cohorts, indicates that tumor volume analysis at 8 weeks may provide an early marker for survival, and contribute to therapeutic decision making by identifying patients who may benefit from additional anticancer therapy after 8 weeks of EGFR-TKI therapy.
引用
收藏
页码:1059 / 1068
页数:10
相关论文
共 55 条
[1]   TUMOR VOLUME IS A PROGNOSTIC FACTOR IN NON-SMALL-CELL LUNG CANCER TREATED WITH CHEMORADIOTHERAPY [J].
Alexander, Brian M. ;
Othus, Megan ;
Caglar, Hale B. ;
Allen, Aaron M. .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2011, 79 (05) :1381-1387
[2]  
[Anonymous], CANC FACTS FIG 2012
[3]   Rebiopsy of Lung Cancer Patients with Acquired Resistance to EGFR Inhibitors and Enhanced Detection of the T790M Mutation Using a Locked Nucleic Acid-Based Assay [J].
Arcila, Maria E. ;
Oxnard, Geoffrey R. ;
Nafa, Khedoudja ;
Riely, Gregory J. ;
Solomon, Stephen B. ;
Zakowski, Maureen F. ;
Kris, Mark G. ;
Pao, William ;
Miller, Vincent A. ;
Ladanyi, Marc .
CLINICAL CANCER RESEARCH, 2011, 17 (05) :1169-1180
[4]   Early Changes in Tumor Size in Patients Treated for Advanced Stage Nonsmall Cell Lung Cancer Do Not Correlate With Survival [J].
Birchard, Katherine R. ;
Hoang, Jenny K. ;
Herndon, James E., Jr. ;
Patz, Edward F., Jr. .
CANCER, 2009, 115 (03) :581-586
[5]   Tumor volume combined with number of positive lymph node stations is a more important prognostic factor than TNM stage for survival of non-small-cell lung cancer patients treated with (chemo)radiotherapy [J].
Dehing-Oberije, Cary ;
De Ruysscher, Dirk ;
van der Weide, Hiska ;
Hochstenbag, Monique ;
Bootsma, Gerben ;
Geraedts, Wiel ;
Pitz, Cordula ;
Simons, Jean ;
Teule, Jaap ;
Rahmy, Ali ;
Thimister, Paul ;
Steck, Harald ;
Lambin, Philippe .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2008, 70 (04) :1039-1044
[6]  
Ding L, 2011, J CLIN ONCOL S, V29
[7]   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
[8]   MET amplification leads to gefitinib resistance in lung cancer by activating ERBB3 signaling [J].
Engelman, Jeffrey A. ;
Zejnullahu, Kreshnik ;
Mitsudomi, Tetsuya ;
Song, Youngchul ;
Hyland, Courtney ;
Park, Joon Oh ;
Lindeman, Neal ;
Gale, Christopher-Michael ;
Zhao, Xiaojun ;
Christensen, James ;
Kosaka, Takayuki ;
Holmes, Alison J. ;
Rogers, Andrew M. ;
Cappuzzo, Federico ;
Mok, Tony ;
Lee, Charles ;
Johnson, Bruce E. ;
Cantley, Lewis C. ;
Janne, Pasi A. .
SCIENCE, 2007, 316 (5827) :1039-1043
[9]   Whole-Tumor Perfusion CT in Patients with Advanced Lung Adenocarcinoma Treated with Conventional and Antiangiogenetic Chemotherapy: Initial Experience [J].
Fraioli, Francesco ;
Anzidei, Michele ;
Zaccagna, Fulvio ;
Mennini, Maria Luisa ;
Serra, Goffredo ;
Gori, Bruno ;
Longo, Flavia ;
Catalano, Carlo ;
Passariello, Roberto .
RADIOLOGY, 2011, 259 (02) :574-582
[10]   The BATTLE to Personalize Lung Cancer Prevention through Reverse Migration [J].
Gold, Kathryn A. ;
Kim, Edward S. ;
Lee, J. Jack ;
Wistuba, Ignacio I. ;
Farhangfar, Carol J. ;
Hong, Waun Ki .
CANCER PREVENTION RESEARCH, 2011, 4 (07) :962-972