Progression-free Survival Decreases with Each Subsequent Therapy in Patients Presenting for Phase I Clinical Trials

被引:26
作者
Bailey, Christopher H. [1 ]
Jameson, Gayle [1 ]
Sima, Chao [2 ]
Fleck, Sharon [1 ]
White, Erica [1 ]
Von Hoff, Daniel D. [1 ,2 ]
Weiss, Glen J. [1 ,2 ]
机构
[1] Virginia G Piper Canc Ctr Clin Trials Scottsdale, Scottsdale, AZ USA
[2] Translat Genom Res Inst TGen, Phoenix, AZ USA
关键词
Progression-free survival; chemotherapy; advanced cancer; systemic therapy; phase I clinical trials; CELL LUNG-CANCER; METASTATIC COLORECTAL-CANCER; OXALIPLATIN-BASED CHEMOTHERAPY; ADVANCED PANCREATIC-CANCER; ADVANCED GASTRIC-CANCER; III TRIAL; 1ST-LINE TREATMENT; 2ND-LINE TREATMENT; GASTROESOPHAGEAL ADENOCARCINOMA; CARBOPLATIN-PACLITAXEL;
D O I
10.7150/jca.3.7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: There is often a finite progression-free interval of time between one systemic therapy and the next when treating patients with advanced cancer. While it appears that progression-free survival (PFS) between systemic therapies tends to get shorter for a number of factors, there has not been a formal evaluation of diverse tumor types in an advanced cancer population treated with commercially-available systemic therapies. Methods: In an attempt to clarify the relationship between PFS between subsequent systemic therapies, we analyzed the records of 165 advanced cancer patients coming to our clinic for consideration for participation in six different phase I clinical trials requiring detailed and extensive past medical treatment history documentation. Results: There were 77 men and 65 women meeting inclusion criteria with a median age at diagnosis of 55.3 years (range 9.4-81.6). The most common cancer types were colorectal (13.9%), other gastrointestinal (11.8%), prostate (11.8%). A median of 3 (range 1-11) systemic therapies were received prior to phase I evaluation. There was a significant decrease in PFS in systemic therapy for advanced disease from treatment 1 to treatment 2 to treatment 3 (p = 0.002), as well as, from treatment 1 through treatment 5 (p < 0.001). Conclusions: In an advanced cancer population of diverse tumor types, we observe a statistically significant decrease in PFS with each successive standard therapy. Identification of new therapies that reverse this trend of decreasing PFS may lead to improved clinical outcomes.
引用
收藏
页码:7 / 13
页数:7
相关论文
共 72 条
[51]   EGF receptor gene mutations are common in lung cancers from "never smokers" and are associated with sensitivity of tumors to gefitinib and erlotinib [J].
Pao, W ;
Miller, V ;
Zakowski, M ;
Doherty, J ;
Politi, K ;
Sarkaria, I ;
Singh, B ;
Heelan, R ;
Rusch, V ;
Fulton, L ;
Mardis, E ;
Kupfer, D ;
Wilson, R ;
Kris, M ;
Varmus, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (36) :13306-13311
[52]   Randomized Phase III Study of Panitumumab With Fluorouracil, Leucovorin, and Irinotecan (FOLFIRI) Compared With FOLFIRI Alone As Second-Line Treatment in Patients With Metastatic Colorectal Cancer [J].
Peeters, Marc ;
Price, Timothy Jay ;
Cervantes, Andres ;
Sobrero, Alberto F. ;
Ducreux, Michel ;
Hotko, Yevhen ;
Andre, Thierry ;
Chan, Emily ;
Lordick, Florian ;
Punt, Cornelis J. A. ;
Strickland, Andrew H. ;
Wilson, Gregory ;
Ciuleanu, Tudor-Eliade ;
Roman, Laslo ;
Van Cutsem, Eric ;
Tzekova, Valentina ;
Collins, Simon ;
Oliner, Kelly S. ;
Rong, Alan ;
Gansert, Jennifer .
JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (31) :4706-4713
[53]   Determinants of tumor response and survival with erlotinib in patients with non-small-cell lung cancer [J].
Pérez-Soler, R ;
Chachoua, A ;
Hammond, LA ;
Rowinsky, EK ;
Huberman, M ;
Karp, D ;
Rigas, J ;
Clark, GM ;
Santabàrbara, P ;
Bonomi, P .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (16) :3238-3247
[54]   Biweekly cetuximab and irinotecan as third-line therapy in patients with advanced colorectal cancer after failure to irinotecan, oxaliplatin and 5-fluorouracil [J].
Pfeiffer, P. ;
Nielsen, D. ;
Bjerregaard, J. ;
Qvortrup, C. ;
Yilmaz, M. ;
Jensen, B. .
ANNALS OF ONCOLOGY, 2008, 19 (06) :1141-1145
[55]   Overall survival with cisplatin-gemcitabine and bevacizumab or placebo as first-line therapy for nonsquamous non-small-cell lung cancer: results from a randomised phase III trial (AVAiL) [J].
Reck, M. ;
von Pawel, J. ;
Zatloukal, P. ;
Ramlau, R. ;
Gorbounova, V. ;
Hirsh, V. ;
Leighl, N. ;
Mezger, J. ;
Archer, V. ;
Moore, N. ;
Manegold, C. .
ANNALS OF ONCOLOGY, 2010, 21 (09) :1804-1809
[56]   Bevacizumab in combination with oxaliplatin-based chemotherapy as first-line therapy in metastatic colorectal cancer:: A randomized phase III study [J].
Saltz, Leonard B. ;
Clarke, Stephen ;
Diaz-Rubio, Eduardo ;
Scheithauer, Werner ;
Figer, Arie ;
Wong, Ralph ;
Koski, Sheryl ;
Lichinitser, Mikhail ;
Yang, Tsai-Shen ;
Rivera, Fernando ;
Couture, Felix ;
Sirzen, Florin ;
Cassidy, Jim .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (12) :2013-2019
[57]   Biweekly cetuximab and irinotecan as second-line therapy in patients with gastro-esophageal cancer previously treated with platinum [J].
Schoennemann, Katrine R. ;
Bjerregaard, Jon K. ;
Hansen, Tine P. ;
De Stricker, Karin ;
Gjerstorff, Morten F. ;
Jensen, Helle A. ;
Vestermark, Lene W. ;
Pfeiffer, Per .
GASTRIC CANCER, 2011, 14 (03) :219-225
[58]   Erlotinib in previously treated non-small-cell lung cancer [J].
Shepherd, FA ;
Pereira, JR ;
Ciuleanu, T ;
Tan, EH ;
Hirsh, V ;
Thongprasert, S ;
Campos, D ;
Maoleekoonpiroj, S ;
Smylie, M ;
Martins, R ;
van Kooten, M ;
Dediu, M ;
Findlay, B ;
Tu, DS ;
Johnston, D ;
Bezjak, A ;
Clark, G ;
Santabárbara, P ;
Seymour, L .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (02) :123-132
[59]   EPIC:: Phase III trial of cetuximab plus irinotecan after fluoropyrimidine and oxaliplatin failure in patients with metastatic colorectal cancer [J].
Sobrero, Alberto F. ;
Maurel, Joan ;
Fehrenbacher, Louis ;
Scheithauer, Werner ;
Abubakr, Yousif A. ;
Lutz, Manfred P. ;
Vega-Villegas, M. Eugenia ;
Eng, Cathy ;
Steinhauer, Ernst U. ;
Prausova, Jana ;
Lenz, Heinz-Josef ;
Borg, Christophe ;
Middleton, Gary ;
Kroening, Hendrik ;
Luppi, Gabriele ;
Kisker, Oliver ;
Zubel, Angela ;
Langer, Christiane ;
Kopit, Justin ;
Burris, Howard A., III .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (14) :2311-2319
[60]   Gefitinib-sensitizing EGFR mutations in lung cancer activate anti-apoptotic pathways [J].
Sordella, R ;
Bell, DW ;
Haber, DA ;
Settleman, J .
SCIENCE, 2004, 305 (5687) :1163-1167