Prognostic factors predictive of response and survival to a modified FOLFOX regimen: Importance of an increased neutrophil count

被引:34
作者
Michael, Michael
Goldstein, David
Clarke, Stephen J.
Milner, Alvin D.
Beale, Phillip
Friedlander, Michael
Mitchell, Paul
机构
[1] Peter MacCallum Canc Ctr, Div Haematol & Med Oncol, Melbourne, Vic 8006, Australia
[2] Prince Wales Hosp, Randwick, NSW 2031, Australia
[3] Sydney Canc Ctr, Camperdown, NSW, Australia
[4] Peter MacCallum Canc Ctr, Ctr Biostat & Clin Trials, Melbourne, Vic, Australia
[5] Austin & Repatriat Med Ctr, Heidelberg, Vic, Australia
关键词
efficacy; 5-fluorouracil; leucovorin; oxaliplatin;
D O I
10.3816/CCC.2006.n.048
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: The aim of this study was to identify prognostic indicators of survival and response in a homogeneous population of chemotherapy-naive patients treated with oxaliplatin as part of 3 successive trials. Patients and Methods: Patient data were derived from 3 successive phase 11 trials evaluating modifications of the FOLFOX4 (oxaliplatin/5-fluorouracil/leucovorin) regimen. Clinical and laboratory prognostic factors were identified from the literature. Multifactor analyses stratified by treatment cohort were performed to identify independent prognostic factors for progression-free survival (PFS), overall survival (OS), and response rate. Results: One hundred thirty-four patients were enrolled across all 3 studies. Reduced PFS (n = 128) was associated with patients with the following characteristics: no previous surgery (P = 0.003); previous adjuvant chemotherapy (P = 0.015); > 1 organ involvement (P = 0.001); baseline absolute neutrophil count (ANC) >= upper limit of normal (P = 0.001); and time from diagnosis to metastases < 9 months (P = 0.043). Poor OS (n = 128) was associated with patients with the following characteristics: performance status > 1 (P < 0.001); > 1 organ involvement (P = 0.0 18); and baseline ANC >= upper limit of normal (P < 0.001). Response rate was related to previous surgery (P = 0.0 17) and performance status (P = 0.02). Conclusion: This analysis has identified the additional prognostic importance of an increased ANC for PFS and OS. Further consideration needs to be given to include markers of systemic inflammation such as ANC as well as relevant cytokine levels in a larger cohort of identically treated patients.
引用
收藏
页码:297 / 304
页数:8
相关论文
共 69 条
[1]   Serum proinflammatory cytokines and its relationship to clinical parameters in lung cancer patients with reactive thrombocytosis [J].
Alexandrakis, MG ;
Passam, FH ;
Perisinakis, K ;
Ganotakis, E ;
Margantinis, G ;
Kyriakou, DS ;
Bouros, D .
RESPIRATORY MEDICINE, 2002, 96 (08) :553-558
[2]  
Becker C, 2005, CELL CYCLE, V4, P217
[3]   Factors predicting efficacy of oxaliplatin in combination with 5-fluorouracil (5-FU) ± folinic acid in a compassionate-use cohort of 481 5-FU-resistant advanced colorectal cancer patients [J].
Bensmaïne, MA ;
Marty, M ;
de Gramont, A ;
Brienza, S ;
Lévi, F ;
Ducreux, M ;
François, E ;
Gamelin, E ;
Bleiberg, H ;
Cvitkovic, E .
BRITISH JOURNAL OF CANCER, 2001, 85 (04) :509-517
[4]   Factors predicting for efficacy of oxaliplatin in combination with 5-fluorouracil (5-FU)±folinic acid (FA) in a compassionate-use cohort of 370 5-FU-resistant advanced colorectal cancer (CRC) patients [J].
Bensmaïne, MA ;
de Gramont, A ;
Brienza, S ;
Marty, M ;
Lévi, F ;
Ducreux, M ;
François, E ;
Gamelin, E ;
Bleiberg, H ;
Bleuzen, P ;
Simon, J ;
Cvitkovic, E .
EUROPEAN JOURNAL OF CANCER, 2000, 36 (18) :2335-2343
[5]   The impact of adding low-dose leucovorin to monthly 5-fluorouracil in advanced colorectal carcinoma: Results of a phase III trial [J].
Borner, MM ;
Castiglione, M ;
Bacchi, M ;
Weber, W ;
Herrmann, R ;
Fey, MF ;
Pagani, O ;
Leyvraz, S ;
Morant, R ;
Pestalozzi, B ;
Hanselmann, S ;
Goldhirsch, A .
ANNALS OF ONCOLOGY, 1998, 9 (05) :535-541
[6]   Oxaliplatin added to 5-fluorouracil-based therapy (5-FU ± FA) in the treatment of 5-FU-pretreated patients with advanced colorectal carcinoma (ACRC):: Results from the European compassionate-use program [J].
Brienza, S ;
Bensmaïne, MA ;
Soulié, P ;
Louvet, C ;
Gamelin, E ;
François, E ;
Ducreux, M ;
Marty, M ;
André, T ;
de Braud, F ;
Bleiberg, H ;
Ségal, V ;
Itzhaki, M ;
Cvitkovic, E .
ANNALS OF ONCOLOGY, 1999, 10 (11) :1311-1316
[7]   Differentiation-dependent expression and mitogenic action of interleukin-6 in human colon carcinoma cells: Relevance for tumour progression [J].
Brozek, W ;
Bises, G ;
Girsch, T ;
Cross, HS ;
Kaiser, HE ;
Peterlik, M .
EUROPEAN JOURNAL OF CANCER, 2005, 41 (15) :2347-2354
[8]   Relation between tumour response to first-line chemotherapy and survival in advanced colorectal cancer: a meta-analysis [J].
Buyse, M ;
Thirion, P ;
Carlson, RW ;
Burzykowski, T ;
Molenberghs, G ;
Piedbois, P .
LANCET, 2000, 356 (9227) :373-378
[9]   Evaluation of a cumulative prognostic score based on the systemic inflammatory response in patients undergoing potentially curative surgery for colorectal cancer [J].
Canna, K ;
McMillan, DC ;
McKee, RF ;
McNicol, AM ;
Horgan, PG ;
McArdle, CS .
BRITISH JOURNAL OF CANCER, 2004, 90 (09) :1707-1709
[10]   Serum interleukin-6 levels reflect the disease status of colorectal cancer [J].
Chung, YC ;
Chang, YF .
JOURNAL OF SURGICAL ONCOLOGY, 2003, 83 (04) :222-226