Serum CA19-9 response as a surrogate for clinical outcome in patients receiving fixed-dose rate gemcitabine for advanced pancreatic cancer

被引:126
作者
Ko, AH
Hwang, J
Venook, AP
Abbruzzese, JL
Bergsland, EK
Tempero, MA
机构
[1] Univ Calif San Francisco, Ctr Comprehens Canc, San Francisco, CA 94115 USA
[2] MD Anderson Canc Ctr, Houston, TX 77030 USA
关键词
pancreatic cancer; CA19-9; gemcitabine; tumour marker; surrogate end point;
D O I
10.1038/sj.bjc.6602687
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The use of serial serum measurements of the carbohydrate antigen 19-9 (CA19-9) to guide treatment decisions and serve as a surrogate end point in clinical trial design requires further validation. We investigated whether CA19-9 decline represents an accurate surrogate for survival and time to treatment failure (TTF) in a cohort of 76 patients with advanced pancreatic cancer receiving fixed-dose rate gemcitabine in three separate studies. Statistically significant correlations between percentage CA19-9 decline and both overall survival and TTF were found, with median survival ranging from 12.0 months for patients with the greatest degree of biomarker decline (> 75%) compared with 4.3 months in those whose CA19-9 did not decline during therapy (P < 0.001). Using specific thresholds, patients with >= 25% decline in CA19-9 during treatment had significantly better outcomes than those who did not ( median survival and TTF of 9.6 and 4.6 months vs 4.4 and 1.5 months; P < 0.001).Similar results were seen using both 50 and 75% as cutoff points. We conclude that serial CA19-9 measurements correlate well with clinical outcomes in this patient population, and that decline in this biomarker should be entertained for possible use as a surrogate end point in clinical trials for the selection of new treatments in this disease. (c) 2005 Cancer Research UK.
引用
收藏
页码:195 / 199
页数:5
相关论文
共 19 条
[1]  
DELVILLANO BC, 1983, CLIN CHEM, V29, P549
[2]  
GRUNEWALD R, 1990, CANCER RES, V50, P6823
[3]  
Halm U, 2000, BRIT J CANCER, V82, P1013
[4]  
Ikeda W, 2001, CANCER-AM CANCER SOC, V91, P490, DOI 10.1002/1097-0142(20010201)91:3<490::AID-CNCR1027>3.0.CO
[5]  
2-L
[6]   Cancer statistics, 2005 [J].
Jemal, A ;
Murray, T ;
Ward, E ;
Samuels, A ;
Tiwari, RC ;
Ghafoor, A ;
Feuer, EJ ;
Thun, MJ .
CA-A CANCER JOURNAL FOR CLINICIANS, 2005, 55 (01) :10-30
[7]   Prognostic value of CA 19-9 levels in patients with carcinoma of the pancreas treated with radiotherapy [J].
Katz, A ;
Hanlon, A ;
Lanciano, R ;
Hoffman, J ;
Coia, L .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1998, 41 (02) :393-396
[8]   COLORECTAL-CARCINOMA ANTIGENS DETECTED BY HYBRIDOMA ANTIBODIES [J].
KOPROWSKI, H ;
STEPLEWSKI, Z ;
MITCHELL, K ;
HERLYN, M ;
HERLYN, D ;
FUHRER, P .
SOMATIC CELL GENETICS, 1979, 5 (06) :957-972
[9]   SPECIFIC ANTIGEN IN SERUM OF PATIENTS WITH COLON-CARCINOMA [J].
KOPROWSKI, H ;
HERLYN, M ;
STEPLEWSKI, Z ;
SEARS, HF .
SCIENCE, 1981, 212 (4490) :53-55
[10]   Predictive value of carbohydrate antigen 19-9 in pancreatic cancer treated with radiochemotherapy [J].
Micke, O ;
Bruns, F ;
Kurowski, R ;
Horst, E ;
deVries, AF ;
Hausler, JW ;
Willich, N ;
Schäfer, U .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2003, 57 (01) :90-97