Efficacy and patterns of failure for locally advanced cancer of the cervix treated with celebrex (celecoxib) and chemoradiotherapy in rtog 0128

被引:38
作者
Gaffney, David K.
Winter, Kathryn
Dicker, Adam P.
Miller, Brigitte
Eifel, Patricia J.
Ryu, Janice
Avizonis, Vilija
Fromm, Mitch
Small, William
Greven, Kathryn
机构
[1] Univ Utah, Huntsman Canc Hosp, Dept Radiat Oncol, Salt Lake City, UT 84132 USA
[2] Radiat Therapy Oncol Grp, Dept Stat, Philadelphia, PA USA
[3] Thomas Jefferson Univ Hosp, Bodine Ctr Canc Treatment, Philadelphia, PA 19107 USA
[4] Wake Forest Univ, Sch Med, Dept Obstet & Gynecol, Winston Salem, NC 27109 USA
[5] Wake Forest Univ, Sch Med, Dept Radiat Oncol, Winston Salem, NC 27109 USA
[6] Univ Texas, MD Anderson Canc Ctr, Dept Radiat Oncol, Houston, TX 77030 USA
[7] Univ CA, Davis Canc Ctr, Dept Radiat Oncol, Sacramento, CA USA
[8] LDS Hosp, Ctr Radiat, Dept Radiat Oncol, Salt Lake City, UT USA
[9] Akron Gen Med Ctr, Dept Radiat Oncol, Akron, OH USA
[10] NW Mem Hosp, Radiat Oncol Ctr, Chicago, IL 60611 USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2007年 / 69卷 / 01期
关键词
cervix; radiotherapy; celecoxib; acute toxicity;
D O I
10.1016/j.ijrobp.2007.02.050
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To determine the efficacy and patterns of initial failure for oral celecoxib, intravenous cisplatin, and 5-fluorouracil and concurrent pelvic radiotherapy in patients with locally advanced cancer of the cervix. Methods and Materials: Patients were treated with concurrent 5-fluorouracil and cisplatin chemotherapy and pelvic radiotherapy and brachytherapy. Celecoxib was prescribed at a dose of 400 mg twice daily for I year beginning on the first day of radiotherapy. The overall and disease-free survival rates were determined. Results: A total of 84 patients were accrued, of whom 78 were eligible. The estimated 2-year disease-free survival and overall survival rate was 69% and 83%, respectively. Of the 78 patients, 24 had treatment failure: 3 with persistent local disease, 9 local only, 2 regional, 4 distant, 1 regional and distant, 1 local and distant, and 2 with local, regional, and distant disease, and 1 had died of cervical cancer without a reported site of first failure and 1 without evidence of disease. Conclusion: At 2 years, the estimated disease-free survival and overall survival rate for patients with advanced cervical cancer who underwent a combination of chemoradiotherapy and celecoxib treatment was 69% and 83%, respectively. Recurrent disease developed in 24 patients, and, of those patients, 18 had a component of locoregional failure as a site of first failure. Thus, locoregional control continues to be problematic after chemoradiotherapy as delivered in our study. The identification of more active biologically targeted therapies is warranted for the treatment of advanced cancer of the cervix. (c) 2007 Elsevier Inc.
引用
收藏
页码:111 / 117
页数:7
相关论文
共 50 条
[1]   Celecoxib for the prevention of colorectal adenomatous polyps [J].
Arber, Nadir ;
Eagle, Craig J. ;
Spicak, Julius ;
Racz, Istvan ;
Dite, Petr ;
Hajer, Jan ;
Zavoral, Miroslav ;
Lechuga, Maria J. ;
Gerletti, Paola ;
Tang, Jie ;
Rosenstein, Rebecca B. ;
Macdonald, Katie ;
Bhadra, Pritha ;
Fowler, Robert ;
Wittes, Janet ;
Zauber, Ann G. ;
Solomon, Scott D. ;
Levin, Bernard .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 355 (09) :885-895
[2]   Increased toxicity and lack of efficacy of rofecoxib in combination with chemotherapy for treatment of metastatic colorectal cancer: A phase II study [J].
Becerra, CR ;
Frenkel, EP ;
Asrfaq, R ;
Gaynor, RB .
INTERNATIONAL JOURNAL OF CANCER, 2003, 105 (06) :868-872
[3]   Celecoxib for the prevention of sporadic colorectal adenomas [J].
Bertagnolli, Monica M. ;
Eagle, Craig J. ;
Zauber, Ann G. ;
Redston, Mark ;
Solomon, Scott D. ;
Kim, KyungMann ;
Tang, Jie ;
Rosenstein, Rebecca B. ;
Wittes, Janet ;
Corle, Donald ;
Hess, Timothy M. ;
Woloj, G. Mabel ;
Boisserie, Frederic ;
Anderson, William F. ;
Viner, Jaye L. ;
Bagheri, Donya ;
Burn, John ;
Chung, Daniel C. ;
Dewar, Thomas ;
Foley, T. Raymond ;
Hoffman, Neville ;
Macrae, Finlay ;
Pruitt, Ronald E. ;
Saltzman, John R. ;
Salzberg, Bruce ;
Sylwestrowicz, Thomas ;
Gordon, Gary B. ;
Hawk, Ernest T. .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 355 (09) :873-884
[4]   A phase I study of 5-fluorouracil, leucovorin, and celecoxib in patients with incurable colorectal cancer [J].
Blanke, CD ;
Mattek, NC ;
Deloughery, TG ;
Koop, DR .
PROSTAGLANDINS & OTHER LIPID MEDIATORS, 2005, 75 (1-4) :169-172
[5]   Phase I/II study of selective cyclooxygenase-2 inhibitor celecoxib as a radiation sensitizer in patients with unresectable brain metastases [J].
Cerchietti, LCA ;
Bonomi, MR ;
Navigante, AH ;
Castro, MA ;
Cabalar, ME ;
Roth, BMC .
JOURNAL OF NEURO-ONCOLOGY, 2005, 71 (01) :73-81
[6]   Increased expression of nitric oxide synthase and cyclooxygenase-2 is associated with poor survival in cervical cancer treated with radiotherapy [J].
Chen, HHW ;
Su, WC ;
Chou, CY ;
Guo, HR ;
Ho, SY ;
Que, J ;
Lee, WY .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2005, 63 (04) :1093-1100
[7]  
Chiarugi V, 1998, INT J MOL MED, V2, P715
[8]   Initial experience combining cyclooxygenase-2 inhibition with chemoradiation for locally advanced pancreatic cancer [J].
Crane, CH ;
Mason, K ;
Janjan, NA ;
Milas, L .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 2003, 26 (04) :S81-S84
[9]   Targeting cyclooxygenase-2 in recurrent non-small cell lung cancer: A phase II trial of celecoxib and docetaxel [J].
Csiki, I ;
Morrow, JD ;
Sandler, A ;
Shyr, Y ;
Oates, J ;
Williams, MK ;
Dang, T ;
Carbone, DP ;
Johnson, DH .
CLINICAL CANCER RESEARCH, 2005, 11 (18) :6634-6640
[10]   Pelvic irradiation with concurrent chemotherapy versus pelvic and para-aortic irradiation for high-risk cervical cancer: An update of radiation therapy oncology group trial (RTOG) 90-01 [J].
Eifel, PJ ;
Winter, K ;
Morris, M ;
Levenback, C ;
Grigsby, PW ;
Cooper, J ;
Rotman, M ;
Gershenson, D ;
Mutch, DG .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (05) :872-880