Systemic treatment of patients who have colorectal cancer and inflammatory bowel disease

被引:13
作者
Goessling, Wolfram
Mayer, Robert J.
机构
[1] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
[3] Massachusetts Gen Hosp, Dept Med, Gastrointestinal Unit, Boston, MA 02114 USA
[4] Childrens Hosp, Stem Cell Program, Boston, MA 02115 USA
[5] Childrens Hosp, Div Hematol Oncol, Boston, MA 02115 USA
关键词
D O I
10.1016/j.gtc.2006.07.006
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Inflammatory bowel disease (IBD) is an acknowledged predisposing factor for the development of intestinal and extraintestinal cancers. In general, an increased risk for colorectal cancer exists for patients who have both ulcerative colitis (UC) and Crohn's disease (CD). Small bowel tumors are extremely rare in the general population, but their incidence is enhanced 40-fold in patients who have CD. UC confers a marginally increased risk for myeloid leukemia, whereas patients who have CD may have a trend toward a higher incidence of lymphoma. This article reviews the therapeutic options for the most common malignant complication, colorectal carcinoma, as well as specific recommendations regarding the impact of the underlying disease upon the tolerance and efficacy of chemotherapy in these patients.
引用
收藏
页码:713 / +
页数:16
相关论文
共 94 条
[1]   IRINOTECAN (CPT-11) HIGH-DOSE ESCALATION USING INTENSIVE HIGH-DOSE LOPERAMIDE TO CONTROL DIARRHEA [J].
ABIGERGES, D ;
ARMAND, JP ;
CHABOT, GG ;
DACOSTA, L ;
FADEL, E ;
COTE, C ;
HERAIT, P ;
GANDIA, D .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1994, 86 (06) :446-449
[2]   Growth of intestinal epithelium in organ culture is dependent on EGF signalling [J].
Abud, HE ;
Watson, N ;
Heath, JK .
EXPERIMENTAL CELL RESEARCH, 2005, 303 (02) :252-262
[3]   Pharmacogenetics of irinotecan:: A promoter polymorphism of UGT1A1 gene and severe adverse reactions to irinotecan [J].
Ando, M ;
Hasegawa, Y ;
Ando, Y .
INVESTIGATIONAL NEW DRUGS, 2005, 23 (06) :539-545
[4]   Oxaliplatin, fluorouracil, and leucovorin as adjuvant treatment for colon cancer [J].
Andre, T ;
Boni, C ;
Mounedji-Boudiaf, L ;
Navarro, M ;
Tabernero, J ;
Hickish, T ;
Topham, C ;
Zaninelli, M ;
Clingan, P ;
Bridgewater, J ;
Tabah-Fisch, I ;
de Gramont, A .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (23) :2343-2351
[5]   Semimonthly versus monthly regimen of fluorouracil and leucovorin administered for 24 or 36 weeks as adjuvant therapy in stage II and III colon cancer:: Results of a randomized trial [J].
André, T ;
Colin, P ;
Louvet, C ;
Gamelin, E ;
Bouche, O ;
Achille, E ;
Colbert, N ;
Boaziz, C ;
Piedbois, P ;
Tubiana-Mathieu, N ;
Boutan-Laroze, A ;
Flesch, M ;
Buyse, M ;
de Gramont, A .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (15) :2896-2903
[6]   Risk of haematopoietic cancer in patients with inflammatory bowel disease [J].
Askling, J ;
Brandt, L ;
Lapidus, A ;
Karlén, P ;
Björkholm, M ;
Löfberg, R ;
Ekbom, A .
GUT, 2005, 54 (05) :617-622
[7]   Critical update and emerging trends in epidermal growth factor receptor targeting in cancer [J].
Baselga, J ;
Arteaga, CL .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (11) :2445-2459
[8]   Epidermal growth factor receptor signaling regulates Bax and Bcl-w expression and apoptotic responses during intestinal adaptation in mice [J].
Bernal, NP ;
Stehr, W ;
Coyle, R ;
Erwin, CR ;
Warner, BW .
GASTROENTEROLOGY, 2006, 130 (02) :412-423
[9]  
Bernstein CN, 2001, CANCER-AM CANCER SOC, V91, P854, DOI 10.1002/1097-0142(20010215)91:4<854::AID-CNCR1073>3.0.CO
[10]  
2-Z