Role of Anti-inflammatory Drugs in the Colorectal Cancer

被引:14
|
作者
Sada, Oumer [1 ]
Ahmed, Kemal [2 ]
Jeldo, Aliye [1 ]
Shafi, Mensur [3 ]
机构
[1] Addis Ababa Univ, Addis Ababa, Ethiopia
[2] Wollo Univ, Dessie, Ethiopia
[3] St Pauls Hosp Millennium Med Coll, Addis Ababa, Ethiopia
关键词
colorectal cancer; NSAID; COX-2; inhibitors; ASPIRIN USE; RANDOMIZED-TRIAL; FOLLOW-UP; CELECOXIB; COLON; RISK; PREVENTION; RECURRENCE; CHEMOPREVENTION; ASSOCIATION;
D O I
10.1177/0018578718823736
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objective: The objective of this review was to systematically review and synthesize evidence regarding benefits of using nonsteroidal anti-inflammatory drugs (NSAIDs) for the treatment of colorectal cancer (CRC). Data Sources: The data sources were MEDLINE, PubMed, NEJM, Google Scholar, and Google searches of references from relevant and eligible trials. Review Methods: We screened abstracts and full-text articles of identified references for eligibility and reviewed randomized controlled trials, cohort studies, and meta-analysis for evidence on benefits of using NSAIDs in CRC treatments. For all extracted data, completeness and relevance were checked. Results: The risk of any adenoma among frequent NSAID users was 26.8% vs 39.9% among placebo subjects who later used NSAIDs sporadically (adjusted relative risk = 0.62, 95% confidence interval [CI] = 0.39-0.98; P trend with NSAID use frequency = .03). Long-term use of aspirin reduces the risk of CRC. Aspirin also reduces the incidence of colon adenomas and mortality, especially when used for >10 years. Rofecoxib is associated with the reduction of CRC; however, it was associated with cardiovascular risk (with an overall unadjusted relative risk of 1.50 [95% CI = 0.76-2.94; P = .24]). Adenoma Prevention with Celecoxib trial shows that, for patients of all genotypes, the estimated cumulative incidence of one or more adenomas by year 3 was 59.8% for those randomized to placebo as compared with 43.3% for those randomized to low-dose (200 mg, twice daily) celecoxib (relative risk [RR] = 0.68; 95% CI = 0.59-0.79; P < .001) and 36.8% for those randomized to high-dose (400 mg, twice daily) celecoxib and 60.7% in placebo group (RR = 0.54; 95% CI = 0.46-0.64; P < .001). Conclusions: The use of COX-2 inhibitors both prior to and after diagnosis of CRC seemed to be mildly associated with the reduction in mortality of patients with CRC. Some literatures state that COX-2 inhibitors might play a synergistic role in adjuvant chemotherapy of FOLFOX regimen. Celecoxib was found to increase the radiosensitization of colon cancer cells.
引用
收藏
页码:168 / 180
页数:13
相关论文
共 50 条
  • [1] The Role of Anti-Inflammatory Drugs in Colorectal Cancer
    Wang, Dingzhi
    DuBois, Raymond N.
    ANNUAL REVIEW OF MEDICINE, VOL 64, 2013, 64 : 131 - 144
  • [2] Colorectal cancer and non-steroidal anti-inflammatory drugs
    Ota, S
    Bamba, H
    Kato, A
    ACTA PHARMACOLOGICA SINICA, 2000, 21 (05): : 391 - 395
  • [3] Nonsteroidal anti-inflammatory drugs and prevention of colorectal cancer.
    Arber N.
    DuBois R.N.
    Current Gastroenterology Reports, 1999, 1 (5) : 441 - 448
  • [4] Nonsteroidal anti-inflammatory drugs (NSAIDS) in colorectal cancer chemoprevention
    Krishnan, K
    Brenner, DE
    CANCER JOURNAL - FRANCE, 1997, 10 (01): : 10 - 16
  • [5] Nonsteroidal anti-inflammatory drugs (NSAIDs) in the prevention of colorectal cancer
    Stockbrügger, RW
    EUROPEAN JOURNAL OF CANCER PREVENTION, 1999, 8 : S21 - S25
  • [6] Chemoprevention of colorectal cancer by non-steroidal anti-inflammatory drugs
    Bus, PJ
    Verspaget, HW
    Lamers, CBHW
    Griffioen, G
    SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 2000, 35 : 101 - 104
  • [7] Bioengineered Colorectal Cancer Drugs: Orally Delivered Anti-Inflammatory Agents
    Urbanska, Aleksandra Malgorzata
    Zhang, Xiaoying
    Prakash, Satya
    CELL BIOCHEMISTRY AND BIOPHYSICS, 2015, 72 (03) : 757 - 769
  • [8] Nonsteroidal anti-inflammatory drugs in colorectal cancer: from prevention to therapy
    P Ricchi
    R Zarrilli
    A di Palma
    A M Acquaviva
    British Journal of Cancer, 2003, 88 : 803 - 807
  • [9] Nonsteroidal anti-inflammatory drugs, COX-2 and colorectal cancer
    Patrignani, P
    TOXICOLOGY LETTERS, 2000, 112 : 493 - 498