全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

A Postauthorization Survey to Document the Therapeutic Management of Oxaliplatin as a First-Line Chemotherapy Regimen in South Africa in Patients with Metastatic Colorectal Cancer

DOI: 10.1155/2014/520701

Full-Text   Cite this paper   Add to My Lib

Abstract:

Oxaliplatin is a standard first-line treatment for metastatic colorectal cancer. The objectives were to document the therapeutic management of oxaliplatin in South Africa, determine the incidence and severity of sensory neuropathy, and record the 2-year survival rate. Meccelox was a prospective, noncontrolled, open label, multicentre, observational survey of adult patients with stage IV metastatic colorectal cancer treated with oxaliplatin-based chemotherapeutic regimens. The study was conducted from August 2007 to November 2011 in 29 sites in South Africa by 66 participating treating physicians. Among the 195 enrolled patients, 61% were treated with FOLFOX regimen (5-fluorouracil/folinic acid plus oxaliplatin) for an average of 12 cycles and 32% patients were treated with XELOX (capecitabine plus oxaliplatin) for an average of 6–8 cycles, with the main reason for discontinuation being completion of the preplanned prescribed regimen. In Meccelox survey, 80% of patients were treated with intent of palliation. Overall 64% of patients reported symptoms of sensory neuropathy. The 2-year survival rate was 30%. Conclusions. Patients received a specified preplanned number of chemotherapy cycles rather than being treated until disease progression or toxicity. Both the incidence of neuropathy and the 2-year survival rate were less than previous reports. 1. Introduction Colorectal cancer constitutes a major health problem worldwide representing the third most commonly diagnosed cancer in males and the second most common in females. Over 1.2 million new cancer cases and over 600,000 deaths occur globally each year [1]. Colorectal cancer can be considered as primarily a disease of the elderly, with more than 40% of cases occurring in patients over the age of 75 years [2]. In South Africa, incidence rates, after being standardized for age, are 8.6 per 100,000 males and 5.5 per 100,000 females, according to the country’s national cancer registry (NCR) [3]. Age-standardised mortality rates in South Africa are 7.7 per 100,000 males and 4.5 per 100,000 females [4]. The most common site for metastases is the liver; synchronous liver metastases occur in 15 to 25% of newly diagnosed patients [5, 6]. Treating with both chemotherapy and surgical resection, overall 5-year survival rates of about 30–40% can now be achieved for patients with metastatic colorectal cancer [5]. Chemotherapy remains the cornerstone therapy for the treatment of metastatic colorectal cancer. First-line therapy for patients with metastatic colorectal cancer is rapidly evolving. Treatment regimens are

References

[1]  A. Jemal, F. Bray, M. M. Center, J. Ferlay, E. Ward, and D. Forman, “Global cancer statistics,” CA: Cancer Journal for Clinicians, vol. 61, no. 2, pp. 69–90, 2011.
[2]  C.-H. K?hne, G. Folprecht, R. M. Goldberg, E. Mitry, and P. Rougier, “Chemotherapy in elderly patients with colorectal cancer,” Oncologist, vol. 13, no. 4, pp. 390–402, 2008.
[3]  N. Mqoqi, P. Kellett, F. Sitas, et al., Cancer in South Africa, 1998-1999, National Cancer Registry of South Africa, Johannesburg, South Africa, 2004.
[4]  M. M. Center, A. Jemal, R. A. Smith, and E. Ward, “Worldwide variations in colorectal cancer,” CA: Cancer Journal for Clinicians, vol. 59, no. 6, pp. 366–378, 2009.
[5]  D. L. Bartlett and E. Chu, “Can metastatic colorectal cancer be cured?” Oncology, vol. 26, no. 3, pp. 266–275, 2012.
[6]  J. Norstein and W. Silen, “Natural history of liver metastases from colorectal carcinoma,” Journal of Gastrointestinal Surgery, vol. 1, no. 5, pp. 398–407, 1997.
[7]  C. Tournigand, T. André, E. Achille et al., “FOLFIRI followed by FOLFOX6 or the reverse sequence in advanced colorectal cancer: a randomized GERCOR study,” Journal of Clinical Oncology, vol. 22, no. 2, pp. 229–237, 2004.
[8]  M. L. Rothenberg, A. M. Oza, R. H. Bigelow et al., “Superiority of oxaliplatin and fluorouracil-leucovorin compared with either therapy alone in patients with progressive colorectal cancer after irinotecan and fluorouracil-leucovorin: interim results of a phase III trial,” Journal of Clinical Oncology, vol. 21, no. 11, pp. 2059–2069, 2003.
[9]  A. de Gramont, A. Figer, M. Seymour et al., “Leucovorin and fluorouracil with or without oxaliplatin as first-line treatment in advanced colorectal cancer,” Journal of Clinical Oncology, vol. 18, no. 16, pp. 2938–2947, 2000.
[10]  S. Giacchetti, B. Perpoint, R. Zidani et al., “Phase III multicenter randomized trial of oxaliplatin added to chronomodulated fluorouracil-leucovorin as first-line treatment of metastatic colorectal cancer,” Journal of Clinical Oncology, vol. 18, no. 1, pp. 136–147, 2000.
[11]  E. Aitini, A. Rossi, P. Morselli et al., “Economic comparison of capecitabine + oxaliplatin and 5-fluorouracil + oxaliplatin in the adjuvant treatment of colon cancer,” Cancer Management and Research, vol. 4, no. 1, pp. 99–103, 2012.
[12]  H. T. Arkenau, D. Arnold, J. Cassidy, et al., “Efficacy of oxaliplatin plus capecitabine or infusional fluorouracil/leucovorin in patients with metastatic colorectal cancer: a pooled analysis of randomized trials,” Journal of Clinical Oncology, vol. 26, pp. 5910–5917, 2008.
[13]  “Common Terminology Criteria for Adverse Events v3. 0 (CTCAE),” 2006.
[14]  M. M. Oken, R. H. Creech, and T. E. Davis, “Toxicology and response criteria of the Eastern Cooperative Oncology Group,” The American Journal of Clinical Oncology: Cancer Clinical Trials, vol. 5, no. 6, pp. 649–655, 1982.
[15]  R. M. Goldberg, M. L. Rothenberg, E. Van Cutsem et al., “The continuum of care: a paradigm for the management of metastatic colorectal cancer,” Oncologist, vol. 12, no. 1, pp. 38–50, 2007.
[16]  J. Y. Douillard, D. Cunningham, A. D. Roth et al., “Irinotecan combined with fluorouracil compared with fluorouracil alone. as first-line treatment for metastatic colorectal cancer: a multicentre randomised trial,” The Lancet, vol. 355, no. 9209, pp. 1041–1047, 2000.
[17]  S. R. Alberts, D. J. Sargent, S. Nair et al., “Effect of oxaliplatin, fluorouracil, and leucovorin with or without cetuximab on survival among patients with resected stage III colon cancer: a randomized trial,” Journal of the American Medical Association, vol. 307, no. 13, pp. 1383–1393, 2012.
[18]  E. Gamelin, L. Gamelin, L. Bossi, and S. Quasthoff, “Clinical aspects and molecular basis of oxaliplatin neurotoxicity: current management and development of preventive measures,” Seminars in Oncology, vol. 29, supplement 15, no. 5, pp. 21–33, 2002.
[19]  A. Grothey, “Oxaliplatin-safety profile: neurotoxicity,” Seminars in Oncology, vol. 30, supplement 15, no. 4, pp. 5–13, 2003.
[20]  J. Cassidy, S. Clarke, E. Díaz-Rubio et al., “XELOX vs FOLFOX-4 as first-line therapy for metastatic colorectal cancer: NO16966 updated results,” British Journal of Cancer, vol. 105, no. 1, pp. 58–64, 2011.

Full-Text

comments powered by Disqus

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133

WeChat 1538708413