Supplementation With Fish Oil Increases First-Line Chemotherapy Efficacy in Patients With Advanced Nonsmall Cell Lung Cancer

被引:162
作者
Murphy, Rachel A.
Mourtzakis, Marina [2 ]
Chu, Quincy S. C. [3 ]
Baracos, Vickie E. [3 ]
Reiman, Tony [4 ]
Mazurak, Vera C. [1 ]
机构
[1] Univ Alberta, Dept Agr Food & Nutr Sci, Div Human Nutr, Li KaShingCtr Hlth Res Innovat 4 126C, Edmonton, AB T6G 2E1, Canada
[2] Univ Waterloo, Dept Kinesiol, Waterloo, ON N2L 3G1, Canada
[3] Univ Alberta, Dept Oncol, Edmonton, AB T6G 2E1, Canada
[4] Dalhousie Univ, Dept Oncol, St John, NB, Canada
关键词
lung cancer; carboplatin; n-3 fatty acids; toxicity; survival; response rate; POLYUNSATURATED FATTY-ACIDS; DOCOSAHEXAENOIC ACID; CPT-11; IRINOTECAN; BREAST-CARCINOMA; CARDIAC TOXICITY; BODY-COMPOSITION; SKELETAL-MUSCLE; DOUBLE-BLIND; VITAMIN-E; TRIAL;
D O I
10.1002/cncr.25933
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Palliative chemotherapy is aimed at increasing survival and palliating symptoms. However, the response rate to first-line chemotherapy in patients with nonsmall cell lung cancer (NSCLC) is less than 30%. Experimental studies have shown that supplementation with fish oil (FO) can increase chemotherapy efficacy without negatively affecting nontarget tissue. This study evaluated whether the combination of FO and chemotherapy (carboplatin with vinorelbine or gemcitabine) provided a benefit over standard of care (SOC) on response rate and clinical benefit from chemotherapy in patients with advanced NSCLC. METHODS: Forty-six patients completed the study, n = 31 in the SOC group and n = 15 in the FO group (2.5 g EPA + DHA/day). Response to chemotherapy was determined by clinical examination and imaging. Response rate was defined as the sum of complete response plus partial response, and clinical benefit was defined as the sum of complete response, partial response, and stable disease divided by the number of patients. Toxicities were graded by a nurse before each chemotherapy cycle. Survival was calculated 1 year after study enrollment. RESULTS: Patients in the FO group had an increased response rate and greater clinical benefit compared with the SOC group (60.0% vs 25.8%, P = .008; 80.0% vs 41.9%, P = .02, respectively). The incidence of dose-limiting toxicity did not differ between groups (P = .46). One-year survival tended to be greater in the FO group (60.0% vs 38.7%; P = .15). CONCLUSIONS: Compared with SOC, supplementation with FO results in increased chemotherapy efficacy without affecting the toxicity profile and may contribute to increased survival. Cancer 2011;117:3774-80. (C) 2011 American Cancer Society.
引用
收藏
页码:3774 / 3780
页数:7
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