Continued cigarette smoking by patients receiving concurrent chemoradiotherapy for limited-stage small-cell lung cancer is associated with decreased survival

被引:182
作者
Videtic, GMM
Stitt, LW
Dar, AR
Kocha, WI
Tomiak, AT
Truong, PT
Vincent, MD
Yu, EW
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dana Farber Canc Inst,Dept Radiat Oncol, Boston, MA 02115 USA
[2] London Reg Canc Ctr, Dept Biometry, London, ON N6A 4L6, Canada
[3] London Reg Canc Ctr, Dept Radiat Oncol, London, ON N6A 4L6, Canada
[4] London Reg Canc Ctr, Dept Med Oncol, London, ON N6A 4L6, Canada
[5] Kingston Reg Canc Ctr, Dept Med Oncol, Kingston, ON, Canada
[6] British Columbia Canc Agcy, Dept Radiat Oncol, Victoria, BC, Canada
[7] Vancouver Isl Canc Ctr, Victoria, BC, Canada
关键词
D O I
10.1200/JCO.2003.10.089
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To determine the impact of continued smoking by patients receiving chemotherapy (CHT) and radiotherapy (RT) for limited-stage small-cell lung cancer (LSCLC) on toxicity and survival. Patients and Methods: A retrospective review was carried out on 215 patients with LSCLC treated between 1989 and 1999. Treatment consisted of six cycles of alternating cyclophosphamide, doxorubicin, vincristine and etoposide, cisplatin (EP). Thoracic RT was concurrent with EP (cycle 2 or 3) only. Patients were known smokers, with their smoking status recorded at the start of chemoradiotherapy (CHT/RT). RT interruption during concurrent CHT/RT was used as the marker for treatment toxicity. Results: Of 215 patients, smoking status was recorded for 186 patients (86.5%), with 79 (42%) continuing to smoke and 107 (58%) abstaining during CHT/RT. RT interruptions were recorded in 38 patients (20.5%), with a median duration of 5 days (range, 1 to 18 days). Median survival for former smokers was greater than for continuing smokers (18 v 13.6 months), with 5-year actuarial overall survival of 8.9% versus 4%, respectively (log-rank P = .0017). Proportion of noncancer deaths was comparable between the two cohorts. Continuing smokers did not have a greater incidence of toxicity-related treatment breaks (P = .49), but those who continued to smoke and also experienced a treatment break had the poorest overall survival (median, 13.4 months; log-rank P = .0014). Conclusion: LSCLC patients who continue to smoke during CHT/RT have poorer survival rates than those who do not. Smoking did not have an impact on the rate of treatment interruptions attributed to toxicity. J Clin Oncol 21:1544-1549. (C) 2003 by American Society of Clinical Oncology.
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页码:1544 / 1549
页数:6
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