Human papillomavirus and prognosis of invasive cervical cancer: A population-based study

被引:121
作者
Schwartz, SM
Daling, JR
Shera, KA
Madeleine, MM
McKnight, B
Galloway, DA
Porter, PL
McDougall, JK
机构
[1] Fred Hutchinson Canc Res Ctr, Epidemiol & Biostat Program, Div Publ Hlth Sci, Seattle, WA 98109 USA
[2] Fred Hutchinson Canc Res Ctr, Program Canc Biol, Div Human Biol, Seattle, WA 98109 USA
[3] Univ Washington, Sch Publ Hlth & Community Med, Dept Biostat, Seattle, WA USA
[4] Univ Washington, Sch Publ Hlth & Community Med, Dept Epidemiol, Seattle, WA USA
[5] Univ Washington, Sch Med, Dept Microbiol, Seattle, WA USA
[6] Univ Washington, Sch Med, Dept Pathol, Seattle, WA USA
关键词
D O I
10.1200/JCO.2001.19.7.1906
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To determine the association between human papillomavirus (HPV) type and prognosis of patients with invasive cervical carcinoma. Patients and Methods: patients diagnosed with International Federation of Gynecology and Obstetrics (FIGO) stage IB to IV cervical cancer between 1986 and 1997 while residents of three Washington State counties were included (n = 399). HPV typing was performed on paraffin-embedded tumor tissue using polymerase chain reaction methods. Patients were observed for a median of 50.8 months. Total mortality (TM) and cervical cancer-specific mortality (CCSM) were determined. Hazards ratios (HR) adjusted for age, stage, and histologic type were estimated using multivariable models. Results: Eighty-six patients held HPV 18-related tumors and 210 patients had HPV 16-related tumors. Cumulative TM among patients with HPV 18-related tumors and among patients with HPV 16-related tumors were 33.7% and 27.6%, respectively; cumulative CCSM in these two groups were 26.7% and 18.1%, respectively. Compared with patients with HPV 16-related cancers, patients with HPV 18-related cancers were at increased risk for TM (HRTM, 2.2; 95% confidence interval [CI], 1.3 to 3.6) and CCSM (HRCCSM, 2.5; 95% CI, 1.4 to 4.4). The HPV18 associations were strongest for patients with FIGO stage IB or IIA disease (HRTM, 3.1; 95% CI, 2.3 to 4.2; and HRCCSM 5.8; 95% CI, 3.9 to 8.7), whereas no associations were observed among patients with FIGO stage IIB to IV disease. Virtually identical associations were found in the subset of patients with squamous cell carcinoma (n = 219). Conclusion: HPV 18-related cervical carcinomas, particularly those diagnosed at an early stage, are associated with a poor prognosis. Elucidating the mechanism or mechanisms underlying this association could lead to new treatment approaches for patients with invasive cervical carcinoma. (C) 2001 by American Society of Clinical Oncology.
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页码:1906 / 1915
页数:10
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