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1 with HIV infection have an elevated risk of anal cancer.
2 PV) 16 and 18 infections cause most cases of anal cancer.
3 y profile and may help to reduce the risk of anal cancer.
4 ce of anal HPV infections that contribute to anal cancer.
5 IV-1)-infected men are at increased risk for anal cancer.
6 ffect on local failure and colostomy rate in anal cancer.
7 usses the issues around screening to prevent anal cancer.
8 oplasia treatment to reduce the incidence of anal cancer.
9 als and recent studies on chemoradiation for anal cancer.
10 of intensity modulated radiation therapy for anal cancer.
11 icant role during posttreatment follow-up of anal cancer.
12 al adenocarcinoma, oropharyngeal cancer, and anal cancer.
13 vaccination and decrease in lifetime risk of anal cancer.
14 lysis to highlight discrepancies relevant to anal cancer.
15 life years, and lifetime risk of developing anal cancer.
16 used to record adverse events using PROs for anal cancer.
17 g men who have sex with men (MSM) and causes anal cancer.
18 -HPV infections, consistent with its role in anal cancer.
19 ximately 6-7 years prior to the diagnosis of anal cancer.
20 me a useful diagnostic tool in patients with anal cancer.
21 ablished prognostic factors in patients with anal cancer.
22 ponse evaluation after chemoradiotherapy for anal cancer.
23 o 90% of anal intraepithelial neoplasias and anal cancers.
24 maviruses (HPVs) cause a large proportion of anal cancers.
25 , 4.5% and 0.7%; lung cancer, 3.4% and 2.8%; anal cancer, 1.5% and 0.05%; colorectal cancer, 1.0% and
27 te ratios of 3.85 (95% CI, 2.32 to 6.37) for anal cancer, 6.68 (95% CI, 3.64 to 12.25) for anal intra
31 esent the results of a case-control study of anal cancer among HIV-infected people in Switzerland.
34 ssary to identify men at the highest risk of anal cancer among those infected with high-risk HPV.
35 good accuracy in posttreatment evaluation of anal cancer and has a relevant impact on patient managem
39 study strengthens evidence that lung cancer, anal cancer, and myeloma are diagnosed at modestly young
40 ar, no history of genital warts or penile or anal cancer, and no current diagnosis of a sexually tran
41 esophageal, cervical, prostate, and possibly anal cancers; and since the 1990s for bone/joint and end
44 llomavirus (HPV) is causally associated with anal cancer, as HPV DNA is detected in up to 90% of anal
45 ity is relatively common before diagnosis of anal cancer but rare for other HPV-related anogenital ca
46 tant at an early stage of the development of anal cancer, but that the neoplastic process becomes irr
48 high-grade anal intraepithelial neoplasia or anal cancer by history or by screening cytology or histo
52 igh-resolution anoscopy-guided ablation) and anal cancer (chemoradiation and possibly intensity-modul
53 seven of 24 individuals) who later developed anal cancer compared with 0.6% of controls (four of 718
55 appeared to be strongest 6-7 years prior to anal cancer diagnosis (OR for <200 vs. >/=500 cells/muL
58 us (HIV)-infected women are at high risk for anal cancer, few data have been published on prevalence
61 Recent studies show that the incidence of anal cancer has increased since the introduction of high
62 with increased cancer-specific mortality for anal cancer, Hodgkin lymphoma, or diffuse large B-cell l
63 an papillomavirus-related cancers, including anal cancer (HR, 2.77; 95% CI, 1.29-5.96) and female gen
64 ention of human papillomavirus (HPV)-induced anal cancer in high-risk populations such as human immun
65 Treatment options for anal dysplasia and anal cancer in HIV-infected individuals are expanding an
66 that in the general population, the risk of anal cancer in HIV-infected patients is still extremely
71 te intensity modulated radiation therapy for anal cancer, in an effort to reduce acute and long-term
72 ulation, used Poisson regression to evaluate anal cancer incidence among subgroups of people with HIV
74 ted standardized incidence ratios to compare anal cancer incidence in people with HIV infection with
77 follow-up between 1996 and 2007, we compared anal cancer incidence rates among 34 189 HIV-infected (5
80 lts Among 447,953 people with HIV infection, anal cancer incidence was much higher than in the genera
83 lications in the areas of colon, rectal, and anal cancers; inflammatory bowel disease; incontinence;
84 e of PVOD in the French population that have anal cancer is 3.9 of 1000 patients, which is much highe
89 infections are common, and the incidence of anal cancer is high in HIV-infected men who have sex wit
94 he use of MMC in a definitive CR regimen for anal cancer is justified, particularly in patients with
99 es occurring in the HIV-positive population, anal cancer is potentially preventable, using methods si
100 omavirus (HPV), primarily HPV type 16 or 18, anal cancer is preceded by high-grade anal intraepitheli
101 incidence of human papillomavirus-associated anal cancer is unacceptably high among HIV-positive men
102 ho have sex with men, are at excess risk for anal cancer, it has been difficult to disentangle the in
103 continue to have high rates of cervical and anal cancer, it is important to continue screening effor
104 ncies, some related to known infections (eg, anal cancer, Kaposi sarcoma) and others unrelated (eg, m
106 gnosis of lung (median, 50 vs. 54 years) and anal cancer (median, 42 vs. 45 years) were significantly
107 nt smoking was significantly associated with anal cancer (odds ratio (OR) = 2.59, 95% confidence inte
111 drivalent HPV vaccine (qHPV) reduces risk of anal cancer/precancerous lesions in young men who have s
122 vention of anal intraepithelial neoplasia or anal cancer related to infection with HPV-6, 11, 16, or
125 human papillomavirus type 16 protein E6 and anal cancer risk, highlighting the role of this viral on
127 pational exposure of healthcare workers; (5) anal cancer screening among men who have sex with men (M
128 ers could help refine clinical approaches to anal cancer screening and prevention for the HIV-infecte
129 All HIV-infected adults should be offered anal cancer screening as part of clinical care at specia
130 ological study to evaluate whether access to anal cancer screening programs may help improve patient
133 Data are insufficient to recommend routine anal cancer screening with anal cytology in persons livi
137 o -1.86; P < .001), whereas the incidence of anal cancer significantly increased (APC, 4.42; 95% CI,
138 to use in clinical research and practice for anal cancer since no questionnaire specific for anal can
139 o reduction in the incidence of cervical and anal cancer since the introduction of highly active anti
140 and substantially elevated risks for second anal cancer (SIR = 120.50) and Kaposi's sarcoma (SIR = 1
142 d cancer survival time with HAART use, while anal cancer survival may have been slightly decreased (R
143 consequence of staging misclassification in anal cancer that we have termed reduced prognostic discr
145 The results of our trial--the largest in anal cancer to date--show that fluorouracil and mitomyci
147 e in longitudinal follow-up of patients with anal cancer treated with (chemo)radiation, the EORTC-QLQ
148 etabolic tumor volume (MTV) in patients with anal cancer treated with definitive chemoradiotherapy.
150 other HPV-related cancers (e.g. cervical and anal cancer), trends over time do not appear to be influ
151 clear, although an ongoing randomized trial (Anal Cancer Trial II) may help clarify the role of cispl
154 In the USA, more than 7200 new cases of anal cancer were diagnosed in 2014 with incidence rising
156 ly been questioned, while the association of anal cancer with AIDS in both males and females is more
157 the general population had an excess risk of anal cancer, with SIRs of 109.8 (95% CI, 84.6 to 140.3),
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