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Showing papers by "Matthew P. Fox published in 2006"


Journal ArticleDOI
TL;DR: Five years of tamoxifen confers a significant benefit beyond 1–2 years of tamxifen, so physicians should ask patients about side effects, other prescriptions, and beliefs about tamoxIFen and should educate them about the benefits of completing adjuvant therapy.
Abstract: To estimate the proportion of older women who fail to complete 5 years of tamoxifen therapy and to identify predictors of non-adherence. We followed 462 women 65-years-old or older with stage I–IIIA breast cancer diagnosed in four US regions between 1996 and 1999 and who initiated tamoxifen therapy. We interviewed patients annually to assess tamoxifen adherence and collected information about predictors of adherence by medical record review, patient interview, and physician questionnaire. Thirty-one percent of patients who started tamoxifen failed to complete the recommended 5-year course. Patients who had initial severe side effects [hazard ratio (HR) per side effect=1.2, 95% confidence interval (CI) 0.97, 1.5] or developed them (HR per new side effect=1.3, 95% CI 1.0, 1.6) were more likely to discontinue. Patients with more prescription medications at baseline were less likely to discontinue (HR per baseline prescription equaled 0.90, 95% CI 0.81, 0.99), whereas patients who added a prescription were more likely to discontinue (HR per new prescription equaled 1.2, 95% CI 1.0, 1.4). Patients with positive views of tamoxifen at baseline (HR for a 10-point higher score=0.93, 95% CI 0.83, 1.0) and an improving view over follow-up (HR for a 10-point positive change=0.93, 95% CI 0.87, 1.0) were less likely to discontinue. Five years of tamoxifen confers a significant benefit beyond 1–2 years of tamoxifen, so physicians should ask patients about side effects, other prescriptions, and beliefs about tamoxifen and should educate them about the benefits of completing adjuvant therapy.

317 citations


Journal ArticleDOI
TL;DR: HIV-infected children with severe pneumonia fail WHO-standard treatment with parenteral penicillin or amoxicillin at day 2 and day 14 more often than do HIV-un Infected children, especially young infants.
Abstract: Objective To determine whether children aged 3–59 months with mild or non-symptomatic human immunodeficiency virus (HIV) infection and WHO-defined severe pneumonia have a higher failure rate than do HIV-uninfected children when treated with the standard WHO treatment of parenteral penicillin or oral amoxicillin. Methods This study was a planned sub-analysis of a randomized trial of 3–59-month-old children presenting with WHO-defined severe pneumonia (the APPIS study). We included two sites with high HIV prevalence in Durban, South Africa and Ndola, Zambia. Primary outcome measures were clinical treatment failure at day 2 and day 14. ClinicalTrials.gov identifier: CT00227331http://www.clinicaltrialsgov/show/NCT00227331). Findings Of the 523 children enrolled, HIV status was known for 464 participants; 106 (23%) of these were infected with HIV. By day 2, 57 (12.3%) children had failed treatment and 110 (23.7%) failed by day 14. Twenty (18.9%) HIV-infected children failed by day 2 compared with 37 (10.3%) uninfected children (adjusted odds ratio (OR) 2.07; 95% confidence interval (CI): 1.07–4.00). Thirty-four (32.1%) HIV-infected children failed treatment by day 14 compared with 76 (21.2%) uninfected children (adjusted OR 1.88; 95% CI: 1.11–3.17). Analysis stratified by age showed that the greatest differential in treatment failure at day 2 and day 14 occurred in the children aged 3–5 months. Conclusions HIV-infected children with severe pneumonia fail WHO-standard treatment with parenteral penicillin or amoxicillin at day 2 and day 14 more often than do HIV-uninfected children, especially young infants. Standard case management of acute respiratory infection (ARI) using WHO treatment guidelines is inadequate in areas of high HIV prevalence and reappraisal of empiric antimicrobial therapy is urgently needed for severe pneumonia associated with HIV-1.

45 citations


Journal ArticleDOI
TL;DR: The mortality rate declined with an increasing number of mammograms, and results are consistent with a protective effect of regular surveillance mammography after completing therapy for early stage breast cancer.
Abstract: Guidelines have been developed for appropriate posttherapy surveillance for breast cancer recurrence. One purpose of posttherapy surveillance is to detect potentially curable local recurrences and new cancers in the opposite breast. The objective of this investigation was to assess the impact of annual mammography on all-cause mortality in breast cancer survivors. We conducted a case-control analysis nested in a cohort of 865 stage I or II breast cancer patients diagnosed from 1996 to 1999. The exposure variable was the number of mammograms received after completing primary therapy. Cases were decedents and we used risk-set sampling to match eight controls to each case on follow-up time. The mortality rate declined with an increasing number of mammograms (p for trend=0.007). The age- and therapy-adjusted odds ratio associating receipt of an additional mammogram, compared with receipt of no mammogram, equaled 0.77 (95% confidence interval [CI] 0.53-1.1). These results are consistent with a protective effect of regular surveillance mammography after completing therapy for early stage breast cancer.

39 citations


Journal ArticleDOI
TL;DR: Design methods for equivalency trials that can substantially increase confidence in claims of equivalence are explored, including how, with commonly used methods, antibiotic equivalency Trials often show that 2 drugs are equivalent when strong differences truly exist.

6 citations



Journal ArticleDOI
TL;DR: Doll R, Peto R. The causes of cancer, case-control studies, and statistical methods in cancer research: A systematic review and meta-analysis.
Abstract: Doll R, Peto R. The causes of cancer. J Nat Cancer Inst 1981;66:1192–312. (see p. 1218). 8 Breslow NE, Day NE. Statistical methods in cancer research. Volume I. The analysis of case-control studies. Publication No. 32 Lyon: International Agency for Research on Cancer, 1980. 9 Mark DM. Deaths attributable to obesity. JAMA 2005;293:1918–19. 10 Parker-Pope T. Trials and errors: In the study of Women’s Health, design flaws raise questions. The Wall Street Journal. February 28, 2006. p. A1. 11 Statistical clinical trials ready for the scrap heap. Letters. The Wall Street Journal. March 13, 2006. p. A19. 12 Gori GB. Considerations on guidelines of good epidemiologic practice. Ann Epidemiol 2002;12:73–8. 13 Feinleib M. New directions for community intervention studies. AJPH 1997;86:1696–8.

1 citations