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Early PSA decrease is an independent predictive factor of clinical failure and specific survival in patients with localized prostate cancer treated by radiotherapy with or without androgen deprivation therapy
Annals of Oncology, 10/16/09
de Crevoisier R et al. – A PSA decline 6 weeks after the start of EBRT when used as monotherapy and 3 months after the start of ADT in patients treated with combined ADT and EBRT is predictive of progression and specific survival.
Methods- 448 patients with prostate cancer received EBRT alone (n = 361, group 1) or ADT followed by EBRT (n = 87, group 2)
- In group 2, ADT initiated 3 months before EBRT
- After baseline PSA determination (PSApreRT), PSA was assessed during the 6th week of the EBRT course (PSA6wRT) in group 1
- In group 2, PSA measured again 3 months after start of ADT, before EBRT (PSAADT-preRT)
- In group 1, median PSA6wRT/PSApreRT 0.72 and median prostate-specific antigen velocity (PSAV) was –1.5 ng/ml/month.
- In multivariate analysis, prognostic groups and PSA6wRT/PSApreRT (or PSAV) independently predicted biochemical failure (BF), clinical failure (CF), and prostate cancer-specific survival
- In group 2, the median PSAADT-preRT was 1.3 ng/ml
- In high-risk group, an undetectable PSAADT-preRT (0.2 ng/ml) predicted BF and CF
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Lymphoma in patients treated with anti-TNF. Results of the 3-year prospective French RATIO registry.
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Activity of fulvestrant in HER2-overexpressing advanced breast cancer
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Risk of dying from prostate cancer in men randomized to screening
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Randomized phase III trial on gemcitabine versus mytomicin in recurrent superficial bladder cancer: Evaluation of efficacy and tolerance
Journal of Clinical Oncology, 10/22/09
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Cancer, 11/03/09
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