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Pathologic features from prostate needle biopsy and prognosis after I-125 brachytherapy
1Department of Radiation Oncology, Memorial Sloan-Kettering Cancer Center, New York, New York, USA.
Radiation Oncology Investigations
|September 4, 1998
Summary
Pretreatment prostate-specific antigen (PSA) levels are the strongest predictor of biochemical failure in early-stage prostate cancer treated with I-125 brachytherapy. Detailed pathology from biopsies offers minimal additional prognostic value.
Area of Science:
- Urology
- Oncology
- Pathology
Background:
- Early-stage prostate cancer treatment often involves I-125 brachytherapy.
- Predicting treatment outcomes is crucial for patient management.
- The role of detailed pathological features in predicting outcomes requires further evaluation.
Purpose of the Study:
- To assess the prognostic value of detailed pathological features on biopsy for predicting outcomes in early-stage prostate cancer patients treated with I-125 brachytherapy.
- To correlate biochemical tumor control rates with pretreatment PSA, Gleason score, tumor volume on biopsy, and perineural invasion.
Main Methods:
- Retrospective review of biopsy slides from 103 patients with T1/T2 prostate cancer and Gleason scores of 4-7 treated with transperineal I-125 implantation.
- Multivariate Cox proportional-hazard analysis was used to identify predictors of biochemical failure (PSA < 1.0 ng/ml).
Main Results:
- Pretreatment PSA > 10 ng/ml was the strongest predictor of biochemical failure (P = 0.013).
- The length of biopsy specimen replaced by tumor showed borderline significance (P = 0.15).
- Gleason score, percent of biopsy tissue replaced by tumor, and perineural invasion were not significant predictors of prognosis.
Conclusions:
- Pretreatment PSA is the most significant predictor of biochemical failure in this patient cohort.
- Detailed pathological assessment of needle biopsies provides limited additional prognostic information beyond pretreatment PSA.
- Significant overlap exists in pathological features among patients with varying biochemical control outcomes.