The use of artificial intelligence technology to predict lymph node spread in men with clinically localized prostate carcinoma

Cancer. 2000 May 1;88(9):2105-9. doi: 10.1002/(sici)1097-0142(20000501)88:9<2105::aid-cncr16>3.0.co;2-3.

Abstract

Background: The current study assesses artificial intelligence methods to identify prostate carcinoma patients at low risk for lymph node spread. If patients can be assigned accurately to a low risk group, unnecessary lymph node dissections can be avoided, thereby reducing morbidity and costs.

Methods: A rule-derivation technology for simple decision-tree analysis was trained and validated using patient data from a large database (4,133 patients) to derive low risk cutoff values for Gleason sum and prostate specific antigen (PSA) level. An empiric analysis was used to derive a low risk cutoff value for clinical TNM stage. These cutoff values then were applied to 2 additional, smaller databases (227 and 330 patients, respectively) from separate institutions.

Results: The decision-tree protocol derived cutoff values of < or = 6 for Gleason sum and < or = 10.6 ng/mL for PSA. The empiric analysis yielded a clinical TNM stage low risk cutoff value of < or = T2a. When these cutoff values were applied to the larger database, 44% of patients were classified as being at low risk for lymph node metastases (0.8% false-negative rate). When the same cutoff values were applied to the smaller databases, between 11 and 43% of patients were classified as low risk with a false-negative rate of between 0.0 and 0.7%.

Conclusions: The results of the current study indicate that a population of prostate carcinoma patients at low risk for lymph node metastases can be identified accurately using a simple decision algorithm that considers preoperative PSA, Gleason sum, and clinical TNM stage. The risk of lymph node metastases in these patients is < or = 1%; therefore, pelvic lymph node dissection may be avoided safely. The implications of these findings in surgical and nonsurgical treatment are significant.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acid Phosphatase / analysis
  • Algorithms
  • Artificial Intelligence*
  • Biopsy, Needle
  • Carcinoma / secondary*
  • Cost Control
  • Databases as Topic
  • Decision Support Techniques
  • Decision Trees
  • False Negative Reactions
  • Humans
  • Lymph Node Excision / adverse effects
  • Lymph Node Excision / economics
  • Lymphatic Metastasis / pathology*
  • Male
  • Neoplasm Staging
  • Prostate-Specific Antigen / analysis
  • Prostatic Neoplasms / pathology*
  • Reproducibility of Results
  • Risk Factors

Substances

  • Acid Phosphatase
  • Prostate-Specific Antigen