Prognostic significance of three novel biologic factors in a clinical trial of adjuvant therapy for node-negative breast cancer

Surgery. 1995 Jun;117(6):601-8. doi: 10.1016/s0039-6060(95)80001-8.

Abstract

Background: Five products of human breast carcinoma cells, including membrane-associated phospholipase A2 (M-PLA2), polymorphonuclear leukocyte elastase (PMN-E), tissue-type plasminogen activator (t-PA), urokinase-type plasminogen activator (u-PA), and endothelin-1 (ET-1), have been implicated in the processes of tumor cell invasion and metastasis in human breast carcinoma. However, the prognostic significance of these factors has not been assessed previously in node-negative breast carcinoma, in which adjuvant treatment is dependent on risk stratification.

Methods: The five products of breast carcinoma cells were measured in 184 patients with node-negative breast carcinoma who were enrolled in the Kumamoto Adjuvant Chemo-Endocrine Therapy for Breast Cancer prospective randomized trial, and the predictive values of these factors for relapse-free and overall survival were evaluated.

Results: M-PLA2, PMN-E, and t-PA were found to be significant independent predictors of relapse-free and overall survival, whereas u-PA and ET-1 were not independently predictive. Further statistical analyses showed that the predictive powers of M-PLA2, PMN-E, and t-PA were additive. A combination of these three factors identified a group of patients (approximately 50% of those who manifested node-negative breast carcinoma) with a favorable prognosis, regardless of the administration of adjuvant therapy.

Conclusions: This study identified three biologic factors that are valuable predictors of survival in node-negative breast carcinoma. A combination of these biologic factors may allow identification of low-risk patients who could be spared adjuvant therapy.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Breast Neoplasms / chemistry*
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / pathology
  • Carcinoma / chemistry*
  • Carcinoma / drug therapy*
  • Carcinoma / pathology
  • Chemotherapy, Adjuvant
  • Disease-Free Survival
  • Endothelins / analysis
  • Female
  • Follow-Up Studies
  • Humans
  • Leukocyte Elastase
  • Mastectomy, Modified Radical
  • Mastectomy, Radical
  • Neoplasm Staging
  • Pancreatic Elastase / analysis*
  • Phospholipases A / analysis*
  • Phospholipases A2
  • Prognosis
  • Prospective Studies
  • Risk Factors
  • Survival Rate
  • Tamoxifen / therapeutic use
  • Tissue Plasminogen Activator / analysis*
  • Urokinase-Type Plasminogen Activator / analysis

Substances

  • Endothelins
  • Tamoxifen
  • Phospholipases A
  • Phospholipases A2
  • Pancreatic Elastase
  • Leukocyte Elastase
  • Tissue Plasminogen Activator
  • Urokinase-Type Plasminogen Activator