Literature DB >> 8197775

Integration of risk factors to allow patient selection for adjuvant systemic therapy in lymph node-negative breast cancer patients.

W C Wood1.   

Abstract

The selection of patients with axillary lymph node-negative breast cancer who should receive adjuvant therapy today is confused by an expanding arsenal of putative prognostic factors. The size of the primary tumor remains the dominant factor in sorting among this group of patients, with general agreement that tumors 1 cm or less should be spared adjuvant systemic therapy outside of a clinical trial. There are a few favorable histologic subgroups that may be added to this excluded group: ductal carcinoma in situ and pure tubular, papillary, and typical medullary tumors. For the larger tumor (generally > 2 cm in diameter, but always > 3 cm), there is little disagreement that adjuvant therapy is indicated. The host of additional prognostic factors are directed mainly toward the group of tumors that fall between these two categories. Nuclear grade, S-phase, and perhaps p53 mutations influence decisions for treatment by their elevation. Although the decision remains with the patient and the recommendation with the mature judgment of the clinician, the prognostic indicators available continue to multiply. That an indicator can retrospectively sort prognosis is of limited interest. It requires prospective validation in another patient population, reproducibility in other laboratories, and multivariate analysis among factors measured on the same population of patients to integrate a factor into clinical decision-making. It is only beginning to be accomplished. The next generation of factors being sought are those that predict for response or lack of response to specific therapies, rather than merely indicating natural history. Estrogen and progesterone receptors are the prototypes of this class of indicators.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 8197775     DOI: 10.1007/bf00348190

Source DB:  PubMed          Journal:  World J Surg        ISSN: 0364-2313            Impact factor:   3.352


  26 in total

1.  Clinical relevance of the urokinase-type and tissue-type plasminogen activators and of their type 1 inhibitor in breast cancer.

Authors:  F Jänicke; M Schmitt; H Graeff
Journal:  Semin Thromb Hemost       Date:  1991-07       Impact factor: 4.180

Review 2.  NIH consensus conference. Treatment of early-stage breast cancer.

Authors: 
Journal:  JAMA       Date:  1991-01-16       Impact factor: 56.272

Review 3.  Steroid receptors, cellular kinetics, and lymph node status as prognostic factors in breast cancer.

Authors:  S E Benner; G M Clark; W L McGuire
Journal:  Am J Med Sci       Date:  1988-07       Impact factor: 2.378

4.  Node-negative breast cancer treated by modified radical mastectomy without adjuvant therapies: variables associated with disease recurrence and survivorship.

Authors:  R A Huseby; H E Ownby; J Frederick; S Brooks; J Russo; M J Brennan
Journal:  J Clin Oncol       Date:  1988-01       Impact factor: 44.544

Review 5.  Immunocytochemical analysis of estrogen receptors in human breast carcinomas. Evaluation of 130 cases and review of the literature regarding concordance with biochemical assay and clinical relevance.

Authors:  D C Allred; M A Bustamante; C O Daniel; H V Gaskill; A B Cruz
Journal:  Arch Surg       Date:  1990-01

6.  Classical prognostic factors in node-negative breast cancer: the DBCG experience.

Authors:  H T Mouridsen; J Andersen; K W Andersen; C Axelsson; M Blichert-Toft; P Dombernowsky; M Hansen; C Krag; M Overgård; B B Rasmussen
Journal:  J Natl Cancer Inst Monogr       Date:  1992

7.  p53 as an independent prognostic marker in lymph node-negative breast cancer patients.

Authors:  R Silvestrini; E Benini; M G Daidone; S Veneroni; P Boracchi; V Cappelletti; G Di Fronzo; U Veronesi
Journal:  J Natl Cancer Inst       Date:  1993-06-16       Impact factor: 13.506

8.  Systemic treatment of early breast cancer by hormonal, cytotoxic, or immune therapy. 133 randomised trials involving 31,000 recurrences and 24,000 deaths among 75,000 women. Early Breast Cancer Trialists' Collaborative Group.

Authors: 
Journal:  Lancet       Date:  1992-01-11       Impact factor: 79.321

9.  Accumulation of p53 tumor suppressor gene protein: an independent marker of prognosis in breast cancers.

Authors:  A D Thor; I I Moore DH; S M Edgerton; E S Kawasaki; E Reihsaus; H T Lynch; J N Marcus; L Schwartz; L C Chen; B H Mayall
Journal:  J Natl Cancer Inst       Date:  1992-06-03       Impact factor: 13.506

10.  Immunocytochemical analysis of estrogen receptors as a predictor of prognosis in breast cancer patients: comparison with quantitative biochemical methods.

Authors:  L B Kinsel; E Szabo; G L Greene; J Konrath; G S Leight; K S McCarty
Journal:  Cancer Res       Date:  1989-02-15       Impact factor: 12.701

View more
  5 in total

1.  Sensitive and reliable PCR and sequencing used to detect p53 point mutations in fine needle aspirates of the breast.

Authors:  G P Howes; J Stephenson; S Humphreys
Journal:  J Clin Pathol       Date:  1996-07       Impact factor: 3.411

2.  Lessons learned from the initial 100 patient experience with sentinel lymph node mapping in the evaluation of breast cancer.

Authors:  G M Fuhrman; E G Burch; G H Farr; T A King; E Farkas; J S Bolton
Journal:  Ochsner J       Date:  2000-01

3.  Ethnicity and birthplace in relation to tumor size and stage in Asian American women with breast cancer.

Authors:  A N Hedeen; E White; V Taylor
Journal:  Am J Public Health       Date:  1999-08       Impact factor: 9.308

4.  Breast cancer size and stage in Hispanic American women, by birthplace: 1992-1995.

Authors:  A N Hedeen; E White
Journal:  Am J Public Health       Date:  2001-01       Impact factor: 9.308

5.  Predicting axillary lymph node metastases in breast carcinoma patients.

Authors:  P L Choong; C J deSilva; H J Dawkins; G F Sterrett; P Robbins; J M Harvey; J Papadimitriou; Y Attikiouzel
Journal:  Breast Cancer Res Treat       Date:  1996       Impact factor: 4.872

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.