Prediction of early course of breast carcinoma by thymidine labeling

The thymidine labeling index (TLI) was measured in vitro in 278 primary breast carcinomas. In 227 operable women treated by radical mastectomy, TLI's below the median of 4.55% carried a probability of relapse of 20% at four years, in contrast to 52% for TLI's above the median (P = 0.0001). The probability of relapse was significantly related to the TLI independent of TNM pathologic stage, axillary lymph nodal status alone, estrogen receptor (ER) content, or menopausal status. The abilities of the TLI and nodal status to predict early relapse were equally strong and independent, whereas other variables tested had less or no independent predictive capacity. The predictive value of the ER content depended largely on its relationship to the TLI, and ER was related to the probability of relapse in the below median TLI group only. The TLI can select a subgroup of node‐negative patients with a relapse‐expectancy of approximately 50% at four years.

[1]  R. Silvestrini,et al.  Cell proliferation and its relationship to clinical features and relapse in breast cancers , 1981 .

[2]  M. Tubiana,et al.  Kinetic parameters and the course of the disease in breast cancer , 1981, Cancer.

[3]  J. Meyer,et al.  Relationships of S-phase fraction of breast carcinoma in relapse to duration of remission, estrogen receptor content, therapeutic responsiveness, and duration of survival. , 1980, Cancer research.

[4]  J. Meyer,et al.  Advanced stage and early relapse of breast carcinomas associated with high thymidine labeling indices. , 1979, Cancer research.

[5]  M. Daidone,et al.  Relationship between proliferative activity and estrogen receptors in breast cancer , 1979, Cancer.

[6]  J. Meyer,et al.  Estrogen receptor assay of carcinomas of the breast by a simplified dextran--charcoal method. , 1978, American journal of clinical pathology.

[7]  Meyer Js,et al.  Subpopulations of breast carcinoma defined by S-phase fraction, morphology, and estrogen receptor content. , 1978 .

[8]  J. Meyer,et al.  In vitro labeling of solid tissues with tritiated thymidine for autoradiographic detection of S-phase nuclei. , 1977, Stain technology.

[9]  C. Redmond,et al.  L‐phenylalanine mustard (L‐PAM) in the management of primary breast cancer: An update of earlier findings and a comparison with those utilizing L‐PAM plus 5‐fluorouracil (5‐FU) , 1977, Cancer.

[10]  G. Bonadonna,et al.  Combination chemotherapy as an adjuvant treatment in operable breast cancer. , 1976, The New England journal of medicine.

[11]  B. Fisher,et al.  The pathology of invasive breast cancer A Syllabus Derived from Findings of the National Surgical Adjuvant Breast Project (Protocol No. 4) , 1975, Cancer.

[12]  C. Redmond,et al.  1-Phenylalanine mustard (L-PAM) in the management of primary breast cancer. A report of early findings. , 1975, The New England journal of medicine.

[13]  E. Kaplan,et al.  Nonparametric Estimation from Incomplete Observations , 1958 .