Table 2.

Elimination of Primary Tumor Cells Isolated From Patients With Breast Cancer During Culture in the Presence of IT

Patient No.Age (yr)Cell SourceReceptor ExpressionTumor Cell Depletion
Erb-B2EGFRAnti–Erb-B2 ITAnti–EGFR-IT
1  61  Ascites  +  * >99.2%  
2  48  Pleural effusion  +  >99.2%  >99.2%  
3  73  Pleural effusion −  +  —  >99.2%  
4  74  Bone marrow  ND +  —  >99.2%  
5  84  Pleural effusion  +  —  75%  
6  49  Ascites  +  −  66% ND  
7  68  Ascites  +  −  74%  73% 
Patient No.Age (yr)Cell SourceReceptor ExpressionTumor Cell Depletion
Erb-B2EGFRAnti–Erb-B2 ITAnti–EGFR-IT
1  61  Ascites  +  * >99.2%  
2  48  Pleural effusion  +  >99.2%  >99.2%  
3  73  Pleural effusion −  +  —  >99.2%  
4  74  Bone marrow  ND +  —  >99.2%  
5  84  Pleural effusion  +  —  75%  
6  49  Ascites  +  −  66% ND  
7  68  Ascites  +  −  74%  73% 

Tumor cells (>60% purity) were cultured in a-MEM/10% FCS for 7 days in the presence of 1,000 ng/mL ITs as described in Materials and Methods. Tumor cells were quantitated by immunohistochemical staining with anticytokeratin antibodies.

Abbreviations: EGFR, EGF receptor; +, receptor expression detectable by Western blot; −, receptor expression undetectable by Western blot; ND, not determined.

*

—, No response detected. Percent values represent the percent depletion of cytokeratin-positive cells in treated cultures compared with untreated control cultures.

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