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. Author manuscript; available in PMC: 2012 Sep 3.
Published in final edited form as: Clin Cancer Res. 2010 Aug 27;16(24):6159–6168. doi: 10.1158/1078-0432.CCR-10-1027

Table 1.

Clinicopathological characteristics of patients and cancers included in study

All patients Patients assessable
for RAD51

n 68 57
Median Age 47 (29-67) 48 (29-67)
Pathology
 IDC 53 45
 ILC 11 9
 Other 2 1
Median tumour size (range mm) 51 (20-110) 53 (21-110)
Grade
 1 1 0
 2 29 25
 3 32 29
Axillary node positive 54% (30/52) 55% (25/45)
ER positive 64% (41/64) 63% (35/55)
HER2 positive 19% (10/52) 18% (9/49)
Menopausal status
 Pre 38 36
 Peri 2 2
 Post 16 14
Chemotherapy
 AC 36 28
 FEC 5 4
 ECisF 14 14
 ECycloF 5 4
 NE 8 7
Tamoxifen 82% (48/58) 79% (43/54)
Clinical response
 CR 12 10
 PR 38 35
 SD 12 7
 PD 3 3
path CR 10% (6/60) 10% (5/49)

Eleven tumours had no proliferation in the post chemotherapy biopsy and were not assessable for RAD51. IDC – Invasive ductal carcinoma; ILC – Invasive lobular carcinoma. Chemotherapy – AC (Doxorubicin, Cyclophosphamide), FEC (Fluorouracil, Epirubicin, Cyclophosphamide), ECisF (Epirubicin, Cisplatin, infusional Fluorouracil), ECycloF (Epirubicin, Cyclophosphamide, infusional Fluorouracil), NE (Navelbine, Epirubuicin) (35, 36). Clinical response; CR – complete response; PR – partial response; SD – stable disease; PD – progressive disease.