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. 2013 Jul 18;109(4):1072–1078. doi: 10.1038/bjc.2013.389

Table 1. Patient characteristics.

  All patients
 
N=87 (%/range)
Median age
56 (27–80)
Tumour type
Ovarian epithelial 80 (92.0)
Fallopian tube 2 (2.3)
Primary peritoneal
5 (5.7)
Stage
II 5 (5.7)
III 48(55.2)
IV
34 (39.1)
BRCA mutation statusa
BRCA1 44 (50.6)
BRCA2 12 (13.8)
Any BRCA mutation 56 (64.4)
Negative
31 (35.6)
History of allergy to medications, environmental factors, foods, and type IV contrast
44 (50.6)
Median platinum-free interval in months
15.9 (5.7–82.4)
Median number of prior carboplatin regimens
2 (0–6)
Median number of prior carboplatin cycles
9 (0–42)
Median number of prior platinum regimensb
2 (1–6)
Median number of prior platinum cyclesb 12 (2–42)
a

One patient had both BRCA1 and 2 mutation and is counted once in ‘any BRCA mutation' cohort; one patient had a BRCAPro of 68% and is counted in ‘any BRCA mutation' cohort, but not in either of ‘BRCA1' or ‘BRCA2' cohorts.

b

Includes both carboplatin and cisplatin chemotherapy. One patient received 3 months of oxaliplatin/gemcitabine/cyclophosphamide therapy before enrolment of our trial, but details were not available and excluded from the total platinum calculations.