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. 2011 Oct 20;9:179. doi: 10.1186/1479-5876-9-179

Table 4.

Proportion of symptomatic TEs according to the type of chemotherapy regimen

% (n/N) (95% CI)
Thromboembolic events Nadroparin Placebo Relative risk

Overall PROTECHT population 2 (15/769) 3.9 (15/381) 0.5 (0.24-1.00)
Chemotherapy regimen containing:
 5-Fluorouracil 2.5 (7/285) 3.3 (5/151) 0.74 (0.24-2.30)
 Cisplatin 2.3 (4/177) 7.0 (6/86) 0.32 (0.09-1.12)
 Gemcitabine 2.6 (4/156) 8.1 (7/86) 0.32 (0.09-1.05)
 Oxaliplatin 0.7 (1/143) 1.1 (1/89) 0.62 (0.04-9.83)
 Docetaxel 1.4 (2/142) 4.5 (3/67) 0.31 (0.05-1.84)
 Carboplatin 0.8 (1/119) 5.5 (3/55) 0.15 (0.02-1.45)
 Epirubicin 0.0 (0/54) 8.3 (2/24) ND
 Adriamycin 0.0 (0/25) 5.3 (1/19) ND
 Irinotecan 3.1 (3/96) 0.0 (0/41) ND
 Vinca alkaloids 2.2 (2/90) 3.7 (1/27) 0.60 (0.06-6.36)
 Capecitabine 0.0 (0/61) 3.3 (1/30) ND
 Etoposide 2.4 (1/41) 11.8 (2/17) 0.21 (0.02-2.14)
 Cyclophosphamide 0.0 (0/33) 5.6 (1/18) ND
Previous Chemotherapy
 Naïve 2.5 (10/405) 5.2 (11/213) 0.48 (0.21-1.11)
 Non-naïve 1.4 (5/364) 2.4 (4/168) 0.58 (0.16-2.12)

No TE events were observed among patients receiving trastuzumab, cetuximab, bevacizumab, liposomal doxorubicin or mitomycin. Abbreviation: ND, not determinable.