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. 2018 Aug 16;35(10):126. doi: 10.1007/s12032-018-1180-x

Table 1.

Patient characteristics, response to sorafenib, and outcome

Pts. nb. Age at diagn. (years) Type of can. Sex Stage at diagn. Nb. sorafenib line therapy CHT parallel to sorafenib Age at sorafenib Length of therapy (days) Best response Time to the best response Toxicity (grades 2–3) Reason for stopping therapy Status at last follow up
1 2.6 ES F Met 1 IFO, TC 4.1 40 PD PD AWD
2 15.7 CHS M Met 4 20.8 56 PR 30 PD DOD
3 19.9 OS F Met 1 VP, IFO 20.5 147 PR 26 Skin Toxicity AWD
4 14.5 OS F Loc 2 21.3 299 PR 66 PD DOD
5 11.0 OS F Loc 6 ADM, GMZ 19.6 214 PR 80 PD DOD
6 18.4 OS M Met 5 27.9 71 PR 35 PD DOD
7 6.7 OS M Met 3 DTIC,VP, CTX 7.6 114 PR 41 PD DOD
8 3.5 CHS M Met 2 VP, CBDCA 4.1 60 PD PD DOD
9 13.6 OS M Met 2 GMZ, DCT 16.2 15 SD 15 Skin Toxicity NED
10 18.5 ES M Met 2 21.9 50 PR 32 PD DOD
11 13.3 OS M Met 1 16.3 13 SD 13 Skin Toxicity NED
12 12.8 OS M Met 1 VP, IFO 13.0 118 PR 69 Surgery DOD

Nb number, ES Ewing sarcoma, OS osteosarcoma, CHS chondrosarcoma, Met metastases, Loc localize, TC topotecan, cyclophosphamide, IFO ifosfamide, GMZ gemcitabine, DCT docetaxel, CTX cyclophosphamide, VP etoposide, ADM adriamycin, DTIC dacarbazine, CBDCA carboplatin, PR partial response, SD stable disease, PD progression disease, DOD death of disease, NED no evidence of disease, AWD alive with disease