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. 2010 Aug 6;3(2):287–293. doi: 10.1159/000318873

Table 1.

Combination chemotherapy in the treatment of aggressive fibromatosis


Study No. of patients Chemotherapeutic agents Response Duration oftherapy Follow-up

Weiss and Lackman 1989 [6] 8 vinblastine and methotrexate 2 CR, 5 PR, ÌMR NR NR

Okuno and Edmonson 2003 [7] 7 cyclophosphamide 600 mg/m2 and doxorubicin 60 mg/m2; mitomycin 8 mg/m2, doxorubicin 40 mg/m2, and cisplatin 60 mg/m2; ifosfamide 2,500 mg/m2 and etoposide 100 mg/m2 Objective disease regression 3 patients, clinical benefit 6 patients 3–12 months 2–8 cycles 3 months-15 years

Patel et al. 1993 [8] 9 doxorubicin 60–90 mg/m2 and dacarbazine 750–1,000 mg/m2 2 CR, 4 PR, 1 MR, 2 SD 5 cycles 28–253 months

Gega et al. 2006 [9] 7 doxorubicin 20 mg/m2 daily and dacarbazine 150 mg/m2 followed by meloxicam 10 mg/m2 3 CR 4 cycles NR

Azzarelli et al. 2001 [10] 30 methotrexate 30 mg/m2 and vinblastine 6 mg/m2 12 PR, 18 SD 38 cycles 6–96 months

Tsukada et al. 1991 [11] 8 adriamycin 50 mg/m2 and cyclophosphamide 250 mg/m2 and vincristine 2 mg/m2 and 5-FU 275 mg/m2; adriamycin 50 mg/m2 and cyclophosphamide 250 mg/m2 and dacarbazine 250 mg/m2 or actinomycin D 2 CR, 1 PR NR NR
Weiss et al. 1999 [15] 17 methotrexate 50 mg parenterally once a week and vinorelbine 20 mg/m2 weekly 3 CR, 7 PR, 2 MR, 3 SD, 2 PD NR NR

Response evaluation according to Response Evaluation Criteria in Solid Tumours (RECIST): CR = complete response; PR = partial response; SD = stable disease; MR = minor response; PD = progressive disease; NR = not reported