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. 2020 Oct 23;5(5):e000860. doi: 10.1136/esmoopen-2020-000860

Table 1.

Patientand treatment characteristics

Characteristic n=338
Age at first ASCT, years
 median (range) (IQR) 37.3 (18.1–69.6) (27.6–49.7)
Histology n %
 Leiomyosarcoma 66 19.5
 Synovial sarcoma 52 15.4
 Angiosarcoma* 40 11.8
 Liposarcoma 34 10.1
 Desmoplastic small round cell tumour 10 3
 other STS† 136 40.2
Tumour grading n %
 Grade 1 4 3.8
 Grade 2 18 17.3
 Grade 3 82 78.8
 missing 234
Remission status before ASCT n %
 Complete response/no evidence of disease 55 20.1
 Partial response 107 39.1
 Stable disease 28 10.2
 Progressive disease 84 30.7
 Missing 64
Year of first ASCT n %
 1996–2000 152 45.0
 2001–2005 111 32.8
 2006–2016 75 22.2
Preparative regimen n %
 PEI/CEI 71 42.5
 Other platinum based 31 18.6
 Melphalan based 42 25.1
 Other 23 13.8
 missing 171
Remission status after last ASCT n %
 Complete response/no evidence of disease 94 58.4
 Partial response 19 11.8
 Stable disease 22 13.7
 Progressive disease 26 16.1
 missing 177

*Including haemangiosarcoma and lymphangiosarcoma.

†Including: fibrosarcoma: n=8, malignant fibrous histiocytoma: n=3, sarcoma NOS: n=2, malignant peripheral nerve sheath tumour: n=2, fibromyxoid sarcoma: n=1, sarcoma not further subclassified: n=120.

ASCT, autologous stem cell transplantation; CEI, Carboplatinum, Etoposide, Ifosfamide; NOS, not otherwise specified; PEI, Cisplatinum, Etoposide, Ifosfamide; STS, soft-tissue sarcoma.