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. Author manuscript; available in PMC: 2024 Nov 15.
Published in final edited form as: Clin Cancer Res. 2024 May 15;30(10):2260–2271. doi: 10.1158/1078-0432.CCR-24-0148

Table 1.

Clinicopathologic summary of soft tissue leiomyosarcoma (STLMS)

Clinicopathologic variables All cases N (%) Primary at Presentation N% Univariate P-value* Multivariate P-value*
Total 195 151
Age (years) 0.511
 ≤ 60 110 (56) 86 (57)
 > 60 85 (44) 65 (43)
Sex 0.489
 Female 124 (64) 96 (64)
 Male 71 (46) 55 (36)
Site 0.566
 Retroperitoneal/intraabdominal/pelvic 145 (74) 110 (73)
 Extremity 37 (20) 31 (21)
 Trunk 13 (6) 10 (7)
Size (cm) 0.229
 ≤ 5 49 (26) 46 (31)
 > 5 to ≤ 10 77 (41) 61 (40)
 > 10 64 (33) 44 (29)
Mitotic rate (per 10 HPF) 0.0039 0.0045
 ≤ 10 96 (49) 70 (46)
 > 10 to ≤ 20 60 (31) 51 (34)
 > 20 39 (20) 30 (20)
Necrosis 0.0371 0.2572
 Present 134 (81) 108 (79)
 Absent 31 (19) 29 (21)
 Unknown 30 14
Progression
 Yes – Distant metastasis 171 (88) 127 (84)
 Yes – Local recurrence 5 (3) 5 (3)
 No 19 (9) 19 (13)
Median survival (months)
 Disease-specific survival 80.1 109
 Progression-free survival 26.3
*

DSS analysis among 151 STLMS primary at presentation