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. Author manuscript; available in PMC: 2009 Aug 17.
Published in final edited form as: Cancer. 2008 Dec 1;113(11):3242–3247. doi: 10.1002/cncr.23929

Table 1.

Clinicopathologic Characteristics of Rhabdomyosarcoma With and Without Anaplasia. (IRSG/COG studies – 1995–1998)

Anaplasia
None (n=474) Focal (n=40) Diffuse (n=32)
AGE (YEARS)
 <1 18 3 (14%) -
 1–9 296 19(6%) 26 (8%)
 10+ 157 18(10%) 6 (3%)
 Unknown 3 - -
RACE
 White 333 24 (6%) 23 (6%)
 Non-white 137 16 (10%) 9 (6%)
SEX
 Male 300 26 (8%) 19 (6%)
 Female 174 14 (7%) 13 (7%)
CLINICAL GROUP
 I 86 10 (10%) 10 (10%)
 II 50 7 (12%) 3 (5%)
 III 249 16 (6%) 8 (3%)
 IV 84 7 (7%) 11 (11%)
 Unknown 4 - 1
STAGE
 1 155 20 (11%) 11 (6%)
 2 76 3 (2%) 5 (6%)
 3 158 10 (6%) 5 (3%)
 4 84 7 (7%) 11 (11%)
 Unknown 1 - -
PRIMARY SITE
All Favorable Sites 163 24 (12%) 13 (7%)
 Orbit 49 4 (7%) 3 (5%)
 Head and neck/non-PM 32 4 (11%) 2 (5%)
 GU, non-bladder/prostate 82 16 (15%) 8 (8%)
All Unfavorable Sites 311 16 (5%) 19 (5%)
 Parameningeal 97 2 (2%) 2 (2%)
 Parameningeal extension 11 1 (8%) 0
 Bladder/prostate 49 2 (4%) 2 (4%)
 Extremity 63 4 (5%) 10 (13%)
 Other 91 7 (7%) 5 (5%)
Tumor Invasiveness
 T1 219 21 (8%) 17 (7%)
 T2 247 19 (7%) 15 (5%)
 Unknown 8 - -
Nodal involvement
 N0 351 28 (7%) 25 (6%)
 N1 93 7 (7%) 6 (6%)
 Unknown 30 5 1
Tumor size
 ≤ 5cm 216 19 (7%) 19 (7%)
 > 5 cm 249 21 (7%) 13 (5%)
 Unknown 9 - -