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Uterine Leiomyosarcoma: 14-year Two-center Experience of 31 Cases

Authors
Kim, WY[Kim, Woo Young]Chang, SJ[Chang, Suk-Joon]Chang, KH[Chang, Ki-Hong]Yoon, JH[Yoon, Jong-Hyuck]Kim, JH[Kim, Jang Hee]Kim, BG[Kim, Byoung-Gie]Bae, DS[Bae, Duk-Soo]Ryu, HS[Ryu, Hee-Sug]
Issue Date
Mar-2009
Publisher
KOREAN CANCER ASSOCIATION
Keywords
Stage; Mitotic count; Adjuvant therapy; Prognostic factor
Citation
CANCER RESEARCH AND TREATMENT, v.41, no.1, pp.24 - 28
Indexed
SCIE
KCI
Journal Title
CANCER RESEARCH AND TREATMENT
Volume
41
Number
1
Start Page
24
End Page
28
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/78414
DOI
10.4143/crt.2009.41.1.24
ISSN
1598-2998
Abstract
Purpose The aim of this study was to evaluate the clinicopathological characteristics of uterine leiomyosarcoma (LMS) and possible prognostic factors. Materials and Methods This study included 31 patients with histologically proven LMS at Samsung Medical Center and Ajou University Hospital between 1994 and 2007. The medical records and available histological slides were reviewed retrospectively. Results The median age was 46 years (range, 32 similar to 63). The most common symptom was vaginal bleeding (11 patients, 35.5%). There were 23 patients with stage I, one patient with stage III, seven patients with stage IV disease. The median follow up time was 29 months (range, 1 similar to 94). The most common recurrence site was lung (5 case), followed by pelvis and upper abdomen (2 case). Nine patients died of disease with a 5-year overall survival rate of 63%. Early tumor stage and mitotic count were the prognostic factor in univariate analysis (p<0.0001 and p=0.0031, respectively), but early tumor stage only was associated with prognosis in multivariate analysis (p=0.010 vs p=0.143). Adjuvant treatment for early stage disease did not decrease the recurrence rate (p=0.1075), but high mitotic count (15>10HPF) had a trend for disease recurrence in early stage LMS (p=0.0859). Conclusion Mitotic count less than 15/HPF in early stage may be related with longer progression-free interval, but we could not reach the conclusion that adjuvant therapy in early stage LMS be effective.
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