TY - JOUR
T1 - Influence of tumor size on outcomes following pelvic exenteration
AU - Smith, B.
AU - Jones, E. L.
AU - Kitano, M.
AU - Gleisner, A. L.
AU - Lyell, N. J.
AU - Cheng, G.
AU - McCarter, M. D.
AU - Abdel-Misih, S.
AU - Backes, F. J.
N1 - Publisher Copyright:
© 2017 Elsevier Inc.
PY - 2017/11
Y1 - 2017/11
N2 - Objective Pelvic exenteration (PE) is often the only curative option for locally advanced or recurrent pelvic malignancies. Despite radical surgery, recurrence risk and morbidity remain high. In this study, we sought to determine tumor size effect on perioperative outcomes and subsequent survival in patients undergoing PE. Methods Retrospective chart review was performed for female patients who underwent PE at two comprehensive cancer centers from 2000 to 2015. Demographics, complications and outcomes were recorded. Statistical analyses were performed using chi-square, student's t-test, logistic regression, non-parametric tests, log-rank test, and Cox proportional hazards. Results Of 151 women who underwent PE, 144 had available pathologic tumor size. Gynecologic oncology, surgical oncology, and urology performed 84, 29, and 31 exenterations, respectively. Tumor dimensions ranged from 0 to 25.5 cm. Perioperative complications, 30-day mortality, reoperation, and readmission rates were not associated with tumor size. Obesity and prior radiation increased risk for major perioperative complication while anterior exenterations decreased risk. Larger tumors were more likely to undergo total pelvic exenteration (OR 1.14; 95%CI 1.03–1.27), have positive margins (OR 1.11; 95%CI 1.02–1.22), and recur (65%, 42% and 20% for tumors > 4 cm, ≤ 4 cm and no residual tumor respectively, p = 0.016). Tumor size > 4 cm and positive margins were associated with worse overall survival amongst gynecologic oncology patients. Conclusion Tumor size was not associated with perioperative morbidity. Larger tumors were associated with positive margins, more extensive resection, and worse survival in gynecologic oncology patients. Larger studies are needed to further understand tumor size impact on PE outcomes within specific tumor types.
AB - Objective Pelvic exenteration (PE) is often the only curative option for locally advanced or recurrent pelvic malignancies. Despite radical surgery, recurrence risk and morbidity remain high. In this study, we sought to determine tumor size effect on perioperative outcomes and subsequent survival in patients undergoing PE. Methods Retrospective chart review was performed for female patients who underwent PE at two comprehensive cancer centers from 2000 to 2015. Demographics, complications and outcomes were recorded. Statistical analyses were performed using chi-square, student's t-test, logistic regression, non-parametric tests, log-rank test, and Cox proportional hazards. Results Of 151 women who underwent PE, 144 had available pathologic tumor size. Gynecologic oncology, surgical oncology, and urology performed 84, 29, and 31 exenterations, respectively. Tumor dimensions ranged from 0 to 25.5 cm. Perioperative complications, 30-day mortality, reoperation, and readmission rates were not associated with tumor size. Obesity and prior radiation increased risk for major perioperative complication while anterior exenterations decreased risk. Larger tumors were more likely to undergo total pelvic exenteration (OR 1.14; 95%CI 1.03–1.27), have positive margins (OR 1.11; 95%CI 1.02–1.22), and recur (65%, 42% and 20% for tumors > 4 cm, ≤ 4 cm and no residual tumor respectively, p = 0.016). Tumor size > 4 cm and positive margins were associated with worse overall survival amongst gynecologic oncology patients. Conclusion Tumor size was not associated with perioperative morbidity. Larger tumors were associated with positive margins, more extensive resection, and worse survival in gynecologic oncology patients. Larger studies are needed to further understand tumor size impact on PE outcomes within specific tumor types.
KW - Pelvic exenteration
KW - Perioperative morbidity
KW - Tumor size
UR - http://www.scopus.com/inward/record.url?scp=85027407156&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85027407156&partnerID=8YFLogxK
U2 - 10.1016/j.ygyno.2017.08.014
DO - 10.1016/j.ygyno.2017.08.014
M3 - Article
C2 - 28822555
AN - SCOPUS:85027407156
SN - 0090-8258
VL - 147
SP - 345
EP - 350
JO - Gynecologic Oncology
JF - Gynecologic Oncology
IS - 2
ER -