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Could the long-term oncological safety of laparoscopic surgery in low-risk endometrial cancer also be valid for the high–intermediate-and high-risk patients? a multi-center Turkish gynecologic oncology group study conducted with 2745 endometrial cancer cases. (TRSGO-end-001)

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SCHOOL OF MEDICINE
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Vardar, Mehmet Ali
Güzel, Ahmet Barış
Taşkın, Salih
Güngör, Mete
Özgül, Nejat
Salman, Coşkun
Küçükgöz-Güleç, Ümran
Khatib, Ghanim
Duender, Ilkkan
Ortaç, Fırat

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Abstract

This study was conducted to compare the long-term oncological outcomes of laparotomy and laparoscopic surgeries in endometrial cancer under the light of the 2016 ESMO-ESGO-ESTRO risk classification system, with particular focus on the high–intermediate-and high-risk categories. Using multicentric databases between January 2005 and January 2016, disease-free and overall survivals of 2745 endometrial cancer cases were compared according to the surgery route (laparotomy vs. laparoscopy). The high–intermediate-and high-risk patients were defined with respect to the 2016 ESMO-ESGO-ESTRO risk classification system, and they were analyzed with respect to differences in survival rates. Of the 2745 patients, 1743 (63.5%) were operated by laparotomy, and the remaining were operated with laparoscopy. The total numbers of high–intermediate- and high-risk endometrial cancer cases were 734 (45%) patients in the laparotomy group and 307 (30.7%) patients in the laparoscopy group. Disease-free and overall survivals were not statistically different when compared between laparoscopy and laparotomy groups in terms of low-, intermediate-, high–intermediateand high-risk endometrial cancer. In conclusion, regardless of the endometrial cancer risk category, long-term oncological outcomes of the laparoscopic approach were found to be comparable to those treated with laparotomy. Our results are encouraging to consider laparoscopic surgery for high–intermediate- and high-risk endometrial cancer cases.

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Multidisciplinary Digital Publishing Institute (MDPI)

Subject

Oncology

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Has Part

Source

Current Oncology

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DOI

10.3390/curroncol28060368

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