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Robotic single site radical hysterectomy plus pelvic lymphadenectomy in gynecological cancers

OBJECTIVE: To evaluate the feasibility and the safety of robotic single-site radical hysterectomy (RSSRH) plus pelvic lymphadenectomy (PL) in endometrial or cervical cancer. METHODS: Patients with endometrial cancer (EC) International Federation of Gynecology and Obstetrics (FIGO) stage II, early ce...

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Autores principales: Vizza, Enrico, Chiofalo, Benito, Cutillo, Giuseppe, Mancini, Emanuela, Baiocco, Ermelinda, Zampa, Ashanti, Bufalo, Arabella, Corrado, Giacomo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Asian Society of Gynecologic Oncology; Korean Society of Gynecologic Oncology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5709528/
https://www.ncbi.nlm.nih.gov/pubmed/29185260
http://dx.doi.org/10.3802/jgo.2018.29.e2
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author Vizza, Enrico
Chiofalo, Benito
Cutillo, Giuseppe
Mancini, Emanuela
Baiocco, Ermelinda
Zampa, Ashanti
Bufalo, Arabella
Corrado, Giacomo
author_facet Vizza, Enrico
Chiofalo, Benito
Cutillo, Giuseppe
Mancini, Emanuela
Baiocco, Ermelinda
Zampa, Ashanti
Bufalo, Arabella
Corrado, Giacomo
author_sort Vizza, Enrico
collection PubMed
description OBJECTIVE: To evaluate the feasibility and the safety of robotic single-site radical hysterectomy (RSSRH) plus pelvic lymphadenectomy (PL) in endometrial or cervical cancer. METHODS: Patients with endometrial cancer (EC) International Federation of Gynecology and Obstetrics (FIGO) stage II, early cervical cancer (ECC) FIGO stage IB1 or locally advanced cervical cancer (LACC) FIGO stage IB2–IIB with clinical response ≥50% after neo-adjuvant chemotherapy (NACT) were enrolled in a prospective cohort trial. All cases were performed using the da Vinci Si Surgical Single Site System(®). RESULTS: Between April 2014 and November 2016, twenty patients were included in our pilot study. Three and 17 patients underwent type B1 or C1 RSSRH plus PL, respectively. The median age of patients was 46 years (range, 36–68 years) and the median body mass index was 23.5 kg/m(2) (range, 19.1–36.3 kg/m(2)). The median total operative time was 190 minutes (range, 90–310 minutes). The median blood loss was 75 mL (range, 20–700 mL) and the median number of pelvic lymph nodes removed was 16 (range, 5–27). No laparoscopic/laparotomic conversions were reported and the median time to discharge was 6 days (range, 4–16 days). No intra-operative complications occurred while 4 (20%) post-operative complications were reported: one pelvic abscess, one lymphorrea, one bowel perforation, and one vaginal dehiscence. CONCLUSION: RSSRH plus PL is technically feasible in patients affected by gynecological cancer.
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spelling pubmed-57095282018-01-01 Robotic single site radical hysterectomy plus pelvic lymphadenectomy in gynecological cancers Vizza, Enrico Chiofalo, Benito Cutillo, Giuseppe Mancini, Emanuela Baiocco, Ermelinda Zampa, Ashanti Bufalo, Arabella Corrado, Giacomo J Gynecol Oncol Original Article OBJECTIVE: To evaluate the feasibility and the safety of robotic single-site radical hysterectomy (RSSRH) plus pelvic lymphadenectomy (PL) in endometrial or cervical cancer. METHODS: Patients with endometrial cancer (EC) International Federation of Gynecology and Obstetrics (FIGO) stage II, early cervical cancer (ECC) FIGO stage IB1 or locally advanced cervical cancer (LACC) FIGO stage IB2–IIB with clinical response ≥50% after neo-adjuvant chemotherapy (NACT) were enrolled in a prospective cohort trial. All cases were performed using the da Vinci Si Surgical Single Site System(®). RESULTS: Between April 2014 and November 2016, twenty patients were included in our pilot study. Three and 17 patients underwent type B1 or C1 RSSRH plus PL, respectively. The median age of patients was 46 years (range, 36–68 years) and the median body mass index was 23.5 kg/m(2) (range, 19.1–36.3 kg/m(2)). The median total operative time was 190 minutes (range, 90–310 minutes). The median blood loss was 75 mL (range, 20–700 mL) and the median number of pelvic lymph nodes removed was 16 (range, 5–27). No laparoscopic/laparotomic conversions were reported and the median time to discharge was 6 days (range, 4–16 days). No intra-operative complications occurred while 4 (20%) post-operative complications were reported: one pelvic abscess, one lymphorrea, one bowel perforation, and one vaginal dehiscence. CONCLUSION: RSSRH plus PL is technically feasible in patients affected by gynecological cancer. Asian Society of Gynecologic Oncology; Korean Society of Gynecologic Oncology 2018-01 2017-09-12 /pmc/articles/PMC5709528/ /pubmed/29185260 http://dx.doi.org/10.3802/jgo.2018.29.e2 Text en Copyright © 2018. Asian Society of Gynecologic Oncology, Korean Society of Gynecologic Oncology https://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Vizza, Enrico
Chiofalo, Benito
Cutillo, Giuseppe
Mancini, Emanuela
Baiocco, Ermelinda
Zampa, Ashanti
Bufalo, Arabella
Corrado, Giacomo
Robotic single site radical hysterectomy plus pelvic lymphadenectomy in gynecological cancers
title Robotic single site radical hysterectomy plus pelvic lymphadenectomy in gynecological cancers
title_full Robotic single site radical hysterectomy plus pelvic lymphadenectomy in gynecological cancers
title_fullStr Robotic single site radical hysterectomy plus pelvic lymphadenectomy in gynecological cancers
title_full_unstemmed Robotic single site radical hysterectomy plus pelvic lymphadenectomy in gynecological cancers
title_short Robotic single site radical hysterectomy plus pelvic lymphadenectomy in gynecological cancers
title_sort robotic single site radical hysterectomy plus pelvic lymphadenectomy in gynecological cancers
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5709528/
https://www.ncbi.nlm.nih.gov/pubmed/29185260
http://dx.doi.org/10.3802/jgo.2018.29.e2
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