Introduction: The aim of our study was to assess the clinical outcome of isolated lymph node recurrence in patients with epithelial ovarian cancer treated by surgery and to analyze the impact of various clinico-pathological factors on prognosis. Material and methods: We conducted a retrospective analysis of all the epithelial ovarian can -cer patients who underwent secondary lymphadenectomy surgery for isolated lymph node recurrence at our institute from 2013 to 2020. Univariate analysis of various factors influ-encing the post-recurrence disease free survival and post-recurrence survival was done using Kaplan-Meier for categorical variables and cox-proportional hazard progression for continuous variables.Results: A total of 21 patients of isolated lymph node recurrence were treated surgically during the study period. The median disease free interval to develop lymph nodal recurrence was 13 months. All the patients achieved complete resection to no gross residual disease without any significant morbidity associated with the procedure. The median post-recurrence disease free survival after treatment of lymph node recurrence was 25 months with 3-year post-recurrence survival of 72% and 3-year overall survival of 85%. Amongst the factors influ-encing post-recurrence disease free survival, young age (< 50 years), para-aortic lymph node dissection at initial surgery and single site of lymph node recurrence were significantly asso-ciated with better prognosis. A single site of lymph node recurrence was associated with significantly better post-recurrence survival.Conclusions: Complete resection is feasible for epithelial ovarian cancer patients presenting with isolated lymph node recurrence, without any significant perioperative morbidity. When combined with postoperative adjuvant chemotherapy, complete resection is associated with favourable survival outcomes. Young age, para-aortic lymph node dissection during primary surgery and single site of lymph node recurrence are associated with better prognosis.& COPY; 2022 Elsevier Masson SAS. All rights reserved.
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Seoul Natl Univ Hosp, Dept Radiat Oncol, Seoul, South KoreaSeoul Natl Univ Hosp, Dept Radiat Oncol, Seoul, South Korea
Lee, T. H.
Shin, H.
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Samsung Med Ctr, Dept Radiat Oncol, Seoul, South KoreaSeoul Natl Univ Hosp, Dept Radiat Oncol, Seoul, South Korea
Shin, H.
Ahn, Y. C.
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Samsung Med Ctr, Dept Radiat Oncol, Seoul, South KoreaSeoul Natl Univ Hosp, Dept Radiat Oncol, Seoul, South Korea
Ahn, Y. C.
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Kang, M. K.
Song, C.
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Seoul Natl Univ, Bundang Hosp, Dept Radiat Oncol, Seongnam, South KoreaSeoul Natl Univ Hosp, Dept Radiat Oncol, Seoul, South Korea
Song, C.
Kim, W. C.
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Inha Univ Hosp, Dept Radiat Oncol, Incheon, South KoreaSeoul Natl Univ Hosp, Dept Radiat Oncol, Seoul, South Korea
Kim, W. C.
Moon, S. H.
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Natl Canc Ctr, Proton Therapy Ctr, Goyang, South KoreaSeoul Natl Univ Hosp, Dept Radiat Oncol, Seoul, South Korea
Moon, S. H.
Kim, J. H.
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Dongsan Med Ctr, Dept Radiat Oncol, Daegu, South KoreaSeoul Natl Univ Hosp, Dept Radiat Oncol, Seoul, South Korea
Kim, J. H.
Cho, J.
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Yonsei Canc Ctr, Dept Radiat Oncol, Seoul, South KoreaSeoul Natl Univ Hosp, Dept Radiat Oncol, Seoul, South Korea
Cho, J.
Park, H. J.
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Hanyang Univ Hosp, Dept Radiat Oncol, Seoul, South KoreaSeoul Natl Univ Hosp, Dept Radiat Oncol, Seoul, South Korea
Park, H. J.
Lee, H. K.
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Jeonju Jesus Hosp, Dept Radiat Oncol, Jeonju, South KoreaSeoul Natl Univ Hosp, Dept Radiat Oncol, Seoul, South Korea
Lee, H. K.
Kim, B. H.
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Seoul Natl Univ, Dept Radiat Oncol, Boramae Med Ctr, Seoul Metropolitan Govt, Seoul, South KoreaSeoul Natl Univ Hosp, Dept Radiat Oncol, Seoul, South Korea
Kim, B. H.
Kim, H. J.
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Seoul Natl Univ Hosp, Dept Radiat Oncol, Seoul, South KoreaSeoul Natl Univ Hosp, Dept Radiat Oncol, Seoul, South Korea