TY - JOUR
T1 - Peritoneal Carcinomatosis of Rare Ovarian Origin Treated by Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy
T2 - A Multi-Institutional Cohort from PSOGI and BIG-RENAPE
AU - the PSOGI Working Group
AU - the BIG-RENAPE Working Group
AU - Mercier, Frédéric
AU - Bakrin, Naoual
AU - Bartlett, David L.
AU - Goere, Diane
AU - Quenet, François
AU - Dumont, Frédéric
AU - Heyd, Bruno
AU - Abboud, Karine
AU - Marolho, Christelle
AU - Villeneuve, Laurent
AU - Glehen, Olivier
AU - Ahrendt, S. A.
AU - Akaishi, E.
AU - Bhatt, A.
AU - Cachin, P.
AU - Ceelen, W.
AU - Edwards, R. P.
AU - Holtzman, M. P.
AU - Kecmanovic, D.
AU - Lee, K. W.
AU - Levine, E. A.
AU - Mehta, S.
AU - Morris, D. L.
AU - Pande, P. K.
AU - Piso, P.
AU - O’Dwyer, S.
AU - Pingpank, J. F.
AU - Rajan, F.
AU - Rau, B.
AU - Spiliotis, J.
AU - Sugarbaker, P.
AU - Teo, M.
AU - Yarema, R.
AU - Yonemura, Y.
AU - Zeh, H. J.
AU - Abba, J.
AU - Arvieux, C.
AU - Bereder, J. M.
AU - Bouzard, D.
AU - Brigand, C.
AU - Carrère, S.
AU - Eveno, C.
AU - Facy, O.
AU - Ferron, G.
AU - Guyon, F.
AU - Kianmanesh, R.
AU - Lo Dico, R.
AU - Lorimier, G.
AU - Marchal, F.
AU - Mariani, P.
N1 - Funding Information:
The collaborators of the PSOGI Working Group included the following: S. A. Ahrendt (Department of Surgical Oncology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA); E. Akaishi (Department of Surgical Oncology, Centro de Oncologia Hospital Sirio Libanes, Sao Paulo, Brazil); A. Bhatt (Department of Surgical Oncology, Fortis Hospitals Limited, Bangalore, India); P. Cachin (Department of Surgery, Akademiska sjukhuset, Uppsala University Hospital, Uppasala, Sweden); W. Ceelen (Department of Gastrointestinal Surgery, Gent University Hospital, Ghent, Belgium); R. P. Edwards (Department of Surgical Oncology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA); M. P. Holtzman (Department of Surgical Oncology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA); D. Kecmanovic (Department of Surgery, First Surgical Clinic, Clinical Center of Serbia, Belgrade, Serbia); K. W. Lee (Department of Surgical Oncology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA); E. A. Levine (Department of Surgical Sciences-Oncology, Wake Forest Baptist Medical Center, Winston Salem, USA); S. Mehta (Division of Peritoneal Surface Oncology, Saifee Hospital, Mumbai, India); D. L. Morris (Department of Surgery, University of New South Wales, Sidney, Australia); P. K. Pande (Department of Surgical Oncology, BLK Superspeciality Hospital, New Delhi, India); P. Piso (Department of Surgery, University of Regensburg, Regensburg, Germany); S. O’Dwyer (Department of Colorectal Surgery, Christie Cancer Center, Manchester, United Kingdom); J. F. Pingpank (Department of Surgical Oncology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA); F. Rajan (Department of Surgical Oncology, Kovai Medical Centre, Coimbatore, India); B. Rau (Department of Surgical Oncology, Charite Campus Mitte University of Berlin, Berlin, Germany); J. Spiliotis (First Department of Surgical Oncology, Metaxa Cancer Memorial Hospital, Piraeus, Greece); P. Sugarbaker (Department of Surgical Oncology, Washington Hospital Center, United States); M. Teo (Department of Surgical Oncology, National Cancer Centre Singapore, Singapore, Singapore); R. Yarema (Department of Oncology and Medical Radiology Danylo Halytsky Lviv National Medical University, Lviv, Ukraine); Y. Yonemura (Department of Surgical Oncology, Organization to Support Peritoneal Dissemination Treatment, Osaka, Japan); H. J. Zeh (Department of Surgical Oncology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA).
Publisher Copyright:
© 2018, Society of Surgical Oncology.
PY - 2018/6/1
Y1 - 2018/6/1
N2 - Purpose: Ovarian cancer is the most common deadly cancer of gynecologic origin. Patients often are diagnosed at advanced stage with peritoneal metastasis. There are many rare histologies of ovarian cancer; some have outcomes worse than serous ovarian cancer. Cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC) can be considered for patients with recurrence. This study was designed to assess the impact of CRS and HIPEC on survival of patient with peritoneal metastasis from rare ovarian malignancy. Methods: A prospective, multicentric, international database was retrospectively searched to identify all patients with rare ovarian tumor (mucinous, clear cells, endometrioid, small cell hypercalcemic, and other) and peritoneal metastasis who underwent CRS and HIPEC through the Peritoneal Surface Oncology Group International (PSOGI) and BIG-RENAPE working group. The postoperative complications, long-term results, and principal prognostic factors were analyzed. Results: The analysis included 210 patients with a median follow-up of 43.5 months. Median overall survival (OS) was 69.3 months, and the 5-year OS was 57.7%. For mucinous tumors, median OS and DFS were not reached at 5 years. For granulosa tumors, median overall survival was not reached at 5 years, and median DFS was 34.6 months. Teratoma or germinal tumor showed median overall survival and DFS that were not reached at 5 years. Differences in OS were not statistically significant between histologies (p = 0.383), whereas differences in DFS were (p < 0.001). Conclusions: CRS and HIPEC may increases long-term survival in selected patients with peritoneal metastasis from rare ovarian tumors especially in mucinous, granulosa, or teratoma histological subtypes.
AB - Purpose: Ovarian cancer is the most common deadly cancer of gynecologic origin. Patients often are diagnosed at advanced stage with peritoneal metastasis. There are many rare histologies of ovarian cancer; some have outcomes worse than serous ovarian cancer. Cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC) can be considered for patients with recurrence. This study was designed to assess the impact of CRS and HIPEC on survival of patient with peritoneal metastasis from rare ovarian malignancy. Methods: A prospective, multicentric, international database was retrospectively searched to identify all patients with rare ovarian tumor (mucinous, clear cells, endometrioid, small cell hypercalcemic, and other) and peritoneal metastasis who underwent CRS and HIPEC through the Peritoneal Surface Oncology Group International (PSOGI) and BIG-RENAPE working group. The postoperative complications, long-term results, and principal prognostic factors were analyzed. Results: The analysis included 210 patients with a median follow-up of 43.5 months. Median overall survival (OS) was 69.3 months, and the 5-year OS was 57.7%. For mucinous tumors, median OS and DFS were not reached at 5 years. For granulosa tumors, median overall survival was not reached at 5 years, and median DFS was 34.6 months. Teratoma or germinal tumor showed median overall survival and DFS that were not reached at 5 years. Differences in OS were not statistically significant between histologies (p = 0.383), whereas differences in DFS were (p < 0.001). Conclusions: CRS and HIPEC may increases long-term survival in selected patients with peritoneal metastasis from rare ovarian tumors especially in mucinous, granulosa, or teratoma histological subtypes.
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U2 - 10.1245/s10434-018-6464-z
DO - 10.1245/s10434-018-6464-z
M3 - Article
C2 - 29637438
AN - SCOPUS:85045132983
SN - 1068-9265
VL - 25
SP - 1668
EP - 1675
JO - Annals of Surgical Oncology
JF - Annals of Surgical Oncology
IS - 6
ER -