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Diagnosis and Management of Peritoneal Metastases from Ovarian Cancer

DOI: 10.1155/2012/541842

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Abstract:

The management and the outcome of peritoneal metastases or recurrence from epithelial ovarian cancer are presented. The biology and the diagnostic tools of EOC peritoneal metastasis with a comprehensive approach and the most recent literatures data are discussed. The definition and the role of surgery and chemotherapy are presented in order to focuse on the controversial points. Finally, the paper discusses the new data about the introduction of cytoreductive surgery and hyperthermic intraperitoneal chemotherapy (HIPEC) in the treatment of advanced epithelial ovarian cancer. 1. Introduction Epithelial ovarian cancer (EOC) affects over 210,000 women and causes 128,000 deaths annually worldwide [1]. This cancer remains the leading cause of death from gynecology malignancy in the USA and was responsible for 14,600 deaths in 2009 [2]. The annual incidence and mortality rates have dropped 1.6% and 0.3% per year on average for the years 1997–2006 [3]. Current standard treatment of EOC is cytoreductive surgery (CRS) in order to remove the primary tumor and debulk any metastatic disease in combination with systemic chemotherapy with paclitaxel and platinum-based agents (carboplatin or cisplatin). Despite this treatment, only 46–49% of women with EOC will survive 5 years [4, 5]. While the incidence is low before the menopause, it rises after that with a median age at the time of diagnosis of 63 years. The lifetime risk of ovarian cancer is 1 in 70, but there are women with much higher risk especially those with germ line mutations of BRCA1 and BRCA2 tumor suppressor genes [6, 7]. If there is a response to systemic chemotherapy, the disease often relapses within 12 to 18 months. The pattern of treatment failure is mostly local-regional, involving only the peritoneum and adjacent intra-abdominal organs. With this natural history, EOC patients may be candidates for local-regional in addition to systemic chemotherapy treatment [8]. 2. Biology of Peritoneal Metastasis from Ovarian Cancer Malignancies that are managed as EOC may have as a primary site the epithelium of the ovary, the peritoneum itself (primary peritoneal adenocarcinoma), or the fallopian tube. They are histologically and clinically similar and are treated in the same fashion [9]. In this paper they are grouped together as EOC. EOC frequently spreads by direct extension from the primary site tumor to neighboring organs such as bladder and large bowel. Also, exfoliated tumor cells detach from the primary tumor and are transported throughout the peritoneal space by peritoneal fluid and disseminate within

References

[1]  American Cancer Society, “Cancer facts and figures,” 2010, http://www.cancer.org/acs/.
[2]  J. Liu and U. A. Matulonis, “New advances in ovarian cancer,” Oncology, vol. 24, no. 8, pp. 691–698, 2010.
[3]  M. J. Horner, L. A. G. Ries, M. Krapcho, et al., SEER Cancer Statistics Review 1975—2006, Bethesda, Md, USA, 2010, http://seer.cancer.gov/csr/1975_2006/.
[4]  A. P. Heintz, F. Odicino, and P. Maisonneuve, “Carcinoma of the ovary FIGO 6th annual report on the results of treatment in Gynecological cancer,” International Journal of Gynecology & Obstetrics, supplement I, pp. 161–192, 2006.
[5]  A. Jemal, R. Siegel, E. Ward, Y. Hao, J. Xu, and M. J. Thun, “Cancer statistics, 2009,” CA Cancer Journal for Clinicians, vol. 59, no. 4, pp. 225–249, 2009.
[6]  A. Gadducci, F. Landoni, E. Sartori et al., “Analysis of treatment failures and survival of patients with fallopian tube carcinoma: a Cooperation Task Force (CTF) study,” Gynecologic Oncology, vol. 81, no. 2, pp. 150–159, 2001.
[7]  F. A. Tavassoli, “Pathology and Genetics of tumors of the breast and Female genital organs,” in World Health Organization Classification of Tumors, F. A. Tavassoli and P. Devilee, Eds., France IARC Press, Lyon, France, 2003.
[8]  J. D. Spiliotis, “Peritoneal carcinomatosis cytoreductive surgery and HIPEC: a ray of hope for cure,” Hepato-Gastroenterology, vol. 57, no. 102-103, pp. 1173–1177, 2010.
[9]  R. S. Tuma, “Origin of ovarian cancer may have implications for screening,” Journal of the National Cancer Institute, vol. 102, no. 1, pp. 11–13, 2010.
[10]  S. M. Eisenkop and N. M. Spirtos, “The clinical significance of occult macroscopically positive retroperitoneal nodes in patients with epithelial ovarian cancer,” Gynecologic Oncology, vol. 82, no. 1, pp. 143–149, 2001.
[11]  AJCC, “Ovary and primary peritoneal carcinoma,” in AJCC Cancer Staging Handbook, pp. 501–506, Spinger, 7th edition, 2009.
[12]  E. Lengyel, “Ovarian cancer development and metastasis,” The American Journal of Pathology, vol. 177, no. 3, pp. 1053–1064, 2010.
[13]  G. P. Gupta and J. Massagué, “Cancer metastasis: building a framework,” Cell, vol. 127, no. 4, pp. 679–695, 2006.
[14]  M. A. Huber, N. Kraut, and H. Beug, “Molecular requirements for epithelial-mesenchymal transition during tumor progression,” Current Opinion in Cell Biology, vol. 17, no. 5, pp. 548–558, 2005.
[15]  S. Elloul, M. B. Elstrand, J. M. Nesland et al., “Snail, slug, and smad-interacting protein 1 as novel parameters of disease aggressiveness in metastatic ovarian and breast carcinoma,” Cancer, vol. 103, no. 8, pp. 1631–1643, 2005.
[16]  K. M. Burleson, L. K. Hansen, and A. P. N. Skubitz, “Ovarian carcinoma spheroids disaggregate on type I collagen and invade live human mesothelial cell monolayers,” Clinical and Experimental Metastasis, vol. 21, no. 8, pp. 685–697, 2005.
[17]  K. M. Burleson, R. C. Casey, K. M. Skubitz, S. E. Pambuccian, T. R. Oegema, and A. P. N. Skubitz, “Ovarian carcinoma ascites spheroids adhere to extracellular matrix components and mesothelial cell monolayers,” Gynecologic Oncology, vol. 93, no. 1, pp. 170–181, 2004.
[18]  J. Sehouli, F. Senyuva, C. Fotopoulou et al., “Intra-abdominal tumor dissemination pattern and surgical outcome in 214 patients with primary ovarian cancer,” Journal of Surgical Oncology, vol. 99, no. 7, pp. 424–427, 2009.
[19]  H. A. Kenny, S. Kaur, L. M. Coussens, and E. Lengyel, “The initial steps of ovarian cancer cell metastasis are mediated by MMP-2 cleavage of vitronectin and fibronectin,” Journal of Clinical Investigation, vol. 118, no. 4, pp. 1367–1379, 2008.
[20]  S. Kaur, H. A. Kenny, S. Jagadeeswaran et al., “β3-integrin expression on tumor cells inhibits tumor progression, reduces metastasis, and is associated with a favorable prognosis in patients with ovarian cancer,” The American Journal of Pathology, vol. 175, no. 5, pp. 2184–2196, 2009.
[21]  L. Chen, S. M. Park, A. V. Tumanov et al., “CD95 promotes tumour growth,” Nature, vol. 465, no. 7297, pp. 492–496, 2010.
[22]  Y. H. Jee, L. S. Mangala, J. Y. Fok et al., “Clinical and biological significance of tissue transglutaminase in ovarian carcinoma,” Cancer Research, vol. 68, no. 14, pp. 5849–5858, 2008.
[23]  N. Nishida, H. Yano, K. Komai, T. Nishida, T. Kamura, and M. Kojiro, “Vascular endothelial growth factor C and vascular endothelial growth factor receptor 2 are related closely to the prognosis of patients with ovarian carcinoma,” Cancer, vol. 101, no. 6, pp. 1364–1374, 2004.
[24]  L. Khalique, A. Ayhan, J. C. Whittaker et al., “The clonal evolution of metastases from primary serous epithelial ovarian cancers,” International Journal of Cancer, vol. 124, no. 7, pp. 1579–1586, 2009.
[25]  AJCC, “Fallopian tube Carcinoma,” in AJCC Cancer Staging Handbook, pp. 501–506, Springer, New York, NY, USA, 2009.
[26]  FIGO, “Current FIGO staging for cancer of the vagina, fallopian tube, ovary and gestational trophoblastic neoplasia,” International Journal of Gynecology & Obstetrics, vol. 105, pp. 3–4, 2009.
[27]  A. Heintz, F. Odicino, P. Maisonneuve, et al., “Carcinoma of the ovary. FIGO 6th annual report of the results of treatment in Gynecological Cancer,” International Journal of Gynecology & Obstetrics, vol. 95, supplement 1, pp. S161–S192, 2006.
[28]  P. Jacquet and P. H. Sugarbaker, “Clinical research methodologies in diagnosis and staging of patients with peritoneal carcinomatosis,” Cancer Treatment and Research, vol. 82, pp. 359–374, 1996.
[29]  B. A. Goff, L. S. Mandel, C. W. Drescher et al., “Development of an ovarian cancer symptom index: possibilities for earlier detection,” Cancer, vol. 109, no. 2, pp. 221–227, 2007.
[30]  M. R. Andersen, B. A. Goff, K. A. Lowe et al., “Use of a Symptom Index, CA125, and HE4 to predict ovarian cancer,” Gynecologic Oncology, vol. 116, no. 3, pp. 378–383, 2010.
[31]  S. A. Cannistra, “Cancer of the ovary,” The New England Journal of Medicine, vol. 351, no. 24, pp. 2519–2529, 2004.
[32]  A. T. Byrne, L. Ross, J. Holash et al., “Vascular endothelial growth factor-trap decreases tumor burden, inhibits ascites, and causes dramatic vascular remodeling in an ovarian cancer model,” Clinical Cancer Research, vol. 9, no. 15, pp. 5721–5728, 2003.
[33]  E. J. Lee, S. H. Kim, Y. H. Kim, and H. J. Lee, “Is CA-125 an additional help to radiologic findings for differentiation borderline ovarian tumor from stage I carcinoma?” Acta Radiologica, vol. 52, no. 4, pp. 458–462, 2011.
[34]  L. S. Bradford and J. O. Schorge, “CA125 screening after risk-reducing salpingo-oophorectomy: are the titers too high, or is it all just too much?” Menopause, vol. 18, no. 2, pp. 123–124, 2011.
[35]  N. B. Rettenmaier, C. R. Rettenmaier, T. Wojciechowski et al., “The utility and cost of routine follow-up procedures in the surveillance of ovarian and primary peritoneal carcinoma: a 16-year institutional review,” British Journal of Cancer, vol. 103, no. 11, pp. 1657–1662, 2010.
[36]  W. Zhang, H. C. Yang, Q. Wang, et al., “Clinical value of combined detection of serum matrix metalloproteinase-9 heparanose and cethepsin for determining ovarian cancer invasion and metastasis,” Anticancer Research, vol. 31, no. 10, pp. 3423–3428, 2011.
[37]  J. H. No, Y. T. Jeon, Y. B. Kim, and Y. S. Song, “Quantitative detection of serum survivin and its relationship with prognostic factors in ovarian cancer,” Gynecologic and Obstetric Investigation, vol. 71, no. 2, pp. 136–140, 2011.
[38]  S. A. Funt, H. Hricak, N. Abu-Rustum, M. Mazumdar, H. Felderman, and D. S. Chi, “Role of CT in the management of recurrent ovarian cancer,” American Journal of Roentgenology, vol. 182, no. 2, pp. 393–398, 2004.
[39]  J. A. Rauh-Hain, A. B. Olawaiye, E. G. Munro et al., “Role of computed tomography in the surgical management of patients with bowel obstruction secondary to recurrent ovarian carcinoma,” Annals of Surgical Oncology, vol. 17, no. 3, pp. 853–860, 2010.
[40]  S. H. Chandrashekhara, S. Thulkar, D. N. Srivastava et al., “Pre-operative evaluation of peritoneal deposits using multidetector computed tomography in ovarian cancer,” British Journal of Radiology, vol. 84, no. 997, pp. 38–43, 2011.
[41]  J. Klostergaard, K. Parga, and R. G. Raptis, “Current and future applications of magnetic resonance imaging (MRI) to breast and ovarian cancer patient management,” Puerto Rico Health Sciences Journal, vol. 29, no. 3, pp. 223–231, 2010.
[42]  S. Kyriazi, D. J. Collins, V. A. Morgan, S. L. Giles, and N. M. deSouza, “Diffusion-weighted imaging of peritoneal disease for noninvasive staging of advanced ovarian cancer,” Radiographics, vol. 30, no. 5, pp. 1269–1285, 2010.
[43]  F. V. Cookley, “Staging ovarian cancer: role of imaging,” Radiologic Clinics of North America, vol. 40, no. 3, pp. 609–636, 2002.
[44]  M. J. Fulham, J. Carter, A. Baldey, R. J. Hicks, J. E. Ramshaw, and M. Gibson, “The impact of PET-CT in suspected recurrent ovarian cancer: a prospective multi-centre study as part of the Australian PET Data Collection Project,” Gynecologic Oncology, vol. 112, no. 3, pp. 462–468, 2009.
[45]  E. Sala, M. Kataoka, N. Pandit-Taskar et al., “Recurrent ovarian cancer: use of contrast-enhanced CT and PET/CT to accurately localize tumor recurrence and to predict patients' survival,” Radiology, vol. 257, no. 1, pp. 125–134, 2010.
[46]  D. S. Chi, F. Musa, F. Dao, et al., “An analysis of patients with bulky advanced stage ovarian, tubal and peritoneal carcinoma treated with primary debulking surgery (PDS) during an identical time period as the randomized EORTC-NCIC trial of PDS vs neo-adjuvant chemotherapy,” Gynecologic Oncology, vol. 124, pp. 10–14, 2012.
[47]  A. du Bois, M. Quinn, T. Thigpen, et al., “2004 consensus statements on the management of ovarian cancer,” Annals of Oncology, vol. 16, no. 8, pp. 7–12, 2005.
[48]  P. Harter, F. Hilpert, S. Mahner, S. Kommoss, F. Heitz, and A. Du Bois, “Role of cytoreductive surgery in recurrent ovarian cancer,” Expert Review of Anticancer Therapy, vol. 9, no. 7, pp. 917–922, 2009.
[49]  P. H. Sugarbaker, “Peritonectomy procedures,” Cancer Treatment and Research, vol. 134, pp. 247–264, 2007.
[50]  J. Spiliotis, A. A. K. Tentes, A. Vaxevanidou et al., “Cytoreductive surgery and hyperthermic intraperitoneal chemotherapy in the management of peritoneal carcinomatosis. Preliminary results and cost from two centers in Greece,” Journal of B.U.ON, vol. 13, no. 2, pp. 205–210, 2008.
[51]  J. Spiliotis, A. Vaxevanidou, A. Datsis, A. Rogdakis, and S. Kekelos, “Peritoneal carcinomatosis: intra-operative and post-operative assessment of patients undergoing cytoreduction and HIPEC,” Hepato-Gastroenterology, vol. 57, no. 102-103, pp. 1052–1059, 2010.
[52]  P. H. Sugarbaker and D. Chang, “Results of treatment of 385 patients with peritoneal surface spread of appendiceal malignancy,” Annals of Surgical Oncology, vol. 6, no. 8, pp. 727–731, 1999.
[53]  A. du Bois, J. Herrstedt, A. C. Hardy-Bessard et al., “Phase III trial of carboplatin plus paclitaxel with or without gemcitabine in first-line treatment of epithelial ovarian cancer,” Journal of Clinical Oncology, vol. 28, no. 27, pp. 4162–4169, 2010.
[54]  R. F. Ozols, B. N. Bundy, B. E. Greer et al., “Phase III trial of carboplatin and paclitaxel compared with cisplatin and paclitaxel in patients with optimally resected stage III ovarian cancer: a Gynecologic Oncology Group study,” Journal of Clinical Oncology, vol. 21, no. 17, pp. 3194–3200, 2003.
[55]  A. du Bois, A. Reuss, E. Pujade-Lauraine, P. Harter, I. Ray-Coquard, and J. Pfisterer, “Role of surgical outcome as prognostic factor in advanced epithelial ovarian cancer: a combined exploratory analysis of 3 prospectively randomized phase 3 multicenter trials: by the arbeitsgemeinschaft gynaekologische onkologie studiengruppe ovarialkarzinom (AGO-OVAR) and the groupe d'Investigateurs nationaux pour les etudes des cancers de l'Ovaire (GINECO),” Cancer, vol. 115, no. 6, pp. 1234–1244, 2009.
[56]  P. Harter and A. du Bois, “The role of surgery in ovarian cancer with special emphasis on cytoreductive surgery for recurrence,” Current Opinion in Oncology, vol. 17, no. 5, pp. 505–514, 2005.
[57]  R. E. Bristow, I. Puri, and D. S. Chi, “Cytoreductive surgery for recurrent ovarian cancer: a meta-analysis,” Gynecologic Oncology, vol. 112, no. 1, pp. 265–274, 2009.
[58]  S. M. Eisenkop, R. L. Friedman, and N. M. Spirtos, “The role of secondary cytoreductive surgery in the treatment of patients with recurrent epithelial ovarian carcinoma,” Cancer, vol. 88, pp. 144–153, 2000.
[59]  J. Sehouli, R. Richter, E. I. Braicu et al., “Role of secondary cytoreductive surgery in ovarian cancer relapse: who will benefit? A systematic analysis of 240 consecutive patients,” Journal of Surgical Oncology, vol. 102, no. 6, pp. 656–662, 2010.
[60]  R. Y. Zang, Z. Y. Zhang, Z. T. Li, et al., “Effect of cytoreductive surgery on survival of patients with recurrent epithelial ovarian cancer,” Journal of Surgical Oncology, vol. 75, pp. 24–30, 2000.
[61]  N. D. Fleming, I. Cass, C. S. Walsh, B. Y. Karlan, and A. J. Li, “CA125 surveillance increases optimal resectability at secondary cytoreductive surgery for recurrent epithelial ovarian cancer,” Gynecologic Oncology, vol. 121, no. 2, pp. 249–252, 2011.
[62]  B. Gronlund, L. Lundvall, I. J. Christensen, J. B. Knudsen, and C. H?gdall, “Surgical cytoreduction in recurrent ovarian carcinoma in patients with complete response to paclitaxel-platinum,” European Journal of Surgical Oncology, vol. 31, no. 1, pp. 67–73, 2005.
[63]  A. A. K. Tentes, O. S. Korakianitis, S. Kakolyris et al., “Cytoreductive surgery and perioperative intraperitoneal chemotherapy in recurrent ovarian cancer,” Tumori, vol. 96, no. 3, pp. 411–416, 2010.
[64]  P. Harter, A. du Bois, M. Hahmann et al., “Surgery in recurrent ovarian cancer: the Arbeitsgemeinschaft Gynaekologische Onkologie (AGO) DESKTOP OVAR trial,” Annals of Surgical Oncology, vol. 13, no. 12, pp. 1702–1710, 2006.
[65]  P. Harter, M. Hahmann, H. J. Lueck et al., “Surgery for recurrent ovarian cancer: role of peritoneal carcinomatosis: exploratory analysis of the DESKTOP i trial about risk factors, surgical implications, and prognostic value of peritoneal carcinomatosis,” Annals of Surgical Oncology, vol. 16, no. 5, pp. 1324–1330, 2009.
[66]  P. Harter, J. Sehouli, A. Reuss et al., “Prospective validation study of a predictive score for operability of recurrent ovarian cancer: the multicenter intergroup study DESKTOP II,” International Journal of Gynecological Cancer, vol. 21, no. 2, pp. 289–295, 2011.
[67]  D. S. Chi, O. Zivanovic, K. L. Levinson et al., “The incidence of major complications after the performance of extensive upper abdominal surgical procedures during primary cytoreduction of advanced ovarian, tubal, and peritoneal carcinomas,” Gynecologic Oncology, vol. 119, no. 1, pp. 38–42, 2010.
[68]  C. Scarabelli, A. Gallo, A. Zarrelli, C. Visentin, and E. Campagnutta, “Systematic pelvic and para-aortic lymphadenectomy during cytoreductive surgery in advanced ovarian cancer: potential benefit on survival,” Gynecologic Oncology, vol. 56, no. 3, pp. 328–337, 1995.
[69]  P. B. Panici, A. Maggioni, N. Hacker et al., “Systematic aortic and pelvic lymphadenectomy versus resection of bulky nodes only in optimally debulked advanced ovarian cancer: a randomized clinical trial,” Journal of the National Cancer Institute, vol. 97, no. 8, pp. 560–566, 2005.
[70]  C. G. Gerestein, G. M. Nieuwenhuyzen-de Boer, M. J. Eijkemans, G. S. Kooi, and C. W. Burger, “Prediction of 30-day morbidity after primary cytoreductive surgery for advanced stage ovarian cancer,” European Journal of Cancer, vol. 46, no. 1, pp. 102–109, 2010.
[71]  L. Woelber, S. Jung, C. Eulenburg et al., “Perioperative morbidity and outcome of secondary cytoreduction for recurrent epithelial ovarian cancer,” European Journal of Surgical Oncology, vol. 36, no. 6, pp. 583–588, 2010.
[72]  C. G. Gerestein, R. A. M. Damhuis, C. W. Burger, and G. S. Kooi, “Postoperative mortality after primary cytoreductive surgery for advanced stage epithelial ovarian cancer: a systematic review,” Gynecologic Oncology, vol. 114, no. 3, pp. 523–552, 2009.
[73]  D. K. Armstrong, B. Bundy, L. Wenzel et al., “Intraperitoneal cisplatin and paclitaxel in ovarian cancer,” The New England Journal of Medicine, vol. 354, no. 1, pp. 34–43, 2006.
[74]  D. S. Dizon, M. L. Hensley, E. A. Poynor et al., “Retrospective analysis of carboplatin and paclitaxel as initial second-line therapy for recurrent epithelial ovarian carcinoma: application toward a dynamic disease state model of ovarian cancer,” Journal of Clinical Oncology, vol. 20, no. 5, pp. 1238–1247, 2002.
[75]  M. K. Parmar, J. A. Ledermann, N. Colombo, et al., “Paclitaxel plus platinum-based chemotherapy versus conventional platinum-based chemotherapy in women with relapsed ovarian cancer the ICON 4/AGO-OVAR 2.2 trial,” The Lancet, vol. 361, pp. 2099–2106, 2003.
[76]  J. Pfisterer, M. Plante, I. Vergote et al., “Gemcitabine plus carboplatin compared with carboplatin in patients with platinum-sensitive recurrent ovarian cancer: an intergroup trial of the AGO-OVAR, the NCIC CTG, and the EORTC GCG,” Journal of Clinical Oncology, vol. 24, no. 29, pp. 4699–4707, 2006.
[77]  G. P. Sfakianos and L. J. Havrilesky, “A review of cost-effectiveness studies in ovarian cancer,” Cancer Control, vol. 18, no. 1, pp. 59–64, 2011.
[78]  P. Benedetti Panici, A. de Vivo, F. Bellati et al., “Secondary cytoreductive surgery in patients with platinum-sensitive recurrent ovarian cancer,” Annals of Surgical Oncology, vol. 14, no. 3, pp. 1136–1142, 2007.
[79]  G. J. Gardner and E. L. Jewell, “Current and future directions of clinical trials for ovarian Cancer,” Cancer Control, vol. 18, no. 1, pp. 44–51, 2011.
[80]  R. A. Burger, “Role of vascular endothelial growth factor inhibitors in the treatment of gynecologic malignancies,” Journal of Gynecologic Oncology, vol. 21, no. 1, pp. 3–11, 2010.
[81]  A. A. Garcia, H. Hirte, G. Fleming et al., “Phase II clinical trial of bevacizumab and low-dose metronomic oral cyclophosphamide in recurrent ovarian cancer: a trial of the California, Chicago, and Princess Margaret Hospital phase II consortia,” Journal of Clinical Oncology, vol. 26, no. 1, pp. 76–82, 2008.
[82]  K. Behbakht, M. W. Sill, K. M. Darcy et al., “Phase II trial of the mTOR inhibitor, temsirolimus and evaluation of circulating tumor cells and tumor biomarkers in persistent and recurrent epithelial ovarian and primary peritoneal malignancies: a Gynecologic Oncology Group study,” Gynecologic Oncology, vol. 123, no. 1, pp. 19–26, 2011.
[83]  Phase II randomized, double blind, multicentre study to assess the efficacy of AZD, 2281 in the treatment of patients with platinum sensitive ovarian cancer following treatment with two or more platinum regimens. NCT00753545, 2010, http://clinicaltrials.gov/ct2/show/NCT00753545.
[84]  A phase II evaluation of belinostat and carboplatin in the treatment of recurrent or persistent platinum—resistant ovarian, fallopian tube, or primary peritoneal cancer. NCT00993616, 2010, http://clinicaltrials.gov/ct2/show/NCT00993616.
[85]  B. W. Loggie, J. M. Sterchi, A. T. Rogers et al., “Intraperitoneal hyperthermic chemotherapy for advanced gastrointestinal and ovarian cancers,” Regional Cancer Treatment, vol. 7, no. 2, pp. 78–81, 1995.
[86]  J. Spiliotis, A. Vaxevanidou, F. Sergouniotis, E. Lambropoulou, A. Datsis, and A. Christopoulou, “The role of cytoreductive surgery and hyperthermic intraperitoneal chemotherapy in the management of recurrent advanced ovarian cancer: a prospective study,” Journal of B.U.ON, vol. 16, no. 1, pp. 74–79, 2011.
[87]  C. W. Helm, S. D. Richard, J. Pan, et al., “HIPEC in ovarian cancer: first report of HYPER-O registry,” International Journal of Gynecological Cancer, vol. 20, no. 1, pp. 61–69, 2010.
[88]  K. Rowan, “Intraperitoneal therapy for ovarian cancer: why has it not become standard?” Journal of the National Cancer Institute, vol. 101, no. 11, pp. 775–777, 2009.
[89]  S. Rufian, F. C. Munoz-Casares, J. Briceno, et al., “Radical surgery—peritonectomy and intra-operative intra-peritoneal chemotherapy for the treatment of peritoneal carcinomatosis in recurrent or primary ovarian cancer,” Journal of Surgical Oncology, vol. 94, no. 4, pp. 316–324, 2006.
[90]  M. Deraco, S. Kusomura, S. Virzi, et al., “Cytoreductive surgery and hyperthermic intra-peritoneal chemotherapy as up front therapy for advanced. EOC: multi-institutional phase II study,” Gynecologic Oncology, vol. 122, no. 2, pp. 215–220, 2011.
[91]  M. Deraco, D. Baratti, B. Laterza et al., “Advanced cytoreduction as surgical standard of care and hyperthermic intraperitoneal chemotherapy as promising treatment in epithelial ovarian cancer,” European Journal of Surgical Oncology, vol. 37, no. 1, pp. 4–9, 2011.
[92]  K. Jaaback and N. Johnson, “Intraperitoneal chemotherapy for the initial management of primary epithelial ovarian cancer,” Cochrane Database of Systematic Reviews, no. 1, Article ID CD005340, 2006.
[93]  I. Vergote, C. G. Trope, F. Amant, et al., “Neo-adjuvant chemotherapy or primary surgery in stage IIIc or IV ovarian cancer,” The New England Journal of Medicine, vol. 363, no. 10, pp. 943–953, 2010.
[94]  J. Spiliotis, E. Halkia, and E. Efstathiou, “Peritoneal carcinomatosis 2011. Is about time for chemosurgery?” Journal of B.U.ON, vol. 16, pp. 400–408, 2011.
[95]  K. Galaal, R. Naik, R. E. Bristow, A. Patel, A. Bryant, and H. O. Dickinson, “Cytoreductive surgery plus chemotherapy versus chemotherapy alone for recurrent epithelial ovarian cancer,” Cochrane Database of Systematic Reviews, vol. 6, Article ID CD007822, 2010.
[96]  “Study comparing tumor debulking surgery versus chemotherapy alone in recurrent platinum-sensitive ovarian cancer,” AGO—OVAR OP4 DESKTOP III, NCT01166737.
[97]  M. Deraco, C. R. Rossi, E. Pennacchioli et al., “Cytoreductive surgery followed by intraperitoneal hyperthermic perfusion in the treatment of recurrent epithelial ovarian cancer: a phase II clinical study,” Tumori, vol. 87, no. 3, pp. 120–126, 2001.
[98]  C. Zanon, R. Clara, I. Chiappino et al., “Cytoreductive surgery and intraperitoneal chemohyperthermia for recurrent peritoneal carcinomatosis from ovarian cancer,” World Journal of Surgery, vol. 28, no. 10, pp. 1040–1045, 2004.
[99]  F. Raspagliesi, S. Kusamura, J. C. Campos Torres et al., “Cytoreduction combined with intraperitoneal hyperthermic perfusion chemotherapy in advanced/recurrent ovarian cancer patients: the experience of National Cancer Institute of Milan,” European Journal of Surgical Oncology, vol. 32, no. 6, pp. 671–675, 2006.
[100]  C. W. Helm, L. Randall-Whitis, R. S. Martin et al., “Hyperthermic intraperitoneal chemotherapy in conjunction with surgery for the treatment of recurrent ovarian carcinoma,” Gynecologic Oncology, vol. 105, no. 1, pp. 90–96, 2007.
[101]  A. Di Giorgio, E. Naticchioni, D. Biacchi et al., “Cytoreductive surgery (peritonectomy procedures) combined with hyperthermic intraperitoneal chemotherapy (HIPEC) in the treatment of diffuse peritoneal carcinomatosis from ovarian cancer,” Cancer, vol. 113, no. 2, pp. 315–325, 2008.
[102]  A. Fagotti, I. Paris, F. Grimolizzi et al., “Secondary cytoreduction plus oxaliplatin-based HIPEC in platinum-sensitive recurrent ovarian cancer patients: a pilot study,” Gynecologic Oncology, vol. 113, no. 3, pp. 335–340, 2009.
[103]  N. Carrabin, F. Mithieux, P. Meeus et al., “Hyperthermic intraperitoneal chemotherapy with oxaliplatin and without adjuvant chemotherapy in stage IIIC ovarian cancer,” Bulletin du Cancer, vol. 97, no. 4, pp. E23–E32, 2010.
[104]  C. W. Helm, “The role of hyperthermic intraperitoneal chemotherapy (HIPEC) in ovarian cancer,” Oncologist, vol. 14, no. 7, pp. 683–694, 2009.
[105]  J. H. Bae, J. M. Lee, K. S. Ryu et al., “Treatment of ovarian cancer with paclitaxel- or carboplatin-based intraperitoneal hyperthermic chemotherapy during secondary surgery,” Gynecologic Oncology, vol. 106, no. 1, pp. 193–200, 2007.
[106]  J. Gori, R. Casta?o, M. Toziano et al., “Intraperitoneal hyperthermic chemotherapy in ovarian cancer,” International Journal of Gynecological Cancer, vol. 15, no. 2, pp. 233–239, 2005.
[107]  A. Fagotti, B. Costantini, G. Vizzielli et al., “HIPEC in recurrent ovarian cancer patients: morbidity-related treatment and long-term analysis of clinical outcome,” Gynecologic Oncology, vol. 122, no. 2, pp. 221–225, 2011.
[108]  R. M. Smeenk, V. J. Verwaal, and F. A. N. Zoetmulder, “Learning curve of combined modality treatment in peritoneal surface disease,” British Journal of Surgery, vol. 94, no. 11, pp. 1408–1414, 2007.
[109]  C. Pomel, G. Ferron, G. Lorimier et al., “Hyperthermic intra-peritoneal chemotherapy using Oxaliplatin as consolidation therapy for advanced epithelial ovarian carcinoma. Results of a phase II prospective multicentre trial. CHIPOVAC study,” European Journal of Surgical Oncology, vol. 36, no. 6, pp. 589–593, 2010.
[110]  J. D. Spiliotis, A. Rogdakis, A. Vaxevanidou, A. Datsis, G. Zacharis, and A. Christopoulou, “Morbidity and mortality of cytoreductive surgery and hyperthermic intraperitoneal chemotherapy in the management of peritoneal carcinomatosis,” Journal of B.U.ON, vol. 14, no. 2, pp. 259–264, 2009.
[111]  Oxford Center for Evidence Based Medicine, 2010, http://www.cebm.net/index.aspx?o=1025.
[112]  J. Spiliotis, E. Halkia, and D. H. Roukos, “Ovarian cancer screening and peritoneal carcinomatosis: standards, “omics” and miRNAs for personalized management,” Expert Review of Molecular Diagnostics, vol. 11, no. 5, pp. 465–467, 2011.

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