Article Data

  • Views 473
  • Dowloads 119

Original Research

Open Access

Secondary cytoreductive surgery, hyperthermic intraperitoneal intraoperative chemotherapy, and chemotherapy alone: a retrospective comparison of alternative approaches in relapsed platinum sensitive ovarian cancer

  • F. Marocco1
  • M. Vaira2
  • A. Milani3
  • S. Genta3
  • F. Maggiorotto1
  • A. Magistris1
  • A. Cinquegrana2
  • M. Robella3
  • M. De Simone3
  • M. Aglietta3
  • R. Ponzone1
  • G. Valabrega3,*,

1Division of Gynecological Oncology, Fondazione del Piemonte per l'Oncologia (FPO) Candiolo Cancer Center (IRCCs), Turin, Italy

2Division of Surgical Oncology, Fondazione del Piemonte per l'Oncologia (FPO)-Candiolo Cancer Center (IRCCs), Turin, Italy

3Division of Medical Oncology, Fondazione del Piemonte per l'Oncologia (FPO)-Candiolo Cancer Center (IRCCs), Turin, Italy

4Department of Oncology, University of Turin Medical School, Turin, Italy

DOI: 10.12892/ejgo3257.2016 Vol.37,Issue 5,October 2016 pp.638-643

Published: 10 October 2016

*Corresponding Author(s): G. Valabrega E-mail: giorgio.valabrega@ircc.it

Abstract

Introduction: The best treatment for relapsed platinum sensitive epithelial ovarian cancer (EOC) is controversial. The aim of the study was to compare progression-free survival (PFS) and overall survival (OS) in platinum-sensitive EOC patients treated with chemotherapy alone (CTA), secondary cytoreductive surgery (SCR) or SCR plus hyperthermic intraperitoneal intraoperative chemotherapy (HIPEC). Materials and Methods: Retrospective analysis of the clinical outcome of 46 EOC patients with at least 30 months of follow-up. Results: Median follow-up time was 32 months for the CTA group, 30 months for the SCR group, and 45 months for the SCR + HIPEC group. Fifteen recurrences were observed in the CTA group, seven in the SCR group, and 16 in the SCR + HIPEC group. The median time elapsed between first and second recurrence (PFI-2) was significantly higher among patients treated with SCR + HIPEC, in comparison with patients treated with CTA (p = 0.012 and p = 0.017, respectively). On the contrary, PFI-2 did not significantly differ between the SCR and SCR + HIPEC groups (p = 0.877). A statistically significant difference in OS favouring SCR + HIPEC in comparison with CTA (p = 0.04) was observed. Conclusions: SCR ± HIPEC compared with CTA improves PFI-2 in patients with platinum-sensitive EOC recurrence. SCR + HIPEC might also improve OS in comparison with CTA. No improvement in favor of SCR + HIPEC vs SCR was observed,. These results further support the need of a randomized trial comparing chemotherapy with SCR ± HIPEC in this setting.

Keywords

Secondary cytoreduction; HIPEC; Platinum sensitive relapse; Ovarian cancer; Platinum based chemotherapy; Cytoreductive surgery.

Cite and Share

F. Marocco,M. Vaira,A. Milani,S. Genta,F. Maggiorotto,A. Magistris,A. Cinquegrana,M. Robella,M. De Simone,M. Aglietta,R. Ponzone,G. Valabrega. Secondary cytoreductive surgery, hyperthermic intraperitoneal intraoperative chemotherapy, and chemotherapy alone: a retrospective comparison of alternative approaches in relapsed platinum sensitive ovarian cancer . European Journal of Gynaecological Oncology. 2016. 37(5);638-643.

References

[1] Bafaloukos D., Linardou H., Aravantinos G., Papadimitriou C., Bamias A., Fountzilas G., et al.: “A randomized phase II study of carboplatin plus pegylated liposomal doxorubicin versus carboplatin plus paclitaxel in platinum sensitive ovarian cancer patients: a Hellenic Cooperative Oncology Group study”. BMC Medicine, 2010, 8, 3.

[2] Chang S.J., Bristow R.E.: “Evolution of surgical treatment paradigms for advanced-stage ovarian cancer: redefining 'optimal' residual disease”. Gynecol. Oncol., 2012, 125, 483.

[3] Boran N., Hizli D., Yilmaz S., Turan T., Celik B., Karabuk E., et al.: “Secondary cytoreductive surgery outcomes of selected patients with paclitaxel/platinum sensitive recurrent epithelial ovarian cancer”. J. Surg. Oncol., 2012, 106, 369.

[4] Luvero D., Milani A., Ledermann J.A.: “Treatment options in recurrent ovarian cancer: latest evidence and clinical potential”. Ther. Adv. Med. Oncol., 2014, 6, 229.

[5] Mutch D.G., Orlando M., Goss T., Teneriello M.G., Gordon A.N., McMeekin S.D., et al.: “Randomized phase III trial of gemcitabine compared with pegylated liposomal doxorubicin in patients with platinum-resistant ovarian cancer”. J. Clin. Oncol., 2007, 25, 2811.

[6] Galaal K., Naik R., Bristow R.E., Patel A., Bryant A., Dickinson H.O.: “Cytoreductive surgery plus chemotherapy versus chemotherapy alone for recurrent epithelial ovarian cancer”. Cochrane Database Syst. Rev., 2010, 6, CD007822.

[7] Bristow R.E., Puri I., Chi D.S.: “Cytoreductive surgery for recurrent ovarian cancer: a meta-analysis”. Gynecol. Oncol., 2009, 112, 265.

[8] Gungor M., Ortac F., Arvas M., Kosebay D., Sonmezer M., Kose K.: “The role of secondary cytoreductive surgery for recurrent ovarian cancer”. Gynecol. Oncol., 2005, 97, 74.

[9] Harter P., Hahmann M., Lueck H.J., Poelcher M., Wimberger P., Ortmann O., 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”. Ann. Surg. Oncol., 2009, 16, 1324.

[10] Lee C.K., Lord S., Grunewald T., Gebski V., Hardy-Bessard A.C., Sehouli J., et al.: “Impact of secondary cytoreductive surgery on survival in patients with platinum sensitive recurrent ovarian cancer: Analysis of the CALYPSO trial”. Gynecol. Oncol., 2015, 136, 18.

[11] Chua T.C., Yan T.D., Saxena A., Morris D.L.: “Should the treatment of peritoneal carcinomatosis by cytoreductive surgery and hyperthermic intraperitoneal chemotherapy still be regarded as a highly morbid procedure?: a systematic review of morbidity and mortality”. Ann. Surg., 2009, 249, 900.

[12] Fagotti A., Costantini B., Petrillo M., Vizzielli G., Fanfani F., Margariti P.A., et al.: “Cytoreductive surgery plus HIPEC in platinum-sensitive recurrent ovarian cancer patients: a case-control study on survival in patients with two year follow-up”. Gynecol. Oncol., 2012, 127, 502.

[13] Cavaliere F., De Simone M., Virzi S., Deraco M., Rossi C.R., Garofalo A., et al.: “Prognostic factors and oncologic outcome in 146 patientswith colorectal peritoneal carcinomatosis treated with cytoreductive surgery combined with hyperthermic intraperitoneal chemotherapy: Italian multicenter study S.I.T.I.L.O”. Eur. J. Surg. Oncol., 2011, 37, 148.

[14] Caneparo A., Massucco P., Vaira M., Maina G., Giovale E., Coggiola M., et al.: “Contamination risk for operators performing semiclosed HIPEC procedure using cisplatin. Eur J Surg Oncol: 2014;40(8):925.

[15] Yan T.D., Black D., Savady R., Sugarbaker P.H.: “A systematic review on the efficacy of cytoreductive surgery and perioperative intraperitoneal chemotherapy for pseudomyxoma peritonei”. Ann. Surg. Oncol., 2007, 14, 484.

[16] Yan T.D., Black D., Savady R., Sugarbaker P.H.: “Systematic review on the efficacy of cytoreductive surgery combined with perioperative intraperitoneal chemotherapy for peritoneal carcinomatosis from colorectal carcinoma”. J. Clin. Oncol., 2006, 24, 4011.

[17] Yan T.D., Welch L., Black D., Sugarbaker P.H.: “A systematic review on the efficacy of cytoreductive surgery combined with perioperative intraperitoneal chemotherapy for diffuse malignancy peritoneal mesothelioma”. Ann. Oncol., 2007, 18, 827.

[18] Jacquet P., Sugarbaker P.H.: “Clinical research methodologies in diagnosis and staging of patients with peritoneal carcinomatosis”. Cancer Treat. Res., 1996, 82, 359.

[19] Sugarbaker P.H.: “Peritonectomy procedures”. Cancer Treat Res., 1996, 82, 235.

[20] De Simone M., Barone R., Vaira M., Aghemo B., Mioli P., Franco C., et al.: “Semi-closed hyperthermic-antiblastic peritoneal perfusion (HAPP) in the treatment of peritoneal carcinosis”. J. Surg. Oncol., 2003, 82, 138.

[21] Rustin G.J., Vergote I., Eisenhauer E., Pujade-Lauraine E., Quinn M., Thigpen T., et al.: “Definitions for response and progression in ovarian cancer clinical trials incorporating RECIST 1.1 and CA 125 agreed by the Gynecological Cancer Intergroup (GCIG)”. Int. J. Gynecol. Cancer, 2011, 21, 419.

[22] Clavien P.A., Barkun J., de Oliveira M.L., Vauthey J.N., Dindo D., Schulick R.D., et al.: “The Clavien-Dindo classification of surgical complications: five-year experience”. Ann. Surg., 2009, 250, 187.

[23] Pfisterer J., Plante M., Vergote I., du Bois A., Hirte H., Lacave A.J., et al.: “Gemcitabine plus carboplatin compared with carboplatin in patients with platinum-sensitive recurrent ovarian cancer: an intergrouptrial of the AGO-OVAR, the NCIC CTG, and the EORTC GCG”. J. Clin. Oncol., 2006, 24, 4699.

[24] Wagner U., Marth C., Largillier R., Kaern J., Brown C., Heywood M., et al.: “Final overall survival results of phase III GCIG CALYPSO trial of pegylated liposomal doxorubicin and carboplatin vs paclitaxel and carboplatin in platinum-sensitive ovarian cancer patients”.Br. J. Cancer, 2012, 107, 588.

[25] Al Rawahi T., Lopes A.D., Bristow R.E., Bryant A., Elattar A., Chattopadhyay S., et al.: “Surgical cytoreduction for recurrent epithelial ovarian cancer”. Cochrane Database Syst. Rev., 2013, 2, CD008765.

[26] Harter P., Sehouli J., Reuss A., Hasenburg A., Scambia G., Cibula D., et al.: “Prospective validation study of a predictive score for operability of recurrent ovarian cancer: the Multicenter Intergroup Study DESKTOP II. A project of the AGO Kommission OVAR, AGO Study Group, NOGGO, AGO-Austria, and MITO”. Int. J. Gynecol. Cancer, 2011, 21, 289.

[27] Oksefjell H., Sandstad B., Trope C.: ‘The role of secondary cytoreduction in the management of the first relapse in epithelial ovarian cancer”. Ann. Oncol., 2009, 20, 286.

[28] Spiliotis J., Vaxevanidou A., Sergouniotis F., Lambropoulou E., DatsisA., Christopoulou A.: “The role of cytoreductive su rgery and hyperthermicintraperitoneal chemotherapy in the management of recurrent advanced ovarian cancer: a prospective study”. J. BUON., 2011, 16, 74.

[29] Munoz-Casares F.C., Rufian S., Rubio M.J., Diaz C.J., Diaz R., Casado A., et al.: “The role of hyperthermic intraoperative intra-peritoneal chemotherapy (HIPEC) in the treatment of peritoneal carcinomatosis in recurrent ovarian cancer”. Clin. Transl. Oncol., 2009, 11, 753.

[30] Harrison M.L., Gore M.E., Spriggs D., Kaye S., Iasonos A., Hensley M., et al.: “Duration of second or greater complete clinical remission in ovarian cancer: exploring potential endpoints for clinical trials”. Gynecol. Oncol., 2007, 106, 469.


Abstracted / indexed in

Science Citation Index Expanded (SciSearch) Created as SCI in 1964, Science Citation Index Expanded now indexes over 9,500 of the world’s most impactful journals across 178 scientific disciplines. More than 53 million records and 1.18 billion cited references date back from 1900 to present.

Biological Abstracts Easily discover critical journal coverage of the life sciences with Biological Abstracts, produced by the Web of Science Group, with topics ranging from botany to microbiology to pharmacology. Including BIOSIS indexing and MeSH terms, specialized indexing in Biological Abstracts helps you to discover more accurate, context-sensitive results.

Google Scholar Google Scholar is a freely accessible web search engine that indexes the full text or metadata of scholarly literature across an array of publishing formats and disciplines.

JournalSeek Genamics JournalSeek is the largest completely categorized database of freely available journal information available on the internet. The database presently contains 39226 titles. Journal information includes the description (aims and scope), journal abbreviation, journal homepage link, subject category and ISSN.

Current Contents - Clinical Medicine Current Contents - Clinical Medicine provides easy access to complete tables of contents, abstracts, bibliographic information and all other significant items in recently published issues from over 1,000 leading journals in clinical medicine.

BIOSIS Previews BIOSIS Previews is an English-language, bibliographic database service, with abstracts and citation indexing. It is part of Clarivate Analytics Web of Science suite. BIOSIS Previews indexes data from 1926 to the present.

Journal Citation Reports/Science Edition Journal Citation Reports/Science Edition aims to evaluate a journal’s value from multiple perspectives including the journal impact factor, descriptive data about a journal’s open access content as well as contributing authors, and provide readers a transparent and publisher-neutral data & statistics information about the journal.

Submission Turnaround Time

Conferences

Top