Article Data

  • Views 834
  • Dowloads 132

Original Research

Open Access

Validation of a treatment-selection rule for patients with advanced stage ovarian cancer

  • R. van de Vrie1,†,*,
  • E. van Werkhoven2,†
  • M. J. Rutten1
  • J. D. Asseler1
  • H. S. van Meurs1
  • D. E. Werter1
  • M. R. Buist1
  • A. H. Zwinderman3
  • C. A. R. Lok4
  • P. M. M. Bossuyt2
  • G. G. Kenter1
  • P. Tajik2,5

1Department of Obstetrics and Gynaecology, Centre for Gynaecologic Oncology Amsterdam, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands

2Biometrics Department, The Netherlands Cancer Institute, Amsterdam, the Netherlands

3Department of Epidemiology, Biostatistics & Bioinformatics, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands

4Department of Gynaecologic Oncology, Centre for Gynaecologic Oncology Amsterdam, Antoni van Leeuwenhoek Hospital, Amsterdam, the Netherlands

5Department of Pathology, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands

DOI: 10.31083/j.ejgo.2020.06.5369 Vol.41,Issue 6,December 2020 pp.1023-1030

Submitted: 29 January 2019 Accepted: 10 May 2020

Published: 15 December 2020

*Corresponding Author(s): R. van de Vrie E-mail: r.vandevrie@amsterdamumc.nl

† These authors contributed equally.

Abstract

Purpose of investigation: To externally validate the rule of Van Meurs et al. for selecting patients with advanced epithelial ovarian cancer for treatment with primary surgery or neoadjuvant chemotherapy (NACT). Materials and Methods: We analysed a historical cohort of 900 consecutive patients with FIGO stage IIIC/IV ovarian cancer treated for advanced stage epithelial ovarian cancer at the Centre of Gynaecologic Oncology Amsterdam between 1998 and 2012. To externally validate the treatment-selection rule of Van Meurs et al. four groups were defined based on metastatic tumour size (smaller or larger than 45 mm) and FIGO stage (IIIC vs. IV). Within these groups, we compared survival outcomes of primary surgery and NACT. Results: Differential treatment benefit in model-defined subgroups based on metastatic tumour size and FIGO stage was confirmed (interaction p = 0.008). Survival after primary surgery was significantly better compared to NACT plus interval debulking surgery for patients in FIGO stage IIIC (p = 0.001) or IV (p = 0.028) with metastases ≤ 45 mm, and those in FIGO stage IIIC with metastases > 45 mm (p = 0.011). Survival was not significantly worse for FIGO stage IV patients with metastases > 45 mm (p = 0.094). In patients with such large metastases, the location (omentum versus elsewhere in the body) was not prognostic (p = 0.44). Conclusion: Our study has externally validated the treatment-selection rule first described by van Meurs et al. Primary surgery was shown to be superior for all patients except for the FIGO stage IV patients with a large metastatic tumour size (> 45 mm), irrespective of localisation of the metastasis.

Keywords

Ovarian cancer; Treatment strategy; Overall survival; FIGO stage; Metastasis.


Cite and Share

R. van de Vrie,E. van Werkhoven,M. J. Rutten,J. D. Asseler,H. S. van Meurs,D. E. Werter,M. R. Buist,A. H. Zwinderman,C. A. R. Lok,P. M. M. Bossuyt,G. G. Kenter,P. Tajik. Validation of a treatment-selection rule for patients with advanced stage ovarian cancer. European Journal of Gynaecological Oncology. 2020. 41(6);1023-1030.

References

[1] Siegel R., Naishadham D., Jemal A.: “Cancer statistics, 2012”. Ca. Cancer J. Clin., 2012, 62, 10-29.

[2] Rutten M.J., Leeflang M.M.G., Kenter G.G., Mol B.W.J., Buist M.: “Laparoscopy for diagnosing resectability of disease in patients with advanced ovarian cancer”. Cochrane Database Syst. Rev., 2014, 21, CD009786.

[3] van Meurs H.S., Tajik P., Hof M.H.P., Vergote I., Kenter G.G., Mol B.W.J., et al.: “Which patients benefit most from primary surgery or neoadjuvant chemotherapy in stage IIIC or IV ovarian cancer? An exploratory analysis of the European organisation for research and treatment of cancer 55971 randomised trial”. Eur. J. Cancer, 2013, 49, 3191-3201.

[4] Makar A.P., Tropé C.G., Tummers P., Denys H., Vandecasteele K.: “Advanced ovarian cancer: primary or interval debulking? five categories of patients in view of the results of randomized trials and tumor biology: Primary debulking surgery and interval debulking surgery for advanced ovarian cancer”. Oncologist, 2016, 21, 745-754.

[5] Vergote I., Tropé C.G., Amant F., Kristensen G.B., Ehlen T., John-son N., et al.: “Neoadjuvant chemotherapy or primary surgery in stage IIIC or IV ovarian cancer”. N. Engl. J. Med., 2010, 363, 943-953.

[6] Kehoe S., Hook J., Nankivell M., Jayson G.C., Kitchener H., Lopes T., et al.: “Primary chemotherapy versus primary surgery for newly diagnosed advanced ovarian cancer (CHORUS): an open-label, randomised, controlled, non-inferiority trial”. Lancet, 2015, 386, 249-257.

[7] Morrison J., Swanton A., Collins S., Kehoe S.: “Chemotherapy versus surgery for initial treatment in advanced ovarian epithelial cancer”. Cochrane Database Syst. Rev., 2007, 117, CD005343.

[8] Vergote I., Tropé C.G., Amant F., Ehlen T., Reed N.S., Casado A.: “Neoadjuvant chemotherapy is the better treatment option in some patients with stage IIIC to IV ovarian cancer”. J. Clin. Oncol., 2011, 29, 4076-4078.

[9] Chi D.S., Bristow R.E., Armstrong D.K., Karlan B.Y.: “Is the easier way ever the better way?”. J. Clin. Oncol., 2011, 29, 4073-4075.

[10] Bristow R.E., Eisenhauer E.L., Santillan A., Chi D.S.: “Delaying the primary surgical effort for advanced ovarian cancer: A systematic review of neoadjuvant chemotherapy and interval cytoreduc-tion”. Gynecol. Oncol., 2007, 104, 480-490.

[11] Vergote I.B., Van Nieuwenhuysen E., Vanderstichele A.: “How to select neoadjuvant chemotherapy or primary debulking surgery in patients with stage IIIC or IV ovarian carcinoma”. J. Clin. Oncol., 2016, 34, 3827-3828.

[12] Vergote I., De Wever I., Tjalma W., Van Gramberen M., Decloedt J., van Dam P.: “Neoadjuvant chemotherapy or primary debulking surgery in advanced ovarian carcinoma: A retrospective analysis of 285 patients”. Gynecol. Oncol., 1998, 71, 431-436.

[13] Wright A.A., Bohlke K., Armstrong D.K., Bookman M.A., Cliby W. A., Coleman R.L., et al.: “Neoadjuvant chemotherapy for newly diagnosed, advanced ovarian cancer: Society of gynecologic oncology and american society of clinical oncology clinical practice guideline”. Gynecol. Oncol., 2016, 143, 3-15.

[14] Rutten M.J., van de Vrie R., Bruining A., Spijkerboer A.M., Mol B. W., Kenter G.G., et al.: “Predicting surgical outcome in patients with international federation of gynecology and obstetrics stage III or IV ovarian cancer using computed tomography”. Int. J. Gynecol. Cancer, 2015, 25, 407-415.

[15] Rutten M.J., van Meurs H.S., van de Vrie R., Gaarenstroom K.N., Naaktgeboren C.A., van Gorp T., et al.: “Laparoscopy to predict the result of primary cytoreductive surgery in patients with advanced ovarian cancer: A randomized controlled trial”. J. Clin. Oncol., 2017, 35, 613-621.

[16] van Driel W.J., Koole S.N., Sikorska K., Schagen van Leeuwen J. H., Schreuder H.W.R., Hermans R.H.M., et al.: “Hyperthermic intraperitoneal chemotherapy in ovarian cancer”. N. Engl. J. Med., 2018, 378, 230-240.

[17] Meyer L.A., Cronin A.M., Sun C.C., Bixel K., Bookman M.A., Cristea M.C., et al.: “Use and effectiveness of neoadjuvant chemotherapy for treatment of ovarian cancer”. J. Clin. Oncol., 2016, 34, 3854-3863.

[18] Fagotti A., Ferrandina G., Fanfani F., Garganese G., Vizzielli G., Carone V., et al.: “Prospective validation of a laparoscopic predictive model for optimal cytoreduction in advanced ovarian carcinoma”. Am. J. Obstet. Gynecol., 2008, 199, 642.e1-642.e6.

[19] Collins G.S., de Groot J.A., Dutton S., Omar O., Shanyinde M., Tajar A., et al.: “External validation of multivariable prediction models: a systematic review of methodological conduct and reporting”. BMC Med. Res. Methodol., 2014, 14, 40.

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