Skip to main content
Log in

Are There Survival Differences Between Women with Equivalent Residual Disease After Interval Cytoreductive Surgery Compared with Primary Cytoreductive Surgery for Advanced Ovarian and Peritoneal Cancer?

  • Gynecologic Oncology
  • Published:
Annals of Surgical Oncology Aims and scope Submit manuscript

Abstract

Objective

The aim of this study was to investigate survival differences between equivalent residual disease [complete gross resection (CGR), minimal residual disease (MRD), suboptimal] at the time of primary debulking surgery (PDS) and interval debulking surgery (IDS).

Methods

The National Cancer Database was used to identify patients from 2010 to 2015 with stage IIIC/IV primary peritoneal or ovarian cancer who had residual disease recorded. Propensity score matching (PSM) was used to correct for differences in characteristics between the PDS and IDS groups.

Results

Of 8683 patients with advanced ovarian cancer, 4493 (52%), 2546 (29%), and 1644 (19%) had CGR, MRD, or suboptimal resection, respectively. From 2010 to 2015, the number of patients undergoing IDS increased 27% (ptrend < 0.001), and there was an 18% increase in CGRs (ptrend = 0.005). The increased use of IDS from 2010 to 2015 was associated with increased CGRs (ptrend = 0.02) and decreased MRD (ptrend = 0.001), but not with decreased suboptimal resections (ptrend = 0.18). IDS, even after PSM, was associated with inferior overall survival [OS; hazard ratio (HR) 1.12, 95% confidence interval (CI) 1.03–1.22, p = 0.008]. A CGR at PDS had prolonged median OS compared with a CGR at IDS (51 vs. 44 months, p < 0.001). Additionally, MRD at PDS had worse median OS compared with a CGR at IDS (41 vs. 44 months, p = 0.03), but improved median OS compared with MRD at IDS (median OS 35 months, p = 0.05).

Conclusion

The use of IDS continues to rise in the US, and is associated with improved surgical outcomes but not necessarily similar oncologic outcomes. There should be continued efforts to improve cytoreductive outcomes in women with advanced ovarian and peritoneal malignancies.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

References

  1. Siegel RL, Miller KD, Jemal A. Cancer statistics, 2018. CA Cancer J Clin. 2018;68(1):7–30. https://doi.org/10.3322/caac.21442.

    Article  PubMed  Google Scholar 

  2. Cannistra SA. Cancer of the ovary. N Engl J Med. 2004;351(24):2519–29. https://doi.org/10.1056/nejmra041842.

    Article  CAS  PubMed  Google Scholar 

  3. Morgan RJ, Armstrong DK, Alvarez RD, et al. Ovarian cancer, version 1.2016, NCCN clinical practice guidelines in oncology. J Natl Compr Cancer Netw. 2016;14(9):1134–63.

    Article  Google Scholar 

  4. Vergote I, Trope CG, Amant F, et al. Neoadjuvant chemotherapy or primary surgery in stage IIIC or IV ovarian cancer. N Engl J Med. 2010;363(10):943–53. https://doi.org/10.1056/nejmoa0908806.

    Article  CAS  PubMed  Google Scholar 

  5. Kehoe S, Hook J, Nankivell M, 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(9990):249–57. https://doi.org/10.1016/s0140-6736(14)62223-6.

    Article  PubMed  Google Scholar 

  6. Schorge JO, Clark RM, Lee SI, Penson RT. Primary debulking surgery for advanced ovarian cancer: Are you a believer or a dissenter? Gynecol Oncol. 2014;135(3):595–605. https://doi.org/10.1016/j.ygyno.2014.10.007.

    Article  PubMed  Google Scholar 

  7. Chi DS, Bristow RE, Armstrong DK, Karlan BY. Is the easier way ever the better way? J Clin Oncol. 2011;29(31):4073–5. https://doi.org/10.1200/jco.2011.35.9935.

    Article  CAS  PubMed  Google Scholar 

  8. Kang S. Neoadjuvant chemotherapy for ovarian cancer: Do we have enough evidence? Lancet. 2015;386(9990):223–4. https://doi.org/10.1016/s0140-6736(14)62259-5.

    Article  PubMed  Google Scholar 

  9. Onda T, Satoh T, Saito T, et al. Comparison of survival between upfront primary debulking surgery versus neoadjuvant chemotherapy for stage III/IV ovarian, tubal and peritoneal cancers in phase III randomized trial: JCOG0602. J Clin Oncol. 2018;36(15 Suppl):5500. https://doi.org/10.1200/jco.2018.36.15_suppl.5500.

    Article  Google Scholar 

  10. Fagotti A, Vizzielli G, Ferrandina G, et al. Survival analyses from a randomized trial of primary debulking surgery versus neoadjuvant chemotherapy for advanced epithelial ovarian cancer with high tumor load (SCORPION trial). J Clin Oncol. 2018;36(15 Suppl):5516. https://doi.org/10.1200/jco.2018.36.15_suppl.5516.

    Article  Google Scholar 

  11. Winchester DP, Stewart AK, Phillips JL, Ward EE. The national cancer data base: past, present, and future. Ann Surg Oncol. 2010;17(1):4–7.

    Article  Google Scholar 

  12. Wright JD, Chen L, Hou JY, et al. Association of hospital volume and quality of care with survival for ovarian cancer. Obstet Gynecol. 2017;130(3):545–53. https://doi.org/10.1097/aog.0000000000002164.

    Article  PubMed  PubMed Central  Google Scholar 

  13. Horner W, Peng K, Pleasant V, et al. Trends in surgical complexity and treatment modalities utilized in the management of ovarian cancer in an era of neoadjuvant chemotherapy. Gynecol Oncol. 2019;154(2):283–9. https://doi.org/10.1016/j.ygyno.2019.05.023.

    Article  PubMed  Google Scholar 

  14. Fisher J, Jones D, Pomposelli F, Upchurch G. Fisher’s mastery of surgery. Philadelphia, PA: Lippincott Williams and Wilkins; 2012. pp. 2–25.

    Google Scholar 

  15. R: A language and environment for statistical computing. R Foundation for Statistical Computing. Vienna: The R Foundation for Statistical Computing; 2014.

  16. Reeve BB, Smith AW, Arora NK, Hays RD. Reducing bias in cancer research: application of propensity score matching. Health Care Financ Rev. 2008;29(4):69–80.

    PubMed  PubMed Central  Google Scholar 

  17. Ridgeway G, McCaffrey D, Morral A, Burgette L, Griffin BA. Toolkit for weighting and analysis of nonequivalent groups: a tutorial for the twang package. Santa Monica, CA: RAND Corporation; 2017.

    Google Scholar 

  18. Sioulas VD, Schiavone MB, Kadouri D, et al. Optimal primary management of bulky stage IIIC ovarian, fallopian tube and peritoneal carcinoma: are the only options complete gross resection at primary debulking surgery or neoadjuvant chemotherapy? Gynecol Oncol. 2017;145(1):15–20. https://doi.org/10.1016/j.ygyno.2017.02.023.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Tate S, Nishikimi K, Kato K, et al. Microscopic diseases remain in initial disseminated sites after neoadjuvant chemotherapy for stage III/IV ovarian, tubal, and primary peritoneal cancer. J Gynecol Oncol. 2020;31(3):e34.

    Article  CAS  Google Scholar 

  20. Hynninen J, Lavonius M, Oksa S, Grénman S, Carpén O, Auranen A. Is perioperative visual estimation of intra-abdominal tumor spread reliable in ovarian cancer surgery after neoadjuvant chemotherapy? Gynecol Oncol. 2013;128(2):229–32.

    Article  Google Scholar 

  21. Aletti GD, Peiretti M. Quality control in ovarian cancer surgery. Best Pract Res Clin Obstet Gynaecol. 2017;41:96–107.

    Article  Google Scholar 

  22. Reuss A, du Bois A, Harter P, et al. TRUST: trial of radical upfront surgical therapy in advanced ovarian cancer (ENGOT ov33/AGO-OVAR OP7). Int J Gynecol Cancer. 2019;29(8):1327–31. https://doi.org/10.1136/ijgc-2019-000682.

    Article  PubMed  Google Scholar 

Download references

Acknowledgment

The data used in the study are derived from a de-identified NCDB file. The American College of Surgeons and the Commission on Cancer have not verified and are not responsible for the analytic or statistical methodology employed, or the conclusions drawn from these data by the investigator.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to David Pierce Mysona MD.

Ethics declarations

Disclosure

David P. Mysona, Sharad Ghamande, Jin-Xiong She, Lynn Tran, Paul Tran, Bunja J. Rungruang, John K. Chan, Victoria Bae-Jump, and Paola A. Gehrig have no conflicts of interest in relation to the submitted work. Outside of the submitted work, Dr Ghamande has received compensation from GlaxoSmithKline for consulting and from Merck as part of their speakers’ bureau. Dr. Chan has received compensation from Acerta, Aravive, Biodesix, Clovis, Janssen/J&J, Oxigen/Mateon, Roche/Genentech, Tesaro, Astra Zeneca, and Eisai.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Mysona, D.P., Ghamande, S., She, JX. et al. Are There Survival Differences Between Women with Equivalent Residual Disease After Interval Cytoreductive Surgery Compared with Primary Cytoreductive Surgery for Advanced Ovarian and Peritoneal Cancer?. Ann Surg Oncol 28, 3605–3615 (2021). https://doi.org/10.1245/s10434-020-09304-w

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1245/s10434-020-09304-w

Navigation