Can the use of perioperative epidural impact survival outcome in women with advanced ovarian cancer?

Can the use of perioperative epidural impact survival outcome in women with advanced ovarian cancer?

Søren Lunde1, Pernille T. Jensen2,3

1Department of Obstetrics and Gynecology, Aalborg University Hospital, Aalborg, Denmark; 2Department of Obstetrics and Gynecology, Odense University Hospital, Odense, Denmark; 3Faculty of Health Science, University of Southern Denmark, Odense, Denmark

Correspondence to: Søren Lunde. Department of Obstetrics and Gynecology, Aalborg University Hospital, Reberbansgade 15, 9000 Aalborg, Denmark. Email:

Comment on: Tseng JH, Cowan RA, Afonso AM, et al. Perioperative epidural use and survival outcomes in patients undergoing primary debulking surgery for advanced ovarian cancer. Gynecol Oncol 2018;151:287-93.

Received: 12 December 2018; Accepted: 14 December 2018; Published: 21 December 2018.

doi: 10.21037/gpm.2018.12.01

The surgical stress response following major surgery is characterized by a physiologic cascade of immunologic and endocrine alterations and an activation of the sympathetic nervous system with release of catecholamines like dopamine, norepinephrine, and epinephrine (1). The stress response is activated by afferent neuronal impulses from the site of tissue injury. The resultant sympathoadrenal response increases secretion of cortisol from the adrenal cortex, which in turn elevates the level of blood glucose via an increased hepatic glycogenolysis, gluconeogenesis, and a decreased peripheral metabolism of glucose. The surgical tissue injury furthermore induces a release of cytokines like interleukin-1, tumor necrosis factor-α and interleukin-6 from leucocytes and fibroblasts which mediates the inflammatory cascade and induces angioneogenesis (2). The surgical stress response is a complex physiologic mechanism, which enables the organism to encounter vast tissue damage. Clinical studies, however, have demonstrated that the release of cytokines and catecholamines induced by the stress response as well as the use of systemic opioids and general anesthesia can inhibit the cell-mediated immunity (CMI) which plays a key role in the recognition of foreign antibodies (3,4). In cancer surgery, this immunosuppressive consequence is problematic seeing that the reduced CMI also affects the recognition of tumor cells thereby promoting micrometastasis (5).

An emerging theory have hypothesized that the use of epidural analgesia could decrease the neuroendocrine and cytokine mediated surgical stress response. Additionally, the use of epidural analgesia could decrease the need for systemic opioids and general anesthesia thereby reducing the negative effect on the CMI (3). Theoretically, the use of epidural analgesia would thereby reduce the level of micrometastasis, thus resulting in improved survival outcome following cancer surgery.

Several retrospective studies and a few randomized controlled trials have investigated this proposed theory over the past decade in numerous cancer diseases [e.g., colorectal cancer (6), breast cancer (7), malignant melanoma (8), prostate cancer (9), urinary bladder cancer (10) and ovarian cancer (11,12)]—mainly with contradictory results. This was further evaluated in a meta-analysis published in 2017 of 28 studies concerning the effect of epidural in various cancer diseases. The meta-analysis concluded that epidural analgesia had no benefit in overall survival (OS), recurrence-free survival, or biochemical recurrence-free survival in cancer patients (3).

Recently, the effect of perioperative epidural in patients undergoing primary debulking surgery for advanced ovarian cancer was addressed in a retrospective cohort study published by Tseng et al. (13). The cohort consisted of 648 patients with FIGO stage IIIB to IV epithelial ovarian cancer who underwent primary debulking surgery from 2005 to 2013 at Memorial Sloan Kettering Cancer Center in New York, USA. Roughly, two thirds of the patients received a perioperative epidural, while one third did not. The decision to place an epidural or not was made by the attending surgeon and anesthesiologist in respect of the patient’s preference. The epidural catheters were all placed preoperatively while infusion started either intraoperatively or immediately postoperatively. Adjuvant chemotherapy was given either as intravenous infusion or in combination with intraperitoneal chemotherapy. Postoperative imaging assessed recurrence and progression and the outcome measures were progression free survival (PFS) and OS. The epidural group had a significantly higher FIGO stage distribution, higher rate of carcinomatosis, and bulky upper abdominal disease compared to the non-epidural group. Complete gross resection was achieved more frequently in the epidural group compared to the non-epidural group (48% vs. 31%). The results showed a significantly higher risk of recurrence, progression, and death in the non-epidural compared to the epidural group with a PFS of 13.9 vs. 20.8 months (P=0.021) and an OS of 41.9 vs. 62.4 months (P<0.001), respectively. The authors suggest this considerable difference in PFS and OS to be the effect of the diminished surgical stress response in patients who received an epidural.

Retrospective studies are prone to a high risk of bias. If unexpected results emerge one must consider potential confounding. During the past two decades several studies and a Cochrane review have confirmed that complete resection of any intraabdominal gross disease (R0) is the most important prognostic factor for survival in women with advanced ovarian cancer (14-18). Further, both the number of residual nodules and the volume of disease have been shown to impact on survival (19).

In the study of Tseng et al. information on complete gross resection and presence of peritoneal carcinomatosis was obtained retrospectively from medical chart review (13). Complete gross resection was defined as cytoreduction leaving tumor nodules measuring 1–10 mm, which is usually defined as R1. Both factors constitute significant confounders. The inaccuracy by retrospective scrutiny of the medical charts for the surgeon’s specification of residual disease cannot be disregarded. Further, it remains unknown whether a single or hundreds of small nodules <10 mm were left and how the patients with different degrees of residual disease were distributed between the two groups. Other inherent confounders could be mentioned: Imbalance between groups regarding the choice of epidural or not, lack of standardized set up related to start and discontinuation of the epidural during the intra- and postoperative phase, different chemotherapy regimens used e.g., only some patients had intraperitoneal chemotherapy while other had intravenous chemotherapy only and this was not balanced between groups.

However, another confounder may be even more important and is likely to jeopardize the internal validity of the study. Recently, in a second paper, the authors discussed the importance of surgeon’s expertise and time related factors with institutional improvement over time in the complete cytoreduction rate (20). In the present study (13), the epidural group had significantly worse baseline disease distribution in critical locations but obtained better surgical outcome than the non-epidural group. This is counterintuitive and draws the reader’s attention. A problematic imbalance between surgeons’ competences and experience within primary debulking surgery in advanced ovarian cancer could explain the findings. The authors therefore include the surgeon as a cluster effect in the Cox proportional Hazard model to account for potential influence of variances in surgeons’ competences. However, considering the indisputable less favorable baseline disease distribution in the epidural group, the results of the survival analyses between epidural groups are still surprising. The close correlation between surgeons’ competences and the rate of R0/R1 after primary debulking surgery in ovarian cancer and the well-known correlation between R0/R1 and survival is likely to introduce multicollinearity in the regression analyses. Hence, despite an attempt to adjust for the differences between groups, the imbalance severely compromises the internal and external validity of the study. Further, multicollinearity is likely to be present and influence the response variable. Hence, it is questioned whether epidural use in the present setting represents a true independent variable as suggested. Surgeons’ competences may play a greater role than accounted for and it could be questioned whether the suggested study design is suitable to evaluate the question of whether perioperative epidural impact survival outcome in women with advanced ovarian cancer.

Having said that the results of the study are interesting and warrant further studies. The mechanisms responsible for the formation of micrometastasis and the complex immunologic aspects of the surgical stress response are yet to be fully understood. Until then, large randomized controlled trials are needed to form an unambiguous conclusion when it comes to the effect of a perioperative epidural on survival outcome in solid tumor cancers.




Conflicts of Interest: The authors have no conflicts of interest to declare.


  1. Desborough JP. The stress response to trauma and surgery. Br J Anaesth 2000;85:109-17. [Crossref] [PubMed]
  2. Sheeran P, Hall GM. Cytokines in anaesthesia. Br J Anaesth 1997;78:201-19. [Crossref] [PubMed]
  3. Grandhi RK, Lee S, Abd-Elsayed A. The Relationship Between Regional Anesthesia and Cancer: A Metaanalysis. Ochsner J 2017;17:345-61. [PubMed]
  4. Ben-Eliyahu S. The promotion of tumor metastasis by surgery and stress: immunological basis and implications for psychoneuroimmunology. Brain Behav Immun 2003;17 Suppl 1:S27-36. [Crossref] [PubMed]
  5. Shakhar G, Ben-Eliyahu S. Potential prophylactic measures against postoperative immunosuppression: could they reduce recurrence rates in oncological patients? Ann Surg Oncol 2003;10:972-92. [Crossref] [PubMed]
  6. Day AR, Smith RVP, Scott MJP. Randomized clinical trial investigating the stress response from two different methods of analgesia after laparoscopic colorectal surgery. Br J Surg 2015;102:1473-9. [Crossref] [PubMed]
  7. Starnes-Ott K, Goravanchi F, Meininger JC. Anesthetic choices and breast cancer recurrence: a retrospective pilot study of patient, disease, and treatment factors. Crit Care Nurs Q 2015;38:200-10. [Crossref] [PubMed]
  8. Gottschalk A, Brodner G, Van Aken HK. Can regional anaesthesia for lymph-node dissection improve the prognosis in malignant melanoma? Br J Anaesth 2012;109:253-9. [Crossref] [PubMed]
  9. Tseng KS, Kulkarni S, Humphreys EB, et al. Spinal anesthesia does not impact prostate cancer recurrence in a cohort of men undergoing radical prostatectomy: an observational study. Reg Anesth Pain Med 2014;39:284-8. [Crossref] [PubMed]
  10. Chipollini J, Alford B, Boulware DC, et al. Epidural anesthesia and cancer outcomes in bladder cancer patients: is it the technique or the medication? A matched-cohort analysis from a tertiary referral center. BMC Anesthesiol 2018;18:157. [Crossref] [PubMed]
  11. Lin L, Liu C, Tan H. Anaesthetic technique may affect prognosis for ovarian serous adenocarcinoma: A retrospective analysis. Br J Anaesth 2011;106:814-22. [Crossref] [PubMed]
  12. de Oliveira GS, Ahmad S, Schink JC. Intraoperative neuraxial anesthesia but not postoperative neuraxial analgesia is associated with increased relapse-free survival in ovarian cancer patients after primary cytoreductive surgery. Reg Anesth Pain Med 2011;36:271-7. [Crossref] [PubMed]
  13. Tseng JH, Cowan RA, Afonso AM, et al. Perioperative epidural use and survival outcomes in patients undergoing primary debulking surgery for advanced ovarian cancer. Gynecol Oncol 2018;151:287-93. [Crossref] [PubMed]
  14. Sørensen SM, Schnack TH, Høgdall C. Impact of residual disease on overall survival in women with Federation of Gynecology and Obstetrics stage IIIB-IIIC vs stage IV epithelial ovarian cancer after primary surgery. Acta Obstet Gynecol Scand 2018. [Epub ahead of print]. [PubMed]
  15. Vergote I, Trimbos BJ. Treatment of patients with early epithelial ovarian cancer. Curr Opin Oncol 2003;15:452-5. [Crossref] [PubMed]
  16. Eisenkop SM, Friedman RL, Wang HJ. Complete cytoreductive surgery is feasible and maximizes survival in patients with advanced epithelial ovarian cancer: a prospective study. Gynecol Oncol 1998;69:103-8. [Crossref] [PubMed]
  17. Markauskas A, Mogensen O, dePont Christensen R. Primary surgery or interval debulking for advanced epithelial ovarian cancer: does it matter? Int J Gynecol Cancer 2014;24:1420-8. [Crossref] [PubMed]
  18. Elattar A, Bryant A, Winter-Roach BA. Optimal primary surgical treatment for advanced epithelial ovarian cancer. Cochrane database Syst Rev 2011.CD007565. [PubMed]
  19. Stoeckle E, Paravis P, Floquet A, et al. Number of residual nodules, better than size, defines optimal surgery in advanced epithelial ovarian cancer. Int J Gynecol Cancer 2004;14:779-87. [Crossref] [PubMed]
  20. Tseng JH, Cowan RA, Zhou Q, et al. Continuous improvement in primary Debulking surgery for advanced ovarian cancer: Do increased complete gross resection rates independently lead to increased progression-free and overall survival? Gynecol Oncol 2018;151:24-31. [Crossref] [PubMed]
doi: 10.21037/gpm.2018.12.01
Cite this article as: Lunde S, Jensen PT. Can the use of perioperative epidural impact survival outcome in women with advanced ovarian cancer? Gynecol Pelvic Med 2018;1:13.