Skip to main content

Surgical staging of apparent early-stage ovarian mucinous carcinoma

Abstract

Objectives

The aim of the study was to explore the rate of upstaging after complete surgical staging among patients with apparent FIGO stage I ovarian mucinous carcinoma.

Methods

Ovarian mucinous carcinoma patients with surgical treatment at the Peking Union Medical College Hospital between October 2020 and January 1994 were retrospectively reviewed.

Results

In total, 163 patients were included in this study. Surgical restaging was performed in 89 patients after initial incomplete surgical staging, and one-step complete surgical staging was performed in 74 patients. Among these initially incompletely staged patients, residual tumors were found in 16 patients (16/89, 17.9%). Among the 19 patients with apparent FIGO stage IA, no patient was found to have residual tumors after incomplete staging surgery, according to the final pathology result of restaging surgery. Ovarian cystectomy (OR=4.932, 95% CI= 1.347–18.058, P=0.016) was an independent risk factor for residual tumors after incomplete staging surgery. Among all 163 patients, upstaging occurred in 15 patients (15/163, 9.2%). Among 44 apparent FIGO stage IA patients, no patient was upstaged to FIGO II–IVB. Moreover, both a history of ovarian mucinous tumor (OR=4.745, 95% CI= 1.132–19.886, P=0.033) and bilateral ovary involvement (OR=9.739, 95% CI= 2.016–47.056, P=0.005) were independent risk factors for upstaging to FIGO stage II–IVB.

Conclusions

For patients with apparent FIGO stage IA disease, the possibility of residual tumors and upstaging is relatively low. For patients with cystectomy, bilateral mucinous carcinomas, or a history of ovarian mucinous tumors, complete staging surgery maintains greater significance.

Introduction

According to the National Comprehensive Cancer Network (NCCN) clinical practice guidelines, for newly diagnosed invasive epithelial ovarian cancer apparently confined to the ovaries, staged as apparent International Federation of Gynecology and Obstetrics (FIGO) stage I, complete surgical staging includes peritoneal cytologic examination, biopsy of any peritoneal surface or adhesion suspicious for harboring metastasis, omentectomy, appendectomy, pelvic lymph nodes, and para-aortic lymph nodes dissection; whether hysterectomy and salpingo-oophorectomy are performed depends on whether fertility is preserved [1]. However, patients with mucinous ovarian carcinoma are typically diagnosed after surgery. Among primary ovarian tumors with diagnostic discordance in the intraoperative frozen section diagnosis of primary ovarian tumor, patients with mucinous carcinoma constitute the majority of discordant cases (40.5%) [2]. For epithelial ovarian cancer, comprehensive surgical staging is recommended to be performed to rule out occult higher-stage disease, because the data show that approximately 30% of patients undergoing complete staging surgery are upstaged [3]. However, in contrast to high-grade serous ovarian cancers, 65–80% of mucinous ovarian cancers are early-stage at diagnosis and appear to progress in a stepwise manner from benign epithelium to a preinvasive lesion to carcinoma [4]. Moreover, in 2019, in a study of “the value of surgical staging in patients with apparent early-stage epithelial ovarian carcinoma,” histology and grade of histology were identified as important factors for upstaging. Patients with serous carcinomas, especially high-grade serous carcinomas, were more frequently upstaged than those with other histological subtypes [5]. The rate of upstaging in mucinous ovarian carcinoma is unclear. Therefore, the aim of our study was to explore the rate of upstaging after complete surgical staging in patients with apparent FIGO stage I mucinous ovarian carcinoma.

Materials and methods

This study was approved by the Peking Union Medical College Hospital Ethics Review Board (S-K1753). Written informed consent for data collection for research purposes was waived due to its retrospective nature, and the data set was deidentified to protect patient privacy.

Mucinous ovarian carcinoma patients with surgical treatment were, retrospectively, reviewed at the Peking Union Medical College Hospital between October 2020 and January 1994. The inclusion criteria were as follows: complete surgical staging performed in our hospital, histological confirmation of mucinous ovarian carcinoma by at least two experienced gynecological pathologists, and apparent stage I disease according to the FIGO 2014 guidelines. The exclusion criteria were as follows: apparent FIGO stage II–IV disease, pathological type of borderline mucinous tumor, borderline tumor with intraepithelial carcinoma, microinvasive carcinoma, seromucinous carcinoma, or metastatic mucinous carcinoma of the ovary.

Apparent FIGO stage I mucinous ovarian carcinoma was defined as tumors apparently limited to the ovaries, by intraoperative evaluation and/or imaging evaluation for those with one-step complete staging surgery, and by both intraoperative evaluation in the initial incomplete surgery and/or imaging evaluation before restaging surgery for those with restaging surgery (Fig. 1). Upgrading was defined as an apparently FIGO stage I carcinoma was found to be a FIGO stage II–IV carcinoma by final pathologic staging.

Fig. 1
figure 1

Methods

Categorical variables are summarized in frequency tables, whereas continuous variables are presented as medians (25–75% percentiles), as appropriate for data distribution. Binary logistic regression was used to explore the possible influential factors of outcomes. Variates with P < 0.1 in the univariate analysis were entered into the multivariate analysis. The data were analyzed using SPSS (version 23, IBM, Armonk, NY). A P value < 0.05 was considered statistically significant (two-tailed hypothesis).

Results

In total, 163 patients were included in this study, and the clinical characteristics of the patients are summarized in Table 1. Restaging surgery was performed in 89 patients after incomplete surgical staging, and one-step complete staging surgery was performed in 74 patients.

Table 1 The clinical characteristics of the patients

For all 163 patients, the detailed information regarding staging surgery scope and staging surgery-associated complications (severe or medically significant, hospitalization or prolongation of hospitalization indicated) is presented in supplementary table 1. Overall, 23 (14.1%) adverse events occurred, with 9 adverse events (10.1%) associated with restaging surgery and 14 (18.9%) associated with one-step complete staging surgery, respectively.

Among the 89 patients in the restaging surgery group, the initial incomplete staging surgery consisted of bilateral adnexectomy in 7 patients, unilateral adnexectomy in 55, ovarian cystectomy in 26, omentectomy in 4, appendectomy in 7, and hysterectomy in 6. Moreover, among these 89 patients, residual tumors were found in 16 patients (16/89, 17.9%) during the completion of restaging surgery by final pathologic confirmation; in other words, residual tumors were present in 16 patients at the prior initial incomplete staging surgery.

FIGO stage IA was defined as a tumor limited to the unilateral ovary (capsule intact), without malignant cells in ascites or peritoneal washings. While FIGO stage non-IA was defined as FIGO stage IB, IC, or undetermined IA/IB/IC, namely, that it was unclear whether the tumor capsule had ruptured.

Regarding the potential risk factors related to the residual tumor after the initial incomplete staging surgery, for 19 patients with apparent FIGO stage IA, no patient was found to have residual tumor confirmed by the final pathology result of restaging surgery, Among the 70 patients with clinical FIGO stage non-IA, as was shown in Table 2, in the univariate analysis, residual tumors were significantly associated with bilateral ovary involvement (P=0.036) and ovarian cystectomy (P=0.004). In the multivariate analysis, ovarian cystectomy (odds ratio [OR] =4.932, 95% confidence interval [CI]=1.347–18.058, P=0.016) remained an independent risk factor for residual tumors after incomplete staging surgery.

Table 2 The potential risk factors for residual tumors after initial incomplete staging surgery

Upstaging was found in 15 patients (15/163, 9.2%) (Table 3). Of those 15 patients, restaging surgery was performed in 10 patients, and one-step complete staging surgery was performed in 5 patients. According to the data for both restaging surgery and one-step complete staging surgery, among the 44 patients with apparent FIGO stage IA, no patient had upstaged to FIGO II–IVB according to the final surgical pathologic result.

Table 3 The information of upstaged patients

Among the 119 patients with apparent FIGO stage non-IA, 15 patients (15/119, 12.6%) were upstaged to II–IVB based on pathologic findings. As is shown in Table 4. in the univariate analysis, upstaging to FIGO stage II–IV was significantly associated with a history of ovarian mucinous tumor (P=0.033) and bilateral ovary involvement (P=0.005). In the multivariate analysis, both a history of ovarian mucinous tumor (OR=4.745, 95% CI= 1.132–19.886, P=0.033) and bilateral ovary involvement (OR=9.739, 95% CI= 2.016–47.056, P=0.005) remained independent risk factors for upstaging to FIGO stage II–IVB.

Table 4 The potential risk factors for up-staging

Discussion

In this study, 9.2% of patients, apparently (clinically) thought to have stage I disease, upstaged to II–IV based on pathologic findings of surgical staging. Among the patients with apparent (clinical) FIGO stage IA and non-IA, the percentages were 0.0% and 12.6%, respectively.

As is shown in supplementary table 2, in previous studies, the percentage ranged from 12.8% to 31.8% [3, 5,6,7]. The percentage in our study is relatively lower than that in previous studies. The reason may be that, in our study, all the included patients had mucinous ovarian carcinoma, whereas the included patients in previous studies had ovarian epithelial carcinoma, with the majority having serous carcinoma. As mentioned before, patients with high-grade serous tumors were more frequently upstaged than those with other histological subtypes [5].

Interestingly, in our study, we found that, for apparent FIGO stage IA patients, no patient with initial incomplete staging surgery, was found to have residual tumor confirmed by the final pathological results of restaging surgery, and no patient with restaging or one-step surgical staging surgery, was found to have been upstage to FIGO stage II–IVB based on the final pathologic result. To some extent, consistent with a previous study, Peiretti M, et al found that surgical restaging seems to result in the upstaging of a considerable number of ovarian granulosa cell tumors, mainly in the initial stage IC group of patients [8].

As we all know, exploring the possible risk factors for residual tumors during the initial incomplete staging surgery is of significance to clinical decision-making.

Unlike clear-cell and endometrioid carcinomas, which are frequently associated with marked adhesion to the surrounding tissues due to endometriosis, mucinous carcinoma may be a possible candidate for cystectomy [9]. However, in our study, after the multivariate analysis, we found that preservation of the tumor-involved ovary, cystectomy, was related to the residual tumor. The reason why cystectomy was related to the residual tumor may be obvious, as it could be explained by the hypothesis that preservation of the tumor-involved ovary may carry a risk of harboring residual tumor within the remaining ovarian tissue. This hypothesis is supported by a large retrospective study [10]. In the above-mentioned study, the patients with cystectomy more frequently showed ovarian relapse than the patients with oophorectomy [10]. Although oophorectomy is considered as an appropriate operation, cystectomy may be an unavoidable option when it is the only surgical procedure available to preserve fertility [9]. In this situation, special care such as rigorous follow-up should be practiced for those patients with ovarian cystectomy.

A few studies have investigated the possible risk factors for up-staging for epithelial ovarian carcinoma [5]. To the best of our knowledge, this is the first study to explore the possible risk factors for up-staging, especially for mucinous ovarian carcinoma, which may have greater significance. Interestingly, in our study, we found that the presence of bilateral mucinous carcinomas was an independent risk factor for up-staging to FIGO stage II–IVB.

Moreover, distinguishing primary or metastatic mucinous carcinoma continues to be diagnostically challenging [11, 12]. It is thought that bilateral mucinous carcinomas may be an indicator for metastatic tumors [11, 13]. In the study of Seidman JD et al, among bilateral ovarian mucinous tumors, 6% (2/31) were primary and 94% (29/31) were metastatic, whereas among unilateral ovarian mucinous tumors, 55% (10/19) were primary and 45% (9/19) were metastatic [13]. For patients with bilateral mucinous carcinomas, complete staging surgery and comprehensive exploration maintain greater significance, which may alter treatment strategies.

Ovarian mucinous carcinomas are thought to grow from benign epithelium to borderline tumor to invasive carcinoma [12]. Previous studies found that the risk factors for borderline mucinous ovarian tumors evolving to carcinoma included residual disease after the initial surgery [14]. Interestingly, in our study, we also found that a history of ovarian mucinous tumors was also an independent risk factor for up-staging to FIGO stage II–IVB.

This study was limited by the inadequate large sample size and its retrospective nature, which could have possibly introduced some degree of bias. The rate of lymph node dissection was relatively low. Considering the rate of lymph node metastasis is less than 2% in cases of apparent early-stage mucinous ovarian cancer [15]. And the opinions, regarding whether the lymph node dissection should be performed in apparently early-stage ovarian mucinous carcinoma, are controversial [16]. In our institution, resection of clinically negative nodes in cases of apparent early-stage mucinous ovarian cancer is not necessary. Moreover, the rate of omentectomy was 98.7%, and the information is presented in supplementary table 1. With normal appearance, omentectomy was not performed in two cases, one being a 12-year-old patient and one being a 28-year-old patient. Despite these limitations, our study revealed several important factors. The primary finding is as regards the percentage of upstaging to FIGO stage II–IVB for apparent FIGO stage I patients. The secondary finding is as regards the potential risk factors for residual tumors and up-staging. The third finding is that for patients with apparent FIGO stage IA disease, the possibility of residual tumors or upstaging is low.

In conclusion, in this study, residual tumors occurred in 17.9% of patients during incomplete staging surgery and 9.2% of patients were upstaged to stage II–IV. Cystectomy was an independent risk factor for residual tumor, and both bilateral mucinous carcinomas and a history of ovarian mucinous tumors were two independent risk factors for upstaging. For patients with apparent FIGO stage IA disease, the possibility of residual tumors and upstaging is relatively low. For patients with cystectomy, bilateral mucinous carcinomas, or a history of ovarian mucinous tumors, complete staging surgery maintains great significance.

Availability of data and materials

Please contact the corresponding author with a request for data.

Abbreviations

FIGO:

International Federation of Gynecology and Obstetrics

CEA:

Carcinoembryonic antigen

CA:

Carbohydrate antigen

OR:

Odds ratio

CI:

Confidence interval

NCCN:

National Comprehensive Cancer Network

References

  1. NCCN Clinical Practice Guidelines in Oncology - Ovarian Cancer Including Fallopian Tube Cancer and Primary Peritoneal Cancer (2021 Version I)[DB/OL]. http://www.nccn.org.

  2. Yoshida H, Tanaka H, Tsukada T, Abeto N, Kobayashi-Kato M, Tanase Y, et al. Diagnostic Discordance in Intraoperative Frozen Section Diagnosis of Ovarian Tumors: A Literature Review and Analysis of 871 Cases Treated at a Japanese Cancer Center. Int J Surg Pathol. 2020:1066896920960518. https://doi.org/10.1177/1066896920960518.

  3. Stier EA, Barakat RR, Curtin JP, Brown CL, Jones WB, Hoskins WJ. Laparotomy to complete staging of presumed early ovarian cancer. Obstet Gynecol. 1996;87(5 Pt 1):737–40. https://doi.org/10.1016/0029-7844(96)00021-x.

    Article  CAS  PubMed  Google Scholar 

  4. Morice P, Gouy S, Leary A. Mucinous Ovarian Carcinoma. N Engl J Med. 2019;380(13):1256–66. https://doi.org/10.1056/NEJMra1813254.

    Article  CAS  PubMed  Google Scholar 

  5. Hengeveld E, Zusterzeel P, Lajer H, Høgdall C, Rosendahl M. The value of surgical staging in patients with apparent early stage epithelial ovarian carcinoma. Gynecol Oncol. 2019;154(2):308–13. https://doi.org/10.1016/j.ygyno.2019.06.006.

    Article  CAS  PubMed  Google Scholar 

  6. Young RC, Decker DG, Wharton JT, Piver MS, Sindelar WF, Edwards BK, et al. Staging laparotomy in early ovarian cancer. JAMA. 1983;250(22):3072–6.

    Article  CAS  Google Scholar 

  7. Buchsbaum HJ, Brady MF, Delgado G, Miller A, Hoskins WJ, Manetta A, et al. Surgical staging of carcinoma of the ovaries. Surg Gynecol Obstet. 1989;169(3):226–32.

    CAS  PubMed  Google Scholar 

  8. Peiretti M, Candotti G, Fais ML, Ricciardi E, Colombo N, Zanagnolo V, et al. Comparison between laparoscopy and laparotomy in the surgical re-staging of granulosa cell tumors of the ovary. Gynecol Oncol. 2020;157(1):85–8. https://doi.org/10.1016/j.ygyno.2019.12.040.

    Article  CAS  PubMed  Google Scholar 

  9. Kajiyama H, Suzuki S, Niimi K, Tamauchi S, Kawai M, Nagasaka T, et al. Oncologic and reproductive outcomes of cystectomy as a fertility-sparing treatment for early-stage epithelial ovarian cancer. Int J Clin Oncol. 2019;24(7):857–62. https://doi.org/10.1007/s10147-019-01416-y.

    Article  PubMed  Google Scholar 

  10. Fruscio R, Corso S, Ceppi L, Garavaglia D, Garbi A, Floriani I, et al. Conservative management of early-stage epithelial ovarian cancer: results of a large retrospective series. Ann Oncol. 2013;24(1):138–44. https://doi.org/10.1093/annonc/mds241.

    Article  CAS  PubMed  Google Scholar 

  11. Yemelyanova AV, Vang R, Judson K, Wu L-S-F, Ronnett BM. Distinction of Primary and Metastatic Mucinous Tumors Involving the Ovary: Analysis of Size and Laterality Data by Primary Site With Reevaluation of an Algorithm for Tumor Classification. Am J Surg Pathol. 2008;32(1):128–38. https://doi.org/10.1097/PAS.0b013e3180690d2d.

    Article  PubMed  Google Scholar 

  12. Babaier A, Ghatage P. Mucinous Cancer of the Ovary: Overview and Current Status. Diagnostics (Basel). 2020;10(1):52. https://doi.org/10.3390/diagnostics10010052.

  13. Seidman JD, Kurman RJ, Ronnett BM. Primary and metastatic mucinous adenocarcinomas in the ovaries: incidence in routine practice with a new approach to improve intraoperative diagnosis. Am J Surg Pathol. 2003;27(7):985–93. https://doi.org/10.1097/00000478-200307000-00014.

    Article  PubMed  Google Scholar 

  14. Morice P, Uzan C, Fauvet R, Gouy S, Duvillard P, Darai E. Borderline ovarian tumour: pathological diagnostic dilemma and risk factors for invasive or lethal recurrence. Lancet Oncol. 2012;13(3):e103–15. https://doi.org/10.1016/s1470-2045(11)70288-1.

    Article  PubMed  Google Scholar 

  15. Morice P, Joulie F, Camatte S, Atallah D, Rouzier R, Pautier P, et al. Lymph node involvement in epithelial ovarian cancer: analysis of 276 pelvic and paraaortic lymphadenectomies and surgical implications. J Am Coll Surg. 2003;197(2):198–205. https://doi.org/10.1016/s1072-7515(03)00234-5.

    Article  PubMed  Google Scholar 

  16. Chen J, Yin J, Li Y, Gu Y, Wang W, Shan Y, et al. Systematic Lymph Node Dissection May Be Abolished in Patients With Apparent Early-Stage Low-Grade Mucinous and Endometrioid Epithelial Ovarian Cancer. Front Oncol. 2021;11:705720.

    Article  Google Scholar 

Download references

Acknowledgements

None.

Funding

No external funding was obtained for this study.

Author information

Authors and Affiliations

Authors

Contributions

Conception and design: ZY, DC, YZ. Acquisition of data: ZY, DC, YZ, KS. Analysis and interpretation of data: ZY, DC, YZ. Manuscript writing: ZY, YZ. Critical review of the manuscript: ZY, DC, YZ, KS. Final approval of manuscript: ZY, DC, YZ, KS.

Corresponding author

Correspondence to Ying Zhang.

Ethics declarations

Ethics approval and consent to participate

This study was approved by Peking Union Medical College Hospital Ethics Review Board (S-K1753). Written informed consent to participate was waived for its retrospective nature.

Consent for publication

Written informed consent for publication was waived for its retrospective nature, and the data set was de-identified to protect patient privacy.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

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

Supplementary Information

Additional file 1: Supplementary table 1

. The information of staging surgery.

Additional file 2: Supplementary table 2

. Previous studies regarding upstaging in ovarian epithelial cancer. FIGO, International Federation of Gynecology and Obstetrics.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Yuan, Z., Zhang, Y., Cao, D. et al. Surgical staging of apparent early-stage ovarian mucinous carcinoma. World J Surg Onc 20, 307 (2022). https://doi.org/10.1186/s12957-022-02758-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12957-022-02758-0

Keywords