J Gastric Cancer.  2011 Mar;11(1):31-37.

Metachronous Ovarian Metastases Following Resection of the Primary Gastric Cancer

Affiliations
  • 1Department of Surgery, Samsung Changwon Hospital, Sungkyunkwan University School of Medicine, Changwon, Korea. ncnanmc@yahoo.co.kr
  • 2Haeundae Paik Hospital, Inje University College of Medicine, Busan, Korea.

Abstract

PURPOSE
We performed this study to evaluate the clinical presentation as well as the proper surgical intervention for ovarian metastasis from gastric cancers and these tumors were identified during postoperative follow-up. This will help establish the optimal strategy for improving the survival of patients with this entity.
MATERIALS AND METHODS
22 patients (3.2%) with ovarian metastasis were noted when performing a retrospective chart review of (693) females patients who had undergone a resection for gastric cancer between 1981 and 2008. The covariates used for the survival analysis were the patient age at the time of ovarian relapse, the size of the tumor, the initial TNM stage of the gastric cancer, the interval to metastasis and the presence of gross residual disease after treatment for Krukenberg tumor. The cumulative survival curves for the patient groups were calculated with the Kaplan-Meier method and they were compared by means of the Log-Rank test.
RESULTS
The average age of the patients was 48.6 years (range: 24 to 78 years) and the average survival time of the 22 patients was 18.8 months (the estimated 3-year survival rate was 15.8%) with a range of 2 to 59 months after the diagnosis of Krukenberg tumor. The survival rate for patients without gross residual disease was longer than that of the patients with gross residual disease (P=0.0003). In contrast, patient age, the size of ovarian tumor, the initial stage of gastric adenocarcinoma, the interval to metastasis and adjuvant chemotherapy were not prognostic indicators for survival after the development of ovarian metastasis.
CONCLUSIONS
Early diagnosis and complete resection are the only possible hope to improve survival. As the 3-year survival rate after resection of Krukenberg tumor is 15.8%, it seems worthwhile to consider performing tumorectomy as the second cytoreduction.

Keyword

Krukenberg tumor; Stomach neoplasms; Survival

MeSH Terms

Adenocarcinoma
Chemotherapy, Adjuvant
Early Diagnosis
Female
Follow-Up Studies
Humans
Krukenberg Tumor
Neoplasm Metastasis
Recurrence
Retrospective Studies
Stomach Neoplasms
Survival Rate

Figure

  • Fig. 1 Overall survival curves for the patients with Krukenberg tumor from gastric cancer. The patients without gross residual disease survived longer than the patients with gross residual disease (P=0.0003).


Reference

1. Wang J, Shi YK, Wu LY, Wang JW, Yang S, Yang JL, et al. Prognostic factors for ovarian metastases from primary gastric cancer. Int J Gynecol Cancer. 2008. 18:825–832.
Article
2. Yada-Hashimoto N, Yamamoto T, Kamiura S, Seino H, Ohira H, Sawai K, et al. Metastatic ovarian tumors: a review of 64 cases. Gynecol Oncol. 2003. 89:314–317.
Article
3. Cheong JH, Hyung WJ, Chen J, Kim J, Choi SH, Noh SH. Survival benefit of metastasectomy for Krukenberg tumors from gastric cancer. Gynecol Oncol. 2004. 94:477–482.
Article
4. Kiyokawa T, Young RH, Scully RE. Krukenberg tumors of the ovary: a clinicopathologic analysis of 120 cases with emphasis on their variable pathologic manifestations. Am J Surg Pathol. 2006. 30:277–299.
5. Sobin LH, Wittekind C, editors. TNM Classification of Malignant Tumours (UICC). 2002. 6th ed. New York: Wiley-Liss;65–68.
6. Kakushima N, Kamoshida T, Hirai S, Hotta S, Hirayama T, Yamada J, et al. Early gastric cancer with Krukenberg tumor and review of cases of intramucosal gastric cancers with Krukenberg tumor. J Gastroenterol. 2003. 38:1176–1180.
Article
7. Nam SY, Choi IJ, Park KW, Kim CG, Lee JY, Kook MC, et al. Effect of repeated endoscopic screening on the incidence and treatment of gastric cancer in health screenees. Eur J Gastroenterol Hepatol. 2009. 21:855–860.
Article
8. Novak C, Gray LA. Krukenberg tumor of the ovary: clinical and pathological study of four cases. Surg Gynecol Obstet. 1938. 66:157–165.
9. Serov SF, Scully RE, Sobin LH. Histological Typing of Ovarian Tumours. International Histological Classification of Tumours. No 9. 1973. Geneva: WHO;17–54.
10. Lerwill MF, Young RH. Ovarian metastases of intestinal-type gastric carcinoma: a clinicopathologic study of 4 cases with contrasting features to those of the Krukenberg tumor. Am J Surg Pathol. 2006. 30:1382–1388.
11. Yoo CH, Noh SH, Shin DW, Choi SH, Min JS. Recurrence following curative resection for gastric carcinoma. Br J Surg. 2000. 87:236–242.
Article
12. Shin DW, Hyung WJ, Noh SH, Min JS. Risk factors for recurrence aft er curative surgery for early gastric cancer. J Korean Gastric Cancer Assoc. 2001. 1:106–112.
Article
13. Berek JS, Natarajan S. Berek JS, editor. Ovarian and fallopian tube cancer. Berek and Novak's Gynecology. 2007. 14th ed. Philadelphia: Lippincott Williams and Wilkins;1457–1547.
14. McGill F, Ritter DB, Rickard C, Kaleya RN, Wadler S, Greston WM. Management of Krukenberg tumors: an 11-year experience and review of literature. Prim Care Update Ob Gyns. 1998. 5:157–158.
Article
15. Kim HK, Heo DS, Bang YJ, Kim NK. Prognostic factors of Krukenberg's tumor. Gynecol Oncol. 2001. 82:105–109.
Article
16. Shen-Gunther J, Mannel RS. Ascites as a predictor of ovarian malignancy. Gynecol Oncol. 2002. 87:77–83.
Article
17. Mateş IN, Iosif C, Bănceanu G, Ionescu M, Peltecu G, Dinu D, et al. Features of Krukenberg-type tumors--clinical study and review. Chirurgia (Bucur). 2008. 103:23–38.
18. Koyama T, Mikami Y, Saga T, Tamai K, Togashi K. Secondary ovarian tumors: spectrum of CT and MR features with pathologic correlation. Abdom Imaging. 2007. 32:784–795.
Article
19. McGill FM, Ritter DB, Rickard CS, Kaleya RN, Wadler S, Greston WM, et al. Krukenberg tumors: can management be improved? Gynecol Obstet Invest. 1999. 48:61–65.
20. Dikken JL, Jansen EP, Cats A, Bakker B, Hartgrink HH, Kranenbarg EM, et al. Impact of extent of surgery and postoperative chemoradiotherapy on recurrence patterns in gastric cancer. J Clin Oncol. 2010. 28:2430–2436.
Article
21. Wagner AD, Grothe W, Haerting J, Kleber G, Grothey A, Fleig WE. Chemotherapy in advanced gastric cancer: a systematic review and meta-analysis based on aggregate data. J Clin Oncol. 2006. 24:2903–2909.
Article
22. Schütt U, Wedell J, Köppen P, Reichmann J. Preventive ovariectomy in colorectal cancer. Chirurg. 1993. 64:1040–1043.
23. Yamamoto M, Baba H, Kakeji Y, Endo K, Ikeda Y, Toh Y, et al. Prognostic significance of tumor markers in peritoneal lavage in advanced gastric cancer. Oncology. 2004. 67:19–26.
Article
Full Text Links
  • JGC
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr