Ovarian Metastasis from Pancreatic Ductal Adenocarcinoma.


Journal

World journal of surgery
ISSN: 1432-2323
Titre abrégé: World J Surg
Pays: United States
ID NLM: 7704052

Informations de publication

Date de publication:
10 2021
Historique:
accepted: 10 06 2021
pubmed: 9 7 2021
medline: 21 9 2021
entrez: 8 7 2021
Statut: ppublish

Résumé

Pancreatic ductal adenocarcinoma (PDAC) has a high propensity for systemic dissemination. Ovarian metastases are rare and poorly described. We identified PDAC cases with ovarian metastasis from a prospectively maintained registry. We reported on the association between outcomes and clinicopathologic factors. Recurrence-free (RFS) and overall survival (OS) were calculated using Kaplan-Meier analysis. Twelve patients with PDAC and synchronous or metachronous ovarian metastases were identified. Nine patients (75%) underwent pancreatectomy for localized PDAC and developed metachronous ovarian recurrence. The median OS for all patients was 25.4 (IQR:15.4-82.9) months. For the nine patients with metachronous ovarian metastasis, the median RFS and OS were 14.2 (IQR:7.2-58.3) and 44.6 (IQR:18.6-82.9) months, respectively. Nodal disease, poor grade, vascular invasion in the pancreatic primary, and bilateral ovarian disease tended to confer worse outcomes. Patients with resected PDAC and ovarian recurrence tend to have a comparable disease course to more common patterns of recurrence. Primaries with nodal disease, poorer grade, vascular invasion, and bilateral ovarian disease were indicative of more aggressive disease biology. The ideal management remains largely unknown, and future collaborative efforts should optimize therapeutic strategies.

Sections du résumé

BACKGROUND
Pancreatic ductal adenocarcinoma (PDAC) has a high propensity for systemic dissemination. Ovarian metastases are rare and poorly described.
METHODS
We identified PDAC cases with ovarian metastasis from a prospectively maintained registry. We reported on the association between outcomes and clinicopathologic factors. Recurrence-free (RFS) and overall survival (OS) were calculated using Kaplan-Meier analysis.
RESULTS
Twelve patients with PDAC and synchronous or metachronous ovarian metastases were identified. Nine patients (75%) underwent pancreatectomy for localized PDAC and developed metachronous ovarian recurrence. The median OS for all patients was 25.4 (IQR:15.4-82.9) months. For the nine patients with metachronous ovarian metastasis, the median RFS and OS were 14.2 (IQR:7.2-58.3) and 44.6 (IQR:18.6-82.9) months, respectively. Nodal disease, poor grade, vascular invasion in the pancreatic primary, and bilateral ovarian disease tended to confer worse outcomes.
CONCLUSION
Patients with resected PDAC and ovarian recurrence tend to have a comparable disease course to more common patterns of recurrence. Primaries with nodal disease, poorer grade, vascular invasion, and bilateral ovarian disease were indicative of more aggressive disease biology. The ideal management remains largely unknown, and future collaborative efforts should optimize therapeutic strategies.

Identifiants

pubmed: 34236477
doi: 10.1007/s00268-021-06209-x
pii: 10.1007/s00268-021-06209-x
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3157-3164

Informations de copyright

© 2021. Société Internationale de Chirurgie.

Références

Siegel RL, Miller KD, Fuchs HE, Jemal A (2021) Cancer statistics, 2021. CA Cancer J Clin 71(1):7–33
doi: 10.3322/caac.21654
Lennon AM, Wolfgang CL, Canto MI et al (2014) The early detection of pancreatic cancer: what will it take to diagnose and treat curable pancreatic neoplasia? Cancer Res 74(13):3381–3389
doi: 10.1158/0008-5472.CAN-14-0734
Hruban RH, Gaida MM, Thompson E et al (2019) Why is pancreatic cancer so deadly? The Pathologist’s View J Pathol 248(2):131–141
pubmed: 30838636
Groot VP, Rezaee N, Wu W et al (2018) Patterns, timing, and predictors of recurrence following pancreatectomy for pancreatic ductal adenocarcinoma. Ann Surg 267(5):936–945
doi: 10.1097/SLA.0000000000002234
Habib JR, Kinny-Köster B, Bou-Samra P et al (2021) Surgical decision making in pancreatic ductal adenocarcinoma: modeling prognosis following pancreatectomy in the era of induction and neoadjuvant chemotherapy. Ann Surg. https://doi.org/10.1097/SLA.0000000000004915 (published online ahead of print, 2021 Apr 9)
doi: 10.1097/SLA.0000000000004915 pubmed: 33843794
Hart WR (2005) Diagnostic challenge of secondary (metastatic) ovarian tumors simulating primary endometrioid and mucinous neoplasms. Pathol Int 55(5):231–243
doi: 10.1111/j.1440-1827.2005.01819.x
Meriden Z, Yemelyanova AV, Vang R, Ronnett BM (2011) Ovarian metastases of pancreaticobiliary tract adenocarcinomas: analysis of 35 cases, with emphasis on the ability of metastases to simulate primary ovarian mucinous tumors. Am J Surg Pathol 35(2):276–288
doi: 10.1097/PAS.0b013e31820508d0
Woopen H, Rolf C, Braicu EI, et al. (2021) Secondary malignancies in long-term ovarian cancer survivors: results of the ‘Carolin meets HANNA’ study. Int J Gynecol Cancer. [published online ahead of print, 2021 Mar 1]. https://doi.org/10.11136/ijgc-2020-002155 .
de Waal YR, Thomas CM, Oei AL, Sweep FC, Massuger LF (2009) Secondary ovarian malignancies: frequency, origin, and characteristics. Int J Gynecol Cancer 19(7):1160–1165
doi: 10.1111/IGC.0b013e3181b33cce
Shah B, Tang W, Karn S (2016) An up-to-date understanding of the “Krukenberg Tumor” mechanism. Adv Reprod Sci 4:31–36
doi: 10.4236/arsci.2016.42005
Al-Agha OM, Nicastri AD (2006) An in-depth look at Krukenberg tumor: an overview. Arch Pathol Lab Med 130(11):1725–1730
doi: 10.5858/2006-130-1725-AILAKT
Kubeček O, Laco J, Špaček J, Petera J, Kopecký J, Kubečková A, Filip S (2017) The pathogenesis, diagnosis, and management of metastatic tumors to the ovary: a comprehensive review. Clin Exp Metastasis 34(5):295–307
doi: 10.1007/s10585-017-9856-8
Shah B, Tang WH, Karn S (2017) Transcoelomic spread and ovarian seeding during ovulation: a possible pathogenesis of Krukenberg tumor. J Cancer Res Ther 13(1):152–153
doi: 10.4103/0973-1482.206234
Young RH (2006) From krukenberg to today: the ever present problems posed by metastatic tumors in the ovary: part I. historical perspective, general principles, mucinous tumors including the krukenberg tumor. Adv Anat Pathol 13(5):205–227
doi: 10.1097/01.pap.0000213038.85704.e4
Classic pages in obstetrics and gynecology: Friedrich Ernst Krukenberg: Fibrosarcoma ovarii mucocellulare (carcinomatodes). Archiv für Gynäkologie, vol 50, pp. 287–321, 1896. Am J Obstet Gynecol. 1973;117(4):575.
Aziz M, Kasi A. Krukenberg Tumor. In: StatPearls. Treasure Island (FL): StatPearls Publishing; January 22, 2021.
Vang R, Gown AM, Barry TS, Wheeler DT, Ronnett BM (2006) Immunohistochemistry for estrogen and progesterone receptors in the distinction of primary and metastatic mucinous tumors in the ovary: an analysis of 124 cases. Mod Pathol 19(1):97–105
doi: 10.1038/modpathol.3800510
Skirnisdottir I, Garmo H, Holmberg L (2007) Non-genital tract metastases to the ovaries presented as ovarian tumors in Sweden 1990–2003: occurrence, origin and survival compared to ovarian cancer. Gynecol Oncol 105(1):166–171
doi: 10.1016/j.ygyno.2006.11.005
Petru E, Pickel H, Heydarfadai M et al (1992) Nongenital cancers metastatic to the ovary. Gynecol Oncol 44(1):83–86
doi: 10.1016/0090-8258(92)90017-D
Kikkawa F, Shibata K, Ino K et al (2002) Preoperative findings in non-gynecologic carcinomas metastasizing to the ovaries. Gynecol Obstet Invest 54(4):221–227
doi: 10.1159/000068388
Kim WY, Kim TJ, Kim SE et al (2010) The role of cytoreductive surgery for non-genital tract metastatic tumors to the ovaries. Eur J Obstet Gynecol Reprod Biol 149(1):97–101
doi: 10.1016/j.ejogrb.2009.11.011
Sal V, Demirkiran F, Topuz S et al (2016) Surgical treatment of metastatic ovarian tumors from extragenital primary sites. Int J Gynecol Cancer 26(4):688–696
doi: 10.1097/IGC.0000000000000673
Hung YP, Liu CJ, Hu YW et al (2015) Secondary primary malignancy risk in patients with ovarian cancer in Taiwan: a nationwide population-based study. Medicine (Baltimore) 94(38):e1626
doi: 10.1097/MD.0000000000001626
Kim HK, Heo DS, Bang YJ, Kim NK (2001) Prognostic factors of Krukenberg’s tumor. Gynecol Oncol 82(1):105–109
doi: 10.1006/gyno.2001.6210
Wang SD, Zhu L, Wu HW, Dai MH, Zhao YP (2020) Pancreatic cancer with ovarian metastases: a case report and review of the literature. World J Clin Cases 8(21):5380–5388
doi: 10.12998/wjcc.v8.i21.5380
Reade CJ, Riva JJ, Busse JW, Goldsmith CH, Elit L (2013) Risks and benefits of screening asymptomatic women for ovarian cancer: a systematic review and meta-analysis. Gynecol Oncol 130(3):674–681
doi: 10.1016/j.ygyno.2013.06.029
Young RH, Hart WR (1989) Metastases from carcinomas of the pancreas simulating primary mucinous tumors of the ovary: a report of seven cases. Am J Surg Pathol 13:748–756
doi: 10.1097/00000478-198909000-00004
Vang R, Ronnett BM (2006) Distinction of primary ovarian mucinous tumors and mucinous tumors metastatic to the ovary: a practical approach with guidelines for prediction of primary site for metastases of uncertain origin. Pathol Case Rev 11(1):18–30
doi: 10.1097/01.pcr.0000196570.96459.9e
Vang R, Gown AM, Barry TS, Wheeler DT, Ronnett BM (2006) Cytokeratins 7 and 20 in primary and secondary mucinous tumors of the ovary: analysis of coordinate immunohistochemical expression profiles and staining distribution in 179 cases. Am J Surg Pathol 30(9):1130–1139
doi: 10.1097/01.pas.0000213281.43036.bb
Vang R, Gown AM, Wu LSF, Barry TS, Wheeler DT, Yemelyanova A, Seidman JD, Ronnett BM (2006) Immunohistochemical expression of CDX2 in primary ovarian mucinous tumors and metastatic mucinous carcinomas involving the ovary: comparison with CK20 and correlation with coordinate expression of CK7. Mod Pathol 19(11):1421–1428
doi: 10.1038/modpathol.3800698
Ji H, Isacson C, Seidman JD, Kurman RJ, Ronnett BM (2002) Immunohistochemistry for cytokeratins 7 and 20, Dpc4, and MUC5AC in the distinction of metastatic mucinous carcinomas in the ovary from primary ovarian mucinous tumors: Dpc4 assists in the identification of metastatic pancreatic carcinomas. Int J Gynecol Pathol 21(4):391–400
doi: 10.1097/00004347-200210000-00009
Falchook GS, Wolff RA, Varadhachary GR (2008) Clinicopathologic features and treatment strategies for patients with pancreatic adenocarcinoma and ovarian metastases. Gynecol Oncol 108(3):515–519
doi: 10.1016/j.ygyno.2007.11.012
Di Marco M, Vecchiarelli S, Macchini M et al (2012) Preoperative gemcitabine and oxaliplatin in a patient with ovarian metastasis from pancreatic cystadenocarcinoma. Case Rep Gastroenterol 6(2):530–537
doi: 10.1159/000341513
van Driel WJ, Koole SN, Sikorska K et al (2018) Hyperthermic intraperitoneal chemotherapy in ovarian cancer. N Engl J Med 378(3):230–240
doi: 10.1056/NEJMoa1708618
Groot VP, Blair AB, Gemenetzis G et al (2019) Isolated pulmonary recurrence after resection of pancreatic cancer: the effect of patient factors and treatment modalities on survival. HPB (Oxford) 21(8):998–1008
doi: 10.1016/j.hpb.2018.12.002

Auteurs

Joseph R Habib (JR)

Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Shamsher Pasha (S)

Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Subhan Khan (S)

Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Benedict Kinny-Köster (B)

Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Sami Shoucair (S)

Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Elizabeth D Thompson (ED)

Department of Pathology, The Sol Goldman Pancreatic Cancer Research Center, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Jun Yu (J)

Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Kelly Lafaro (K)

Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Richard A Burkhart (RA)

Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

William R Burns (WR)

Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Brigitte M Ronnett (BM)

Department of Pathology, The Sol Goldman Pancreatic Cancer Research Center, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Christopher L Wolfgang (CL)

Department of Surgery, New York University School of Medicine and NYU-Langone Medical Center, New York, NY, USA.

Ralph H Hruban (RH)

Department of Pathology, The Sol Goldman Pancreatic Cancer Research Center, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Jin He (J)

Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Elliot K Fishman (EK)

Department of Radiology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Ammar A Javed (AA)

Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA. ajaved1@jhmi.edu.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH