4.7 Article

Serous tubal Intraepithelial carcinoma: Its potential role in primary peritoneal serous carcinoma and serous cancer prevention

Journal

JOURNAL OF CLINICAL ONCOLOGY
Volume 26, Issue 25, Pages 4160-4165

Publisher

AMER SOC CLINICAL ONCOLOGY
DOI: 10.1200/JCO.2008.16.4814

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Funding

  1. National Cancer Institute [P50 CA10500 [SPORE]]
  2. D. Cramer, principal investigator [NCI KO8 CA108748]
  3. R. Drapkin, principal investigator [NCI 1R21CA124688- 01A1]
  4. C. P. C., principal investigator
  5. Charlotte Geyer Foundation (C. P. C., principal investigator)
  6. Columbia Hospital for Women Research Foundation (C. P. C., principal investigator)
  7. Dana-Farber Cancer Institute
  8. Francis Ward Paine
  9. TSA Pemberton Funds from the Division of Women's and Perinatal Pathology, Brigham and Women's Hospital

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Purpose A diagnosis of primary peritoneal serous carcinoma (PPSC) requires exclusion of a source in other reproductive organs. Serous tubal intraepithelial carcinoma (STIC; stage 0) has been described in asymptomatic women with BRCA mutations and linked to a serous cancer precursor in the fimbria. This study examined the frequency of STIC in PPSC and its clinical outcome in BRCA-positive women. Patients and Methods Presence or absence of STIC was recorded in consecutive cases meeting the 2001 WHO criteria for PPSC, including 26 patients with nonuniform sampling of the fallopian tubes (group 1) and 19 patients with complete tubal examination (group 2; sectioning and extensively examining the fimbriated end, or SEE-FIM protocol). In selected cases, STIC or its putative precursor and the peritoneal tumor were analyzed for p53 mutations (exons 1 to 11). Outcome of STIC was ascertained by literature review. Result Thirteen (50%) of 26 PPSCs in group 1 involved the endosalpinx, with nine STICs (35%). Fifteen (79%) of 19 cases in group 2 contained endosalpingeal involvement, with nine STICs (47%). STIC was typically fimbrial and unifocal, with variable invasion of the tubal wall. In five of five cases, the peritoneal and tubal lesion shared an identical p53 mutation. Of 10 reported STICs in BRCA-positive women, all patients were without disease on follow-up. Conclusion The fimbria is the source of nearly one half of PPSCs, suggesting serous malignancy originates in the tubal mucosa but grows preferentially at a remote peritoneal site. The generally low risk of recurrence in stage 0 (STIC) disease further underscores STIC as a possible target for early serous cancer detection and prevention.

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