Serous Tubal Intraepithelial Carcinoma: Its Potential Role in Primary Peritoneal Serous Carcinoma and Serous Cancer Prevention

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 stud...

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Veröffentlicht in:Journal of clinical oncology 2008-09, Vol.26 (25), p.4160-4165
Hauptverfasser: CARLSON, Joseph W, MIRON, Alexander, JARBOE, Elke A, PARAST, Mana M, HIRSCH, Michelle S, LEE, Yonghee, MUTO, Michael G, KINDELBERGER, David, CRUM, Christopher P
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container_end_page 4165
container_issue 25
container_start_page 4160
container_title Journal of clinical oncology
container_volume 26
creator CARLSON, Joseph W
MIRON, Alexander
JARBOE, Elke A
PARAST, Mana M
HIRSCH, Michelle S
LEE, Yonghee
MUTO, Michael G
KINDELBERGER, David
CRUM, Christopher P
description 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. 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. 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. 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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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. 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. 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. 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. 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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. 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.</abstract><cop>Baltimore, MD</cop><pub>American Society of Clinical Oncology</pub><pmid>18757330</pmid><doi>10.1200/JCO.2008.16.4814</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Biological and medical sciences
Cystadenocarcinoma, Serous - diagnosis
Cystadenocarcinoma, Serous - etiology
Cystadenocarcinoma, Serous - prevention & control
Disease Progression
Exons
Fallopian Tube Neoplasms - diagnosis
Fallopian Tube Neoplasms - etiology
Fallopian Tube Neoplasms - prevention & control
Fallopian Tubes - pathology
Female
Genes, BRCA1
Genes, BRCA2
Genes, p53
Gynecologic Cancer
Humans
Medical sciences
Mutation
Peritoneal Neoplasms - diagnosis
Peritoneal Neoplasms - etiology
Peritoneal Neoplasms - prevention & control
Treatment Outcome
Tumor Suppressor Protein p53 - genetics
Tumors
title Serous Tubal Intraepithelial Carcinoma: Its Potential Role in Primary Peritoneal Serous Carcinoma and Serous Cancer Prevention
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