Survey to assess the feasibility of establishing a gynecologic specimen bank for research
Would you consider your practice to be primarily:
academic (primary activity within medical school teaching hospital or research institute)
private laboratory (not at the hospital)
private hospital (not affiliated with a medical center or research institute)
laboratory affiliated with managed health organization
What is the approximate annual surgical pathology specimen volume at the laboratory where you practice (if multiple, give largest):
<10K
10-25K
>25-50K
>50K
What proportion of these specimens are gynecologic?
<10%
10-20%
>20-50%
>50-100%
Does your laboratory have a subspecialty sign-out with a designated gynecologic section?
No
Yes
Does your laboratory receive risk-reducing surgery specimens from women at high-risk for gynecologic disease/cancer? If so, estimate annual number?
No
Yes (annual number: ___)
How are specimens for the following specific indications processed?
Clinical Indication |
SEE-Fim (Sectioning and Extensively Examining of the Fimbria) |
Submit fimbria |
Submit ovaries |
Endometrium |
High-Grade Serous Cancer Stage I, II, IIIAi |
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Risk-reducing salpingo-oophorectomy or salpingectomy |
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Surgery for benign indications, first sections reveal equivocal or definite STIC (serous tubal intraepithelial carcinoma), epithelial atypia in ovary or clinically occult cancer |
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Surgery for benign indications, first sections reviewed are negative |
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Does your laboratory stain sections of fimbria for Ki67, p53 or other markers (check all that apply):
On every specimen?
On every risk-reducing salpingo-oophorectomy or salpingectomy specimen?
On selected risk-reducing salpingo-oophorectomy or salpingectomy specimens based on H&E review?
On early stage high-grade serous cancer?
Markers not evaluated
Would your laboratory consider providing de-identified blocks and matched pathology reports to a national specimen bank organized by the National Cancer Institute (NCI) to provide access to researchers throughout the world? Possible specimens would include risk-reducing salpingo-oophorectomy or salpingectomy, early high-grade serous cancer (HGSC), serous tubal intraepithelial carcinoma (STIC), and a minor percentage (10%) of total benign tubes and ovaries.
No
Yes
Other comments/clarifications?
File Type | application/msword |
Author | National Cancer Institute |
Last Modified By | Bailey, Karla (NIH/NCI) [E] |
File Modified | 2016-05-13 |
File Created | 2016-02-23 |