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. Author manuscript; available in PMC: 2015 Dec 1.
Published in final edited form as: Cancer Epidemiol Biomarkers Prev. 2014 Dec;23(12):2681–2687. doi: 10.1158/1055-9965.EPI-14-0490

Table 3. Responses of biospecimen researchers to questions on the SEER Residual Tissue Repository (RTR).

A. Background of biospecimen research questionnaire respondents
Q1. If you conduct scientific research, please indicate your primary affiliation. (174 responses)

Academic 117 (67%)

Government 24 (14%)

Other 33 (19%)

Q2. Have you worked with biospecimens from the SEER RTR in the past? (159 responses)

Yes 30 (19%)

No 129 (81%)

Q3. If you are aware of the SEER RTR but have not worked with this resource in the past, please indicate why and continue with Question 8. (90 responses)

Plan to apply once preliminary results are obtained or obtain funding 36 (40%)

Did not meet research needs 28 (31%)

Unaware of RTR resource 15 (17%)

Other 11 (12%)
B. Responses of SEER Biospecimen researchers on SEER RTR research use and potential (n = 30)
Q4. If you answered YES to question 2, what were your research objectives in using the SEER RTR resource? (26 responses)

Biomarker identification/validation 8 (31%)

Whole-genome analysis 7 (27%)

Multivariate molecular profiling 6 (23%)

Other 5 (19%)

Q5. Did the SEER RTR resource enable you to achieve your research goals? (22 responses)

Yes 19 (86%)

No 3 (14%)

Q6a. Please comment on any advantages (strengths) of using the SEER RTR as a research resource. (24 responses)

Population coverage 10 (42%)

Number of biospecimens 7 (29%)

SEER annotation (demographic, clinical, and survival data) 4 (17%)

Cost/speed of access (convenience) 3 (13%)

Q6b. Please comment on any disadvantages (weaknesses) of using the SEER RTR as a research resource. (22 responses)

Insufficient sample size 8 (36%)

Incomplete QC documentation 8 (36%)

Incomplete clinical annotation 6 (27%)

Q7. Please provide suggestions for improving your ability to access and utilize the SEER RTR biospecimens and associated data. (24 responses)

Increase number of biospecimens 6 (25%)

Improve efficiency of access to biospecimens and associated data 6 (25%)

Streamline application process (IRB/MTA) 5 (21%)

Increase RTR funding/staff 4 (17%)

More targeted annotation of clinical data 3 (13%)
C. Future development of SEER biospecimen resources
Q8. Please elaborate on specific research objectives that you would like to see addressed in the future using the SEER RTR. (43 responses)

Prognostic studies 14 (33%)

Other 12 (28%)

Biomarker identification/validation 9 (21%)

Molecular profiling for tumor classification 8 (19%)

Q9. Please comment on methods or techniques that could be used to assess the tissue quality of SEER RTR biospecimens to enhance their utility for advanced research applications, such as next-generation sequencing. (25 responses)

Sample QC* 16 (64%)

Pathology review 3 (12%)

Upgraded annotation 3 (12%)

Age-matched control 2 (8%)

Adjacent tissue samples 1 (4%)

Q10. Please indicate the importance of the following standard SEER data items for research using SEER RTR biospecimens. (70 responses, selection of multiple categories allowed)

Tissue collection, processing, and storage 41 (58%)

Type of treatment 39 (56%)

Age of specimens 37 (52%)

Risk factors 30 (42%)

Type of health insurance 3 (4%)
*

Immunohistochemistry, In situ hybridization, Polymerase chain reaction