Proposed Collection; Comment Request; Follow-Up of Kidney Cancer Patients From the Central European Multicenter Case-Control Study, 65387-65388 [E8-26086]
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Federal Register / Vol. 73, No. 213 / Monday, November 3, 2008 / Notices
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[FR Doc. E8–26139 Filed 10–31–08; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Proposed Collection; Comment
Request; Follow-Up of Kidney Cancer
Patients From the Central European
Multicenter Case-Control Study
SUMMARY: In compliance with the
requirement of section 3506(c)(2)(A) of
the Paperwork Reduction Act of 1995,
for opportunity for public comment on
proposed data collection projects, the
National Cancer Institute (NCI), the
National Institutes of Health (NIH) will
publish periodic summaries of proposed
projects to be submitted to the Office of
Management and Budget (OMB) for
review and approval.
Proposed Collection: Title: Follow-up
of Kidney Cancer Patients from the
Central European Multicenter CaseControl Study. Type of Information
Collection Request: New. Need and Use
of Information Collection: The purpose
of this questionnaire is to obtain
information on the 5-year survival status
of kidney cancer patients that were
enrolled in a Central European CaseControl Study of Kidney Cancer that
was conducted between 2001–2004. The
aim is to assess survival, the prevalence
of recurrent disease and progression,
and to investigate patient, tumor and
genetic determinants of survival among
cases. The questionnaire will collect
information on patient related factors,
tumor related factors not collected
during the initial study, and the type of
treatment(s) received since the patients
were last contacted for the case-control
study. This questionnaire adheres to
The Public Health Service Act, section
412 (42 U.S.C. 285a–1) and section 413
(42 U.S.C. 285a–2), which authorizes
the Division of Cancer Epidemiology
and Genetics of the National Cancer
Institute (NCI) to establish and support
programs for the detection, diagnosis,
prevention and treatment of cancer; and
to collect, identify, analyze and
disseminate information on cancer
research, diagnosis, prevention and
E:\FR\FM\03NON1.SGM
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65388
Federal Register / Vol. 73, No. 213 / Monday, November 3, 2008 / Notices
treatment. Frequency of Response:
Once. Affected Public: Individuals. Type
of Respondents: Individuals that had
previously participated in the Central
European Renal Cancer Case-Control
Study between 2001–2004 and
physician abstractors. The estimated
total annual burden hours requested is
296. The annualized cost to respondents
is estimated at $5174. There are no
additional capital costs, operating costs,
and/or maintenance costs to report.
TABLE 1—ESTIMATES OF ANNUAL BURDEN HOURS
Average
time per
response
(minutes/
hour)
Annual
burden
hours
Number of
respondents
Frequency
of response
Patients ............................................................................................................................
Families (NOK) ................................................................................................................
Physicians ........................................................................................................................
200
240
10
1
1
1
40/60
40/60
15/60
133.33
160.00
2.50
Totals ........................................................................................................................
450
....................
....................
295.83
Type of respondents
Request for Comments: Written
comments and/or suggestions from the
public and affected agencies are invited
on one or more of the following points:
(1) Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
function of the agency, including
whether the information will have
practical utility; (2) Evaluate the
accuracy of the agency’s estimate of the
burden of the proposed collection of
information, including the validity of
the methodology and assumptions used;
(3) Enhance the quality, utility, and
clarity of the information to be
collected; and (4) Minimize the burden
of the collection of information on those
who are to respond, including the use
of appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms of
information technology.
To
request more information on the
proposed project or to obtain a copy of
the data collection plans and
instruments, contact Lee E. Moore, PhD,
MPH, Investigator/Epidemiologist,
Occupational and Environmental
Epidemiology Branch, Division of
Cancer Epidemiology and Genetics,
National Cancer Institute, NIH, DHHS,
Executive Plaza South, Room 8102,
6120 Executive Blvd., EPS–MSC 7240,
Bethesda, MD 20892–7270 or call nontoll-free number 301–496–6427 or email your request, including your
address to: moorele@mail.nih.gov.
Comments Due Date: Comments
regarding this information collection are
best assured of having their full effect if
received within 60 days of the date of
this publication.
sroberts on PROD1PC70 with NOTICES
FOR FURTHER INFORMATION CONTACT:
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Dated: October 24, 2008.
Vivian Horovitch-Kelley,
NCI Project Clearance Liaison Office,
National Institutes of Health.
[FR Doc. E8–26086 Filed 10–31–08; 8:45 am]
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limitations imposed by the review and
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E:\FR\FM\03NON1.SGM
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Agencies
[Federal Register Volume 73, Number 213 (Monday, November 3, 2008)]
[Notices]
[Pages 65387-65388]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-26086]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Proposed Collection; Comment Request; Follow-Up of Kidney Cancer
Patients From the Central European Multicenter Case-Control Study
SUMMARY: In compliance with the requirement of section 3506(c)(2)(A) of
the Paperwork Reduction Act of 1995, for opportunity for public comment
on proposed data collection projects, the National Cancer Institute
(NCI), the National Institutes of Health (NIH) will publish periodic
summaries of proposed projects to be submitted to the Office of
Management and Budget (OMB) for review and approval.
Proposed Collection: Title: Follow-up of Kidney Cancer Patients
from the Central European Multicenter Case-Control Study. Type of
Information Collection Request: New. Need and Use of Information
Collection: The purpose of this questionnaire is to obtain information
on the 5-year survival status of kidney cancer patients that were
enrolled in a Central European Case-Control Study of Kidney Cancer that
was conducted between 2001-2004. The aim is to assess survival, the
prevalence of recurrent disease and progression, and to investigate
patient, tumor and genetic determinants of survival among cases. The
questionnaire will collect information on patient related factors,
tumor related factors not collected during the initial study, and the
type of treatment(s) received since the patients were last contacted
for the case-control study. This questionnaire adheres to The Public
Health Service Act, section 412 (42 U.S.C. 285a-1) and section 413 (42
U.S.C. 285a-2), which authorizes the Division of Cancer Epidemiology
and Genetics of the National Cancer Institute (NCI) to establish and
support programs for the detection, diagnosis, prevention and treatment
of cancer; and to collect, identify, analyze and disseminate
information on cancer research, diagnosis, prevention and
[[Page 65388]]
treatment. Frequency of Response: Once. Affected Public: Individuals.
Type of Respondents: Individuals that had previously participated in
the Central European Renal Cancer Case-Control Study between 2001-2004
and physician abstractors. The estimated total annual burden hours
requested is 296. The annualized cost to respondents is estimated at
$5174. There are no additional capital costs, operating costs, and/or
maintenance costs to report.
Table 1--Estimates of Annual Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
time per Annual
Type of respondents Number of Frequency response burden
respondents of response (minutes/ hours
hour)
----------------------------------------------------------------------------------------------------------------
Patients.................................................... 200 1 40/60 133.33
Families (NOK).............................................. 240 1 40/60 160.00
Physicians.................................................. 10 1 15/60 2.50
---------------------------------------------------
Totals.................................................. 450 ........... ........... 295.83
----------------------------------------------------------------------------------------------------------------
Request for Comments: Written comments and/or suggestions from the
public and affected agencies are invited on one or more of the
following points: (1) Evaluate whether the proposed collection of
information is necessary for the proper performance of the function of
the agency, including whether the information will have practical
utility; (2) Evaluate the accuracy of the agency's estimate of the
burden of the proposed collection of information, including the
validity of the methodology and assumptions used; (3) Enhance the
quality, utility, and clarity of the information to be collected; and
(4) Minimize the burden of the collection of information on those who
are to respond, including the use of appropriate automated, electronic,
mechanical, or other technological collection techniques or other forms
of information technology.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the data collection plans and
instruments, contact Lee E. Moore, PhD, MPH, Investigator/
Epidemiologist, Occupational and Environmental Epidemiology Branch,
Division of Cancer Epidemiology and Genetics, National Cancer
Institute, NIH, DHHS, Executive Plaza South, Room 8102, 6120 Executive
Blvd., EPS-MSC 7240, Bethesda, MD 20892-7270 or call non-toll-free
number 301-496-6427 or e-mail your request, including your address to:
moorele@mail.nih.gov.
Comments Due Date: Comments regarding this information collection
are best assured of having their full effect if received within 60 days
of the date of this publication.
Dated: October 24, 2008.
Vivian Horovitch-Kelley,
NCI Project Clearance Liaison Office, National Institutes of Health.
[FR Doc. E8-26086 Filed 10-31-08; 8:45 am]
BILLING CODE 4140-01-P