HR 4450 · 110th Congress 2007–2009, ended

Pediatric, Adolescent, and Young Adult Cancer Survivorship Research and Quality of Life Act of 2007

Fact sheet

Latest action · Dec 11, 2007 Referred to the Subcommittee on Health.

Progress

Where this bill reached, and when. A stage with no date was not reached; one that failed a vote and later carried shows the date it carried.

  1. IntroducedDec 11, 2007
  2. Passed HouseNot reached
  3. Passed SenateNot reached
  4. To the PresidentNot reached
  5. Became lawNot reached

Summary

Pediatric, Adolescent, and Young Adult Cancer Survivorship Research and Quality of Life Act of 2007 - Amends the Public Health Service Act to direct the Secretary of Health and Human Services, acting through the Director of the Centers for Disease Control and Prevention (CDC), to expand and intensify CDC's cancer control programs. Requires the Secretary to: (1) provide guidance to states, in collaboration with the Director of the National Cancer Institute (NCI), on interventions that may be incorporated into state cancer control programs to improve the long-term health status of childhood cancer survivors; (2) encourage states to incorporate strategies for improving their care into their comprehensive cancer plans; (3) collaborate with the NCI Director to improve or develop systems for tracking cancer survivors; and (4) enhance control programs to include a focus on childhood cancer survivorship.

Directs the NCI Director to: (1) coordinate National Institutes of Health (NIH) activities regarding cancer survivorship; (2) make grants for research regarding pediatric cancer survivors and health disparities in cancer survivorship within minority populations; (3) conduct or support research to evaluate followup care for childhood cancer survivors; and (4) make grants to establish pilot programs to develop, study, or evaluate model systems for monitoring and caring for cancer survivors.

Directs the Secretary to make grants to: (1) establish or improve training programs for health care professionals to improve followup care for young cancer survivors and to ensure that such care is linguistically and culturally competent; (2) pay costs incurred during the first four years of operating a clinic for comprehensive long-term followup services for childhood cancer survivors; and (3) improve physical and psychosocial care for such survivors.

Cosponsors 40

Members who signed on, in the order they did. Signatures ran from Dec 11, 2007 to Nov 19, 2008, with 1 there on the day it was introduced.

SeatCosponsorSigned on
R-CAMary BonoOriginalDec 11, 2007
D-VARobert C. "Bobby" ScottFeb 13, 2008
D-TNSteve CohenFeb 13, 2008
D-AZRaúl M. GrijalvaMar 3, 2008
D-NJSteven R. RothmanMar 31, 2008
D-CAZoe LofgrenMar 31, 2008
R-OHDeborah PryceApr 9, 2008
D-CALois CappsApr 9, 2008
D-MDElijah E. CummingsApr 17, 2008
D-VAJames P. MoranApr 17, 2008
D-CAJoe BacaApr 17, 2008
D-VARick BoucherApr 17, 2008
D-NYEdolphus TownsApr 23, 2008
R-VAFrank R. WolfApr 23, 2008
D-NYJohn J. HallApr 23, 2008

Actions 3

Everything that happened, newest first.

  1. Dec 11, 2007Introduced in House
  2. Dec 11, 2007Referred to the House Committee on Energy and Commerce.
  3. Dec 11, 2007Referred to the Subcommittee on Health.

Related bills 1

Companion bills and other measures the record links to this one.

Subjects

Assigned by the Library of Congress. Policy area: Health.

Text 1

Each version as it was printed, newest first.

  1. Dec 11, 2007Introduced in House

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Everything here is as published by Congress: the summary is the Congressional Research Service's, the action wording is the clerks', and the subjects are the Library of Congress's. How far it got is read from the actions themselves, taking the most recent one of each kind, so a bill that failed a vote and later passed is shown as having passed. Records come from this bill on Congress.gov and govinfo.gov.