III
118th CONGRESS
2d Session
S. RES. 775
IN THE SENATE OF THE UNITED STATES
July 30, 2024
Ms. Stabenow submitted the following resolution; which was referred to the Committee on Health, Education, Labor, and Pensions
RESOLUTION
Expressing support for the designation of July 15, 2024, as “National Leiomyosarcoma Awareness Day”.
Whereas leiomyosarcoma is a malignant sarcoma subtype, 1 of 70 to 100 such subtypes, that arises in smooth muscle and has several subtypes itself due to its vascularity and bone invasion;
Whereas leiomyosarcoma is designated by the National Institutes of Health as a rare form of cancer;
Whereas leiomyosarcoma is largely resistant to standard chemotherapy treatments, radiation treatments, and immunotherapy trials, with 40-year-old chemotherapy treatments still in use;
Whereas leiomyosarcoma affects all age groups, including children, young adults, the middle-aged, and the elderly, and all genders;
Whereas leiomyosarcoma is diagnosed in more than 2,000 individuals in the United States each year;
Whereas, with respect to leiomyosarcoma, research and clinical trials remain complicated and extremely costly due to the difficulty of recruiting patients;
Whereas survival and longevity for individuals with leiomyosarcoma has not significantly improved for at least 30 years;
Whereas multidisciplinary care coordination teams, because of their expertise and experience, are critical to the health of leiomyosarcoma patients;
Whereas researchers continue to strive to improve quality of life for leiomyosarcoma patients, improve outcomes in clinical trials, and promote enhanced survivorship; and
Whereas increased education and awareness about sarcoma and leiomyosarcoma will contribute to the well-being of the communities of the United States: Now, therefore, be it
That the Senate—
supports the designation of July 15, 2024, as National Leiomyosarcoma Awareness Day
;
recognizes the challenges faced by leiomyosarcoma patients; and
commends the dedication of organizations, volunteers, researchers, and caregivers across the United States working to improve the quality of life of leiomyosarcoma patients and their families.