5 results match your criteria: "Cancer Centers of Northern Arizona Healthcare[Affiliation]"
Brachytherapy
November 2024
Cancer Centers of Northern Arizona Healthcare, Sedona, AZ. Electronic address:
Introduction: Accelerated partial breast irradiation with high dose rate brachytherapy treats early-stage carcinoma. Strut-adjusted volume implant applicators are inserted into the cavity post-lumpectomy. For an unstable applicator, changes in distance are seen each day between struts.
View Article and Find Full Text PDFInt J Radiat Oncol Biol Phys
December 2021
Department of Radiation Oncology, University of California Los Angeles, Los Angeles, California.
Int J Radiat Oncol Biol Phys
April 2022
Cedars Sinai Medical Centre, Los Angeles, California.
Purpose: We report efficacy of a prospective phase 2 trial (NCT00450411) of salvage low-dose-rate (LDR) prostate brachytherapy (BT) for local failure (LF) after prior external beam radiation therapy (EBRT) with minimum 5-years' follow-up.
Methods And Materials: Eligible patients had low/intermediate risk prostate cancer (PCa) before EBRT and biopsy-proven LF >30 months after EBRT, with prostate-specific antigen <10 ng/mL and no regional/distant disease. The primary endpoint, late gastrointestinal and genitourinary adverse events (Common Terminology Criteria for Adverse Events v3.
Gland Surg
December 2019
Department of Surgery, Kearney Breast Center, Vancouver, WA, USA.
Background: In breast cancer treatment, marking the tumor bed is an important aspect of the surgical component of therapy. Clear delineation of the tumor bed allows radiation oncologists a defined target for planning and delivering postoperative radiation therapy (XRT). Tumor bed marking also allows radiographic follow-up of the tumor bed on subsequent breast imaging.
View Article and Find Full Text PDFBrachytherapy
April 2018
Ascenture MPTR, PLLC, New York City, NY.
Purpose: To evaluate the use of a polymer-encapsulated palladium-103 ( Pd) source with a unique linear radioactive distribution in prostate brachytherapy. This feasibility study assessed dosimetry, ease and efficiency of use, and side effects. The number of needles required for adequate coverage was the primary end point.
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