MXMelody Xu
Papers(2)
Feasibility and Clini…Cancer control and to…
Collaborators(10)
Sarah Kutika NyagabonaSikudhani MuyaSurbhi GroverBeatrice Paul MushiBenjamin LiCheukkai B. HuiChinmayi Aryasomayaju…Christopher H. ChapmanDong Joo RheeElia Mmbaga
Institutions(5)
University Of Califor…Muhimbili University …University Of Pennsyl…Kaiser PermanenteBanner Md Anderson Ca…

Papers

Cancer control and toxicity results of chemoradiation for cervical cancer using a three-fraction HDR brachytherapy boost.

Brachytherapy is essential for treating locally advanced cervical cancer, but many patients do not receive it due to the resource-intensive nature of the treatment. This study assessed cancer control and toxicity following an accelerated 3-fraction brachytherapy protocol. We identified patients with cervical cancer who received high-dose-rate (HDR) brachytherapy in three fractions as part of chemoradiation at Kaiser Permanente Northern California from 2012-2020. Treatment details, oncologic outcomes and toxicity were determined retrospectively using available medical records. The primary outcome was local recurrence (LR). Secondary outcomes included disease-free survival (DFS), overall survival (OS), and grade ≥3 gastrointestinal (GI), urinary, and gynecologic toxicities. Among 199 patients (median age 52 years), 46.2% had Stage I-II and 53.8% had Stage III-IV disease. The median total radiotherapy duration was 50 days, with ≥5 cycles of cisplatin received by 86.9%. HDR brachytherapy (median dose 2400 cGy/3 fractions) was combined with EBRT, achieving D90% ≥8000 cGy (EQD2) to the high-risk clinical target volume in 92.6% of patients. At 2 years, LR was 5.6%, DFS 66.2%, and OS 80.2%, with lower DFS and OS in patients over 60 or with Stage III-IV disease (p < 0.001). Grade ≥3 toxicities occurred in 9.0% of patients, primarily GI (6.5% grade 3, 1.0% grade 4-5). Urinary and gynecologic grade three toxicities were 1.5% and 1.0%, respectively, with no grade 4-5 events. A 3-fraction brachytherapy protocol demonstrated local control, DFS, and OS comparable to historical controls while maintaining high grade toxicity rates <10%. This approach reduces resource use and may improve treatment access for cervical cancer patients.

15Works
2Papers
14Collaborators
Uterine Cervical NeoplasmsBreast Neoplasms

Education

2016

Resident Physician

University of California · Radiation Oncology

2010

MD

University of Pennsylvania Perelman School of Medicine

2016

Intern Physician

Kaiser Permanente Northern California · Internal Medicine

2015

Masters of Translational Research

University of Pennsylvania

Country

US