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Full-Text Articles in Radiation Medicine
Clinical Outcomes Of Neoadjuvant Chemoimmunotherapy Vs. Chemoradiotherapy In Operable Non-Small Cell Lung Cancer, Tal Sherman, Nikta Nair, Marli Meller, Raleigh Anderson, Guillermo Jimenez, Elizaveta Flevora, Charalambos Solomides, Rita Axelrod, Sarah Gordon, Ida Micaily, Maria Werner-Wasik, Sung Whang, Tyler Grenda, Olugbenga Okusanya, Nathaniel R. Evans, Iii, Nilanjan Haldar, Erik Blomain
Clinical Outcomes Of Neoadjuvant Chemoimmunotherapy Vs. Chemoradiotherapy In Operable Non-Small Cell Lung Cancer, Tal Sherman, Nikta Nair, Marli Meller, Raleigh Anderson, Guillermo Jimenez, Elizaveta Flevora, Charalambos Solomides, Rita Axelrod, Sarah Gordon, Ida Micaily, Maria Werner-Wasik, Sung Whang, Tyler Grenda, Olugbenga Okusanya, Nathaniel R. Evans, Iii, Nilanjan Haldar, Erik Blomain
Department of Radiation Oncology Posters
Introduction
- Non-small cell lung cancer (NSCLC) accounts for ~85% of lung cancers and remains the leading cause of cancer death.
- Surgery is curative for early-stage disease, but recurrence rates remain high.
- CheckMate-816 trial established neoadjuvant chemo-immunotherapy (chemo-IO) as a new standard for resectable NSCLC, demonstrating improved pathologic response and event-free survival.
- PACIFIC trial showed the survival benefit of consolidative immunotherapy after chemoradiotherapy (chemo-RT) in unresectable stage III NSCLC, highlighting the synergy between radiation and immune checkpoint blockade.
- Despite these advances, there is little comparative data on the role of chemo-IO versus chemo-RT in the neoadjuvant, operable setting.
- Objective: To compare …
Anatomically Accurate, Low-Cost 3d-Printed Nasopharynx Simulator For Nasolaryngoscopy Training, Tal Sherman, Robert Walker, Voichita Bar-Ad, Firas Mourtada
Anatomically Accurate, Low-Cost 3d-Printed Nasopharynx Simulator For Nasolaryngoscopy Training, Tal Sherman, Robert Walker, Voichita Bar-Ad, Firas Mourtada
Department of Radiation Oncology Posters
Introduction
- Flexible nasopharyngolaryngoscopy (NPL) is a core diagnostic and procedural skill in otolaryngology, radiation oncology, and related specialties. Early mastery is essential for safe patient care, but traditional training is limited by:
- Reliance on patient encounters, which may cause discomfort and restrict practice opportunities.
- High cost of commercial simulators(often $3,000–$5,000), restricting access across many programs.
- Lack of anatomical accuracyin available models, limiting their educational value.
- Gap: There is currently no accessible, anatomically faithful, and affordable tool for widespread trainee use.
- Objective: To design, fabricate, and validate a low-cost, anatomically accurate 3D-printed simulator for training in flexible NPL
Organ-Specific Dosimetry Following Radiopharmaceutical Therapy For Metastatic Prostate Cancer, Frank J. Arturi, Nilanjan Haldar, Shray Jain, Gia Nguyen, Jessie Dinome, Firas Mourtada, Lydia J. Wilson, Phd
Organ-Specific Dosimetry Following Radiopharmaceutical Therapy For Metastatic Prostate Cancer, Frank J. Arturi, Nilanjan Haldar, Shray Jain, Gia Nguyen, Jessie Dinome, Firas Mourtada, Lydia J. Wilson, Phd
Department of Radiation Oncology Posters
Introduction
- Radiopharmaceutical Therapy (RPT) uses radioactive agents to target cancer at the cellular level
- Lu-177 targeting prostate-specific membrane antigen (PSMA), known as 177Lu- PSMA-617, can be used to treat metastatic, castration-resistant prostate cancer (mCRPC)
- 177Lu-PSMA-617 treatments use a standard dose and treatment regimen for all patients
- Patients exhibit different side effects and tumor response during treatment
Inducing Accelerated Lung Toxicity In Mice Using A Partial Arc Sbrt Technique, Andrew Gerry, Charita Kunta, Noelle Francois, Tiziana Deangelis, Anuradha Shastri, Nicole Simone, Reza Taleei
Inducing Accelerated Lung Toxicity In Mice Using A Partial Arc Sbrt Technique, Andrew Gerry, Charita Kunta, Noelle Francois, Tiziana Deangelis, Anuradha Shastri, Nicole Simone, Reza Taleei
Department of Radiation Oncology Posters
Background
- Radiation-induced pulmonary fibrosis (RIPF) is a frequent outcome of thoracic radiation therapy, constraining safe tumor radiation dosage. Various animal models, such as mice, rats, and pigs, have been devised to study RIPF
- Current methods for inducing lung fibrosis in mice involve whole lung irradiation with doses between 2-20 Gy. These methods used fixed anterior and posterior (AP/PA) x-ray beams at 0º and 180º with analysis typically commencing 24 to 52 weeks post-radiation
- Current methods are unrepresentative of modern radiation therapy techniques and are limited by the associated long latency of RIPF