s_cid=mm7045e1_w † † COVID-19 was confirmed with laboratory detection of SARS-CoV-2 by reverse transcription-polymerase chain reaction or antigen test. § § Patients with MIS-C as the reason for hospitalization included patients who met the clinical case definition for MIS-C (clinically severe illness requiring hospitalization in a person aged <21 years with fever, laboratory evidence of inflammation, multisystem [≥2] organ involvement and no alternative plausible diagnosis, and evidence of current or recent SARS-CoV-2 infection by reverse transcription polymerase chain reaction, serology or antigen test, or COVID-19 exposure within the 4 weeks preceding symptom onset [https:// emergency.cdc.gov/han/2020/han00432.asp]) and were hospitalized for diagnosis and management of MIS-C, based on chart review.
Background
We evaluated priorities, expectations, and regret among patients treated on a phase II trial of de‐escalated chemoradiation for human papillomavirus (HPV)‐positive oropharyngeal cancer.
Methods
Eligibility included stage III/IV squamous cell carcinoma of the oropharynx, p16‐positivity, age ≥18 years, and Zubrod score 0‐1. Participants were surveyed with validated measures evaluating their treatment experience.
Results
Twenty‐four of 27 (89%) patients participated with a median follow‐up of 24 months. Twenty‐three subjects (96%) selected “being cured” or “living as long as possible” as top priority. No patient reported any regret about the decision to enroll on a de‐escalation protocol. Sixteen participants (67%) found retrospectively reported long‐term swallowing function to be either better than or as originally expected.
Conclusions
These data offer a baseline landscape of perspectives and priorities for patients treated with de‐escalation for HPV‐positive oropharyngeal carcinoma and provide support to the fundamental premise underlying ongoing efforts to establish a new standard of care.
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