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Recruiting Phase 2 NCT06702033

The Minimalist Trial-2

Trial Parameters

Condition HPV-Related Oropharynx Squamous Cell Carcinoma
Sponsor Washington University School of Medicine
Study Type INTERVENTIONAL
Phase Phase 2
Enrollment 142
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2025-04-10
Completion 2030-04-30
Interventions
Radiation therapyCisplatinSurgery

Brief Summary

Head and neck squamous cell carcinoma (HNSCC) is the sixth most common cancer. Oropharynx SCC (OPSCC) is a common sub-type of HNSCC. Each year, 16,000 new cases of OPSCC are diagnosed in the USA. Most cases of OPSCC (\>90%) are caused by the human papillomavirus (HPV) and are often cured with current therapy. However, patients treated with surgery followed by postoperative adjuvant chemotherapy and radiation therapy (POA(C)RT) still experience substantial morbidity. In this highly curable disease, current clinical research interest is focused on investigation of de-escalated therapy, with the goal to reduce treatment-related adverse events (AEs) while maintaining a low recurrence rate. In this study, patients with HPV-related OPSCC will undergo resection of the primary tumor site and involved/at-risk regional neck nodes. Based on the pathology report, patients will be assigned to: * Arm 1 (de-POACRT-42 Gy) * Arm 2A (de-POART-42 Gy) * Arm 2B (de-POART-37.8 Gy) * Arm 2C (de-POACRT-30 Gy). All patients with high-risk pathology will be assigned to Arm 1 whereas patients with intermediate-risk pathology will be randomized (1:1:1) to Arm 2A, Arm 2B, or Arm 2C. Patients with highest-risk pathology and low-risk pathology will be removed from the trial after surgery and will be advised to pursue standard of care options.

Eligibility Criteria

Inclusion Criteria: * Histologically or cytologically confirmed HPV-related, clinical stages I-II OPSCC (8th edition of AJCC/UICC Staging Manual) or HPV-related neck node with unknown primary. Clinical T1N0M0 and T2N0M0 disease are excluded. HPV-related may be defined by p16 IHC stain and/or HPV-High Risk RNA ISH/HPV DNA genotyping by PCR, using standard definitions of positive and negative test results. * Planned resection of the primary tumor site by a transoral approach (TORS, TLM, or conventional surgery). * Planned unilateral or contralateral selective neck dissection. * ECOG PS 0-2. * Adequate organ and marrow function defined as: * Creatinine clearance ≥ 50 mL/min. * ANC ≥ 1.0 K/cumm. * Platelet count ≥100 K/cumm. * At least 18 years of age. * Women of childbearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control, abstinence) prior to study entry and for the duration of participation. Should a woman become pregnant or suspec

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