Could One-Sided radiation be safer for throat cancer patients?
NCT ID NCT06167291
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether people with throat cancer on one side of the neck can safely receive radiation to only that side, instead of both sides. The goal is to reduce side effects from unnecessary radiation. About 8 participants with early-stage HPV-related tonsil or tongue base cancer are being studied.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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8 people
The number who actually took part.
- Started
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Apr 2024
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Newly diagnosed histopathologically-proven p16+ and/or HPV+ HNSCC of the base of tongue or faucial tonsil * cT1-2N0-1 per AJCC 8th edition staging. * Tumor does not cross midline, and must be \>1cm from midline * For tonsil tumors, the primary may extend onto the palate or into the BOT but still be \>1cm from midline * No evidence of contralateral neck disease on contrast MRI, CT Head/Neck, PET/CT, or lymphoscintigraphy nor retropharyngeal lymphadenopathy. * Able to undergo lymphoscintigraphy procedure * No contraindications for SLNM, adjuvant chemotherapy, RT nor adjuvant/definitive radiotherapy. * ECOG 0-1 * Age \>18 years * Ability to understand and the willingness to sign a written informed consent document. Exclusion Criteria * Previous HN Cancer except small skin cancers. * Any retropharyngeal lymphadenopathy on either MRI, CT, or PET/CT * Contralateral neck nodal disease radiographically detected per routine diagnostic imaging or SPECT-CT. * Distant metastatic spread at the time of inclusion * Chemotherapy or surgery (for the present tumor), prior to inclusion. * Previous radiation treatment in the head and neck region, for any reason, except for cutaneous lesions that would not lead to overlap with definitive bilateral neck irradiation * Recurrent or second primary tumor in the head and neck region * Non-tongue base or non-faucial tonsil primaries * Prior history of regionally advanced or distant spread cancers * Pregnancy or no active contraception for pre-menopausal women * Known hypersensitivity to iodine or nanocolloid injection * Having any condition (physical, mental, sociological) that interferes with the informed consent procedure and follow-up schedules Has a diagnosis of active scleroderma, lupus, or other rheumatologic disease which in the opinion of the treating radiation oncologist precludes safe radiation therapy
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Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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MD Anderson Cancer Center
Houston, Texas, 77030, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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