Ignite Creation Date:
2026-03-26 @ 3:19 PM
Ignite Modification Date:
2026-03-30 @ 2:39 AM
Study NCT ID:
NCT07418034
Status:
NOT_YET_RECRUITING
Last Update Posted:
2026-02-18
First Post:
2026-02-10
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
A Single Arm Phase II Trial in p16-positive Oropharynx Cancer of Selective Dose De-escalation of nodAl VolumEs at Minimal Risk and Primary Site Disease (SAVED)
Sponsor:
University of Maryland, Baltimore
Organization:
Study Overview
Official Title:
A Single Arm Phase II Trial in p16-positive Oropharynx Cancer of Selective Dose De-escalation of nodAl VolumEs at Minimal Risk and Primary Site Disease (SAVED)
Status:
NOT_YET_RECRUITING
Status Verified Date:
2026-02
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
SAVED
Brief Summary:
Patients with human papillomavirus (HPV)-related oropharyngeal cancer generally have very good outcomes. Patients' treatment responses depend more on their individual cancer characteristics and personal risk factors than on the specific type of treatment they receive. However, the different treatments used for this cancer can cause significant side effects. Because outcomes are often favorable regardless of treatment type, reducing treatment-related side effects should be a priority when choosing care.
Studies have reported that lowering radiation doses for some patients can reduce side effects while still effectively controlling the cancer.
Patients with this type of head and neck cancer typically receive either surgery or radiation as their first treatment.
For patients who receive surgery first, radiation to the surgical area and nearby neck lymph nodes is often recommended afterward. In these patients, the study will test whether lowering the radiation dose to low-risk lymph nodes on the side of the neck opposite the tumor can reduce side effects while still effectively controlling the cancer (Method A).
For patients who receive radiation as their first treatment, the study will test one or both of two radiation approaches aimed at reducing both short-term and long-term side effects. These approaches include reduced lymph node radiation (Method A, described above) and a tumor dose reduction approach (Method B), which lowers the radiation dose delivered directly to the tumor.
Information such as tumor size, the number of cancerous or suspicious lymph nodes, and risk factors like smoking history will be used to determine which patients may be eligible for reduced lymph node radiation (Method A), reduced tumor radiation (Method B), or both. Patients who may qualify for tumor dose reduction (Method B), either alone or combined with Method A, will need an additional blood test called a circulating tumor DNA (ctDNA) test to determine eligibility.
The ctDNA test measures small amounts of tumor-related DNA in the blood, which are often elevated at the time of diagnosis. Studies have shown that cancer is more likely to return when ctDNA levels remain positive after treatment. This study will evaluate whether ctDNA levels measured before and during treatment can help identify patients who can safely receive lower radiation doses to the tumor (Method B).
Overall, this study aims to safely evaluate two radiation de-escalation approaches in order to lessen short- and long-term side effects while maintaining excellent cancer control.
Studies have reported that lowering radiation doses for some patients can reduce side effects while still effectively controlling the cancer.
Patients with this type of head and neck cancer typically receive either surgery or radiation as their first treatment.
For patients who receive surgery first, radiation to the surgical area and nearby neck lymph nodes is often recommended afterward. In these patients, the study will test whether lowering the radiation dose to low-risk lymph nodes on the side of the neck opposite the tumor can reduce side effects while still effectively controlling the cancer (Method A).
For patients who receive radiation as their first treatment, the study will test one or both of two radiation approaches aimed at reducing both short-term and long-term side effects. These approaches include reduced lymph node radiation (Method A, described above) and a tumor dose reduction approach (Method B), which lowers the radiation dose delivered directly to the tumor.
Information such as tumor size, the number of cancerous or suspicious lymph nodes, and risk factors like smoking history will be used to determine which patients may be eligible for reduced lymph node radiation (Method A), reduced tumor radiation (Method B), or both. Patients who may qualify for tumor dose reduction (Method B), either alone or combined with Method A, will need an additional blood test called a circulating tumor DNA (ctDNA) test to determine eligibility.
The ctDNA test measures small amounts of tumor-related DNA in the blood, which are often elevated at the time of diagnosis. Studies have shown that cancer is more likely to return when ctDNA levels remain positive after treatment. This study will evaluate whether ctDNA levels measured before and during treatment can help identify patients who can safely receive lower radiation doses to the tumor (Method B).
Overall, this study aims to safely evaluate two radiation de-escalation approaches in order to lessen short- and long-term side effects while maintaining excellent cancer control.
Detailed Description:
This research study is designed for people with HPV-related head and neck cancer who are being treated with either surgery followed by radiation or radiation as their first treatment. Patients with this type of cancer generally have excellent outcomes, but the treatments can cause significant short- and long-term side effects. Because cancer control is often very good regardless of the specific treatment approach, this study focuses on whether radiation doses can be safely reduced to lessen side effects while still effectively controlling the cancer.
Most patients receive either surgery or radiation as their initial treatment, based on discussions with their medical team. For patients who have surgery first, radiation is often recommended afterward to the surgical area and nearby lymph nodes in the neck. Traditionally, this includes radiation to lymph nodes on both sides of the neck, even the side opposite the tumor. This study will evaluate whether lowering the radiation dose to low-risk lymph nodes on the side opposite the tumor can reduce side effects without compromising cancer control. This approach is called reduced lymph node radiation (Method A).
For patients who receive radiation as their first treatment, radiation is typically given to both the tumor and lymph nodes on both sides of the neck. In these patients, the study will evaluate one or two radiation-reduction strategies. In addition to reduced lymph node radiation (Method A), the study will also examine tumor dose reduction (Method B), which lowers the amount of radiation delivered directly to the tumor itself. Some patients may receive one of these approaches, while others may be eligible for both. Eligibility for these radiation-reduction approaches is based on individual cancer characteristics, such as tumor size, the number of involved lymph nodes, and risk factors like smoking history.
For patients who may qualify for tumor dose reduction (Method B), an additional blood test called a circulating tumor DNA (ctDNA) test is used. This test measures small amounts of tumor DNA in the blood. Studies suggest that patients whose ctDNA levels are negative after treatment are less likely to have their cancer return. In this study, ctDNA testing before treatment and partway through radiation will help identify patients who may be able to safely stop radiation earlier than usual (Method B).
Participants in the study are followed closely as part of their routine cancer care. This includes regular clinic visits, imaging, and physical exams. This also includes research procedures such as questionnaires about symptoms and quality of life. Some participants will also provide additional research-related blood samples to help researchers better understand which factors may predict treatment response and long-term outcomes in the future.
Up to 132 patients will take part in this study at the University of Maryland Medical System. Participation is voluntary, and treatment decisions-such as whether to have surgery or radiation and whether to receive chemotherapy-are made by the patient and their medical team, not determined by the study. However, the study procedures will determine participants' eligibility for and use of one or both of the two radiation reduction approaches.
The goal of this research is to improve future care by identifying safe ways to reduce radiation and treatment-related side effects while maintaining excellent cancer control.
Most patients receive either surgery or radiation as their initial treatment, based on discussions with their medical team. For patients who have surgery first, radiation is often recommended afterward to the surgical area and nearby lymph nodes in the neck. Traditionally, this includes radiation to lymph nodes on both sides of the neck, even the side opposite the tumor. This study will evaluate whether lowering the radiation dose to low-risk lymph nodes on the side opposite the tumor can reduce side effects without compromising cancer control. This approach is called reduced lymph node radiation (Method A).
For patients who receive radiation as their first treatment, radiation is typically given to both the tumor and lymph nodes on both sides of the neck. In these patients, the study will evaluate one or two radiation-reduction strategies. In addition to reduced lymph node radiation (Method A), the study will also examine tumor dose reduction (Method B), which lowers the amount of radiation delivered directly to the tumor itself. Some patients may receive one of these approaches, while others may be eligible for both. Eligibility for these radiation-reduction approaches is based on individual cancer characteristics, such as tumor size, the number of involved lymph nodes, and risk factors like smoking history.
For patients who may qualify for tumor dose reduction (Method B), an additional blood test called a circulating tumor DNA (ctDNA) test is used. This test measures small amounts of tumor DNA in the blood. Studies suggest that patients whose ctDNA levels are negative after treatment are less likely to have their cancer return. In this study, ctDNA testing before treatment and partway through radiation will help identify patients who may be able to safely stop radiation earlier than usual (Method B).
Participants in the study are followed closely as part of their routine cancer care. This includes regular clinic visits, imaging, and physical exams. This also includes research procedures such as questionnaires about symptoms and quality of life. Some participants will also provide additional research-related blood samples to help researchers better understand which factors may predict treatment response and long-term outcomes in the future.
Up to 132 patients will take part in this study at the University of Maryland Medical System. Participation is voluntary, and treatment decisions-such as whether to have surgery or radiation and whether to receive chemotherapy-are made by the patient and their medical team, not determined by the study. However, the study procedures will determine participants' eligibility for and use of one or both of the two radiation reduction approaches.
The goal of this research is to improve future care by identifying safe ways to reduce radiation and treatment-related side effects while maintaining excellent cancer control.
Study Oversight
Has Oversight DMC:
True
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?: