Resectable Head and Neck Squamous Cell Carcinoma Clinical Trial
— HART-HNOfficial title:
A Phase I Study of Hypofractionated Adjuvant Radiotherapy for Resected Head and Neck Cancers (HART-HN)
The primary purpose of this study is to determine the safe reduction of the treatment fractions to 10, 8, or 5, that may be delivered safely in resected head and neck squamous cell carcinoma (HNSCC) patients with intermediate pathologic risk features.
| Status | Recruiting |
| Enrollment | 18 |
| Est. completion date | January 2026 |
| Est. primary completion date | January 2025 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility | Inclusion Criteria: 1. Patients 18 years or older with gross totally resected (R0 resection) Human papillomavirus (HPV) -negative squamous cell carcinoma of the head and neck (squamous cell carcinoma of the larynx, hypopharynx, oropharynx, oral cavity, nasal cavity, paranasal sinuses or carcinoma of unknown head/neck primary) who have at least 1 of the following intermediate risk factors for adjuvant radiation: 1. Pathologic Node Positive Disease 2. Perineural Invasion 3. Oral cavity cancer with depth of invasion of at least 5 mm 4. Lymphovascular Space Invasion 5. Pathologic T3 or T4 disease 2. Zubrod performance status 0-2. 3. Patients must have the psychological ability and general health that permits completion of the study requirements and required follow up. 4. Inclusion of Covid-19 positive patients will be based on standard institutional protocol. 5. Female patients must meet one of the following: - Postmenopausal for at least one year before the screening visit, or - Surgically sterile (i.e. undergone a hysterectomy or bilateral oophorectomy), or - If subject is of childbearing potential (defined as not satisfying either of the above two criteria), agree to practice two acceptable methods of contraception (combination methods requires use of two of the following: diaphragm with spermicide, cervical cap with spermicide, contraceptive sponge, male or female condom, hormonal contraceptive) from the time of signing of the informed consent form through 90 days after the last dose of study agent, AND o Agree to practice true abstinence when this is in line with the preferred and usual lifestyle of the subject. (Periodic abstinence [e.g., calendar, ovulation, symptom-thermal, post ovulation methods] and withdrawal are not acceptable contraception methods). 6. Male patients, even if surgically sterilized (i.e., status post vasectomy), must agree to one of the following: - Practice effective barrier contraception during the entire study period and through 60 calendar days after the last dose of study agent, OR - Must also adhere to the guidelines of any study-specific pregnancy prevention program, if applicable, OR o Agree to practice true abstinence when this is in line with the preferred and usual lifestyle of the subject. (Periodic abstinence [e.g., calendar, ovulation, symptom-thermal, post ovulation methods] and withdrawal are not acceptable methods of contraception.) 7. Ability to understand a written informed consent document, and the willingness to sign it. Exclusion Criteria: 1. Pathologic evidence of extranodal extension. 2. Pathologic evidence of a final positive margin (R1 resection) or gross residual disease (R2 resection). 3. HPV-positive squamous cell carcinoma. 4. Prior invasive malignancy within the past 3 years (except for non-melanomatous skin cancer, and early stage treated prostate cancer). 5. Life expectancy less than 12 months. 6. Performance status Zubrod = 3. 7. Patients with prior radiation therapy to the head and neck Note: Prior external beam radiotherapy is excluded, but Iodine 131 is allowed. 8. Prior systemic therapy, including cytotoxic chemotherapy, biologic/targeted therapy, or immune therapy for the study cancer. 9. Body weight = 30 kg. 10. Any of the following severe laboratory abnormalities within 14 days of registration, unless corrected prior to it: Sodium < 130 mmol/L or > 155 mmol/L; Potassium < 3.5 mmol/L or > 6 mmol/L; Fasting glucose < 40 mg/dl or > 400 mg/dl; Serum calcium (ionized or adjusted for albumin) < 7 mg/dl or > 12.5 mg/dl; Magnesium < 0.9 mg/dl or > 3 mg/dl. 11. Unstable angina and/or congestive heart failure requiring hospitalization within 3 months prior to Step 1 registration. 12. Transmural myocardial infarction within three months prior to Step 1 registration. 13. Medical or psychiatric illness which would compromise the patient's ability to tolerate treatment or limit compliance with study requirements. 14. Pregnancy or women of childbearing potential and men who are sexually active and not willing/able to use medically acceptable forms of contraception during treatment and for 6 months after radiation, this exclusion is necessary because the treatment involved in this study may be significantly teratogenic. Women who are breastfeeding are also excluded. |
| Country | Name | City | State |
|---|---|---|---|
| United States | Froedtert & the Medical College of Wisconsin | Milwaukee | Wisconsin |
| Lead Sponsor | Collaborator |
|---|---|
| Medical College of Wisconsin |
United States,
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Kumar AMS, Miller J, Hoffer SA, Mansur DB, Coffey M, Lo SS, Sloan AE, Machtay M. Postoperative hypofractionated stereotactic brain radiation (HSRT) for resected brain metastases: improved local control with higher BED10. J Neurooncol. 2018 Sep;139(2):449-454. doi: 10.1007/s11060-018-2885-6. Epub 2018 May 10. — View Citation
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| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Maximum-tolerated Radiation Dose | This will be determined as the radiation dose with the minimum number of fractions at which there is no more than a 33% rate of dose-limiting toxicity (DLT) up to 12 months after completion of radiation treatment using the TITE-CRM design. | 12 months | |
| Primary | Incidence of Dose-Limiting Toxicities | This measure is the number of subjects experiencing a dose-limiting toxicity. A dose-limiting toxicity is defined as an inability to complete radiation treatment within 30 days of the start of radiotherapy that is not deemed to be related to disease progression; OR an unacceptable toxicity within one year of treatment (Grade 4+ toxicity) that is probably or definitely related to radiation treatment as determined by the treating physician or a death within one year of treatment that is probably or definitely related to treatment. | 12 months | |
| Secondary | Overall Survival | This measure is the number of subjects alive at one year following the conclusion of scheduled radiation therapy. | One year | |
| Secondary | Locoregional progression | This measure is the number of subjects showing disease progression in the head and neck by response evaluation criteria in solid tumors (RECIST) criteria. | One year | |
| Secondary | MD Anderson Dysphagia Inventory Global Score | This measure comprises a single five-item, Likert-style question with responses ranging from 'Strongly Agree' to 'Strongly Disagree'. A higher score ('Strongly Agree') corresponds to a worse outcome. | Baseline, up to 2 weeks during radiotherapy, weeks 2, 4 and 6 following radiation therapy; months 3, 6, 9 and 12 following radiation therapy. | |
| Secondary | MD Anderson Dysphagia Inventory Composite Score | This measure comprises 19 five-item, Likert-style questions with responses ranging from 'Strongly Agree' to 'Strongly Disagree'. Questions are worded such that higher scores ('Strongly Agree') corresponds to worse traits or more severe symptoms. | Baseline, up to 2 weeks during radiotherapy, weeks 2, 4 and 6 following radiation therapy; months 3, 6, 9 and 12 following radiation therapy. | |
| Secondary | MD Anderson Dysphagia Inventory Score (Emotional) | This measure is the score for the "emotional" domain comprising a subset of five-item, Likert-style questions of the MD Anderson Dysphagia Inventory Composite tool that assesses symptoms relevant to emotional health. Responses range from 'Strongly Agree' to 'Strongly Disagree'. Questions are worded such that higher scores ('Strongly Agree') correspond to worse traits or more severe symptoms. | Baseline, up to 2 weeks during radiotherapy, weeks 2, 4 and 6 following radiation therapy; months 3, 6, 9 and 12 following radiation therapy. | |
| Secondary | MD Anderson Dysphagia Inventory Score (Functional) | This measure is the score for the "functional" domain comprising a subset of five-item, Likert-style questions of the MD Anderson Dysphagia Inventory Composite tool that assesses symptoms relevant to the ability to function in daily life activities. Responses range from 'Strongly Agree' to 'Strongly Disagree'. Questions are worded such that higher scores ('Strongly Agree') correspond to worse traits or more severe symptoms. | Baseline, up to 2 weeks during radiotherapy, weeks 2, 4 and 6 following radiation therapy; months 3, 6, 9 and 12 following radiation therapy. | |
| Secondary | MD Anderson Dysphagia Inventory Score (Physical) | This measure is the score for the "physical" domain comprising a subset of five-item, Likert-style questions of the MD Anderson Dysphagia Inventory Composite tool that assesses symptoms relevant to the ability to perform physical activities. Responses range from 'Strongly Agree' to 'Strongly Disagree'. Questions are worded such that higher scores ('Strongly Agree') correspond to worse traits or more severe symptoms. | Baseline, up to 2 weeks during radiotherapy, weeks 2, 4 and 6 following radiation therapy; months 3, 6, 9 and 12 following radiation therapy. | |
| Secondary | Functional Assessment of Cancer Therapies- Head and Neck (FACT-HN) | Quality of life scale with 4 sub-scales and 12 items each related specifically to head and neck cancer quality of life. The Physical Health scale has 7 items, each rated 0-4. Scores range from 0-28 with a lower score indicating better quality of life. The Social Well Being scale has 7 items, each rated 0-4. Scores range from 0-28 with a higher score indicating better quality of life. The Emotional Well Being scale has 6 items, each rated 0-4. Scores range from 0-24 with a lower score indicating better quality of life. The Functional scale has 7 items, each rated 0-4. Scores range from 0-28 with a higher score indicating better quality of life. The remaining 12 items are all scored as 0-4 each, range for each item 0-4 with higher or lower score indicating better quality life depending on each individual item. | Baseline, up to 2 weeks during radiotherapy, weeks 2, 4 and 6 following radiation therapy; months 3, 6, 9 and 12 following radiation therapy. | |
| Secondary | Functional Assessment of Cancer Therapies- Head and Neck (Physical Well-being) | The Physical Well-being scale has seven items, each rated 0-4. Scores range from 0-28 with a lower score indicating better quality of life. | Baseline, up to 2 weeks during radiotherapy, weeks 2, 4 and 6 following radiation therapy; months 3, 6, 9 and 12 following radiation therapy. | |
| Secondary | Functional Assessment of Cancer Therapies- Head and Neck (Social/Family Well-being) | The Social Well-being scale has seven items, each rated 0-4. Scores range from 0-28 with a higher score indicating better quality of life. | Baseline, up to 2 weeks during radiotherapy, weeks 2, 4 and 6 following radiation therapy; months 3, 6, 9 and 12 following radiation therapy. | |
| Secondary | Functional Assessment of Cancer Therapies- Head and Neck (Emotional Well-being) | The Emotional Well-being scale has 6 items, each rated 0-4. Scores range from 0-24 with a lower score indicating better quality of life. | Baseline, up to 2 weeks during radiotherapy, weeks 2, 4 and 6 following radiation therapy; months 3, 6, 9 and 12 following radiation therapy. | |
| Secondary | Functional Assessment of Cancer Therapies- Head and Neck (Functional Well-being) | The Functional Well-being scale has 7 items, each rated 0-4. Scores range from 0-28 with a higher score indicating better quality of life. | Baseline, up to 2 weeks during radiotherapy, weeks 2, 4 and 6 following radiation therapy; months 3, 6, 9 and 12 following radiation therapy. |
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