Removing the Planning Tumor Volume From Radiation Therapy for the Treatment of Head and Neck Squamous Cell Carcinoma
Pilot Study of the Elimination of Planning Tumor Volume (PTV) in Head and Neck Squamous Cell Carcinoma (HNSCC)
This clinical trial studies the side effects and how well removing the planning tumor volume (PTV) from radiation therapy (RT) works in treating patients with head and neck squamous cell carcinoma (HNSCC). Standard therapy for HNSCC often involves giving RT with chemotherapy; however, this approach is associated with a high level of short- and long-term side effects. RT uses high energy x-rays, particles, or radioactive seeds to kill tumor cells and shrink tumors. RT is planned to be delivered based on three volumes of the tumor. The first is the gross tumor volume which is the area of the tumor that can be seen, felt, or measured on imaging. The second is the clinical tumor volume which includes the gross tumor volume as well as area beyond this to account for disease that cannot be seen on imaging and may have spread. The third is the PTV which includes an area beyond both the gross tumor volume and clinical tumor volume to account for errors that may happen during RT, such as setup error or movement. As the area between the clinical tumor volume and PTV is not cancer and current advances in RT have improved RT accuracy, researchers think that removing PTV from RT may lower side effects while still being an effective treatment. Removing the PTV from RT may safe, tolerable, and/or effective in treating patients with HNSCC.
調査の概要
状態
状態
条件
条件
- 頭頸部扁平上皮がん
- 中咽頭扁平上皮がん
- 臨床病期 III HPV 媒介 (p16 陽性) 中咽頭癌 AJCC v8
- III期の下咽頭がんAJCC v8
- III期の喉頭がん AJCC v8
- ステージ III 中咽頭 (p16 陰性) がん AJCC v8
- 下咽頭扁平上皮がん
- 喉頭扁平上皮がん
- 臨床ステージ I HPV 媒介 (p16 陽性) 中咽頭がん AJCC v8
- 臨床病期 II HPV 媒介 (p16 陽性) 中咽頭癌 AJCC v8
- ステージ IVA 下咽頭がん AJCC v8
- IVA 期の喉頭がん AJCC v8
- ステージ IVA 中咽頭 (p16 陰性) がん AJCC v8
- ステージ IVB 中咽頭 (p16 陰性) がん AJCC v8
- ステージ I 下咽頭がん AJCC v8
- ステージ II 下咽頭がん AJCC v8
- II期喉頭がん AJCC v8
- ステージ II 中咽頭 (p16 陰性) がん AJCC v8
- ステージ I 喉頭がん AJCC v8
- ステージ 0 中咽頭 (p16 陰性) 癌 AJCC v8
- ステージ I 中咽頭 (p16 陰性) 癌 AJCC v8
介入・治療
介入・治療
詳細な説明
PRIMARY OBJECTIVES:
I. Describe the effect of eliminating PTV on locoregional control and marginal recurrence at 6 months in patients with HNSCC undergoing definitive RT, with or without chemotherapy.
II. Describe the effect of PTV on early toxicity, PRO (patient reported outcomes) and QOL (quality of life) in patients with HNSCC undergoing definitive RT, with or without chemotherapy.
SECONDARY OBJECTIVES:
I. Describe the effect of eliminating PTV on locoregional control at 2 and 5 years in patients with HNSCC undergoing definitive RT, with or without chemotherapy.
II. Describe the patterns of failure when eliminating PTV at 3 months, 2 years and 5 years in patients with HNSCC undergoing definitive RT, with or without chemotherapy.
III. Describe the effect of eliminating PTV on later toxicity in patients with HNSCC undergoing definitive RT, with or without chemotherapy.
IV. Describe the effect of eliminating PTV on later PRO (patient reported outcomes) and QOL (quality of life) in patients with HNSCC undergoing definitive RT, with or without chemotherapy.
V. Describe differences in dosimetric comparison plans with and without PTV in patients with HNSCC undergoing definitive RT, with or without chemotherapy.
VI. Describe the effect of eliminating PTV on marginal recurrence rate at 2 and 5 years in patients with HNSCC undergoing definitive RT, with or without chemotherapy.
OUTLINE:
Patients undergo intensity-modulated radiation therapy (IMRT) or image-guided radiation therapy (IGRT) without PTV 5-6 times a week for thirty-five treatment fractions over 6-7 weeks in the absence of disease progression or unacceptable toxicity. Patients may also receive concurrent chemotherapy on study. Additionally, patients undergo computed tomography (CT), fludeoxyglucose F-18 (FDG)-positron emission tomography (PET)/CT, and laryngopharyngoscopy during screening and CT or FDG-PET/CT during follow up.
After completion of study treatment, patients are followed up every 3 months during years 1-2 and then every 6 months during years 3-5.
研究の種類
研究の種類
入学 (推定)
入学
段階
段階
- 適用できない
連絡先と場所
研究場所
-
-
California
-
Duarte、California、アメリカ、91010
- City of Hope Medical Center
-
主任研究者:
- Arya Amini
-
コンタクト:
- Arya Amini
- 電話番号:626-218-2247
- メール:aamini@coh.org
-
-
参加基準
適格基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
-
Documented informed consent of the participant and/or Legally Authorized Representative
- Assent, when appropriate, will be obtained and documented for adults lacking capacity per institutional guidelines
-
Age: ≥ 18 years
-
Eastern Cooperative Oncology Group (ECOG) ≤ 2
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Pathologically (histologically or cytologically) proven diagnosis of squamous cell carcinoma (including the histological variants papillary squamous cell carcinoma and basaloid squamous cell carcinoma but not neuroendocrine phenotype) of the oropharynx (tonsil, base of tongue, soft palate, or oropharyngeal walls), larynx and hypopharynx; cytologic diagnosis from a cervical lymph node is sufficient in the presence of clinical evidence of a primary tumor in the oropharynx. Clinical evidence should be documented, may consist of palpation, imaging, or endoscopic evaluation, and should be sufficient to estimate the size of the primary (for T stage)
-
No metastatic disease and eligible for definitive radiation based on the following diagnostic workup:
- General history and physical examination within 56 days prior to registration
- Exam with laryngopharyngoscopy (mirror or in office direct procedure acceptable) within 70 days prior to registration
- FDG -PET/CT (with or without contrast) within 60 days prior to registration
- Diagnostic CT scan of neck (with contrast and of diagnostic quality) within 60 days prior to registration
-
Planning to undergo definitive radiation (with or without chemotherapy)
-
Women of childbearing potential (WOCBP): negative urine or serum pregnancy test. If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required
-
Agreement by females and males of childbearing potential to use an effective method of birth control or abstain from heterosexual activity for the course of the study through at least 6 months after the last dose of protocol therapy
- Childbearing potential defined as not being surgically sterilized (men and women) or have not been free from menses for > 1 year (women only)
Exclusion Criteria:
-
Recurrent disease
-
T1-T2 glottic cancers
-
Definitive clinical or radiologic evidence of metastatic diseases
-
Cancers considered to be from an oral cavity site (oral tongue, floor mouth, alveolar ridge, buccal or lip), or the nasopharynx, even if p16-positive, or histologies of adenosquamous, verrucous, or spindle cell carcinomas
-
Gross total excision of both primary and nodal disease; this includes tonsillectomy, local excision of primary site, and nodal excision that removes all clinically and radiographically evident disease. In other words, to participate in this protocol, the patient must have clinically or radiographically evident gross disease for which disease response can be assessed. Patients with unknown primary or resected primary are eligible if gross nodal disease is present
-
Patients with simultaneous primary cancers or separate bilateral primary tumor sites are excluded with the exception of patients with bilateral tonsil cancers
-
Prior radiotherapy to the region of the study cancer that would result in overlap of radiation therapy fields
-
Chemotherapy, radiation therapy, biological therapy, immunotherapy within 21 days or five half-lives (whichever is shorter for non-radiation therapy) prior to day 1 of protocol therapy
-
Severe, active co-morbidity defined as follows:
-
Acute bacterial or fungal infection requiring intravenous antibiotics at the time of registration
-
Chronic obstructive pulmonary disease exacerbation or other respiratory illness requiring hospitalization or precluding study therapy within 30 days of registration
-
Hepatic insufficiency resulting in clinical jaundice and/or coagulation defects
-
Acquired immune deficiency syndrome (AIDS) based upon current Centers for Disease Control and Prevention (CDC) definition with immune compromise. Human immunodeficiency virus (HIV)-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months are eligible. HIV testing is not required for entry into this protocol. The need to exclude patients with AIDS from this protocol is necessary because the treatments involved in this protocol may be significantly immunosuppressive. Protocol-specific requirements may also exclude immuno-compromised patients
-
For patients with evidence of chronic hepatitis B virus (HBV) infection, the HBV viral load must be undetectable on suppressive therapy, if indicated. Hepatitis B testing is not required for entry into this protocol
- Note: Known positive test for hepatitis B virus surface antigen (HBV sAg) indicating acute or chronic infection would make the patient ineligible unless the viral load becomes undetectable on suppressive therapy. Patients who are immune to hepatitis B (anti-Hepatitis B surface antibody positive) are eligible (e.g. patients immunized against hepatitis B)
-
Patients with a history of hepatitis C virus (HCV) infection must have been treated and cured. For patients with HCV infection who are currently on treatment for the hepatitis, they are eligible if they have an undetectable HCV viral load. Hepatitis C testing is not required for entry into this protocol
- Note: Known positive test for hepatitis C virus ribonucleic acid (HCV RNA) indicating acute or chronic infection would make the patient ineligible unless the viral load becomes undetectable on suppressive therapy
-
-
Clinically significant uncontrolled illness
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Females only: Pregnant or breastfeeding
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Any other condition that would, in the Investigator's judgment, contraindicate the patient's participation in the clinical study due to safety concerns with clinical study procedures
-
Prospective participants who, in the opinion of the investigator, may not be able to comply with all study procedures (including compliance issues related to feasibility/logistics)
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
アーム数
武器と介入
参加者グループ / アーム参加者グループ / アーム |
介入・治療介入・治療 |
|---|---|
|
実験的:Treatment (RT without PTV)
Patients undergo IMRT or IGRT without PTV 5-6 times a week for thirty-five treatment fractions over 6-7 weeks in the absence of disease progression or unacceptable toxicity. Patients may also receive concurrent chemotherapy on study. Additionally, patients undergo CT, FDG-PET/CT, and laryngopharyngoscopy during screening and CT or FDG-PET/CT during follow up. |
Ancillary studies Given concurrent chemotherapy
他の名前:
Undergo CT and/or FDG-PET/CT
他の名前:
Undergo laryngopharyngoscopy
他の名前:
Undergo FDG-PET/CT
他の名前:
Undergo IGRT without PTV
他の名前:
Undergo IMRT without PTV
他の名前:
|
この研究は何を測定していますか?
主要な結果の測定
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Percent of patients experiencing locoregional recurrence and marginal recurrence
時間枠:At 6 months post-radiation therapy
|
Will be summarized using descriptive statistics. Will be calculated using the number of patients local or regional recurrence and marginal recurrence divided by the total number of treated/evaluable subjects. Point estimates and two-sided 95% exact binomial confidence intervals will be reported. As secondary analyses, time to locoregional recurrence will be measured from completion of radiation therapy to the first documented local or regional recurrence. The cumulative incidence of locoregional recurrence at 3 months, 2 years, and 5 years will be estimated. Patients alive and free of locoregional recurrence will be censored at the date of their last contact. Point estimates and two-sided 95% confidence intervals will be reported. |
At 6 months post-radiation therapy
|
|
Incidence of treatment-related adverse events
時間枠:From start of treatment to three months post-radiation therapy
|
As assessed by Common Terminology Criteria for Adverse Events (CTCAE) version (v) 6.0, delineated by grade and attribution. Observed toxicities will be summarized by incidence, type, severity, and attribution. |
From start of treatment to three months post-radiation therapy
|
|
Change in Functional Assessment of Cancer Therapy Head and Neck Questionnaire (FACT-H&N) v4.0 scores
時間枠:From baseline to end of treatment and 3 months post-radiation therapy
|
At each post-baseline time point, the observed score and change from baseline will be summarized using descriptive statistics, together with the mean change and its two-sided 95% confidence interval. The number of patients with available assessments will be reported at each time point. (Generalized) linear mixed-effects models may be used to characterize changes over time for exploratory analyses. |
From baseline to end of treatment and 3 months post-radiation therapy
|
|
Change in Eastern Cooperative Oncology Group (ECOG) performance status
時間枠:From baseline to end of treatment and 3 months post-radiation therapy
|
At each post-baseline time point, the observed score and change from baseline will be summarized using descriptive statistics, together with the mean change and its two-sided 95% confidence interval. The number of patients with available assessments will be reported at each time point. (Generalized) linear mixed-effects models may be used to characterize changes over time for exploratory analyses. |
From baseline to end of treatment and 3 months post-radiation therapy
|
二次結果の測定
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Locoregional recurrence rate
時間枠:At 2 and 5 years post-radiation therapy
|
Will be summarized using descriptive statistics. Will be calculated using the number of patients local or regional recurrence and marginal recurrence divided by the total number of treated/evaluable subjects. Point estimates and two-sided 95% exact binomial confidence intervals will be reported. As secondary analyses, time to locoregional recurrence will be measured from completion of radiation therapy to the first documented local or regional recurrence. The cumulative incidence of locoregional recurrence at 3 months, 2 years, and 5 years will be estimated. Patients alive and free of locoregional recurrence will be censored at the date of their last contact. Point estimates and two-sided 95% confidence intervals will be reported. |
At 2 and 5 years post-radiation therapy
|
|
Local recurrence rates
時間枠:At 3 months, 2 years, and 5 years post-radiation therapy
|
Will be summarized using descriptive statistics. Will be calculated using the number of patients local recurrence divided by the total number of treated/evaluable subjects. Point estimates and two-sided 95% exact binomial confidence intervals will be reported. As secondary analyses, time to local recurrence will be measured from completion of radiation therapy to the first documented local recurrence. The cumulative incidence of local recurrence at 3 months, 2 years, and 5 years will be estimated. Patients alive and free of local recurrence will be censored at the date of their last contact. Point estimates and two-sided 95% confidence intervals will be reported. |
At 3 months, 2 years, and 5 years post-radiation therapy
|
|
Regional recurrence rates
時間枠:At 3 months, 2 years, and 5 years post-radiation therapy
|
Will be summarized using descriptive statistics. Will be calculated using the number of patients regional recurrence divided by the total number of treated/evaluable subjects. Point estimates and two-sided 95% exact binomial confidence intervals will be reported. As secondary analyses, time to regional recurrence will be measured from completion of radiation therapy to the first documented regional recurrence. The cumulative incidence of regional recurrence at 3 months, 2 years, and 5 years will be estimated. Patients alive and free of regional recurrence will be censored at the date of their last contact. Point estimates and two-sided 95% confidence intervals will be reported. |
At 3 months, 2 years, and 5 years post-radiation therapy
|
|
Incidence of treatment-related adverse events
時間枠:From start of treatment to 1 year post-radiation therapy
|
As assessed by CTCAE v6.0, delineated by grade and attribution. Observed toxicities will be summarized by incidence, type, severity, and attribution. |
From start of treatment to 1 year post-radiation therapy
|
|
Change in FACT-H&N v4.0 scores
時間枠:From baseline to 6, 9, and 12 months post-radiation therapy
|
At each post-baseline time point, the observed score and change from baseline will be summarized using descriptive statistics, together with the mean change and its two-sided 95% confidence interval. The number of patients with available assessments will be reported at each time point. (Generalized) linear mixed-effects models may be used to characterize changes over time for exploratory analyses. |
From baseline to 6, 9, and 12 months post-radiation therapy
|
|
Change in ECOG performance status
時間枠:From baseline to 6, 9, and 12 months post-radiation therapy
|
At each post-baseline time point, the observed score and change from baseline will be summarized using descriptive statistics, together with the mean change and its two-sided 95% confidence interval. The number of patients with available assessments will be reported at each time point. (Generalized) linear mixed-effects models may be used to characterize changes over time for exploratory analyses. |
From baseline to 6, 9, and 12 months post-radiation therapy
|
|
Prespecified dosimetric parameters for organs at risk
時間枠:At time of radiation therapy (Up to 6-7 weeks)
|
Will be summarized separately for the delivered plan without planning tumor volume (PTV) and the comparison plan generated using PTV. Because both plans are generated for the same patient, the dosimetric quantity will be the within-patient difference between plans. Any formal paired comparisons will be considered exploratory. |
At time of radiation therapy (Up to 6-7 weeks)
|
協力者と研究者
協力者
協力者
捜査官
捜査官
- 主任研究者:Arya Amini、City of Hope Medical Center
研究記録日
主要日程の研究
研究開始 (推定)
研究開始
一次修了 (推定)
一次修了
研究の完了 (推定)
研究の完了
試験登録日
最初に提出
最初に提出
QC基準を満たした最初の提出物
QC基準を満たした最初の提出物
最初の投稿 (実際)
最初の投稿
学習記録の更新
投稿された最後の更新 (実際)
投稿された最後の更新
QC基準を満たした最後の更新が送信されました
QC基準を満たした最後の更新が送信されました
最終確認日
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
その他の研究ID番号
- 25155
- P30CA033572 (米国 NIH グラント/契約)
- NCI-2026-07861 (レジストリ識別子:CTRP (Clinical Trial Reporting Program))
- 25155 (その他の識別子:City of Hope Medical Center)
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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