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临床试验/NCT04392622
NCT04392622招募中1 期

A Phase I Study of d-Limonene With Concurrent Radiation and Platinum Based Chemotherapy for Xerostomia Prevention in Locally Advanced Head and Neck Squamous Cell Carcinoma (HNSCC)

Stanford University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2021年2月15日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
招募中
入组人数
40
试验地点
1
主要终点
Dose limiting Toxicity

研究概览

简要总结

This study explores the safety of d-limonene, a commercially-available dietary supplement (food) as a potential therapeutic for the severe dry mouth (xerostomia) experienced by patients with head and neck cancer as a side effect of their anti-cancer treatment.

详细描述

Primary Objective:To determine the maximum tolerated dose (MTD) of d limonene when combined with radiation and platinum based chemotherapy in subjects with loco regionally advanced head and neck squamous cell carcinoma (HNSCC) based upon dose limiting toxicity (DLT)

Secondary Objective:

  • To evaluate the feasibility and subject compliance with adjuvant administration of d limonene daily up to a maximum of 4 months after completion of chemoradiation
  • To correlate the level of d-limonene measured in the plasma to the dose levels(s) administered to the subject
  • To correlate the level of d limonene measured in the plasma to saliva flow rate and xerostomia questionnaire scores in subjects enrolled in this trial

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Sequential
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Histologically or cytologically confirmed diagnosis of advanced loco regional squamous cell carcinoma of the nasopharynx (AJCC v8 Stage II IV); oropharynx (AJCC v8 Stage I III for HPV+ cancer, excluding T1 2N0; AJCC v8 Stage III IV for Human papillomavirus (HPV) negative cancer); larynx (AJCC v8 Stage III to IV); or hypopharynx (AJCC v8 Stage III to IV), scheduled to undergo chemoradiation. Patients with squamous cell carcinoma of the head and neck from an unknown primary site with involved nodes (N1 to 3) also qualify.
  • Scheduled to received definitive RT with concurrent platinum based chemotherapy at Stanford
  • Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0 to 1
  • Must be able to swallow d limonene gelcaps at the time of enrollment.
  • Adequate hepatic function within 2 weeks prior to registration defined as follows: Bilirubin ≤ 2 mg/dL; aspartate aminotransferase (AST) or alanine aminotransferase (ALT) < 3 times the upper limit of normal
  • Adequate hematologic function within 2 weeks prior to registration defined as follows:
  • Absolute neutrophil count (ANC): ≥ 1,500/mm3
  • Platelets: ≥ 100,000/mm3
  • Hemoglobin: ≥ 8.0 g/dL (Note: The use of transfusion or other intervention to achieve Hgb ≥ 8.0 g/dL is acceptable).
  • Adequate renal function defined as follows:
  • Serum creatinine ≤ 1.5 mg/dL within 2 weeks prior to registration or creatinine clearance (CC) ≥ 50 mL/min within 2 weeks prior to registration determined by 24 hour collection or estimated by Cockcroft Gault formula:
  • CCr male = [(140 - age) x (wt in kg)] [(Serum Cr mg/dL) x (72)] CCr female = 0.85 x (CrCl male)
  • Negative serum pregnancy test within 2 weeks prior to registration and agreement to use a birth control method during the entire duration of d limonene treatment for women of childbearing potential
  • Ability to understand and the willingness to sign a written informed consent document

排除标准

  • History of allergic reactions attributed to citrus fruits
  • Pregnant or lactating

研究组 & 干预措施

d-limonene -2gram

Experimental

2 gram d-limonene orally, once daily delivered during chemoradiation

干预措施: Xerostomia questionnaire (Other)

d-limonene -8gram

Experimental

8 gram d-limonene orally, as 4 grams 2 times daily delivered during chemoradiation

干预措施: Intensity modulated radiotherapy (IMRT) (Radiation)

d-limonene -2gram

Experimental

2 gram d-limonene orally, once daily delivered during chemoradiation

干预措施: Intensity modulated radiotherapy (IMRT) (Radiation)

d-limonene -4gram

Experimental

4 gram d-limonene orally, as 2 grams 2 times daily delivered during chemoradiation

干预措施: Intensity modulated radiotherapy (IMRT) (Radiation)

d-limonene -4gram

Experimental

4 gram d-limonene orally, as 2 grams 2 times daily delivered during chemoradiation

干预措施: Xerostomia questionnaire (Other)

d-limonene -6gram

Experimental

6 gram d-limonene orally, as 3 grams 2 times daily delivered during chemoradiation

干预措施: Intensity modulated radiotherapy (IMRT) (Radiation)

d-limonene -6gram

Experimental

6 gram d-limonene orally, as 3 grams 2 times daily delivered during chemoradiation

干预措施: Xerostomia questionnaire (Other)

d-limonene -8gram

Experimental

8 gram d-limonene orally, as 4 grams 2 times daily delivered during chemoradiation

干预措施: Xerostomia questionnaire (Other)

de-escalation dose d-limonene -6gram

Experimental

6 gram d-limonene orally, as 3 grams 2 times daily delivered during chemoradiation

干预措施: Intensity modulated radiotherapy (IMRT) (Radiation)

de-escalation dose d-limonene -6gram

Experimental

6 gram d-limonene orally, as 3 grams 2 times daily delivered during chemoradiation

干预措施: Xerostomia questionnaire (Other)

de-escalation dose d-limonene -4gram

Experimental

4 gram d-limonene orally, as 2 grams 2 times daily delivered during chemoradiation

干预措施: Intensity modulated radiotherapy (IMRT) (Radiation)

de-escalation dose d-limonene -4gram

Experimental

4 gram d-limonene orally, as 2 grams 2 times daily delivered during chemoradiation

干预措施: Xerostomia questionnaire (Other)

de-escalation dose d-limonene -2gram

Experimental

2 gram d-limonene orally, once daily delivered during chemoradiation

干预措施: Intensity modulated radiotherapy (IMRT) (Radiation)

de-escalation dose d-limonene -2gram

Experimental

2 gram d-limonene orally, once daily delivered during chemoradiation

干预措施: Xerostomia questionnaire (Other)

d-limonene -2gram

Experimental

2 gram d-limonene orally, once daily delivered during chemoradiation

干预措施: D-Limonene Gelcaps (Drug)

d-limonene -4gram

Experimental

4 gram d-limonene orally, as 2 grams 2 times daily delivered during chemoradiation

干预措施: D-Limonene Gelcaps (Drug)

d-limonene -6gram

Experimental

6 gram d-limonene orally, as 3 grams 2 times daily delivered during chemoradiation

干预措施: D-Limonene Gelcaps (Drug)

d-limonene -8gram

Experimental

8 gram d-limonene orally, as 4 grams 2 times daily delivered during chemoradiation

干预措施: D-Limonene Gelcaps (Drug)

de-escalation dose d-limonene -6gram

Experimental

6 gram d-limonene orally, as 3 grams 2 times daily delivered during chemoradiation

干预措施: D-Limonene Gelcaps (Drug)

de-escalation dose d-limonene -4gram

Experimental

4 gram d-limonene orally, as 2 grams 2 times daily delivered during chemoradiation

干预措施: D-Limonene Gelcaps (Drug)

de-escalation dose d-limonene -2gram

Experimental

2 gram d-limonene orally, once daily delivered during chemoradiation

干预措施: D-Limonene Gelcaps (Drug)

d-limonene -2gram

Experimental

2 gram d-limonene orally, once daily delivered during chemoradiation

干预措施: Cisplatin (Drug)

d-limonene -4gram

Experimental

4 gram d-limonene orally, as 2 grams 2 times daily delivered during chemoradiation

干预措施: Cisplatin (Drug)

d-limonene -6gram

Experimental

6 gram d-limonene orally, as 3 grams 2 times daily delivered during chemoradiation

干预措施: Cisplatin (Drug)

d-limonene -8gram

Experimental

8 gram d-limonene orally, as 4 grams 2 times daily delivered during chemoradiation

干预措施: Cisplatin (Drug)

de-escalation dose d-limonene -6gram

Experimental

6 gram d-limonene orally, as 3 grams 2 times daily delivered during chemoradiation

干预措施: Cisplatin (Drug)

de-escalation dose d-limonene -4gram

Experimental

4 gram d-limonene orally, as 2 grams 2 times daily delivered during chemoradiation

干预措施: Cisplatin (Drug)

de-escalation dose d-limonene -2gram

Experimental

2 gram d-limonene orally, once daily delivered during chemoradiation

干预措施: Cisplatin (Drug)

结局指标

主要结局

Dose limiting Toxicity

时间窗: 9 weeks

Dose limiting toxicity is defined as d-limonene related toxicity causing: * Greater than 1 week delay in completing the radiation course. * Inability to receive ≥ 66 Gy of radiotherapy. * Inability to receive at least 200 mg/m2 of total cisplatin equivalent dose or a total area under the curve (AUC) of 10 for carboplatin equivalent dose due to toxicity related to d-limonene Grade 3 or higher diarrhea that is attributable to the study drug. * Grade 3 abdominal pain that is attributable to the study drug. The outcome will be reported as the number of participants per dose level who experience any DLT (a number without dispersion / variance).

次要结局

  • Feasibility of adjuvant d-limonene administration(4 months)
  • Xerostomia toxicity(12 months post completion of chemoradiation)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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