A Clinical and Biological Umbrella Protocol for Smoker or Non-smoker Patients With Oral Potentially Malignant Lesions (OPML) or Head and Neck Squamous Cell Carcinoma (HNSCC) (IHNPACT UMBRELLA)
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 53
- 试验地点
- 20
- 主要终点
- Biomarkers
研究概览
简要总结
This is a multicenter minimal risk or burden prospective 3-cohort follow-up and monitoring study that aims to collect clinical, socio-psychological, medico-economics data and biospecimens for patients with oral potentially malignant lesions (OPML) or resectable head and neck squamous cell carcinoma (HNSCC) :
- Cohort A: OPML patients.
- Cohort B (specific design): smokers (adults who have smoked at least 100 cigarettes in their lifetime) motivated to quit - either current smokers (who currently smokes cigarettes every day (daily) or some days (nondaily)) or former smokers (adults who have smoked at least 100 cigarettes in their lifetime, but say they currently do not smoke) who stops smoking within 3 months prior to the diagnosis - with a resectable HNSCC requiring postoperative radiotherapy or chemoradiation.
- Cohort C: Patients with resectable HNSCC non-eligible to cohort B.
The primary objective of this study is the identification of biomarkers (predictive of malignant transformation or second primary tumor) and new strategies for prevention and therapy, mainly through extensive genomic, epigenomic and immune characterization of OPML and HNSCC.
详细描述
The long-term goal of this study is to reduce the incidence of HNSCC which may impact as well other smoking-related cancers. It may be interesting to foster excellent translational research towards the target of reducing the incidence of HNSCC by developing a global and personalized approach for prevention and treatment of HNSCC. The only way to reach this goal is to develop an ambitious program that coordinates the efforts of experts from various fields (surgeons, medical oncologists and addictologists, scientists, sociologists and economists) that will work together toward the same goal.
This study intends to gather a large scale clinical, sociological, psychological data gathering combined to a unique set of biospecimens collected prospectively including oral preneoplastic disease and resectable HNSCC. This represents a unique setting to develop multidisciplinary studies including a translational research component (validation and discovery of biomarkers, high throughput molecular studies to understand the dynamics of molecular changes and identify new strategies for prevention), a sociopsychological component and an addiction component that aim to increase the percentage of patients entering a process of weaning, as well as a medico-economics component that intend to evaluate the impact of new approaches that may emerge from our work.
In summary, this study proposes to prospectively collect clinical, sociopsychological, medico-economics data and biospecimens in patients included in 3 different cohorts. Cohort A will include patients with OPML, either from smokers/drinkers (S/D) or non-smokers/non-drinkers (NS/ND), while cohort B and C will include patients with HNSCC eligible to upfront surgical resection. Patients in cohort B will be included in an interventional randomized clinical trial evaluating an intensive and sustained smoking cessation program.
In patients with OPML, no standard workup and treatment plan is recommended. OPMLs biopsy is important to identify patients with high grade dysplasia and in situ carcinoma who should undergo surgical resection of the OMPLs if possible. Although LOH status in OPML biopsies or buccal brushes has been evaluated in this population as a biomarker of risk to develop oral cancer, it is not routinely performed. More studies are required to validate their value as a biomarker of risk in a prospective setting and to identify the best set of biomarkers. In smokers and/or excessive alcohol drinkers, it is critical to counsel and help patients quit and it should be part of the standard of care. Unfortunately, this is not always the case. Studies of chemopreventive agents have not resulted in the development of an intervention that can be considered as standard of care.
Despite the accumulated knowledge, no comprehensive molecular characterization of OPML is available. Identification of new targets for prevention and therapy, mainly with genomic, epigenomic and immune characterization of OPML is critical. Cohort A will allow to prospectively collect clinical information and biospecimens (biopsies, buccal brushes and saliva). These unique resources will allow to confirm the value of LOH as a biomarker of risk and develop standardized procedures for sample processing that can be transferred in the routine setting, validate or identify other biomarkers and improve risk assessments beyond LOH, to understand the spatial and temporal dynamics of molecular changes that may help predicting oral cancer risk, identify relevant targets and suggest new chemoprevention strategies including immunoprevention interventions. Furthermore, patients included in this cohort will benefit from standardized care plans and state of the art smoking and alcohol cessation programs according to current recommendations, and will be given the opportunity to participate in future chemoprevention studies that may be embedded in the near future in the umbrella protocol.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 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
- 否
入选标准
- •Age ≥ 18 years at the day of consenting to the study (or at the day of randomization for cohort B patients not included in the global study)
- •Patients with OPML: at least one lesion ≥ 5 mm (Cohort A only)
- •Patients with surgically resectable HNSCC not treated with preoperative chemotherapy, pT1-4 N0-3 M0 (Cohort B only)
- •Patients with surgically resectable HNSCC not treated with preoperative chemotherapy and non-eligible to cohort B (Cohort C only)
- •PS ECOG ≤ 1
- •Treatment plan incorporating surgery and radiation therapy (or at the day of randomization for cohort B patients not included in the global study)
- •Smoker = Adult who have smoked at least 100 cigarettes in his/her lifetime (Cohort B only)
- •Current smoker (who currently smokes cigarettes every day (daily) or some days (nondaily)) or former smoker (who says he/she doesn't smoke) who stops smoking within 3 months prior to diagnosis (Cohort B only)
- •Motivation to quit smoking evaluated by the Richmond test (Cohort B only)
- •Without subordination motivation to quit smoking (Cohort B only)
- •Covered by a medical insurance
- •Signed and dated informed consent document indicating that the patient has been informed of all the pertinent aspects of the trial prior to enrolment
排除标准
- •Non-stabilized cognitive disorder
- •Synchronous malignancy (Cohort A only)
- •History of malignant disease outside the upper aerodigestive tract, except skin carcinoma
- •Substance use disorder other than smoking (cigarette and cannabis) and alcohol (Cohort B only)
- •Use of nicotine replacement therapy, bupropion, varenicline on last 3 months (Cohort B only)
- •Undergoing on last 3 months' behavioral and cognitive therapy for smoking cessation (Cohort B only)
- •Patient included in a clinical trial evaluating interventions for smoking cessation (Cohort B only)
- •Any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule
- •Pregnant or breastfeeding woman
结局指标
主要结局
Biomarkers
时间窗: Month 6, Month 12, Month 24, Month 36, Month 48, Month 60 from inclusion
Prevalence of LOH and/or other candidate biomarkers in OPML and normal mucosa : study of their spatial and temporal dynamic changes and explore their association with the risk of developing oral cavity squamous cell carcinoma, recurrent disease or second primary tumor (blood samples, buccal biopsies, buccal cells)
次要结局
- alcohol quit(Month 6, Month 12, Month 24, Month 36, Month 48, Month 60 from inclusion)
- smoking quit(Month 6, Month 12, Month 24, Month 36, Month 48, Month 60 from inclusion)
- cannabis quit(Month 6, Month 12, Month 24, Month 36, Month 48, Month 60 from inclusion)
- Preclinical models of oral mucosa(Month 6, Month 12, Month 24, Month 36, Month 48, Month 60 from inclusion)
- Preclinical models of OPML(Month 6, Month 12, Month 24, Month 36, Month 48, Month 60 from inclusion)
- Preclinical models of HNSCC(Month 6, Month 12, Month 24, Month 36, Month 48, Month 60 from inclusion)
- Efficacy of intensive and sustained smoking cessation program(Month 6, Month 12 after randomization)
- Time to smoking resumption(Month 6, Month 12, Month 24, Month 36, Month 48, Month 60 after randomization)
- Patients' preference to the 2 smoking cessation programs(Month 12 after randomization)
- Health-related quality of life(Month 6, Month 12 after randomization)
