The Oral Microbiome as a Prognostic Tool in Oral Malignant and Premalignant Lesions and in Medication Related Osteonecrosis of the Jaw

NCT ID: NCT03418454

Last Updated: 2020-01-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

150 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-12-14

Study Completion Date

2021-12-31

Brief Summary

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Oral squamous cell carcinoma (OSCC) is the most common malignant tumor of the head and neck, and its incidence has increased in recent years. Extensive surgery with neck dissection and chemo/radio/ targeted therapy is the current treatment for OSCC, and despite great progress in chemotherapy, radiotherapy, and targeted therapy in the last three decades, the prognosis of OSCC is still poor due to aggressive local invasion and metastasis, which lead to recurrence. Postoperative tumor recurrence confers a poor prognosis in OSCC and a poor quality of life. The 5-year survival rate is over 90% in OSCC patients without recurrence and 30% in patients with recurrence, with a median survival of 76.8 months in patients without recurrence and 42.5 months in patients with recurrence . Therefore, it is important to identify biomarkers that may predict the postoperative recurrence of OSCC. Also, some of the OSCC are preceded by precursor lesions. In the oral cavity the most common lesions recognized as potentially malignant are leukoplakia and erythroplakia, but it is also apparent that as many as 50% of OSCC arise from apparently clinically normal mucosa. The prognostic significance of an individual lesion is difficult to determine. At present therefore, the gold standard for the assessment of oral potentially malignant lesions is microscopic evaluation of haematoxylin and eosin stained sections for the presence of architectural and cytological changes, which are generally referred to as oral epithelial dysplasia (OED). The human microbiome is defined as the collective genomes of the microbes (composed of bacteria, bacteriophages, fungi, protozoa and viruses) that live inside and on the human body, and there are approximately 10 microbes and 100 microbial genes for each human cell and gene respectively. With the advent of next generation sequencing technology, the Human Microbiome Project delineated the composition of healthy microbial communities associated to different body sites in healthy individuals, including the oral cavity \[Human microbiome consortium\]. As opposed to a normal (healthy) microbiome, a disrupted microbiome or dysbiosis represents the lack of equilibrium, and is hypothetically related to disease. Interestingly, the healthy oral microbiome shows relative intraindividual stability over time, suggesting that differences in microbiome profiles may serve as useful tools for the identification of disease states. The working hypothesis is that in OSCC patients, the oral microbiome is altered in comparison to healthy individuals and certain microbial signatures are characteristic of healthy versus disease. In addition, in precursor conditions, i.e., oral epithelial dysplasia (OED), a partial alteration in the composition of the microbiome may predict the progression to malignancy.Also, during treatment, it could be that specific microbial signatures are associated with incomplete eradication, tendency to local recurrence or metastatic potential.Correlations to local recurrence (LR), distant metastases (DM) or disease free survival (DFS) adjusted to clinicopathologic correlations will be sought. In this study, buccal mucosa samples will be collected from patients with OSCC, OED and from healthy individuals , after signing for informed consent, according to Helsinki protocol. Routine pathologic diagnosis will be performed by expert Pathology physicians in our center. Data will be correlated to demographic and clinical data obtained from medical records. This will be carried out in line with institutional ethical guidelines.

Detailed Description

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Conditions

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Oral Squamous Cell Carcinoma Medication Related Osteonecrosis of the Jaw Oral Epithelial Dysplasia

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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Oral Squamous Cell Carcinoma

Buccal mucosa samples for Extraction of BACTERIAL DNA

Buccal mucosa samples for Extraction of BACTERIAL DNA

Intervention Type DIAGNOSTIC_TEST

Sampling of the buccal mucosa after informed consent and prior to routine treatment. Similar sampling on follow up after 3,6,9,12 months.

Extracted BACTERIAL DNA (and not human DNA) from clinical samples will be sequenced and analyzed for the 16s rRNA (BACTERIAL ribosome).

Oral Epithelial Dysplasia

Buccal mucosa samples for Extraction of BACTERIAL DNA

Buccal mucosa samples for Extraction of BACTERIAL DNA

Intervention Type DIAGNOSTIC_TEST

Sampling of the buccal mucosa after informed consent and prior to routine treatment. Similar sampling on follow up after 3,6,9,12 months.

Extracted BACTERIAL DNA (and not human DNA) from clinical samples will be sequenced and analyzed for the 16s rRNA (BACTERIAL ribosome).

Control: Healthy age matched patients

Buccal mucosa samples for Extraction of BACTERIAL DNA

Buccal mucosa samples for Extraction of BACTERIAL DNA

Intervention Type DIAGNOSTIC_TEST

Sampling of the buccal mucosa after informed consent and prior to routine treatment. Similar sampling on follow up after 3,6,9,12 months.

Extracted BACTERIAL DNA (and not human DNA) from clinical samples will be sequenced and analyzed for the 16s rRNA (BACTERIAL ribosome).

Osteonecrosis of the Jaw

Buccal mucosa samples for Extraction of BACTERIAL DNA

Buccal mucosa samples for Extraction of BACTERIAL DNA

Intervention Type DIAGNOSTIC_TEST

Sampling of the buccal mucosa after informed consent and prior to routine treatment. Similar sampling on follow up after 3,6,9,12 months.

Extracted BACTERIAL DNA (and not human DNA) from clinical samples will be sequenced and analyzed for the 16s rRNA (BACTERIAL ribosome).

Underlying disease, no necrosis of the jaw

Buccal mucosa samples for Extraction of BACTERIAL DNA

Buccal mucosa samples for Extraction of BACTERIAL DNA

Intervention Type DIAGNOSTIC_TEST

Sampling of the buccal mucosa after informed consent and prior to routine treatment. Similar sampling on follow up after 3,6,9,12 months.

Extracted BACTERIAL DNA (and not human DNA) from clinical samples will be sequenced and analyzed for the 16s rRNA (BACTERIAL ribosome).

Interventions

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Buccal mucosa samples for Extraction of BACTERIAL DNA

Sampling of the buccal mucosa after informed consent and prior to routine treatment. Similar sampling on follow up after 3,6,9,12 months.

Extracted BACTERIAL DNA (and not human DNA) from clinical samples will be sequenced and analyzed for the 16s rRNA (BACTERIAL ribosome).

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* Patients biopsied with OSCC
* Patients biopsied with oral premalignant lesions
* Patients biopsied with osteonecrosis of the jaw
* healthy age matched patients that visit the oral and maxillofacial clinic for other purposes such as extraction, reactive lesions

Exclusion Criteria

* Patients receiving antimicrobial treatment in the previous 3 months
* Patients receiving radiotherapy
* Patients receiving chemo/immunotherapy
Minimum Eligible Age

20 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Barzilai Medical Center

OTHER

Sponsor Role lead

Responsible Party

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Irit Allon

DMD, PhD, Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Barzilai medical Center

Ashkelon, , Israel

Site Status RECRUITING

Countries

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Israel

Central Contacts

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Irit Allon, MD, Phd

Role: CONTACT

972-52-3609727

Facility Contacts

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Irit Alon, MD, Phd

Role: primary

972-52-3609727

References

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Other Identifiers

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BRZ 0062-17 CTIL

Identifier Type: -

Identifier Source: org_study_id

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