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Neoplastic Cells, Circulating clinical trials

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NCT ID: NCT03979339 Recruiting - Ovarian Cancer Clinical Trials

Feasibility of a New Technology for Isolating Circulating Tumour Cells

CTC-SMMiL-E
Start date: March 11, 2020
Phase: N/A
Study type: Interventional

This is a prospective interventional single-site research with a collection of biological samples. The primary objective of the trial is to assess the ability of the "new technology" to isolating circulating tumor cells (CTC) in selected cancer patients. Five groups will be constitued: at first the Group 0: Healthy volunteers included for the spike-in test; and then the four groups, Group1: Metastatic HER2-positive breast cancer; Group 2: Advanced CA-125 positive ovarian cancer; Group 3: Metastatic PSA-positive castrate-resistant prostate cancer; Group 4: Healthy volunteers included as control). In each group, the percentage of cases with identified circulating tumor cells will be estimated.

NCT ID: NCT03917524 Recruiting - Clinical trials for Oral Cavity Squamous Cell Carcinoma

Feasibility of CTCs Isolation for Transcriptomes and Genome Wide Associated Analysis in Post-OP High Risk OSCC Patients.

CTC
Start date: August 1, 2015
Phase:
Study type: Observational [Patient Registry]

Anti-cancer treatments have been thought to be closely related to their unique genetic alterations. In the past few years, the investigator have used cDNA microarray to delineate the transcriptome profiles of differentially-expressed genes between OSCC tumors and normal epithelium. By supervised hierarachical clustering analysis, the investigator further analyzed and validated the differentially-expressed genes for OSCC tumors. In the investigators' previous research, the investigators have used this strategy to analyze the potential tissue proteins associated with OSCC tumors, indicating the feasibility of this strategy. However, gene detection is a great limitation and challenge in CTCs researches owing to the small number of isolated cells by traditional methods. Fortunately, by means of the investigators' developing high-purity CTCs isolation techniques, some preliminary data implied that isolated CTCs by this method could achieve the criteria of Whole-genome analysis (WGA), which brings the investigators' passion for further investigation.

NCT ID: NCT03843450 Recruiting - Clinical trials for Early Detection of Cancer

Culture System for Isolating Circulating Tumor Cells

Start date: January 29, 2019
Phase:
Study type: Observational

This culture system utilizes the special affinity difference of biomedical material coating for different cells to achieve the effect of isolating cancer cells from the blood sample. The coating of the system has the characteristic that to make the WBCs adhesion, but the cancer cells in the blood sample suspend in the culture medium, which achieves the effect of separating cancer cells from the blood. The supernatant with the cancer cells can further be isolated from the cultural system for related analysis and detection to achieve early diagnosis and screening.

NCT ID: NCT03821909 Recruiting - Pancreatic Cancer Clinical Trials

Acquisition of Portal Venous CTCs and Exosomes From Patients With Pancreatic Cancer by EUS

CTCs
Start date: August 1, 2018
Phase:
Study type: Observational

The investigators are going to explore the diagnostic and prognostic value of circulating tumor cells and exosomes extracted from the portal venous blood obtained with endoscopic ultrasound in pancreatic cancer patients.

NCT ID: NCT03809403 Recruiting - Colorectal Cancer Clinical Trials

Influence of the Surgical Technique Used for Colectomies on the Concentration of Circulating Tumor DNA and the Presence of Circulating Tumor Cells: Comparison of the "no Touch" Technic With Either First Clamping of the Mesenteric Vessels or First Mobilization of the Tumor Followed by Clamping.

ADNCHIR
Start date: February 5, 2019
Phase:
Study type: Observational

Colectomy is the most commonly used therapeutic approach for the treatment of non-metastatic colorectal cancer. This approach is generally very effective however the rate of recurrence and the appearance of metachronous metastasis remains a major problem in the postoperative period. One of the hypothesis that can explain this tumor progression is the dissemination of tumor cells at the time of tumor mobilization. In this work, we wish to verify this hypothesis by comparing two surgical technics used in our department for left or right colectomies: respectively either first section of the mesenteric vessels followed by the mobilization of the tumor or first mobilization of the tumor followed by the section of the mesenteric vessels. To evaluate the dissemination, we will study two disseminations markers that have shown their prognostic value: i) circulating tumor cells (which represent a direct marker of dissemination) and ii) tumor circulating DNA (which is an indirect marker) but has the advantage of being more representative of all tumor clones and therefore the tumor burden released into the blood at the time of surgery).

NCT ID: NCT03797053 Recruiting - Melanoma Clinical Trials

Ex Vivo Expansion of Circulating Tumor Cells as a Model for Cancer Predictive Pharmacology

EXPEVIVO-CTC
Start date: April 6, 2015
Phase:
Study type: Observational

Several studies conducted over the past decade have shown that Circulating tumor cells (CTCs) can be used as a marker for predicting disease progression and survival in patients with early or metastatic cancer. A high number of CTCs correlate with aggressive disease, increased metastasis and decreased survival rates. Knowledge of metastasis mechanisms was mainly obtained from mouse models with CTCs after orthotopic transplants. The only possibility to study the patient's CTC subpopulations is to carry out ex-vivo expansion and develop an animal model with CTC xenograft. Because circulating blood collection is simple and non-invasive, CTCs can be used as a marker to track disease progression and survival in real time. CTCs could also guide therapeutic choice.

NCT ID: NCT03772496 Recruiting - Diagnoses Disease Clinical Trials

Diagnostic Significance of CTCs in Patients With Thyroid Nodules (Circulating Tumor Cells)

CTCs
Start date: July 25, 2018
Phase: N/A
Study type: Interventional

Thyroid nodule patients with suggestion of fine needle aspiration biopsy (FNAB) offered by ultrasound are enrolled in the study. CTCs tested by Optimizing method and FNAB will be performed simultaneously. This is a double blind trial which pathologists and inspectors of CTCs don't know the result of each other. Surgical pathology and diagnostic results of FNAB is the primary endpoint and comparison will be made to see if CTCs combined with ultrasound can get similar diagnostic performance as FNAB. The diagnostic results of FNAB included Bethesda class II and more than V which are defined as benign and malignant, respectively.

NCT ID: NCT03744962 Recruiting - Endometrial Cancer Clinical Trials

MSI in Circulatory DNA of Endometrial Cancer

Start date: November 10, 2018
Phase:
Study type: Observational

This study aims to analyze the microsatellite instability (MSI) in the circulatory tumor DNA and in the tumor tissue in the patients diagnosed with uterine endometrial cancer. These data will be used for the study of "Cohort Study of Universal Screening for Lynch Syndrome in Chinese Patients of Endometrial Cancer" (NCT03291106, clinicaltrials.gov).

NCT ID: NCT03655015 Recruiting - Lung Neoplasm Clinical Trials

Patient-derived Organoid Model and Circulating Tumor Cells for Treatment Response of Lung Cancer

Start date: October 16, 2018
Phase:
Study type: Observational

Create a living biobank of PDOs from Stage I-III lung cancer patients.

NCT ID: NCT03511859 Recruiting - Breast Cancer Clinical Trials

Detecting Circulating Tumor Cells (CTCs) and Cell Free DNA (cfDNA) in Peripheral Blood of Breast Cancer (BC) Patients to Develop the Clinical Application for Early Detection and Diagnostics

Start date: November 16, 2017
Phase:
Study type: Observational

Utilization of circulating-tumor-cell (CTC) and cell free DNA (cfDNA) as novel and noninvasive tests for diagnosis confirmation, therapy selection, and cancer surveillance is a rapidly growing area of interest. In the wake of FDA approval of a liquid biopsy test, it is important for clinicians to acknowledge the obvious clinical utility of liquid biopsy for cancer management throughout the course of the disease.