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Rectal Neoplasms clinical trials

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NCT ID: NCT03867799 Active, not recruiting - Clinical trials for Metastatic Colorectal Cancer

iSCORE: Immunotherapy Sequencing in COlon and REctal Cancer

Start date: March 27, 2019
Phase: Phase 2
Study type: Interventional

This is a single-arm, single centre open-label, phase II interventional clinical trial of combination immunotherapy with Nivolumab and Relatlimab in mCRC.

NCT ID: NCT03867409 Completed - Colo-rectal Cancer Clinical Trials

The United States Healthy Living Study

Start date: November 5, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to pilot test the efficacy of a patient-centered, tailored message intervention delivered via virtual human technology for increasing colorectal cancer (CRC) screening within guidelines. Although participation is not limited to these groups, the study team is particularly interested in the feasibility of the intervention for reaching racial/ethnic minority and rural patients.

NCT ID: NCT03854890 Not yet recruiting - Rectal Cancer Clinical Trials

Fluorescent Lymphography-Guided Lymphadenectomy In Laparoscopic Proctectomy

Start date: July 1, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the number of lymph nodes retrieved with or without the use of intraoperative fluorescence lymphography in laparoscopic radical resection of rectal cancer.

NCT ID: NCT03854799 Completed - Colon Rectal Cancer Clinical Trials

Immunotherapy In Locally Advanced Rectal Cancer

AVANA
Start date: April 1, 2019
Phase: Phase 2
Study type: Interventional

Preoperative CTRT is considered the standard of care in the management of LARC. Preoperative CTRT approach results in significant tumor downstaging and local control with a complete pathological response rate of about 15% even if additional therapeutic strategies should be explored to improve outcomes, expecially for T4 cancers. Immunotherapy with PD-1/PD-L1 immunocheckpoint blockade (ICB), turned out a breakthrough in cancer treatment among different tumor types, including CRC. An ICB strategy could lead up to a 40% of response in metastatic CRC with deficient mismatch repair (MMR) status. Unfortunately, the activity of ICBs in MMR proficient mCRC is extremely low but it might be improved using immunomodulatory strategies as demonstrated by Bendell et al. In this context, the role of RT in revert the tolerance to a low neoantigen-burden (such as in MMR proficient CRCs) by the induction of antigen release from the tumour and activation of dendritic cells leading to a CD8+ T lymphocyte-mediated anticancer immune response has been widely elucidated. Moreover, antineoplastic agents can be exploited to target other crucial cellular effectors of immunosuppressive tumor microenvironment (i.e. regulatory T cells and myeloid-derived suppressor cells). In line with these evidences, Hecht et al. have recently reported that in rectal cancer patients, neoadjuvant CTRT increases PD-L1 expression in tumor cells, strongly suggesting a neoadjuvant combinatory strategy with RT and PD-1/PD-L1 pathway blockade. The integration of immunotherapy in the neoadjuvant setting (instead of adjuvant one) for the management of LARC is also supported by preclinical findings showing that in metastatic breast cancer mice models, neoadjuvant immunotherapy is superior in inducing long-term survivors, compared with adjuvant strategy with a greater magnitude of tumor-specific T cell expansion in neoadjuvant treated mice and a better anti-tumor T cell-mediated immune response. On the basis of such considerations, there is a strong biological and clinical rationale for testing the addition of avelumab, an anti-PD-L1 moab, to capecitabine-based CTRT in patients with technically resectable, LARC. The aim of this strategy is to lead to significant improvements of pCR and, ultimately, patients' survival.

NCT ID: NCT03853733 Completed - Rectal Cancer Clinical Trials

Hypofractionated Palliative Radiotherapy in Patients With Advanced Non-operable Rectal Cancer

Start date: October 1, 2016
Phase:
Study type: Observational

Many patients with rectal cancer were not candidates for surgical resection because advanced age, comorbidities, or multiple synchronous metastases. In this scenario only comfort measures or different palliative radiotherapy regimens are applied, from single doses to treatments lasting several weeks. The aim of this prospective study is to describe the preliminary results of our protocol of hypofractionated palliative radiotherapy in patients with non-operable rectal cancer.

NCT ID: NCT03846882 Recruiting - Rectal Cancer Clinical Trials

FDG - PET / MRI in Patients With Rectal Cancer

RECTOPET
Start date: December 1, 2015
Phase:
Study type: Observational

The combination of FDG-PET/CT and MRI at staging of rectal cancer in diagnosis is currently very little studied. The investigator have a unique opportunity to study this. Hypothetically, with PET/MR as one hybrid imaging method, alternatively as an additional method, it could increase the accuracy of rectal cancer of moderate and high risk type, especially at primary N-staging, but also in assessing other important prognostic factors such as T-staging, peritoneal involvement, metastasis to lateral lymph nodes, EMVI and MRF involvement. The same reasoning applies to the assessment of tumor regression after CRT. In the study, PET/MR is compared with PET/CT, diagnostic CT and MRI to evaluate the additional value of the hybrid imaging PET/MRI. The investigator also plan to evaluate how immunological, proliferative and prognostic biomarkers in blood and tumor tissue correlate with the radiological findings, and if the combination biomarker and radiology can provide additional prognostic information.

NCT ID: NCT03846726 Completed - Rectal Cancer Clinical Trials

Treatment Strategy for Rectal Cancer Patients With Complete Clinical Response

Start date: January 1, 2018
Phase:
Study type: Observational

This was a propensity-score matched observational analysis, comparing the oncological outcome of surgical resection vs watch and wait apporach for rectal cancer patients with a cCR.

NCT ID: NCT03843957 Completed - Cancer Clinical Trials

Effectiveness and Implementation of mPATH-CRC

Start date: October 31, 2019
Phase: N/A
Study type: Interventional

Study Investigators are conducting this study to learn how to best implement a new iPad program in clinical practice.

NCT ID: NCT03840239 Active, not recruiting - Rectal Cancer Clinical Trials

TNT to Increase the Clinical Complete Response Rate for Distal LARC

TESS
Start date: December 25, 2018
Phase: Phase 2
Study type: Interventional

This is a open-label, single-arm study to investigate the safety and efficacy of total neoadjuvant treatment (TNT) in patients with locally advanced resectable rectal cancer.

NCT ID: NCT03826862 Recruiting - Rectal Cancer Clinical Trials

Lateral Lymph Node Dissection for Middle-low Rectal Cancer

Start date: October 1, 2018
Phase: N/A
Study type: Interventional

The investigators will perform CT three-dimension reconstruction for middle-low rectal cancer patients who have enlarged lateral lymph nodes to recognize the variance of pelvic vessels, by which to help reduce operative time and blood loss, localize the lateral lymph nodes, improve the lymph node harvested and positive rate. Besides, The investigators will label the vessels near the interested node to achieve node-by-node for further investigation.