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Chemotherapy Effect clinical trials

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NCT ID: NCT04232748 Recruiting - Weight Loss Clinical Trials

Change in Body Weight During Treatment of Advanced Colorectal Cancer

Start date: January 1, 2019
Phase:
Study type: Observational

Colorectal cancer (CRC) is a significant and growing health burden in Hong Kong. According to data from Hong Kong Cancer Registry, CRC ranked the first in incidence and the second in mortality, with around 5,000 new cases diagnosed and more than 2,000 cancer-related mortality in 2014. The investigators aim to evaluate the association between serial weight change during first line treatment and outcomes in patients with metastatic CRC.

NCT ID: NCT04110769 Recruiting - Pancreatic Cancer Clinical Trials

Development of Biomarker for the Evaluation of Response After Neoadjuvant Therapy in Patients With Pancreatic Cancer

Start date: July 17, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to identify and apply biomarkers that can provide better information than previous imaging and blood tests when evaluating the response after neoadjuvant chemotherapy in pancreatic cancer patients who require neoadjuvant therapy before surgery.

NCT ID: NCT04089748 Recruiting - Bladder Cancer Clinical Trials

Basal Tumours in Bladder Cancer, Response to chemoTherapy

BoBCaT
Start date: February 27, 2019
Phase:
Study type: Observational

Determine the sensitivity/resistance to chemotherapy of the various subgroups of muscle-invasive bladder cancers, including the basal subgroup (about 25% of these tumours) according to 4 different classifications based on molecular or immunohistochemical classifiers.

NCT ID: NCT04042298 Recruiting - Breast Cancer Clinical Trials

Microvascular Function in Patients Undergoing 5-Fluorouracil Chemotherapy

Start date: June 25, 2019
Phase:
Study type: Observational

The primary aim of this study is to investigate potential differences in vascular function between patients receiving 5-Fluorouracil (5-FU) chemotherapy, patients receiving chemotherapies other than 5-FU, cancer survivors who were treated with 5-FU, and an age and sex matched control. 5-FU is the third most commonly administered chemotherapeutic agent and its use is associated with the second most occurrences of cardiotoxicity. Despite the known cardiotoxic effects of 5-FU, it's effects on the human vasculature are not well understood. To achieve the goals of this project Laser Doppler flowmetry (LDF) will be used to assess blood flow within the skin microcirculation of the forearm in cancer patients who have received 5-Fluoruracil within the past 30 days (Experimental Group), cancer patients receiving radiotherapy and/or chemotherapy other than 5-Fluorouracil, and an age and sex matched control (Control Group). LDF utilizes a small (~3 cm) non-invasive sensor placed on the skin. The sensor shines light into the skin, and upon contact with red blood cells (RBCs), the light is reflected and scattered. This information is used to evaluate microvascular blood flow and has previously been used in clinical populations.

NCT ID: NCT03985891 Recruiting - Chemotherapy Effect Clinical Trials

The Efficacy of JS001 Combined With Chemotherapy in Patients With Locally Advanced Colon Cancer

JSFOL
Start date: December 16, 2020
Phase: Phase 1/Phase 2
Study type: Interventional

Colon cancer is one of the most lethal malignancies, and colorectal cancer ranks the fifth leading cause of tumor-related mortality in China. FOLFOX is the recommended adjuvant/ neoadjuvant treatment for advanced colon cancer. JS001, as the first Chinese produced anti-PD-1 monoclonal antibody, has been approved by CFDA. This study aims to assess the safety and efficacy of JS001 in combination with FOLFOX as adjuvant/neoadjuvant treatment for patients with locally advanced colon cancer.

NCT ID: NCT03792269 Recruiting - Chemotherapy Effect Clinical Trials

Intraperitoneal and System Chemotherapy Versus XELOX as First-line Chemotherapy for mCRC

Start date: January 1, 2016
Phase: Phase 2
Study type: Interventional

XELOX as first-line treatment regimen has limited efficacy against patients with metastatic colorectal cancer (mCRC). Peritoneal metastasis is one of the most lethal factor for mCRC. Intraperitoneal chemotherapy has became a widely accepted strategy in the treatment of peritoneal dissemination. We hypothesized that combined multi-channel administration, such as intraperitoneal chemotherapy, oral chemotherapy, and intravenous chemotherapy, can produce better results than XELOX for first-line treatment for mCRC patients.

NCT ID: NCT03683407 Recruiting - Chemotherapy Effect Clinical Trials

Effect of Chemotherapy on TMB in NSCLC

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

Tumor mutation burden is identified as an important biomarkers for predicting PD-1/PD-L1 inhibitors in advanced Non-Small Cell Lung Cancer. Several previous clinical trials have demonstrated that chemotherapy could enhance the efficacy of PD-1/L1 immunotherapy in NSCLC such as Checkmate-227, Impower-150, Keynote-189, etc. Pre-clincial experiment shows that chemotherapy could increase CD8 TIL infiltration in tumor microenvironment, activate T cell immune reaction. However, it remains unclear whether chemotherapy could affect tumor mutation burden in advanced NSCLC patients. The present study aims to evaluate whether tumor mutation burden will change after receiving chemotherapy in advanced NSCLC patients.

NCT ID: NCT03650205 Recruiting - Heart Failure Clinical Trials

Ivabradine to Prevent Anthracycline-induced Cardiotoxicity

IPAC
Start date: January 22, 2019
Phase: N/A
Study type: Interventional

Anthracyclines are associated with cardiotoxic effects. Previous studies suggest that enalapril, and or carvedilol, protect against cardiovascular effects of these drugs. Ivabradine selectively reduces heart rate through inhibition of the cardiac pace maker IF channel, thus prolonging the duration of spontaneous depolarization in the sinus node. Additionally, ivabradine might preserve myocardial perfusion without negative inotropic effect and probably maintain cardiac contractility despite the reduction of heart rate. Ivabradine has been shown to improve outcome in patients with heart failure and angina. The aim of this study is to evaluate whether ivabradine might prevent anthracycline-induced cardiotoxicity.

NCT ID: NCT03633734 Recruiting - Chemotherapy Effect Clinical Trials

Efficacy Evaluation of Sequential Treatment With AG and Modified Folfirinox in Metastatic Pancreatic Adenocarcinoma

Start date: July 1, 2018
Phase: Phase 1/Phase 2
Study type: Interventional

The prognosis of pancreatic cancer is extremely poor. Current guidelines recommend Nab-paclitaxel, Gemcitabine and modified Folfirinox as the first-line chemotherapeutic regimen. Studies have shown that sequential chemotherapeutic regimen can effectively delay the drug resistance and improve the effect of chemotherapy. Here investigators intend to assess the effect of sequential treatment with Nab-paclitaxel plus Gemcitabine and modified Folfirinox on metastatic pancreatic adenocarcinoma.

NCT ID: NCT03626610 Recruiting - Surgery Clinical Trials

Prehabilitation of Patients With oEsophageal Malignancy Undergoing Peri-operative Treatment

Pre-EMPT
Start date: November 2016
Phase: N/A
Study type: Interventional

'Pre-EMPT' - A cohort-controlled, interventional study to assess the effects of a pre-emptive exercise programme, or 'prehabilitation', in patients undergoing peri-operative chemotherapy for adenocarcinoma of the lower oesophagus and gastro-oesophageal junction.