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Carcinoma, Non-Small-Cell Lung clinical trials

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NCT ID: NCT01951469 Recruiting - Clinical trials for Non-small Cell Lung Cancer

Gefitinib With or Without Chemotherapy in Brain Metastases From Non-small Cell Lung Cancer

Start date: January 2016
Phase: Phase 3
Study type: Interventional

This is a multi-center phase III randomized controlled study to assess the efficacy of Gefitinib alone and Gefitinib combination with Pemetrexed/platinum on patients with brain metastasis from non-small cell lung cancer(NSCLC) harboring EGFR mutation type by intracranial PFS(iPFS),also PFS ,DCR and OS.The side effect is evaluated as well.

NCT ID: NCT01932229 Recruiting - NSCLC Clinical Trials

An Open Label Study of BIBW 2992/Afatinib in Advanced Non-Small Cell Lung Cancer Patients Pre-treated With Erlotinib or Gefitinib

Start date: February 2013
Phase: Phase 2
Study type: Interventional

Advanced lung cancer (non-small cell lung cancer) with a mutation in the EGFR (epidermal growth factor receptor) gene, which have disease progression after treatment with an EGFR inhibitor (erlotinib or gefitinib), and have progression of disease also after treatment with chemotherapy will be recruited. The trial has only one arm, of afatinib daily treatment. Blood and exhaled breath samples will be collected for investigations aiming to identify factors that predict response to afatinib.

NCT ID: NCT01930474 Recruiting - Clinical trials for Non Small Cell Lung Cancer Patients

Analysis of Plasma Tumor DNA in Lung Cancer Patients

Start date: July 2013
Phase: N/A
Study type: Observational

The presence of genetic alterations in the tyrosine kinase domain of the oncogene (eg. EGFR and ALK) is associated with the clinical response to tyrosine kinase inhibitors (TKIs) in patients with non-small cell lung cancers. Therefore, the detection of altered genetic alterations is useful for predicting the treatment response for TKIs in non-small cell lung cancer patients. However, good quality tumor tissues are available only in <50% of patients with inoperable lung cancer for mutation analysis. In this study, the investigators will detect and quantify the genetic alterations in plasma. the investigators will investigate if the serial measurement of cancer-derived genetic alterations in plasma can provide a means for monitoring disease progression, as well as treatment response. In addition the investigators will analysis the resistant mechanism of TKIs and chemotherapy with plasma tumor DNA.

NCT ID: NCT01929200 Recruiting - Clinical trials for Non-small-cell Lung Cancer

Icotinib as Adjuvant Therapy in Treating Non-small-cell Lung Cancer Patients With Positive EGFR Mutation

Start date: August 2013
Phase: Phase 2
Study type: Interventional

This study is designed to evaluate the efficacy of icotinib as adjuvant therapy in treating such patients. The primary endpoint is to compare the recurrence-free survival after 1-year or 2-year treatment with icotinib.

NCT ID: NCT01926483 Recruiting - Clinical trials for Non-small Cell Lung Cancer Stage IIIA

Phase II Trial of Regimen for Stage III (N2) NSCLC Using Induction Treatment Followed by Resection

ZTOG-1202
Start date: March 2013
Phase: Phase 2
Study type: Interventional

The investigators hypothesized that the Neoadjuvant Chemoradiotherapy was a beneficial treatment for Patients with Stage IIIA-N2 Non-Small Cell Lung Cancer, so we try to evaluate the security of treatment, the QoL of patients and the influence to the PFS and OS.

NCT ID: NCT01926171 Recruiting - Clinical trials for Non-small-cell Lung Cancer

Icotinib With Whole Brain Radiation Therapy in NSCLC Patients With Brain Metastases

Start date: June 2013
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of icotinib in combination with whole brain radiotherapy for NSCLC patients with brain metastases. The primary endpoint is objective response rate of intracranial lesions.

NCT ID: NCT01902875 Recruiting - Clinical trials for Non Small Cell Lung Cancer

Preconditioning Chemotherapy Combination With Cytokine Induced Killer Cell (CIK) Immunotherapy

Start date: June 2013
Phase: N/A
Study type: Observational

This clinical Trial is proposed to explore whether preconditioning chemotherapy of Paclitaxel+cisplatin(TP)regimen combined with autologous adoptive CIK cell immunotherapy could benefit NSCLC patients with a better clinical outcome.

NCT ID: NCT01891708 Recruiting - Clinical trials for Non Small Cell Lung Cancer

VEGFRs Predict Bevacizumab Benefit in Advanced Non Small Cell Lung Cancer

Start date: June 2013
Phase: N/A
Study type: Observational [Patient Registry]

a. VEGFRs may be the biomarker which can predict the effect of bevacizumab in non small cell lung cancer

NCT ID: NCT01891123 Recruiting - Breast Cancer Clinical Trials

Explore the Individual Treatment of Docetaxel and Paclitaxel in NSCLC, NPC and BRC by PK-guided Dosing Strategy

Start date: June 2013
Phase: N/A
Study type: Interventional

As cytotoxic agents, DTX and PTX have a narrow therapeutic window. BSA dosing leads to great inter-individual PK variability, which is a major contributor for severe toxicity, especially in East-Asian populations. DTX exposures measured by area under plasma concentration-time curve (AUC), PTX exposures measured by the time above a plasma concentration of 0.05 µmol/L (TC>0.05), are the most biologic effects associated PK parameters for DTX and PTX, respectively, which could positively predict related toxicities such as neutropenia, peripheral neuropathy, etc. So, we conducted a randomized clinical trial to compare the effect on related toxicities and efficacy of PK-guided dosing strategy and BSA dosing strategy.

NCT ID: NCT01885754 Recruiting - Clinical trials for Non-Small-cell Lung Cancer

Characterization of Peripheral Muscle Function in Patients With Non-small-cell Lung Cancer

Start date: February 2013
Phase: N/A
Study type: Observational

Rationale: With 1.6 million new cases diagnosed each year and 1.3 million deaths, lung cancer is the leading cancer-related death worldwide and it represents a pressing health issue. Patients with lung cancer are more likely to experience cachexia, a severe debilitating disorder causing fatigue, weight loss, muscle wasting and associated with reduced physical function, increased chemotherapy toxicity and reduced survival. This syndrome occurring in about 80% of advanced cancer patients is the direct cause of death in about 20% of cases. However, despite the importance of cachexia in lung cancer, its mechanisms ans its relation with muscle function and effort tolerance are still unknown. Aim: To explore muscle function, signaling pathways and its relationship to impaired functional capacity of patients with non-small-cell lung cancer(NSCLC); depending of whether they have cachexic state at diagnosis. Methods: This study will be conducted at the Institut universitaire de cardiologie et de pneumologie de Québec. 56 patients newly diagnosed of NSCLC will be recruited and separated whether or not they have a cachexic state. The evaluation will need two visits separated by 5 days. During the evaluation the following tests will be done: - Anthropometric measures - Level of daily physical activity - Pulmonary function test - Maximal incremental cardiopulmonary exercise test on ergocycle - Endurance test on ergocycle - Muscle function tests - Magnetic stimulation - Quadriceps biopsy