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Neoplasms, Second Primary clinical trials

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NCT ID: NCT03777930 Not yet recruiting - Clinical trials for Cancer, Therapy-Related

The Evaluation of Curative Effect on Treatment of Tumor Above Thalidomide Combined With Megestrol

Start date: December 10, 2018
Phase: Phase 4
Study type: Interventional

To observe the effect of thalidomide combined with megestrol acetate on lymphocyte, inflammatory factor regulation and nutritional status in patients with advanced malignant tumors.

NCT ID: NCT03754530 Not yet recruiting - Clinical trials for Non-Small Cell Lung Cancer

Icotinib Combined With Radiation Therapy For NSCLC Patients With Brain Metastases and EGFR Mutation

Start date: December 1, 2018
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy of icotinib in combination with radiotherapy for NSCLC patients with brain metastases. The primary endpoint is PFS of intracranial lesions

NCT ID: NCT03753685 Not yet recruiting - Brain Metastases Clinical Trials

X-396(Ensartinib) Capsules in ALK-Positive NSCLC Patients With Brain Metastases

Start date: December 2018
Phase: Phase 2
Study type: Interventional

To assess efficacy and safety of oral X-396 (Ensartinib) capsule in Chinese ALK-positive NSCLC patients with brain metastases, eligible patients will be enrolled with objective responses being primary outcome measures.

NCT ID: NCT03638765 Not yet recruiting - Brain Metastases Clinical Trials

Dendritic Cell Therapy for Brain Metastases From Breast- or Lung Cancer

Start date: November 2018
Phase: Phase 1
Study type: Interventional

The study will use an Ommaya reservoir that drains into brain metastases to deliver activated, autolous dendritic cells to the tumor lesion, for patients who are 18 - 75 years old who have brain metastases from either lung cancer or breast cancer. The primary objective of the study is to evaluate the safety and feasibility of administering DCVax-Direct to patients with metastatic tumors in the brain. The secondary objectives are to determine tumor response, the rate of intracranial recurrence (IR), the rate of neurologic deaths, decline in neuro-cognitive functioning and overall survival. Approximately 10 patients with injectable metastatic brain tumors will be enrolled initially in a dose escalation scheme, with the expectation to enroll a total of 24 patients.

NCT ID: NCT03613181 Not yet recruiting - Brain Metastases Clinical Trials

ANG1005 in Leptomeningeal Disease From Breast Cancer

ANGLeD
Start date: December 2023
Phase: Phase 3
Study type: Interventional

This is an open-label Phase 3 study to see if ANG1005 can prolong survival compared to a Physician Best Choice control in HER2-negative breast cancer patients with newly diagnosed leptomeningeal disease and previously treated brain metastases.

NCT ID: NCT03591666 Not yet recruiting - Adenocarcinoma Clinical Trials

A Study of Anlotinib in Recurrent/Metastatic Head and Neck Adenocarcinomas

Start date: July 15, 2018
Phase: Phase 2
Study type: Interventional

This is a non-randomized, phase II, open label study of anlotinib hydrochloride capsules in recurrent/metastatic adenocarcinomas of head and neck. The primary purpose of this study is to evaluate the efficacy of anlotinib.

NCT ID: NCT03356600 Not yet recruiting - Brain Metastases Clinical Trials

Apatinib Plus Radiotherapy for Patients With Brain Metastases From Non-small-cell Lung Cancer

Start date: December 2017
Phase: Phase 2
Study type: Interventional

To observe the effectiveness and safety of apatinib combined with radiotherapy for brain metastasis from non-small cell lung cancer patients

NCT ID: NCT02847754 Not yet recruiting - Clinical trials for Vertebral Bony Metastases

Differentiated Resistance Training of the Paravertebral Muscles in Patients With Unstable Spinal Bone Metastasis Under Concomitant Radiotherapy

DISPO-2
Start date: August 2016
Phase: Phase 2
Study type: Interventional

Standard indications for palliative radiation of bony metastases include pain, spinal cord compression, and impending pathologic fractures. Palliative radiation therapy serves to reduce pain, improve quality of life, and avoid complications. Tailored training of the paravertebral musculature may support Radiation therapy and improve above named factors. DISPO-2 was designed to investigate the impact of tailored physical exercise in patients with unstable vertebral metastases as compared to manual therapy (massage etc.). The trial includes patients with painful unstable bony metastases, patients with spinal cord compression or impending pathological fractures are excluded. The investigations are carried out in a prospective randomized controlled phase-II parallel group design.

NCT ID: NCT02832830 Not yet recruiting - Clinical trials for Vertebral Bony Metastases

Image-guided and Intensity-modulated Radiotherapy Versus External Beam Radiotherapy for Patients With Spine Metastases

IRON-1
Start date: August 2016
Phase: Phase 2
Study type: Interventional

The aim of this explorative trial is to verify the comparability of a fractionated intensity modulated radiotherapy with a conventional radiotherapy related to quality of life on the one hand and to evaluate toxicity, re-calcification and stability of vertebral body as well as pain relief and local response for palliative patients with painful spinal bone metastases on the other hand. This is a single-center, prospective randomized controlled trial with parallel-group design to determine the quality of life after RT in patients with spinal bone metastases. Two different techniques were evaluated: intensity modulated radiotherapy (IMRT) and fractionated conventional external beam RT with 10×3 Gy each. Experimental intervention: IMRT 10 x 3 Gy Control intervention: 3D-RT 10 x 3 Gy

NCT ID: NCT02832765 Not yet recruiting - Clinical trials for Vertebral Bony Metastases

Intensity-modulated Radiotherapy With Integrated-boost in Patients With Spinal Bone Metastases

IRON-2
Start date: September 2016
Phase: Phase 2
Study type: Interventional

The primary goal of the study is to determine the local control-rate after radiotherapy (RT) with and without simultaneous integrated boost (SIB) concepts in patients with bone metastases of the spine. Further study objectives are survival, and clinical parameters such as pain, quality of life (QoL) and fatigue. We expect an improvement in local control and consecutively an increased re-sclerotization of the bone metastasis due to a higher biological dose in the tumor area. Therefore patients could benefit in quality-of-life, pain relief and mobility.