Chemotherapy Followed by Surgery and Neoadjuvant Hemothoracic Intensity Modified Radiation Therapy (IMRT) for Patients With Malignant Pleural Mesothelioma
Status: | Recruiting |
---|---|
Conditions: | Lung Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 2/8/2019 |
Start Date: | March 18, 2016 |
End Date: | December 2020 |
Contact: | Karlyn Pierson, RN |
Email: | pierson.karlyn@mayo.edu |
Phone: | 507-293-0807 |
The purpose of this study is to determine the response rate and overall survival in patients
that have been diagnosed with mesothelioma and will undergo chemotherapy, surgery and
intensity modified radiation therapy (IMRT) as part of their standard of care.
that have been diagnosed with mesothelioma and will undergo chemotherapy, surgery and
intensity modified radiation therapy (IMRT) as part of their standard of care.
The investigators will consent patients that have been diagnosed with mesothelioma and will
undergo chemotherapy followed by surgery and then IMRT as their standard of care. The
investigators will collect data from past and future medical records as well as data
regarding their health status for their lifetime by reviewing life status, treatment status
and CT scans.
undergo chemotherapy followed by surgery and then IMRT as their standard of care. The
investigators will collect data from past and future medical records as well as data
regarding their health status for their lifetime by reviewing life status, treatment status
and CT scans.
Inclusion Criteria:
- Subject provides informed consent
- Subject is >18 years of age
- Subject is deemed competent for making medical decisions
- Subject is scheduled to undergo chemotherapy followed by surgery and then IMRT
- Subject is a surgical candidate
- A negative pregnancy test is required in women of child-bearing potential, as standard
of care.
Exclusion Criteria:
•Subject is <18 years old.
We found this trial at
1
site
200 First Street SW
Rochester, Minnesota 55905
Rochester, Minnesota 55905
507-284-2511
Principal Investigator: Dennis A Wigle, MD, PhD
Phone: 507-538-1960
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