Sensitivity Clinical Trial
Official title:
Combining Genomics and Imageomics to Predict the Sensitivity of Neoadjuvant Pemetrexed and Cisplatin Chemotherapy in Patients With Lung Adenocarcinoma
Verified date | December 2021 |
Source | Shanghai Zhongshan Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Combining genomics and imageomics to predict the sensitivity of neoadjuvant pemetrexed and cisplatin chemotherapy in patients with lung adenocarcinoma
Status | Not yet recruiting |
Enrollment | 50 |
Est. completion date | December 31, 2024 |
Est. primary completion date | December 31, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility | Inclusion Criteria: - 1. Aged between 18 and 75 years; - 2. Lung adenocarcinoma; - 3. The patient is able to receive neoadjuvant pemetrexed and cisplatin chemotherapy - 4 .The patient is able to understand and comply with the study and has provided written informed consent. Exclusion Criteria: - 1. Patients with a history of lung surgery; - 2. Postoperative pathology showed non-primary lung cancer; - 3. Patients with a history of other tumors; - 4. Patients with severe complications (coronary heart disease, valvular heart disease, end-stage renal disease, severe liver cirrhosis); - 5. Unable to cooperate with the researchers because of dementia or cognitive decline - 6. Other situations that are not in conformity with the standards and requirements of this trial. |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Shanghai Zhongshan Hospital |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Tumor Regression Grade | 1-2 Weeks after enrollment (after Surgery) |
Status | Clinical Trial | Phase | |
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