Health Condition 1: C148- Malignant neoplasm of overlappingsites of lip, oral cavity and pharynx Health Condition 2: C349- Malignant neoplasm of unspecifiedpart of bronchus or lung
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Lung (NSCLC) and oral (OSCC) cancer patients (Histo-pathologically diagnosed) who are slated to undergo anti-PD L1/ neoadjuvant or palliative chemotherapy. 2.Patients can provide sufficient tissues/blood for molecular analysis. 3.Consent from patients for utilization of their tissues and blood for this study.
Exclusion criteria
Exclusion criteria: 1.Pregnant women and patients under the age of 18 2.Those who are unfit to provide biopsy samples as per protocol 3.Those who refuse to consent to tissues being provided for research as per this protocol
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.To develop a method to predict response to anti-PDL 1/ neoadjuvant/ palliative chemo therapy in lung and oral cancer patients. 2.to confirm/ validate/ improve the method to predict response to anti-PDL 1/ palliative/ neoadjuvant chemo therapy in lung and oral cancer patientsTimepoint: At the end of study | — |
Secondary
| Measure | Time frame |
|---|---|
| NaTimepoint: NA | — |
Countries
India
Contacts
Tata Memorial Hospital