unresectable recurrent solid tumor
Conditions
Interventions
None listed
Sponsors
Shitara Kohei
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Willing to participate in the "XXXX". 2) Written consent has been obtained from the patient for this ancillary study. 3) Age 18 years or older on the date consent is obtained.
Exclusion criteria
Exclusion criteria: 1) Patients who are regarded as inappropriate for enrollment by investigators.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Correlation of objective response rate or disease control rate with biomarkers | — |
Secondary
| Measure | Time frame |
|---|---|
| Progression-free survival, duration of response, duration of treatment success, correlation of biomarkers with overall survival, etc. | — |
Contacts
Public ContactHiromichi Nakajima
National Cancer Center Hospital East
Outcome results
None listed