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Clinical Trials/KCT0002264
KCT0002264
Recruiting
N/A

Identification of predictive biomarkers for treatment outcome in patients with advanced hepatocellular carcinoma

Overview

Phase
N/A
Intervention
Not specified
Conditions
Diseases of the digestive system
Sponsor
Yonsei University Health System, Severance Hospital
Enrollment
100
Status
Recruiting
Last Updated
7 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
7 years ago
Study Type
Observational Study
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • ? unresectable primary liver cancer
  • ? Age 20 years old or older
  • ? Whole body performance (ECOG) 0\-2
  • ? Child\-Pugh score is B or more
  • ? Minimum volume of normal liver without tumor invasion\> 1000cm3
  • ? Minimum distance between target and organ at risk (eg duodenum, stomach) \= 0\.5cm
  • ? Adequate \*LFT (\*AST / \*ALT \<5 x upper limit of normal, total bilirubin\> \<3 mg / dl, albumin\> 2\.5 g / dL, normal \*PT / \*PTT)
  • ? Adequate renal function (creatinine \<1\.8 mg / dl or \*Ccr\> 50 ml / min)
  • ? \*BM reserve (\*ANC \=1500 / mm3, \*PLT \=50000 / mm3, \*Hb\> 9 g / dl)
  • ? lesion that can be measured or evaluated on CT

Exclusion Criteria

  • ? Those who can not perform respiratory training for treatment design
  • ? Patients with a history of previous abdominal radiation therapy
  • ? Those who can not receive consent before treatment
  • ? Those who do not agree to contraception as a pregnant patient

Outcomes

Primary Outcomes

Not specified

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