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Observation of the Impact of Radiotherapy With or Without Chemotherapy in the Value of Peripheral Blood Lymphocyte Subsets for Patients With Thoracic Cancer

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

This study is an observation, single center study to evaluate the alternations and prognostic value of peripheral blood lymphocyte (PBL) in patients diagnosed with thoracic cancers, including lung cancer, esophageal squamous cell carcinoma and thymic epithelial carcinoma underwent radiotherapy with or without chemotherapy.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

⁃ Age at least 18 years. ECOG PS 0-1. Pathologically confirmed NSCLC, esophageal squamous cell carcinoma or thymic epithelial tumor.

⁃ Life expectancy of more than 3 months. Patients with no indications for palliative radiotherapy in the opinion of the investigator.

⁃ Patients with a prior history of surgery are eligible if they have recovered adequately from the toxicity and/or complications of surgery.

⁃ Signed informed consent for the use of fresh tumor biopsies before and during the treatment.

⁃ Women of childbearing age and men must agree to use effective contraception during the trial.

⁃ Adequate organ function within 1 week prior to the enrollment:

• Adequate bone marrow function: hemoglobin ≥80g/L, white blood cell (WBC) count ≥ 4.0 \* 10 \^ 9/L or neutrophil count ≥ 1.5 \* 10 \^ 9/L, and platelet count ≥ 100 \* 10 \^ 9/L;

• Adequate hepatic function: total bilirubin \< 1.5 x upper limit of normal (ULN). Note: If total bilirubin is \> 1.5 x ULN, direct bilirubin must ≤ ULN, Aspartate aminotransferase (AST) and Alanine aminotransferase (ALT) ≤2.5 ULN;

• Adequate renal function: serum creatinine ≤ 1.5 x ULN or creatinine clearance ≥ 50 mL/min;

Locations
Other Locations
China
Fudan University Shanghai Cancer Center
RECRUITING
Shanghai
Time Frame
Start Date: 2012-01-01
Estimated Completion Date: 2026-12
Participants
Target number of participants: 500
Related Therapeutic Areas
Sponsors
Leads: Shanghai Cancer Hospital, China

This content was sourced from clinicaltrials.gov