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Total-body PET/CT Imaging Using the uEXPLORER in Non-small Cell Lung Cancer Patients Treated by Induction Chemotherapy Plus Nivolumab and Definitive Concurrent Chemoradiotherapy

Completed
Conditions
Non-small Cell Lung Cancer
Interventions
Device: Total body PET/CT (uExplorer)
Registration Number
NCT04654234
Lead Sponsor
Sun Yat-sen University
Brief Summary

The prospective study aims to explore the value of total-body PET/CT dynamic imaging (uExplorer) in assessing tumor metabolic heterogeneity and predicting prognosis for patients with locally advanced, unresectable non-small cell lung cancer (stage III) treated by neoadjuvant chemotherapy plus nivolumab and definitive concurrent chemoradiation therapy.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
15
Inclusion Criteria
  • Provision of signed, written and dated informed consent prior to any study specific procedures;
  • Patients aged 18~75 years old;
  • had histologically or cytologically confirmed non-small cell lung cancer;
  • Without prior chemotherapy, radiotherapy, surgery, targeted therapy or immunotherapy;
  • Life expectancy ≥12 weeks;
  • World Health Organization (WHO) Performance Status of 0 or 1;
  • had unresectable stage III disease according to the 8th edition of the American Joint Committee on Cancer staging system;
  • Women should be non-breast feeding during the study period;
  • Women of reproductive age (WOCBP) must agree to comply with the contraceptive method during the study treatment and for a period of 5 months following the last administration of the study treatment;
  • Men who have sex with WOCBP must agree to comply with the contraceptive method during the study treatment and for 7 months after the last administration of the study treatment;
  • Absolute neutrophil count ≥1500/uL, hemoglobin ≥9.0mg/dL, platelet ≥100000/uL;
  • Serum creatinine clearance >50 mL/min by the Cockcroft-Gault formula (Cockcroft and Gault 1976);
  • Serum bilirubin ≤1.5 x upper limit of normal (ULN), Aspartate Transaminase(AST) and Alanine Transaminase(ALT) ≤2.5 x ULN;
  • Forced expiratory volume in 1 second (FEV1) ≥800ml;
Exclusion Criteria
  • Concurrent enrollment in another clinical study, unless it is an observational(non-interventional) clinical study;
  • Mixed small cell and non-small cell lung cancer histology;
  • Prior exposure to any anti-programmed cell death protein(PD)-1 or anti- PD-L1 antibody;
  • Active or prior documented autoimmune disease within the past 2 years;
  • Active or prior documented inflammatory bowel disease (eg. Crohn's disease, ulcerative colitis);
  • History of primary immunodeficiency;
  • Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, uncontrolled hypertension, unstable angina pectoris, cardiac arrhythmia, active peptic ulcer disease or gastritis, active bleeding diatheses;
  • History of another primary malignancy within 5 years, except for adequately treated basal or squamous cell carcinoma of the skin or cancer of the cervix in situ and the disease under study;
  • Female patients who are pregnant, breast-feeding or male or female patients of reproductive potential who are not employing an effective method of birth control;
  • Any situation not suitable for this study judged by researchers;

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Total-body PET/CT (uExplorer)Total body PET/CT (uExplorer)Patients with locally advanced NSCLC will receive total-body PET/CT (uExplorer) scans before, during and after the treatment
Primary Outcome Measures
NameTimeMethod
Patlak-Ki (Ki)From enrollment to 1 year after radiotherapy

The prognostic role of Patlak-Ki and its dynamic change during treatment

Secondary Outcome Measures
NameTimeMethod
standardized uptake value (SUV)From enrollment to 1 year after radiotherapy

The prognostic role of SUV and its dynamic change during treatment

metabolic tumor volume (MTV)From enrollment to 1 year after radiotherapy

The prognostic role of MTV and its dynamic change during treatment

total lesion glycolysis (TLG)From enrollment to 1 year after radiotherapy

The prognostic role of TLG and its dynamic change during treatment

Trial Locations

Locations (1)

Hui Liu

🇨🇳

Guangzhou, Guangdong, China

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