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Clinical Trials/NCT06629714
NCT06629714
Completed
Not Applicable

Cohort Studies of Impact of Pretreatment Emotional on Survival and the Predictive Role of Peripheral Blood Metabolic and Inflammatory Markers in Immunotherapy Response Among Treatment-Naïve, Advanced and Inoperable Gastroesophageal and Non-Small-Cell Lung Cancer Patients

Anhui Medical University1 site in 1 country196 target enrollmentOctober 16, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
Anhui Medical University
Enrollment
196
Locations
1
Primary Endpoint
Cohort 1 & 2: Progression-free survival (PFS)
Status
Completed
Last Updated
3 months ago

Overview

Brief Summary

This is the prospective, observational cohort study to explore the impact of pretreatment emotional distress on survival and the predictive role of peripheral blood metabolic and inflammatory markers in immunotherapy response among treatment-naïve, advanced and inoperable Gastroesophageal Cancer (GEC) and non-small-cell lung cancer (NSCLC).

Detailed Description

This is the prospective, observational cohort study to explore the impact of pretreatment emotional distress on survival and the predictive role of peripheral blood metabolic and inflammatory markers in immunotherapy response among treatment-naïve, advanced and inoperable Gastroesophageal Cancer (GEC) and Non-Small-Cell Lung Cancer (NSCLC). Eligible patients were administered first-line treatment with either immune checkpoint inhibitor or a combination of immunotherapy and chemotherapy upon enrollment. This study will have 2 cohorts: * Cohort 1: A prospective, observational cohort study to explore the impact of pretreatment emotional distress on survival and the predictive role of peripheral blood metabolic and inflammatory markers in immunotherapy response among treatment-naïve, advanced and inoperable GEC patients. * Cohort 2: A prospective, observational cohort study to explore the impact of pretreatment emotional distress on survival and the predictive role of peripheral blood metabolic and inflammatory markers in immunotherapy response among treatment-naïve, advanced and inoperable NSCLC patients.

Registry
clinicaltrials.gov
Start Date
October 16, 2020
End Date
April 20, 2025
Last Updated
3 months ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Anhui Medical University
Responsible Party
Principal Investigator
Principal Investigator

Huaidong Cheng

Professor

Anhui Medical University

Eligibility Criteria

Inclusion Criteria

  • Cohort 1 \& 2
  • Inclusion Criteria:
  • Meet the diagnostic criteria for cancer (including esophageal, gastric, GEJ or NSCLC) through clinical, pathological, and imaging examinations;
  • Karnofsky Performance Status (KPS) score should be equal to or greater than 80 points;
  • Unresectable locally advanced or metastatic;
  • Systematic treatments naive ( e. g., chemotherapy, anti-angiogenic drugs, targeted drugs, and immunotherapy);
  • Presence of at least one measurable lesion according to the Response Evaluation Criteria in Advanced Solid Tumors version 1.1 (RECIST v1.1);
  • Receiving PD-1/PD-L1 inhibitors monotherapy or combination with chemotherapy;
  • Informed and agreed to participate in the study;
  • Required to complete the questionnaire independently or with assistance from others if needed;

Exclusion Criteria

  • Oncogene-driver positive;
  • Combined with other malignant tumors in the past 3 years;
  • Concurrent acute or chronic psychiatric disorders;
  • Current receiving anti-depressive or anti-anxiety therapy or other psychotropic drugs;
  • Previous treatment with other clinical drug trials;
  • Patients with symptomatic brain metastasis;
  • Severe intellectual disabilities or other communication difficulties that hindered normal interaction.

Outcomes

Primary Outcomes

Cohort 1 & 2: Progression-free survival (PFS)

Time Frame: 4 year

Time from the beginning of first-line immunotherapy to the first progression (PD) or death in patients

Secondary Outcomes

  • Value of Neutrophils to lymphocytes ratio (NLR)(0 day, 6 weeks)
  • Value of eosinophil fraction(0 day, 6 weeks)
  • Value of Platelet-lymphocyte ratio (PLR)(0 day, 6 weeks)
  • Value of Monocyte-lymphocyte ratio (MLR)(0 day, 6 weeks)
  • Value of Systemic immune inflammation index (SII)(0 day, 6 weeks)
  • Value of Pan-immune inflammation value (PIV)(0 day, 6 weeks)
  • Value of prognostic nutritional index (PNI)(0 day, 6 weeks)
  • Value of Blood glucose(0 day, 6 weeks)
  • Value of Triglycerides(0 day, 6 weeks)
  • Value of Total cholesterol(0 day, 6 weeks)
  • Value of Albumin(0 day, 6 weeks)
  • Disease Control Rate (DCR)(1 year)

Study Sites (1)

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