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NCT06629714Completed

Impact of Pretreatment Emotional Distress on Survival and the Predictive Role of Peripheral Biomarkers in Immunotherapy Response Among Gastroesophageal and Lung Cancer Patients

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

Source: ClinicalTrials.gov · Last updated 13 Jan 2026

Brief summary (registry, in English)

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).

Status (registry)
Completed
Study type
Observational
Enrollment
196 (actual)
First submitted
4 Oct 2024
Start date
16 Oct 2020
Primary completion date
20 Apr 2025
Lead sponsor
Anhui Medical University
Diseases
Lung cancer
NCT number
NCT06629714

What you commit to

  • Study type: Observational
  • Participants enrolled: 196
  • From 16 Oct 2020 to the primary completion date, 20 Apr 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study design.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • 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;

Other illness

  • Combined with other malignant tumors in the past 3 years;

Other

  • Oncogene-driver positive;
  • Patients with symptomatic brain metastasis;
  • Severe intellectual disabilities or other communication difficulties that hindered normal interaction.

Who the study is looking for

  • 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;
  • Legal age, 18 years or older.

Criteria the registry did not label

  • Cohort 1 \& 2

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Second Affiliated hospital of Anhui Medical University
Coordinator of this site? Confirm its status
HefeiChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.