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Stage III NSCLC RWE in Chinese Patients

AstraZeneca logo

AstraZeneca

Status

Completed

Conditions

Carcinoma, Non-Small-Cell Lung

Study type

Observational

Funder types

Industry

Identifiers

NCT04023812
D4194R00009

Details and patient eligibility

About

The objectives of this study are to assess molecular testing, treatment patterns and associated clinical outcomes in Chinese patients with treatment-naïve stage III non-small cell lung cancer (NSCLC) in real world setting. This study is a prospective, non-interventional study. It is descriptive in nature and does not attempt to test any specific a priori hypotheses.

Enrollment

500 patients

Sex

All

Ages

18 to 130 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male or female aged 18 years or older.
  • Provision of informed consent prior to any study specific procedures.
  • Histologically or cytologically confirmed locally advanced, stage III NSCLC (according to version 8 of the International Association for the Study of Lung Cancer Staging Manual in Thoracic Oncology; IASLC Staging Manual in Thoracic Oncology).

Exclusion criteria

  • Enrolment in studies that prohibit any participation in this observational study.

    • Patients may be concurrently enrolled in unblinded clinical trials, but not blinded clinical trials in which the treatment being administered is unknown.
  • Prior surgery, radiotherapy or systemic therapy for NSCLC, including chemotherapy, targeted therapy, anti-angiogenesis, etc.

Trial design

500 participants in 2 patient groups

Cohort 1
Description:
Cohort 1, including patients without surgical resection, will be defined as unresectable stage III NSCLC
Cohort 2
Description:
Cohort 2,including patients with surgical resection, will be defined as resectable stage III NSCLC

Trial contacts and locations

25

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Data sourced from clinicaltrials.gov

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