Skip to content

A study to understand patient characteristics and treatment of stage III non-small-cell lung cancer patients

A multi-country, multi-centre, observational, retrospective study to reveal the patient characteristics, disease burden, treatment patterns and patient journey of stage III non-small-cell lung cancer patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2018/10/016221
Enrollment
2000
Registered
2018-10-31
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: C342- Malignant neoplasm of middle lobe,bronchus or lung Health Condition 2: C348- Malignant neoplasm of overlappingsites of bronchus and lung

Interventions

None listed

Sponsors

AstraZeneca Pharma India Limited
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Provision of informed consent by the patient or next of kin/legal representative (for deceased patients at study entry, unless a waiver was granted), according to local regulations 2. Adult male or female (18 years old or according to age of majority as defined by local regulations) 3. First ever diagnosis of lung cancer (absence of previous diagnosis of lung cancer, including small cell lung cancer [SCLC] and NSCLC) in the patientââ?¬•s medical records 4. Primary diagnosis of stage III NSCLC, confirmed by pathology, between 01 January 2013 and 31 December 2017 5. Available medical records at the participating site reflect at least 9 months of follow-up from the index date (unless patient died within the first 9 months of diagnosis)

Exclusion criteria

Exclusion criteria: 1. Patients with a concomitant cancer at the time of diagnosis of stage III NSCLC, except for non-metastatic non-melanoma skin cancers or in situ or benign neoplasms. A cancer will be considered concomitant if it occurs within 5 years of NSCLC diagnosis 2. Patients initially diagnosed with stage I-II NSCLC who have progressed to stage III

Design outcomes

Primary

MeasureTime frame
Overall survival (OS) The length of time from stage III NSCLC diagnosis (index date) or time of therapy initiation to death due to any cause.Timepoint: 9 months

Secondary

MeasureTime frame
Progression-free survival (PFS)The length of time from time of therapy initiation to documented disease progression (as available in the medical record) or death due to any cause, whichever occurs first.Timepoint: 9 months

Countries

Australia, Egypt, India, Indonesia, Malaysia, Singapore

Contacts

Public ContactAmit Kumar

AstraZeneca Pharma India Ltd

kirtan.bhatt@astrazeneca.com919886266442

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026