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Genetic variations as predictors of outcome and toxicity in non-small-cell lung cancer patients undergoing chemoradiation or chemotherapy with platinum agents.

Genetic variations as predictors of outcome and toxicity in non-small-cell lung cancer patients undergoing chemoradiation or chemotherapy with platinum agents. - Pharmacogenetics lung cancer - PGx-Lung cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON47255
Enrollment
350
Registered
2015-08-17
Start date
2016-02-16
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

lung cancer Non-small-cell lung cancer

Interventions

None listed

Sponsors

Sint Antonius Ziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: * Diagnosed with NSCLC (stage II-IV) * Age *18 year * Received or starting with chemoradiation or chemotherapy with platinating agents (carboplatin, cisplatin)

Exclusion criteria

Exclusion criteria: * Unable to give informed consent * Patients with cognitive impairment or those who are not able to read or write Dutch (because of difficulties in completing questionnaires)

Design outcomes

Primary

MeasureTime frame
Esophagitis (grade 1-4), nephrotoxicity (grade 1-4), neurotoxicity (grade 1-4) and genetic markers. All toxicities will be graded according to *National Cancer Institute Common Terminology Criteria for Adverse Events* (NCI CTCAE), v4.0.

Secondary

MeasureTime frame
Survival time is defined as survival from date of diagnosis in months. Besides, patient-reported outcomes and quality of life will be compared at 4 points in time (before treatment, after 3 months of treatment, after 6 months and 1 year follow-up). Skeletel muscle mass measured on available (PET)CT scans.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)