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Erlotinib and chemotherapy for advanced lung cancer. The NVALT-17 study

A randomized phase III study of erlotinib compared to intercalated erlotinib with cisplatinum pemetrexed as first-line therapy for advanced EGFR mutated non-small-cell lung cancer. The NVALT-17 study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON27429
Enrollment
150
Registered
2014-01-22
Start date
2014-03-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Advanced EGFR mutated non-small-cell lung cancer

Interventions

Treatment with erlotinib or cisplatin-pemetrexed-erlotinib.

Sponsors

Stichting NVALT studies Luijbenstraat 15 5211 BR Den Bosch The Netherlands
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • Histologically/cytologically proven stage III or IV NSCLC. • Tumor treatment-naive. • Documented activating EGFR mutation in exon 18, 19 or exon 21. • Measurable disease. • Age ≥ 18 years. • Males and females. • ECOG Performance Status of 0 – 3. • Life expectancy > 12 weeks. • Adequate contraception for females of childbearing potential. • Adequate contraception for male participants.

Exclusion criteria

Exclusion criteria: • Documented brain metastasis.• Concomitant treatment with experimental medicines, potent CYP3A4 inhibitors or inducers. • Previous cytotoxic chemotherapy for lung cancer less than 2 years before study entry. • For curatively treated lung cancer: (adjuvant) chemotherapy or chemo-radiotherapy less than 12 month prior to the study entry. • Pregnancy or lactation.

Design outcomes

Primary

MeasureTime frame
Progression free survival.

Secondary

MeasureTime frame
Objective response rate and disease control rate, overall survival, safety.

Contacts

Public ContactT.J.N. Hiltermann

Universitair Medisch Centrum Groningen Longziekten AA11 Postbus 30001

t.j.n.hiltermann@umcg.nl+31 (0)50 3612357

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)