A Study of Lazertinib as Consolidation Therapy in Patients With Locally Advanced, Unresectable, EGFR-Mutant Non-Small Cell Lung Cancer (Stage III) Following Chemoradiation Therapy (PLATINUM)

Sung Yong Lee

Status and phase: Enrolling; Phase 2

Conditions: EGFR Positive Non-small Cell Lung Cancer; Non-small Cell Lung Cancer Stage III; Non-squamous Non-small-cell Lung Cancer

Treatments: Drug: Lazertinib

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT05338619

Korea-Lazertinib-CCRT

LASER IIT-010 (Other Grant/Funding Number)

Details and patient eligibility

About

The "PACIFIC" trial confirmed that the consolidation therapy with durvalumab in patients with stage III, locally advanced, unresectable NSCLC that had not progressed after definitive platinum-based chemoradiation therapy improved the progression-free survival (PFS) by about 17 months. However, in PACIFIC, no significant differences between durvalumab and placebo were observed in PFS. Unmet need remains in development of successful consolidation therapy following chemoradiation therapy in patients with EGFR-mutant stage III unresectable NSCLC.

A recent "ADAURA" study showed that Osimertinib as an adjuvant therapy after surgery significantly prolonged disease-free survival in EGFR mutation-positive patients. Lazertinib, like Osimertinib, is a third-generation EGFR TKI agent and has shown excellent anticancer effects in preclinical studies and in early clinical settings. Based on these results of the 3rd generation EGFR TKI, Lazertinib, it is expected that there is a clinical benefit Lazertinib as consolidation therapy.

This study aims to investigate the clinical benefits of Lazertinib (Trade name: LECLAZA Tab) consolidation therapy for patients with EGFR mutation-positive, unresectable stage III NSCLC after definitive platinum-based chemoradiation therapy.

Full description

This study is designed as a prospective, open-label, single-arm, multicenter, phase II, investigator-initiated trial. A total of 77 patients will participate in the study who have undergone definitive platinum-based concurrent chemoradiation therapy and have no disease progression. Patients are to be enrolled within 1 to 42 days after concurrent chemoradiation therapy and to be administrated with lazertinib 240mg oral once daily until disease progression, or unacceptable toxicity. Patients will visit every 8 weeks and perform CT/MRI tumor evaluation by investigator, and will be followed up for survival every 3 months by phone thereafter. Patients will be followed up till maximum of appropriately 4 years of which 3 years since the last patient enrollment must be.

Enrollment: 77 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. 18 years and older
2. Histologically and cytologically confirmed diagnosis of non-small cell lung cancer (NSCLC) non-squamous cell carcinoma who present with locally advanced, unresectable, Stage III disease
3. ECOG PS 0,1
4. Expected life expectancy of 6 months and more
5. Patients who have received at least 2 cycles of definitive platinum-based concurrent chemoradiation therapy (CCRT) and who must be within 1 to 42 days after completion of radiation therapy
6. Patients must not have had disease progression during or following CCRT
7. Patients with adequate organ and bone marrow function
8. Patients who give in written consent voluntarily to participate in this study

Exclusion criteria

1. History of interstitial lung disease, drug-induced interstitial lung disease, or radiation interstitial pneumonia
2. History of other primary malignancy
3. Mixed small cell and NSCLC histology
4. Prior treatment with EGFR-TKI Therapy
5. Unresolved toxicity of CTCAE grade 2 or higher following chemoradiation
6. Current history of CTCAE grade 2 or higher pneumonia prior to chemoradiation therapy
7. Patients with severe hypersensitivity to active ingredient or excipient of the investigational medicinal product
8. Pregnant or breastfeeding patients
9. Patients who do not agree to contraception with medically acceptable method for at least 6 months after the end of study intervention treatment
10. Patients who participated in clinical trials within 4 weeks before participating in this study
11. Judgment by the investigator that the patient is unsuitable to participate in this study

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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77 participants in 1 patient group

Lazertinib

Experimental group

Description:

Lazertinib 240mg, oral, QD

Treatment:

Drug: Lazertinib