A Phase III, Open-Label Study of Maintenance Lurbinectedin in Combination With Atezolizumab Compared With Atezolizumab in Participants With Extensive-Stage Small-Cell Lung Cancer
Sponsor: Hoffmann-La Roche
ClinicalTrials ID:NCT05091567
Study GO43104 is a Phase III trial evaluating lurbinectedin plus atezolizumab versus atezolizumab alone as maintenance therapy in ES-SCLC. Participants must show ongoing response or stable disease post-induction with carboplatin, etoposide, and atezolizumab. In the maintenance phase, atezolizumab is given at 1200 mg, and lurbinectedin at 3.2 mg/m², both every 21 days.
Patient Parameters
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Program Overview
Study GO43104 is a Phase III, randomized, open-label, multicenter study of lurbinectedin in combination with atezolizumab compared with atezolizumab alone administered as maintenance therapy in participants with extensive-stage small-cell lung cancer (ES-SCLC) after first-line induction therapy with carboplatin, etoposide, and atezolizumab. The study consists of 2 phases: an induction phase and a maintenance phase. Participants need to have an ongoing response or stable disease per the Response Evaluation Criteria in Solid Tumor (RECIST) v1.1 criteria after completion of 4 cycles of carboplatin, etoposide, and atezolizumab induction treatment in order to be considered for eligibility screening for the maintenance phase. Eligible participants will be randomized in a 1:1 ratio to receive either lurbinectedin plus atezolizumab or atezolizumab in the maintenance phase.
Eligibility Criteria
Inclusion Criteria for the Induction Phase:
- ECOG PS of 0 or 1
- No prior systemic therapy for ES-SCLC
- Treatment-free for at least 6 months since last chemo/radiotherapy, among those treated (with curative intent) with prior chemo/radiotherapy for limited-stage SCLC
- Histologically or cytologically confirmed ES-SCLC
- Adequate hematologic and end-organ function to receive 4 cycles of induction treatment with carboplatin, etoposide and atezolizumab
- Measurable disease, as defined by RECIST v1.1
- Negative HIV test and no evidence of active Hepatitis B or Hepatitis C at screening
Exclusion Criteria for the Induction Phase:
- Presence or history of CNS metastases
- Active or history of autoimmune disease or deficiency
- History of malignancies other than SCLC within 5 years prior to enrollment
- Prior treatment with CD137 agonists or immune checkpoint blockade therapies, including anti-CTLA-4, anti-PD-1, and anti-PD-L1 therapeutic antibodies, or lurbinectedin or trabectedin
- History of idiopathic pulmonary fibrosis, organizing pneumonia, drug induced pneumonitis, or idiopathic pneumonitis, or evidence of active pneumonitis on screening chest computed tomography (CT) scan
- Treatment with investigational therapy within 28 days prior to enrollment
Inclusion Criteria for the Maintenance Phase:
- ECOG PS of 0 or 1
- Ongoing response or stable disease per RECIST 1.1 after 4 cycles of induction therapy
- Toxicities attributed to prior induction anti-cancer therapy or PCI resolved to Grade <=1
- Adequate hematologic and end-organ function
Exclusion Criteria for the Maintenance Phase:
- Presence or history of CNS metastases
- Receiving consolidative chest radiation
- Severe infection within 2 weeks prior to randomization into the maintenance
- Treatment with therapeutic oral or IV antibiotics at the time of randomization
Locations
| FACILITY | ZIP | CITY | STATE |
|---|---|---|---|
| Northwest Georgia Oncology Centers, a Service of WellStar Cobb Hospital | 30060 | Marietta | Georgia |
| Illinois Cancer Care | 61615 | Peoria | Illinois |
| New England Cancer Specialists | 04074 | Scarborough | Maine |
| Dana Farber Cancer Institute | 02215 | Boston | Massachusetts |
| Cancer & Hematology Centers of Western Michigan | 49503 | Grand Rapids | Michigan |
| Mercy Research - St. Louis | 63141 | St Louis | Missouri |
| Clinical Research Alliance | 11590 | Westbury | New York |
| The Mark H. Zangmeister Ctr | 43219 | Columbus | Ohio |
| Fox Chase Cancer Center | 19111 | Philadelphia | Pennsylvania |
| Rhode Island Hospital | 02903 | Providence | Rhode Island |
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