A Study to Investigate the Efficacy of Durvalumab Plus Tremelimumab in Combination With Chemotherapy Compared With Pembrolizumab in Combination With Chemotherapy in Metastatic Non-Small Cell Lung Cancer (NSCLC) Patients

Carcinoma, Non-Small-Cell Lung Clinical Trial

— TRITON  

Official title:

A Phase IIIb, Randomized, Multicenter, Open-label Study to Assess the Efficacy of Durvalumab Plus Tremelimumab Versus Pembrolizumab in Combination With Platinum-Based Chemotherapy for First-Line Treatment in Metastatic Non-Small Cell Lung Cancer Patients With Non-Squamous Histology Who Have Mutations and/or Co-mutations in STK11, KEAP1, or KRAS (TRITON).

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06008093
• Other study ID #: D419ML00003
• Status: Recruiting
• Phase: Phase 3
• Start date: April 4, 2024
• Est. completion date: March 12, 2031

Study information

• Verified date: June 2024
• Source: AstraZeneca
• Contact: AstraZeneca Clinical Study Information Center
• Phone: 1-877-240-9479
• Email: information.center[@]astrazeneca.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of the study is to assess the efficacy of durvalumab plus tremelimumab in combination with chemotherapy compared with pembrolizumab in combination with chemotherapy in metastatic NSCLC patients with non-squamous histology who have mutations and/or co-mutations in STK11, KEAP1, or KRAS.

Description:

A trial to learn if durvalumab plus tremelimumab with chemotherapy is safe and how well it works compared to pembrolizumab with chemotherapy in participants with metastatic non-small cell lung cancer with certain genetic mutations. INFORMATION FOR TRIAL PARTICIPANTS: Researchers are looking for a better way to treat people who have metastatic NSCLC and tumors with STK11, KEAP1, or KRAS genetic mutations. Most people learn they have NSCLC after it has already become metastatic, and it can no longer be treated with surgery. Based on previous trials, researchers think durvalumab plus tremelimumab with chemotherapy could help participants more than the current standard treatment, which is pembrolizumab with chemotherapy. Durvalumab and tremelimumab are designed to work by helping the immune system recognize and kill cancer cells. In this trial, researchers want to learn more about how well durvalumab plus tremelimumab with chemotherapy works in people with metastatic NSCLC and genetic mutations that can cause the cancer to be less responsive to treatment. This trial is planned to have 280 participants. These participants will be randomly divided into one of two groups: - One group will receive durvalumab plus tremelimumab with chemotherapy - One group will receive pembrolizumab with chemotherapy Durvalumab, tremelimumab, pembrolizumab, and chemotherapy are given as an injection over time into a vein, also called an IV infusion. Chemotherapy will be one of the following regimens: pemetrexed plus cisplatin or pemetrexed plus carboplatin. This is an open-label trial. This means that each participant will know which trial treatment they receive, and the doctors and trial staff will also know. Researchers will measure and compare: - How long participants live during the trial - How long participants live during the trial without their cancer getting worse - How many participants' tumors respond to treatment - How long participants' tumor responses last - How long before participants need to start a different treatment type Researchers will also keep track of all the medical problems participants have during the trial and monitor their safety. Participants will be in this trial for up to approximately 4 years. They will stop receiving trial treatment if they no longer benefit from it or they stop participating for another reason. Participants will visit their trial site every 3 to 4 weeks. At most visits, participants will: - Have a physical exam and answer questions about any medications they are taking or any medical problems they have - Receive their trial treatment - Give blood and urine samples - Have pictures of their tumors taken using CT or MRI scans

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 280
• Est. completion date: March 12, 2031
• Est. primary completion date: August 17, 2027
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 130 Years

Eligibility

Inclusion Criteria:

• Histologically or cytologically documented Stage IV non-squamous NSCLC not amenable to curative surgery or radiation.
• Participants must have tumors with STK11 or KEAP1 or KRAS mutations. Co-mutations are also allowed.
• Participants must have tumors that lack activating epidermal growth factor receptor mutations and ALK fusions.
• No prior chemotherapy or any other systemic therapy for metastatic NSCLC. Participants who have received prior platinum-containing adjuvant, neoadjuvant, or definitive chemoradiation for advanced disease are eligible, provided that progression has occurred > 6 months from end of last therapy.
• No prior exposure to immune-mediated therapy excluding therapeutic anti-cancer vaccines, within 12 months to randomization.
• WHO/ECOG performance status of 0 or 1 at enrollment and randomization.
• Minimum life expectancy = 12 weeks at randomization.
• At least 1 lesion, not previously irradiated, that qualifies as a RECIST 1.1 target lesion at baseline and can be accurately measured at baseline as = 10 mm in the longest diameter with Computed Tomography (CT)/CT- Positron Emission Tomography or Magnetic Resonance Imaging and that is suitable for accurate repeated measurements as per RECIST 1.1 guidelines.
• Adequate organ and bone marrow function:
• Negative pregnancy test (urine or serum) for women of child-bearing potential
• Female participants must be 1 year post-menopausal, surgically sterile, or using one highly effective form of birth control
• Male and Female participants and their partners must use an acceptable method of contraception.
• Body weight of > 30 kg

Exclusion Criteria:

• Any evidence of acute or uncontrolled diseases or history of allogeneic organ transplant.
• Mixed small cell lung cancer and NSCLC histology.
• Major surgical procedure within 28 days prior to the first dose of the study intervention or an anticipated need for major surgery during the study.
• Active or prior documented autoimmune or inflammatory disorders (including inflammatory bowel disease [eg, colitis or Crohn's disease], systemic lupus erythematosus, sarcoidosis, granulomatosis with polyangiitis, Graves' disease, rheumatoid arthritis [requiring immunosuppressive systemic therapy, eg, methotrexate, steroids], hypophysitis, uveitis, etc), autoimmune pneumonitis and autoimmune

myocarditis. The following are exceptions to this criterion:

• Participants with vitiligo or alopecia.
• Participants with hypothyroidism (eg, following Hashimoto syndrome) stable on hormone replacement.
• Any chronic skin condition that does not require systemic therapy.
• Participants without active disease in the last 5 years may be included but only after consultation with the Study Clinical Lead.
• Participants with celiac disease controlled by diet alone.
• Medical contraindication to platinum-based doublet chemotherapy.
• History of another primary malignancy except:
• Malignancy treated with curative intent with no known active disease = 2 years before the first dose of study intervention and of low potential risk for recurrence
• Adequately resected non-melanoma skin cancer and curatively treated in situ disease.
• Persistent toxicities (Common Terminology Criteria for Adverse Events [CTCAE] Grade = 2) caused by previous anti-cancer therapy, alopecia and vitiligo are excluded toxicities.
• Participants with Grade = 2 neuropathy can be considered based on Investigator's judgement. Participants with irreversible toxicity that is not reasonably expected to be exacerbated by treatment with study intervention in the opinion of the Investigator may be included (eg, hearing loss).
• Spinal cord compression unless asymptomatic and stable.
• Participant meets the following:
• Symptomatic congestive heart failure, unstable angina pectoris, uncontrolled cardiac arrhythmia (multifocal premature ventricular contractions, bigeminy, trigeminy, ventricular tachycardia), which requires treatment (CTCAE Grade 3), symptomatic or uncontrolled atrial fibrillation despite treatment, or asymptomatic sustained ventricular tachycardia. Participants with atrial fibrillation controlled by medication or arrhythmias controlled by pacemakers may be permitted based on the Investigator judgement with cardiologist consultation recommended.
• Any concurrent chemotherapy, investigational product, biologic, or hormonal therapy for cancer treatment. Concurrent use of hormonal therapy for non-cancer-related conditions (eg, hormone replacement therapy) is acceptable.
• No radiation therapy is allowed, unless it is 1) definitive radiation that had been administered at least 6 months prior, 2) palliative radiation to brain, with associated criteria for stability or lack of symptoms, or 3) palliative radiation to painful bony lesions (this must comprise less than 30% of the bone marrow)
• Patients with suspected brain metastases at screening should have an intravenous (IV) contrast-enhanced MRI (preferred) or IV contrast-enhanced CT/CT-PET of the brain prior to study entry. If brain metastases are detected patients must be treated before

randomization. Randomization is only permitted if patients with brain metastases have:

• Confirmed stable condition
• Returned neurologically to baseline Brain metastases will not be recorded as RECIST target lesions at baseline.
• History of leptomeningeal carcinomatosis.
• Known to have tested positive for active tuberculosis infection
• Known active hepatitis infection, positive HCV antibody, HBsAg, or anti-HBc, at screening. Participants with a past or resolved HBV infection (defined as the presence of anti-HBc and absence of HBsAg) are eligible. Participants positive for HCV antibody are eligible only if PCR is negative for HCV RNA. Participants co-infected with HBV and HCV, or co-infected with HBV and HDV, namely: HBV positive (presence of HBsAg and/or anti-HBcAb with detectable HBV DNA); AND
• HCV positive (presence of anti-HCV antibodies); OR
• HDV positive (presence of anti-HDV antibodies).
• Known human immunodeficiency virus (HIV) infection that is not well controlled.
• Current or prior use of immunosuppressive medication within 14 days before the first

dose of study intervention. The following are exceptions to this criterion:

• Intranasal, inhaled, topical steroids or local steroid injections (eg, intra-articular injection).
• Systemic corticosteroids at physiologic doses not to exceed 10 mg/day of prednisone or its equivalent.
• Steroids as premedication for hypersensitivity reactions (eg, CT scan premedication, premedication for chemotherapy) or a single dose for palliative purpose (eg, pain control).
• Receipt of live attenuated vaccine within 30 days prior to the first dose of study intervention.
• Concurrent enrollment in another clinical study, unless it is an observational (non-interventional) clinical study or the follow-up period of an interventional study.
• Participants with a known hypersensitivity to any of the study interventions or any of the excipients of the products.
• For females only: Currently pregnant (confirmed with positive pregnancy test) or breast-feeding, or who are planning to become pregnant. Female participants should refrain from breastfeeding from enrolment throughout the study and until up to 14 months after the last dose of cisplatin or 180 days after pemetrexed or 90 days after tremelimumab or durvalumab or pembrolizumab, whichever is longer; and during treatment with carboplatin.

Related Conditions & MeSH terms

• Carcinoma, Non-Small-Cell Lung
• Lung Neoplasms

Intervention

Drug:
• Durvalumab
Participants will receive intravenous (IV) Durvalumab q3w for four 21-day cycles. Durvalumab will also be given during the maintenance phase q4w until disease progression or unacceptable toxicity and at week 16.
• Tremelimumab
Participants will receive IV Tremelimumab q3w for four 21-day cycles. Tremelimumab will also be given during the maintenance therapy phase at week 16.
• Pemetrexed
Participants will receive IV pemetrexed q3w for four 21-day cycles and q4w until disease progression or unacceptable toxicity. During the maintenance therapy phase, participants may receive an additional cycle of pemetrexed, where applicable, at Week 16.
• Pembrolizumab
Participants will receive IV pembrolizumab q3w for four 21-day cycles and q3w until disease progression or unacceptable toxicity for up to 24 months.
• Carboplatin
Participants will receive IV Carboplatin on Day 1 of each 21-day cycle for 4 cycles.
• Cisplatin
Participants will receive IV Cisplatin on Day 1 of each 21-day cycle for 4 cycles.
• Pemetrexed
Participants will receive IV pemetrexed q3w for four 21-day cycles and q3w until disease progression or unacceptable toxicity for up to 24 months.

Locations

Country	Name	City	State
United States	Research Site	Albany	Georgia
United States	Research Site	Albany	New York
United States	Research Site	Anchorage	Alaska
United States	Research Site	Atlanta	Georgia
United States	Research Site	Atlanta	Georgia
United States	Research Site	Austin	Texas
United States	Research Site	Bethesda	Maryland
United States	Research Site	Billings	Montana
United States	Research Site	Birmingham	Alabama
United States	Research Site	Bismarck	North Dakota
United States	Research Site	Bronx	New York
United States	Research Site	Chandler	Arizona
United States	Research Site	Charlottesville	Virginia
United States	Research Site	Chicago	Illinois
United States	Research Site	Cleveland	Ohio
United States	Research Site	Columbus	Ohio
United States	Research Site	Columbus	Georgia
United States	Research Site	Dallas	Texas
United States	Research Site	Dallas	Texas
United States	Research Site	Dayton	Ohio
United States	Research Site	Denton	Texas
United States	Research Site	Detroit	Michigan
United States	Research Site	Evansville	Indiana
United States	Research Site	Fairfax	Virginia
United States	Research Site	Farmington Hills	Michigan
United States	Research Site	Fort Lauderdale	Florida
United States	Research Site	Fort Worth	Texas
United States	Research Site	Hershey	Pennsylvania
United States	Research Site	Houston	Texas
United States	Research Site	Houston	Texas
United States	Research Site	Irvine	California
United States	Research Site	Jupiter	Florida
United States	Research Site	Kansas City	Missouri
United States	Research Site	Kansas City	Missouri
United States	Research Site	La Jolla	California
United States	Research Site	Lexington	Kentucky
United States	Research Site	Lexington	Kentucky
United States	Research Site	Loma Linda	California
United States	Research Site	Los Alamitos	California
United States	Research Site	Los Angeles	California
United States	Research Site	Los Angeles	California
United States	Research Site	Maywood	Illinois
United States	Research Site	Memphis	Tennessee
United States	Research Site	Memphis	Tennessee
United States	Research Site	Milwaukee	Wisconsin
United States	Research Site	Nashville	Tennessee
United States	Research Site	New Hyde Park	New York
United States	Research Site	New York	New York
United States	Research Site	New York	New York
United States	Research Site	Northport	New York
United States	Research Site	Ocala	Florida
United States	Research Site	Oklahoma City	Oklahoma
United States	Research Site	Orlando	Florida
United States	Research Site	Philadelphia	Pennsylvania
United States	Research Site	Providence	Rhode Island
United States	Research Site	Richmond	Virginia
United States	Research Site	Saint Louis	Missouri
United States	Research Site	Saint Paul	Minnesota
United States	Research Site	San Antonio	Texas
United States	Research Site	Santa Monica	California
United States	Research Site	Shirley	New York
United States	Research Site	Stony Brook	New York
United States	Research Site	Syracuse	New York
United States	Research Site	Tampa	Florida
United States	Research Site	Toledo	Ohio
United States	Research Site	Urbana	Illinois
United States	Research Site	Washington	District of Columbia
United States	Research Site	Washington	District of Columbia
United States	Research Site	Westwood	Kansas
United States	Research Site	Worcester	Massachusetts

Sponsors (1)

Lead Sponsor	Collaborator
AstraZeneca

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Overall survival (OS)	OS is defined as the time from randomization until death due to any cause in all participants.	From randomization until death, withdrawal of consent, or the end of the study (approximately 48 months)
Primary	OS in subset of randomized participants with STK11 or KEAP1 mutations and/or co-mutations	OS is defined as the time from randomization until death due to any cause in participants with STK11 or KEAP1 mutations and/or co-mutations.	From randomization until death, withdrawal of consent, or the end of the study (approximately 48 months)
Secondary	Overall survival at 12 months	OS is defined as the time from randomization until death due to any cause in all participants. The measure of interest is survival rate with corresponding 95% CI at 12 months landmark.	At 12 months
Secondary	Overall survival at 24 months	OS is defined as the time from randomization until death due to any cause in all participants. The measure of interest is survival rate with corresponding 95% CI at 24 months landmark.	At 24 months
Secondary	Overall survival at 12 months in subset of randomized participants with STK11 or KEAP1 mutation and/or co mutations.	OS is defined as the time from randomization until death due to any cause. The measure of interest is survival rate with corresponding 95% CI at 12 months landmark.	At 12 months
Secondary	Overall survival at 24 months in subset of randomized participants with STK11 or KEAP1 mutation and/or co mutations.	OS is defined as the time from randomization until death due to any cause. The measure of interest is survival rate with corresponding 95% CI at 24 months landmark.	At 24 months
Secondary	Overall survival in subset of randomized participants whose PD-L1 status is PD-L1 TC < 1%	OS is defined as the time from randomization until death due to any cause.	From randomization until death, withdrawal of consent, or the end of the study (approximately 48 months)
Secondary	Overall survival at 12 months in subset of randomized participants whose PD-L1 status is PD-L1 TC < 1%	OS is defined as the time from randomization until death due to any cause. The measure of interest is survival rate with corresponding 95% CI at 12 months landmark.	At 12 months
Secondary	Overall survival at 24 months in subset of randomized participants whose PD-L1 status is PD-L1 TC < 1%	OS is defined as the time from randomization until death due to any cause. The measure of interest is survival rate with corresponding 95% CI at 24 months landmark.	At 24 months
Secondary	Progression-free survival (PFS)	PFS is defined as the time from randomization until the date of confirmed PD (per Response Evaluation Criteria in Solid Tumours, Version 1.1 [RECIST 1.1] as assessed by the Investigator) or death due to any cause (in the absence of progression) in all participants.	From randomization until disease progression, death, withdrawal of consent, or end of study (approximately 48 months)
Secondary	Objective response rate (ORR)	ORR is defined as the proportion of participants with a confirmed objective tumour response (complete response [CR] or partial response [PR]) as determined by the investigator per RECIST 1.1 in all participants who have measurable disease at baseline.	From randomization until disease progression, or the last evaluable assessment in the absence of progression (approximately 48 months)
Secondary	Duration of response (DOR)	DOR is defined as the time from the date of first documented confirmed response until the date of documented progression (per RECIST 1.1, as assessed by the Investigator) or death due to any cause (in the absence of disease progression) in all participants who have confirmed objective response.	From first documented response until documented progression (approximately 48 months)
Secondary	Time to First Subsequent Therapy (TFST)	TFST is defined as the time from randomization until the start date of the first subsequent anti-cancer therapy after discontinuation of randomized study intervention, or death due to any cause in all participants.	From randomization until the start date of the first subsequent anti-cancer therapy after discontinuation of randomized study intervention or death [approx. up to 48 months]
Secondary	Number of participants with adverse events (AEs) and serious adverse events (SAEs).	To assess the safety and tolerability of durvalumab plus tremelimumab plus chemotherapy compared with pembrolizumab plus chemotherapy in participants with non-squamous histology who have metastatic NSCLC with mutations and/or co-mutations in STK11, KEAP1, or KRAS.	From screening until the follow-up period is completed [approx. up to 48 months]