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Platinum-based Chemotherapy
Chemotherapy + Nivolumab for Small Cell Lung Cancer
Phase 2
Waitlist Available
Led By Ticiana A Leal
Research Sponsored by National Cancer Institute (NCI)
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
No patients with specific autoimmune diseases, neuromuscular paraneoplastic syndromes, or conditions requiring systemic treatment with corticosteroids or immunosuppressive medications
No patients with symptomatic interstitial lung disease or severe hypersensitivity reaction to study drug components
Must not have
Patients are ineligible if they received a live, attenuated vaccine within 4 weeks before randomization
Patients must NOT have uncontrolled intercurrent illness including ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, uncontrolled cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
Timeline
Screening 3 weeks
Treatment Varies
Follow Up every 6 weeks for 6 months, then every 8 weeks until 1 year, and then every 12 weeks until being off treatment or end of observation. thereafter every 3 months if < 2 years from registration, every 6 months for years 2-3, and yearly up to 3 years 9 months
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing whether adding nivolumab to standard chemotherapy improves treatment for patients with extensive stage small cell lung cancer. The chemotherapy drugs kill or stop the growth of cancer cells, while nivolumab helps the immune system attack the cancer. Nivolumab is an immunotherapy drug that has shown promise in treating various cancers, including non-small cell lung cancer and melanoma.
Who is the study for?
This trial is for adults with extensive stage small cell lung cancer who haven't had prior treatment. They must have normal organ and marrow function, no severe allergies to monoclonal antibodies or study drugs, and not be on other investigational agents. Women of childbearing age and sexually active men must use contraception.
What is being tested?
The trial tests if adding Nivolumab (an immunotherapy drug) to standard chemotherapy (Cisplatin/Carboplatin and Etoposide) improves outcomes in patients with extensive stage small cell lung cancer compared to chemotherapy alone.
What are the potential side effects?
Possible side effects include allergic reactions, immune system-related issues affecting organs, fatigue, nausea, low blood counts increasing infection risk. Nivolumab may also cause skin problems or hormonal gland changes.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I do not have autoimmune diseases or conditions needing steroids or immunosuppressants.
Select...
I do not have lung disease causing symptoms or severe allergies to the study drug.
Select...
My blood tests and liver/kidney function are within required ranges.
Select...
I have no severe allergies to monoclonal antibodies or the study drug's components.
Select...
I have extensive stage small cell lung cancer and can undergo systemic therapy.
Select...
I have not received chemotherapy or biologic therapy for my extensive stage small cell lung cancer.
Select...
I haven't received drugs targeting my immune system to treat cancer.
Select...
I do not have lung disease that causes symptoms or could affect lung toxicity tests.
Select...
I am fully active or can carry out light work.
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I have been cancer-free for at least 2 years if I had another cancer.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have not received a live vaccine in the last 4 weeks.
Select...
I do not have any severe illnesses or social situations that would stop me from following the study's requirements.
Select...
I do not have cancer that has spread to the lining of my brain and spinal cord.
Select...
I am not HIV-positive or not on combination antiretroviral therapy.
Select...
I am not pregnant or breast-feeding.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ every 6 weeks for 6 months, then every 8 weeks until 1 year, and then every 12 weeks until being off treatment or end of observation. thereafter every 3 months if < 2 years from registration, every 6 months for years 2-3, and yearly up to 3 years 9 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~every 6 weeks for 6 months, then every 8 weeks until 1 year, and then every 12 weeks until being off treatment or end of observation. thereafter every 3 months if < 2 years from registration, every 6 months for years 2-3, and yearly up to 3 years 9 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Progression-free Survival (PFS)
Secondary study objectives
Overall Survival (OS)
Response Rate
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Arm A (nivolumab, CE)Experimental Treatment4 Interventions
Patients receive nivolumab IV over 30 minutes on day 1, carboplatin IV over 30-60 minutes on day 1 or cisplatin IV over 60-120 minutes on day 1, and etoposide IV over 60-120 minutes on days 1-3. Treatment repeats every 21 days for up to 4 cycles in the absence of disease progression or unacceptable toxicity. Patients continue to receive nivolumab IV over 30 minutes every 2 weeks for up to 2 years.
Group II: Arm B (CE)Active Control3 Interventions
Patients receive carboplatin IV over 30-60 minutes on day 1 or cisplatin IV over 60-120 minutes on day 1, and etoposide IV over 60-120 minutes on days 1-3. Treatment repeats every 21 days for up to 4 cycles in the absence of disease progression or unacceptable toxicity.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Carboplatin
2014
Completed Phase 3
~6120
Cisplatin
2013
Completed Phase 3
~3120
Etoposide
2010
Completed Phase 3
~2960
Nivolumab
2014
Completed Phase 3
~5220
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for Small Cell Lung Cancer (SCLC) include chemotherapy and immunotherapy. Chemotherapy agents like cisplatin, carboplatin, and etoposide work by killing cancer cells, inhibiting their division, and preventing their spread.
Immunotherapy, such as Nivolumab, employs monoclonal antibodies to enhance the immune system's ability to recognize and attack cancer cells, while also interfering with tumor cell growth and spread. This multi-faceted approach is crucial for SCLC patients as it targets the cancer through different mechanisms, potentially leading to better treatment outcomes and improved survival rates.
Cancer Vaccines and Oncolytic Viruses Exert Profoundly Lower Side Effects in Cancer Patients than Other Systemic Therapies: A Comparative Analysis.Nivolumab for the treatment of small cell lung cancer.Focus on Nivolumab in NSCLC.
Cancer Vaccines and Oncolytic Viruses Exert Profoundly Lower Side Effects in Cancer Patients than Other Systemic Therapies: A Comparative Analysis.Nivolumab for the treatment of small cell lung cancer.Focus on Nivolumab in NSCLC.
Find a Location
Who is running the clinical trial?
National Cancer Institute (NCI)Lead Sponsor
13,906 Previous Clinical Trials
41,011,872 Total Patients Enrolled
Ticiana A LealPrincipal InvestigatorECOG-ACRIN Cancer Research Group
1 Previous Clinical Trials
27 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I do not have autoimmune diseases or conditions needing steroids or immunosuppressants.I do not have lung disease causing symptoms or severe allergies to the study drug.You have a positive test for hepatitis B virus or hepatitis C virus, meaning you have an active or long-lasting infection.I have not received a live vaccine in the last 4 weeks.I do not have any severe illnesses or social situations that would stop me from following the study's requirements.I do not have cancer that has spread to the lining of my brain and spinal cord.My blood tests and liver/kidney function are within required ranges.I do not have an active autoimmune or neuromuscular disorder, except for manageable conditions like type I diabetes or hypothyroidism.I am not HIV-positive or not on combination antiretroviral therapy.I have no severe allergies to monoclonal antibodies or the study drug's components.I have extensive stage small cell lung cancer and can undergo systemic therapy.I have not received chemotherapy or biologic therapy for my extensive stage small cell lung cancer.I am using contraception or abstaining from sex to prevent pregnancy.I haven't received drugs targeting my immune system to treat cancer.Patients must have a way to measure their disease according to specific guidelines.I do not have lung disease that causes symptoms or could affect lung toxicity tests.I am fully active or can carry out light work.You have never had an allergic reaction to drugs that are similar to nivolumab or other drugs used in the study.I am not pregnant or breast-feeding.I have been cancer-free for at least 2 years if I had another cancer.
Research Study Groups:
This trial has the following groups:- Group 1: Arm B (CE)
- Group 2: Arm A (nivolumab, CE)
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Small Cell Lung Cancer Patient Testimony for trial: Trial Name: NCT03382561 — Phase 2
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