ACTIVE_NOT_RECRUITING

Atezolizumab Immunotherapy With or Without Tiragolumab for Patients With Unresectable Stage III NSCLC

Conditions

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This is a phase II trial of neoadjuvant and adjuvant atezolizumab with or without tiragolumab in conjunction with chemoradiotherapy for unresectable stage III NSCLC.

Official Title

Randomized Phase II Trial of Neoadjuvant and Adjuvant Atezolizumab With or Without Tiragolumab in Conjunction With Chemoradiotherapy for Unresectable Stage III NSCLC

Quick Facts

Study Start:2023-12-07

Study Completion:2026-11

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:ACTIVE_NOT_RECRUITING

Study ID

NCT05798663

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
1. Newly pathologically proven diagnosis of stage IIIA/B/C (per AJCC 8) NSCLC 2. Age at least 18 years. 3. Availability of a representative tumor specimen that is suitable for BOTH determination of PD-L1 status via local testing and, independently, other required correlative study biomarkers. Tissue submission should include: 1. A representative FFPE tumor specimen in a paraffin block, along with an associated pathology report, which will be sent to the biorepository. If institutional policy prevents the submission of a block, refer to the Correlative Science Manual (CSM) for alternative submission instructions. 2. If archival tumor tissue is unavailable or is determined to be unsuitable for required testing, tumor tissue must be obtained from a biopsy performed at screening. Questions about biopsy adequacy should be directed to the study team. 3. Patients may still be eligible after these two points (3a and 3b) have been attempted/considered, at the discretion of the AFT Study Team. 4. No active autoimmune disease or uncontrolled infection 5. FEV1 ≥ 1.2L or \> 40% predictive 6. No underlying heart or lung disease precluding treatment per protocol. 7. Measurable (RECIST v1.1) stage IIIA, IIIB or IIIC disease per AJCC 8. 8. Patients must be considered unresectable or inoperable. Patients who decline surgery for stage III NSCLC are also eligible. Patients with nodal recurrence after surgery for early-stage NSCLC are eligible if the following criteria are met: * No prior systemic therapy or radiation for this lung cancer * Prior curative-intent surgery at least 3 months prior to the nodal recurrence Note: Patients may be medically unfit for surgery, (e.g., due to general anesthesia risk), but remain fit for chemoradiotherapy. Thus, the criterion does not necessarily have to exclude all patients who are medically unfit for surgery. 9. Stage III A/B/C disease (per AJCC 8) with minimum diagnostic evaluation to include: * History/physical examination within 4 weeks * Contrast enhanced CT of the chest including upper abdomen (or CT without contrast if contrast is medically contraindicated) within 4 weeks * MRI of the brain with contrast (or CT with contrast if MRI is medically contraindicated) within 6 weeks * PET/CT skull to thigh within 6 weeks If pleural fluid is visible on CT scan, thoracentesis to exclude malignancy should be obtained unless the effusion is too small to tap in which case the patient is eligible. 10. Patients must be at least 4 weeks from major surgery and must be fully recovered. 11. Adequate hematologic and end organ function, defined by the following laboratory results obtained within 14 days prior to the first study treatment (Cycle 1, Day 1); if repeat labs are obtained on or prior to C1D1 they must re-meet eligibility criteria to treat): * ANC ≥ 1500 cells/µL * WBC counts \> 2500/ µ L * Lymphocyte count ≥ 500/ µ L * Platelet count ≥ 100,000/ µ L * Hemoglobin ≥ 9.0 g/dL (patients may be transfused to meet this criterion). * Total bilirubin ≤ 1.5 ⋅ upper limit of normal (ULN) with the following exception: * Patients with known Gilbert disease who have serum bilirubin level ≤ 3 ⋅ ULN may be enrolled. * AST, ALT and Alkaline phosphatase ≤ 2.5 ⋅ ULN * Serum albumin ≥ 25 g/L (2.5 g/dL) * For patients not receiving therapeutic anticoagulation: INR and aPTT ≤ 1.5 ⋅ ULN * For patients receiving therapeutic anticoagulation: stable anticoagulant regimen * Serum creatinine ≤ 1.5 ⋅ ULN or creatinine clearance ≥ 45 mL/min on the basis of the Cockcroft-Gault glomerular filtration rate estimation: * (140 - age) ⋅ (weight in kg) ⋅ (0.85 if female) 72 ⋅ (serum creatinine in mg/dL) 12. Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1. 13. Negative HIV test at screening with the following exception: patients with a positive HIV test at screening are eligible provided they are stable on anti-retroviral therapy, have a CD4+ T-cell count \> 200/vL, and have an undetectable viral load. 14. Negative hepatitis B surface antigen (HBsAg) test at screening 15. Positive hepatitis B surface antibody (HBsAb) test at screening, or negative HBsAb at screening accompanied by either of the following: * Negative total hepatitis B core antibody (HBcAb) * Positive total HBcAb test followed by quantitative hepatitis B virus (HBV) DNA \< 500 IU/mL * The HBV DNA test will be performed only for patients who have a negative HBsAg test, a negative HBsAb test, and a positive total HBcAb test. 16. Negative hepatitis C virus (HCV) antibody test at screening, or positive HCV antibody test followed by a negative HCV RNA test at screening. The HCV RNA test will be performed only for patients who have a positive HCV antibody test. 17. Non-pregnant and non-nursing. The effect of atezolizumab and tiragolumab on the fetus is unknown. 18. For women of childbearing potential: agreement to remain abstinent (refrain from heterosexual intercourse) or use contraception, and agreement to refrain from donating eggs, as defined below: * Women must remain abstinent (refrain from heterosexual intercourse) or use contraceptive methods with a failure rate of \< 1% per year during the treatment period and for 90 days after the final dose of tiragolumab, 5 months after the final dose of atezolizumab, and 6 months after the final dose of paclitaxel, pemetrexed, gemcitabine, carboplatin or cisplatin. Women must refrain from donating eggs during this same period. * A woman is considered to be of childbearing potential if she is postmenarchal, has not reached a postmenopausal state (≥ 12 continuous months of amenorrhea with no identified cause other than menopause), and is not permanently infertile due to surgery (i.e., removal of ovaries, fallopian tubes, and/or uterus) or another cause as determined by the investigator (e.g., Müllerian agenesis). The definition of childbearing potential may be adapted for alignment with local guidelines or regulations. * Examples of contraceptive methods with a failure rate of \< 1% per year include bilateral tubal ligation, male sterilization, hormonal contraceptives that inhibit ovulation, hormone-releasing intrauterine devices, and copper intrauterine devices. * The reliability of sexual abstinence should be evaluated in relation to the duration of the clinical trial and the preferred and usual lifestyle of the patient. Periodic abstinence (e.g., calendar, ovulation, symptothermal, or postovulation methods) and withdrawal are not adequate methods of contraception. If required per local guidelines or regulations, locally recognized adequate methods of contraception and information about the reliability of abstinence will be described in the local Informed Consent Form. * Women of childbearing potential (WOCBP) must be willing to use 2 methods of birth control or be surgically sterile, or abstain from heterosexual activity for the course of the study through 6 months after the last dose of study medication. Patients of childbearing potential are those who have not been surgically sterilized or have not been free of menses \> 1 year. 19. For men: agreement to remain abstinent (refrain from heterosexual intercourse) or use a condom, and agreement to refrain from donating sperm, as defined below: * With a female partner of childbearing potential, men who are not surgically sterile must remain abstinent or use a condom plus an additional contraceptive method that together result in a failure rate of \< 1% per year during the treatment period, for 90 days after the final dose of tiragolumab, and for 6 months after the final dose of paclitaxel and/or carboplatin. Men must refrain from donating sperm during this same period. * With a pregnant female partner, men must remain abstinent or use a condom during the treatment period for 90 days after the final dose of tiragolumab, and for 6 months after the final dose of paclitaxel or carboplatin to avoid exposing the embryo. * The reliability of sexual abstinence should be evaluated in relation to the duration of the clinical trial and the preferred and usual lifestyle of the patient. Periodic abstinence (e.g., calendar, ovulation, symptothermal, or postovulation methods) and withdrawal are not adequate methods of contraception. If required per local guidelines or regulations, locally recognized adequate methods of contraception and information about the reliability of abstinence will be described in the local Informed Consent Form. * Male patients must agree to use an adequate method of contraception starting with the first dose of study therapy through 6 months after the last dose of study therapy Men who would like to father a child after study treatment initiation should be advised regarding the conservation of sperm prior to treatment because of the possibility of irreversible infertility resulting from chemotherapies used in this study. 20. Patients are capable of giving informed consent and/or have an acceptable surrogate capable of giving consent on the subject's behalf.	1. Active autoimmune disease. 2. Greater than minimal, exudative, or cytologically positive pleural effusions. 3. Involved contralateral hilar nodes. 4. More than 10% unintentional weight loss within the past month. 5. Prior invasive malignancy (except non-melanomatous skin cancer) unless disease free for a minimum of 3 years; non-invasive conditions such as carcinoma in situ of the breast, localized prostate cancer or thyroid nodules, carcinoma in situ of the oral cavity or cervix are all permissible. 6. Prior systemic chemotherapy for the study cancer; note that prior chemotherapy for a different cancer is allowable. 7. Prior radiotherapy to the region of the study cancer that would result in clinically significant overlap of radiation therapy fields. 8. Prior severe infusion reaction to a monoclonal antibody. 9. Significant history of uncontrolled cardiac disease; i.e., uncontrolled hypertension, unstable angina, myocardial infarction within the last 6 months, uncontrolled congestive heart failure, and cardiomyopathy with decreased ejection fraction. 10. Acute bacterial or fungal infection requiring intravenous antibiotics at the time of registration or within 2 weeks of cycle 1 day 1. * Severe active infection, including, but not limited to, hospitalization for complications of infection, bacteremia, or severe pneumonia, or any active infection that, in the opinion of the investigator, could impact patient safety * Treatment with therapeutic oral or IV antibiotics within 2 weeks prior to initiation of study treatment * Patients receiving prophylactic antibiotics (e.g., to prevent a urinary tract infection or chronic obstructive pulmonary disease exacerbation) are eligible for the study 11. Chronic Obstructive Pulmonary Disease exacerbation or other respiratory illness requiring hospitalization or precluding study therapy within 30 days before registration. 12. Hepatic insufficiency resulting in clinical jaundice and/or coagulation defects. 13. Acquired Immune Deficiency Syndrome (AIDS) based upon current CDC definition; note, HIV testing is required for entry into this protocol due to the immunologic basis for induction treatment. 14. Uncontrolled or symptomatic hypercalcemia (ionized calcium \> 1.5 mmol/L, calcium \> 12 mg/dL or corrected serum calcium \> ULN). 15. Prior allogeneic stem cell or solid organ transplantation. 16. Pregnancy, lactation, or inability or unwillingness to use medically acceptable forms of contraception if pregnancy is a risk. 17. Any history of allergic reaction to paclitaxel or other taxanes, or to carboplatin. 18. Uncontrolled neuropathy grade 2 or greater regardless of cause. 19. Any approved or unapproved anticancer therapy, including chemotherapy, hormonal therapy, or radiotherapy, within 3 weeks prior to initiation of study treatment; however, the following are allowed: * Hormone-replacement therapy or oral contraceptives * Herbal therapy \> 1 week prior to Cycle 1, Day 1 (herbal therapy intended as anticancer therapy must be discontinued at least 1 week prior to Cycle 1, Day 1) 20. Known clinically significant liver disease, including active viral, alcoholic, or other hepatitis; cirrhosis; fatty liver; and inherited liver disease. * Patients with past or resolved hepatitis B infection (defined as having a negative hepatitis B surface antigen \[HBsAg\] test and a positive anti-HBc \[antibody to hepatitis B core antigen\] antibody test) are eligible. * Patients positive for hepatitis C virus (HCV) antibody are eligible only if polymerase chain reaction (PCR) is negative for HCV RNA. 21. Known hypersensitivity to Chinese hamster ovary cell products or other recombinant human antibodies. 22. Inability to comply with study and follow-up procedures. 23. History of active autoimmune disease, including but not limited to systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease, vascular thrombosis associated with antiphospholipid syndrome, Wegener's granulomatosis, Sjögren's syndrome, Bell's palsy, Guillain-Barré syndrome, multiple sclerosis, autoimmune thyroid disease, vasculitis, or glomerulonephritis. 1. Patients with a history of autoimmune hypothyroidism on a stable dose of thyroid replacement hormone may be eligible. 2. Patients with controlled Type 1 diabetes mellitus on a stable insulin regimen may be eligible. 3. Patients with eczema, psoriasis, lichen simplex chronicus of vitiligo with dermatologic manifestations only (e.g., patients with psoriatic arthritis would be excluded) are permitted provided that they meet the following conditions: * Patients with psoriasis must have a baseline ophthalmologic exam to rule out ocular manifestations. * Rash must cover less than 10% of body surface area (BSA). * Disease is well controlled at baseline and only requiring low potency topical steroids (e.g., hydrocortisone 2.5%, hydrocortisone butyrate 0.1%, fluocinolone 0.01%, desonide 0.05%, alclometasone dipropionate 0.05%). * No acute exacerbations of underlying condition within the last 6 months (not requiring psoralen plus ultraviolet A radiation \[PUVA\], methotrexate, retinoids, biologic agents, oral calcineurin inhibitors; high potency or oral steroids). 24. History of idiopathic pulmonary fibrosis, pneumonitis (including drug induced), organizing pneumonia (i.e., bronchiolitis obliterans, cryptogenic organizing pneumonia, etc.), or evidence of active pneumonitis on screening chest computed tomography (CT) scan. 25. Any other diseases, metabolic dysfunction, physical examination finding, or clinical laboratory finding giving reasonable suspicion of a disease or condition that contraindicates the use of an investigational drug or that may affect the interpretation of the results or render the patient at high risk from treatment complications. 26. Active tuberculosis. 27. Major surgical procedure within 28 days prior to Cycle 1, Day 1 or anticipation of need for a major surgical procedure during the course of the study. 28. Administration of a live, attenuated vaccine within 4 weeks before Cycle 1, Day 1 or anticipation that such a live, attenuated vaccine will be required during the study. 29. Illness or condition that may interfere with a patient's capacity to understand, follow, and/or comply with study procedures. 30. Treatment with systemic immunostimulatory agents (including, but not limited to, interferon and IL-2) within 4 weeks or 5 drug-elimination half-lives (whichever is longer) prior to initiation of study treatment. 31. Treatment with systemic immunosuppressive medication (including, but not limited to, corticosteroids, cyclophosphamide, azathioprine, methotrexate, thalidomide, and anti-tumor necrosis factor- TNF-α agents) within 2 weeks prior to initiation of study treatment, or anticipation of need for systemic immunosuppressive medication during study treatment, with the following exceptions: * Patients who received acute, low-dose systemic immunosuppressant medication or a one-time pulse dose of systemic immunosuppressant medication (e.g., 48 hours of corticosteroids for a contrast allergy) are eligible for the study after Medical Monitor confirmation has been obtained. * Patients who received mineralocorticoids (e.g., fludrocortisone), corticosteroids for chronic obstructive pulmonary disease (COPD) or asthma, or low-dose corticosteroids for orthostatic hypotension or adrenal insufficiency are eligible for the study. 32. Tumors with known EGFR mutations or ALK fusion positive/mutations. However, tumors do not need to be tested specifically for these alterations for trial eligibility. 33. Positive Epstein-Barr virus (EBV) viral capsid antigen immunoglobulin M (IgM) test at screening; should be confirmed with PCR testing. 34. Prior treatment with CD137 agonists or immune checkpoint blockade therapies, including anti-CTLA-4, anti-PD-1, anti-TIGIT, and anti-PD-L1 therapeutic antibodies procedures. 35. Treatment with systemic immunostimulatory agents (including but not limited to interferon \[IFN\]-α or interleukin \[IL\]-2) within 4 weeks or 5 drug-elimination half-lives of the drug (whichever is shorter) prior to Cycle 1, Day 1. 36. Treatment with investigational agent within 42 days prior to Cycle 1, Day 1 (or within 5 half-lives of the investigational product, whichever is longer). 37. Treatment with systemic immunosuppressive medications (including but not limited to prednisone, cyclophosphamide, azathioprine, methotrexate, thalidomide, or anti-tumor necrosis factor \[anti-TNF\] agents) within 2 weeks prior to Cycle 1, Day 1. 1. Patients who have received acute, low-dose, systemic immunosuppressant medications (e.g., a one-time dose of dexamethasone for nausea) may be enrolled. 2. The use of inhaled corticosteroids and mineralocorticoids (e.g., fludrocortisone) for patients with orthostatic hypotension or adrenocortical insufficiency is allowed. 3. The use of prednisone premedication required prior to iodinated contrast for CT scans is allowed. 38. History of severe allergic, anaphylactic, or other hypersensitivity reactions to chimeric or humanized antibodies or fusion proteins.

Inclusion Criteria

Exclusion Criteria

1. Newly pathologically proven diagnosis of stage IIIA/B/C (per AJCC 8) NSCLC
2. Age at least 18 years.
3. Availability of a representative tumor specimen that is suitable for BOTH determination of PD-L1 status via local testing and, independently, other required correlative study biomarkers. Tissue submission should include:
1. A representative FFPE tumor specimen in a paraffin block, along with an associated pathology report, which will be sent to the biorepository. If institutional policy prevents the submission of a block, refer to the Correlative Science Manual (CSM) for alternative submission instructions.
2. If archival tumor tissue is unavailable or is determined to be unsuitable for required testing, tumor tissue must be obtained from a biopsy performed at screening. Questions about biopsy adequacy should be directed to the study team.
3. Patients may still be eligible after these two points (3a and 3b) have been attempted/considered, at the discretion of the AFT Study Team.
4. No active autoimmune disease or uncontrolled infection
5. FEV1 ≥ 1.2L or \> 40% predictive
6. No underlying heart or lung disease precluding treatment per protocol.
7. Measurable (RECIST v1.1) stage IIIA, IIIB or IIIC disease per AJCC 8.
8. Patients must be considered unresectable or inoperable. Patients who decline surgery for stage III NSCLC are also eligible. Patients with nodal recurrence after surgery for early-stage NSCLC are eligible if the following criteria are met:
* No prior systemic therapy or radiation for this lung cancer
* Prior curative-intent surgery at least 3 months prior to the nodal recurrence Note: Patients may be medically unfit for surgery, (e.g., due to general anesthesia risk), but remain fit for chemoradiotherapy. Thus, the criterion does not necessarily have to exclude all patients who are medically unfit for surgery.
9. Stage III A/B/C disease (per AJCC 8) with minimum diagnostic evaluation to include:
* History/physical examination within 4 weeks
* Contrast enhanced CT of the chest including upper abdomen (or CT without contrast if contrast is medically contraindicated) within 4 weeks
* MRI of the brain with contrast (or CT with contrast if MRI is medically contraindicated) within 6 weeks
* PET/CT skull to thigh within 6 weeks If pleural fluid is visible on CT scan, thoracentesis to exclude malignancy should be obtained unless the effusion is too small to tap in which case the patient is eligible.
10. Patients must be at least 4 weeks from major surgery and must be fully recovered.
11. Adequate hematologic and end organ function, defined by the following laboratory results obtained within 14 days prior to the first study treatment (Cycle 1, Day 1); if repeat labs are obtained on or prior to C1D1 they must re-meet eligibility criteria to treat):
* ANC ≥ 1500 cells/µL
* WBC counts \> 2500/ µ L
* Lymphocyte count ≥ 500/ µ L
* Platelet count ≥ 100,000/ µ L
* Hemoglobin ≥ 9.0 g/dL (patients may be transfused to meet this criterion).
* Total bilirubin ≤ 1.5 ⋅ upper limit of normal (ULN) with the following exception:
* Patients with known Gilbert disease who have serum bilirubin level ≤ 3 ⋅ ULN may be enrolled.
* AST, ALT and Alkaline phosphatase ≤ 2.5 ⋅ ULN
* Serum albumin ≥ 25 g/L (2.5 g/dL)
* For patients not receiving therapeutic anticoagulation: INR and aPTT ≤ 1.5 ⋅ ULN
* For patients receiving therapeutic anticoagulation: stable anticoagulant regimen
* Serum creatinine ≤ 1.5 ⋅ ULN or creatinine clearance ≥ 45 mL/min on the basis of the Cockcroft-Gault glomerular filtration rate estimation:
* (140 - age) ⋅ (weight in kg) ⋅ (0.85 if female) 72 ⋅ (serum creatinine in mg/dL)
12. Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1.
13. Negative HIV test at screening with the following exception: patients with a positive HIV test at screening are eligible provided they are stable on anti-retroviral therapy, have a CD4+ T-cell count \> 200/vL, and have an undetectable viral load.
14. Negative hepatitis B surface antigen (HBsAg) test at screening
15. Positive hepatitis B surface antibody (HBsAb) test at screening, or negative HBsAb at screening accompanied by either of the following:
* Negative total hepatitis B core antibody (HBcAb)
* Positive total HBcAb test followed by quantitative hepatitis B virus (HBV) DNA \< 500 IU/mL
* The HBV DNA test will be performed only for patients who have a negative HBsAg test, a negative HBsAb test, and a positive total HBcAb test.
16. Negative hepatitis C virus (HCV) antibody test at screening, or positive HCV antibody test followed by a negative HCV RNA test at screening. The HCV RNA test will be performed only for patients who have a positive HCV antibody test.
17. Non-pregnant and non-nursing. The effect of atezolizumab and tiragolumab on the fetus is unknown.
18. For women of childbearing potential: agreement to remain abstinent (refrain from heterosexual intercourse) or use contraception, and agreement to refrain from donating eggs, as defined below:
* Women must remain abstinent (refrain from heterosexual intercourse) or use contraceptive methods with a failure rate of \< 1% per year during the treatment period and for 90 days after the final dose of tiragolumab, 5 months after the final dose of atezolizumab, and 6 months after the final dose of paclitaxel, pemetrexed, gemcitabine, carboplatin or cisplatin. Women must refrain from donating eggs during this same period.
* A woman is considered to be of childbearing potential if she is postmenarchal, has not reached a postmenopausal state (≥ 12 continuous months of amenorrhea with no identified cause other than menopause), and is not permanently infertile due to surgery (i.e., removal of ovaries, fallopian tubes, and/or uterus) or another cause as determined by the investigator (e.g., Müllerian agenesis). The definition of childbearing potential may be adapted for alignment with local guidelines or regulations.
* Examples of contraceptive methods with a failure rate of \< 1% per year include bilateral tubal ligation, male sterilization, hormonal contraceptives that inhibit ovulation, hormone-releasing intrauterine devices, and copper intrauterine devices.
* The reliability of sexual abstinence should be evaluated in relation to the duration of the clinical trial and the preferred and usual lifestyle of the patient. Periodic abstinence (e.g., calendar, ovulation, symptothermal, or postovulation methods) and withdrawal are not adequate methods of contraception. If required per local guidelines or regulations, locally recognized adequate methods of contraception and information about the reliability of abstinence will be described in the local Informed Consent Form.
* Women of childbearing potential (WOCBP) must be willing to use 2 methods of birth control or be surgically sterile, or abstain from heterosexual activity for the course of the study through 6 months after the last dose of study medication. Patients of childbearing potential are those who have not been surgically sterilized or have not been free of menses \> 1 year.
19. For men: agreement to remain abstinent (refrain from heterosexual intercourse) or use a condom, and agreement to refrain from donating sperm, as defined below:
* With a female partner of childbearing potential, men who are not surgically sterile must remain abstinent or use a condom plus an additional contraceptive method that together result in a failure rate of \< 1% per year during the treatment period, for 90 days after the final dose of tiragolumab, and for 6 months after the final dose of paclitaxel and/or carboplatin. Men must refrain from donating sperm during this same period.
* With a pregnant female partner, men must remain abstinent or use a condom during the treatment period for 90 days after the final dose of tiragolumab, and for 6 months after the final dose of paclitaxel or carboplatin to avoid exposing the embryo.
* The reliability of sexual abstinence should be evaluated in relation to the duration of the clinical trial and the preferred and usual lifestyle of the patient. Periodic abstinence (e.g., calendar, ovulation, symptothermal, or postovulation methods) and withdrawal are not adequate methods of contraception. If required per local guidelines or regulations, locally recognized adequate methods of contraception and information about the reliability of abstinence will be described in the local Informed Consent Form.
* Male patients must agree to use an adequate method of contraception starting with the first dose of study therapy through 6 months after the last dose of study therapy Men who would like to father a child after study treatment initiation should be advised regarding the conservation of sperm prior to treatment because of the possibility of irreversible infertility resulting from chemotherapies used in this study.
20. Patients are capable of giving informed consent and/or have an acceptable surrogate capable of giving consent on the subject's behalf.

1. Active autoimmune disease.
2. Greater than minimal, exudative, or cytologically positive pleural effusions.
3. Involved contralateral hilar nodes.
4. More than 10% unintentional weight loss within the past month.
5. Prior invasive malignancy (except non-melanomatous skin cancer) unless disease free for a minimum of 3 years; non-invasive conditions such as carcinoma in situ of the breast, localized prostate cancer or thyroid nodules, carcinoma in situ of the oral cavity or cervix are all permissible.
6. Prior systemic chemotherapy for the study cancer; note that prior chemotherapy for a different cancer is allowable.
7. Prior radiotherapy to the region of the study cancer that would result in clinically significant overlap of radiation therapy fields.
8. Prior severe infusion reaction to a monoclonal antibody.
9. Significant history of uncontrolled cardiac disease; i.e., uncontrolled hypertension, unstable angina, myocardial infarction within the last 6 months, uncontrolled congestive heart failure, and cardiomyopathy with decreased ejection fraction.
10. Acute bacterial or fungal infection requiring intravenous antibiotics at the time of registration or within 2 weeks of cycle 1 day 1.
* Severe active infection, including, but not limited to, hospitalization for complications of infection, bacteremia, or severe pneumonia, or any active infection that, in the opinion of the investigator, could impact patient safety
* Treatment with therapeutic oral or IV antibiotics within 2 weeks prior to initiation of study treatment
* Patients receiving prophylactic antibiotics (e.g., to prevent a urinary tract infection or chronic obstructive pulmonary disease exacerbation) are eligible for the study
11. Chronic Obstructive Pulmonary Disease exacerbation or other respiratory illness requiring hospitalization or precluding study therapy within 30 days before registration.
12. Hepatic insufficiency resulting in clinical jaundice and/or coagulation defects.
13. Acquired Immune Deficiency Syndrome (AIDS) based upon current CDC definition; note, HIV testing is required for entry into this protocol due to the immunologic basis for induction treatment.
14. Uncontrolled or symptomatic hypercalcemia (ionized calcium \> 1.5 mmol/L, calcium \> 12 mg/dL or corrected serum calcium \> ULN).
15. Prior allogeneic stem cell or solid organ transplantation.
16. Pregnancy, lactation, or inability or unwillingness to use medically acceptable forms of contraception if pregnancy is a risk.
17. Any history of allergic reaction to paclitaxel or other taxanes, or to carboplatin.
18. Uncontrolled neuropathy grade 2 or greater regardless of cause.
19. Any approved or unapproved anticancer therapy, including chemotherapy, hormonal therapy, or radiotherapy, within 3 weeks prior to initiation of study treatment; however, the following are allowed:
* Hormone-replacement therapy or oral contraceptives
* Herbal therapy \> 1 week prior to Cycle 1, Day 1 (herbal therapy intended as anticancer therapy must be discontinued at least 1 week prior to Cycle 1, Day 1)
20. Known clinically significant liver disease, including active viral, alcoholic, or other hepatitis; cirrhosis; fatty liver; and inherited liver disease.
* Patients with past or resolved hepatitis B infection (defined as having a negative hepatitis B surface antigen \[HBsAg\] test and a positive anti-HBc \[antibody to hepatitis B core antigen\] antibody test) are eligible.
* Patients positive for hepatitis C virus (HCV) antibody are eligible only if polymerase chain reaction (PCR) is negative for HCV RNA.
21. Known hypersensitivity to Chinese hamster ovary cell products or other recombinant human antibodies.
22. Inability to comply with study and follow-up procedures.
23. History of active autoimmune disease, including but not limited to systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease, vascular thrombosis associated with antiphospholipid syndrome, Wegener's granulomatosis, Sjögren's syndrome, Bell's palsy, Guillain-Barré syndrome, multiple sclerosis, autoimmune thyroid disease, vasculitis, or glomerulonephritis.
1. Patients with a history of autoimmune hypothyroidism on a stable dose of thyroid replacement hormone may be eligible.
2. Patients with controlled Type 1 diabetes mellitus on a stable insulin regimen may be eligible.
3. Patients with eczema, psoriasis, lichen simplex chronicus of vitiligo with dermatologic manifestations only (e.g., patients with psoriatic arthritis would be excluded) are permitted provided that they meet the following conditions:
* Patients with psoriasis must have a baseline ophthalmologic exam to rule out ocular manifestations.
* Rash must cover less than 10% of body surface area (BSA).
* Disease is well controlled at baseline and only requiring low potency topical steroids (e.g., hydrocortisone 2.5%, hydrocortisone butyrate 0.1%, fluocinolone 0.01%, desonide 0.05%, alclometasone dipropionate 0.05%).
* No acute exacerbations of underlying condition within the last 6 months (not requiring psoralen plus ultraviolet A radiation \[PUVA\], methotrexate, retinoids, biologic agents, oral calcineurin inhibitors; high potency or oral steroids).
24. History of idiopathic pulmonary fibrosis, pneumonitis (including drug induced), organizing pneumonia (i.e., bronchiolitis obliterans, cryptogenic organizing pneumonia, etc.), or evidence of active pneumonitis on screening chest computed tomography (CT) scan.
25. Any other diseases, metabolic dysfunction, physical examination finding, or clinical laboratory finding giving reasonable suspicion of a disease or condition that contraindicates the use of an investigational drug or that may affect the interpretation of the results or render the patient at high risk from treatment complications.
26. Active tuberculosis.
27. Major surgical procedure within 28 days prior to Cycle 1, Day 1 or anticipation of need for a major surgical procedure during the course of the study.
28. Administration of a live, attenuated vaccine within 4 weeks before Cycle 1, Day 1 or anticipation that such a live, attenuated vaccine will be required during the study.
29. Illness or condition that may interfere with a patient's capacity to understand, follow, and/or comply with study procedures.
30. Treatment with systemic immunostimulatory agents (including, but not limited to, interferon and IL-2) within 4 weeks or 5 drug-elimination half-lives (whichever is longer) prior to initiation of study treatment.
31. Treatment with systemic immunosuppressive medication (including, but not limited to, corticosteroids, cyclophosphamide, azathioprine, methotrexate, thalidomide, and anti-tumor necrosis factor- TNF-α agents) within 2 weeks prior to initiation of study treatment, or anticipation of need for systemic immunosuppressive medication during study treatment, with the following exceptions:
* Patients who received acute, low-dose systemic immunosuppressant medication or a one-time pulse dose of systemic immunosuppressant medication (e.g., 48 hours of corticosteroids for a contrast allergy) are eligible for the study after Medical Monitor confirmation has been obtained.
* Patients who received mineralocorticoids (e.g., fludrocortisone), corticosteroids for chronic obstructive pulmonary disease (COPD) or asthma, or low-dose corticosteroids for orthostatic hypotension or adrenal insufficiency are eligible for the study.
32. Tumors with known EGFR mutations or ALK fusion positive/mutations. However, tumors do not need to be tested specifically for these alterations for trial eligibility.
33. Positive Epstein-Barr virus (EBV) viral capsid antigen immunoglobulin M (IgM) test at screening; should be confirmed with PCR testing.
34. Prior treatment with CD137 agonists or immune checkpoint blockade therapies, including anti-CTLA-4, anti-PD-1, anti-TIGIT, and anti-PD-L1 therapeutic antibodies procedures.
35. Treatment with systemic immunostimulatory agents (including but not limited to interferon \[IFN\]-α or interleukin \[IL\]-2) within 4 weeks or 5 drug-elimination half-lives of the drug (whichever is shorter) prior to Cycle 1, Day 1.
36. Treatment with investigational agent within 42 days prior to Cycle 1, Day 1 (or within 5 half-lives of the investigational product, whichever is longer).
37. Treatment with systemic immunosuppressive medications (including but not limited to prednisone, cyclophosphamide, azathioprine, methotrexate, thalidomide, or anti-tumor necrosis factor \[anti-TNF\] agents) within 2 weeks prior to Cycle 1, Day 1.
1. Patients who have received acute, low-dose, systemic immunosuppressant medications (e.g., a one-time dose of dexamethasone for nausea) may be enrolled.
2. The use of inhaled corticosteroids and mineralocorticoids (e.g., fludrocortisone) for patients with orthostatic hypotension or adrenocortical insufficiency is allowed.
3. The use of prednisone premedication required prior to iodinated contrast for CT scans is allowed.
38. History of severe allergic, anaphylactic, or other hypersensitivity reactions to chimeric or humanized antibodies or fusion proteins.

Contacts and Locations

Principal Investigator

Helen Ross, MD

STUDY_CHAIR

Rush University

Evanthia Galanis, MD

PRINCIPAL_INVESTIGATOR

Alliance Foundation Trials, LLC.

Study Locations (Sites)

University of California San Diego Moores Cancer Center

La Jolla, California, 92037

United States

Kaiser Permanente Oakland Medical Center

Oakland, California, 94611

United States

Kaiser Permanente Roseville Medical Center

Roseville, California, 95661

United States

Kaiser Permanente San Francisco Medical Center

San Francisco, California, 94115

United States

Kaiser Permanente Santa Clara Medical Center

Santa Clara, California, 95051

United States

Kaiser Permanente Vallejo Medical Center

Vallejo, California, 94589

United States

Rush University Medical Center

Chicago, Illinois, 60612

United States

Washington University Siteman Cancer Center

St Louis, Missouri, 63110

United States

Missouri Baptist Medical Center

St Louis, Missouri, 63131

United States

University of Nebraska Medical Center

Omaha, Nebraska, 68198

United States

New Hampshire Oncology - Hematology, PA

Manchester, New Hampshire, 03103

United States

Hematology Oncology Associates of Central New York, P.C.

East Syracuse, New York, 13057

United States

SUNY Upstate Medical University

Syracuse, New York, 13210

United States

Ohio State University

Columbus, Ohio, 43210

United States

University of Wisconsin

Madison, Wisconsin, 53792

United States

Collaborators and Investigators

Sponsor: Alliance Foundation Trials, LLC.

Helen Ross, MD, STUDY_CHAIR, Rush University
Evanthia Galanis, MD, PRINCIPAL_INVESTIGATOR, Alliance Foundation Trials, LLC.

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-12-07

Study Completion Date2026-11

Study Record Updates

Study Start Date2023-12-07

Study Completion Date2026-11

Terms related to this study

Additional Relevant MeSH Terms

NSCLC