Testing the Addition of a Type of Drug Called Immunotherapy to the Usual Chemotherapy Treatment for Non-Small Cell Lung Cancer, ALCHEMIST Trial
This phase III ALCHEMIST trial tests the addition of pembrolizumab to usual chemotherapy for the treatment of stage IIA, IIB, IIIA or IIIB non-small cell lung cancer that has been removed by surgery. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body’s immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Chemotherapy drugs, such as cisplatin, pemetrexed, carboplatin, gemcitabine hydrochloride, and paclitaxel, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving pembrolizumab with usual chemotherapy may help increase survival times in patients with stage IIA, IIB, IIIA or IIIB non-small cell lung cancer.
Eligibility
Inclusion Criterea
- A female of childbearing potential is a sexually mature female who:
* Has not undergone a hysterectomy or bilateral oophorectomy; or
* Has not been naturally postmenopausal for at least 12 consecutive months (i.e., has had menses at any time in the preceding 12 consecutive months)
- Previously registered to A151216
- Central and/or local testing of EGFR with no EGFR exon 19 deletion or EGFR L858 R mutation (applicable to non-squamous patients only)
- Central and/or local testing of ALK with no ALK rearrangement (failed testing is considered negative) (applicable to non-squamous patients only)
- Central and/or local testing of PD-L1 immunohistochemistry (IHC) using one of the following assays: DAKO 22C3, DAKO 28-8, EIL3N or SP263
* Note: Central testing of EGFR was discontinued as of A081801 Update 10; central testing of ALK and PD-L1 will continue. Local testing results by a local CLIA certified laboratory is required for EGFR and acceptable for ALK. The report must indicate the result as well as the CLIA number of the laboratory that performed the assay. Local result of PD-L1 by DAKO 22C3, Dako 28-8, EIL3N or SP263 are acceptable for enrollment on A081801. Patients with local results for EGFR, ALK and PD-L1 still need to be registered to A151216 and follow all the submissions requirements but do NOT need to wait for the results to proceed to A081801 registration.
- Completely resected stage IIA, IIB IIIA or IIIB (T3-4N2) non-small cell lung cancer (NSCLC) (squamous or non-squamous) with negative margins (complete R0 resection). Patients will be staged according to the 8th edition of the American Joint Committee on Cancer (AJCC) Staging Manual, 2017
* Note: Patients with pathologic N2 disease, completely resected, are eligible. However, patients known to have N2 disease prior to surgery are not eligible; guidelines do not recommend up-front surgery for this population
- Complete recovery from surgery. Registration to A081801 must be 30-77 days following surgery
- No prior neoadjuvant or adjuvant therapy for current lung cancer diagnosis
- No prior allogeneic tissue/solid organ transplant
- Patients must NOT have uncontrolled intercurrent illness including, but not limited to, serious ongoing or active infection, symptomatic congestive heart failure, uncontrolled cardiac arrhythmia, unstable angina pectoris, that would limit compliance with study requirements
- No current pneumonitis or history of (non-infectious) pneumonitis that required steroids
- Human immunodeficiency virus (HIV)-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months are eligible for this trial
- Age >= 18 years
- Eastern Cooperative Oncology Group (ECOG) performance status (PS): 0-1
- No active auto-immune disease that has required systemic treatment within the last 2 years (e.g., disease-modifying agents, corticosteroids, or immunosuppressive drugs). Replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid release therapy for adrenal or pituitary insufficiency) is not considered a form of systemic treatment
- Not pregnant and not nursing, because this study involves an agent that has known genotoxic, mutagenic and teratogenic effects
* Therefore, for women of childbearing potential only, a negative pregnancy test done =< 7 days prior to registration is required
- No patients with a “currently active” second malignancy that is progressing or has required active treatment within the last 3 years. Participants with non-melanoma skin cancers or carcinoma in situ (e.g., breast carcinoma or cervical cancer in situ) that have undergone potentially curative therapy are eligible
- No hypersensitivity (>= grade 3) to pembrolizumab and/or any of its excipients
- No live vaccine within 30 days prior to registration. Examples of live vaccines include, but are not limited to, the following: measles, mumps, rubella, varicella/zoster (chicken pox), yellow fever, rabies, Bacillus Calmette–Guerin (BCG), and typhoid vaccine. Seasonal influenza vaccines for injection are generally killed virus vaccines and are allowed; however, intranasal influenza vaccines (e.g., FluMist) are live attenuated vaccines and are not allowed
- No known history of hepatitis B (defined as hepatitis B surface antigen [HBsAg] reactive) or known hepatitis C virus (defined as HCV ribonucleic acid [RNA] [qualitative] is detected) infection
- Absolute neutrophil count (ANC) >= 1,500/mm^3
- Platelet count >= 100,000/mm^3
- Hemoglobin >= 8 gm/dl
- Calculated (Calc.) creatinine clearance >= 45 mL/min
- Total bilirubin =< 1.5 x upper limit of normal (ULN)
- Aspartate aminotransferase (AST) / alanine aminotransferase (ALT) =< 2.5 x upper limit of normal (ULN)
Participating Clinics
GenesisCare USA - Fort Apache
OptumCare Cancer Care at Seven Hills
Radiation Oncology Associates
Comprehensive Cancer Centers of Nevada-Horizon Ridge
Cancer and Blood Specialists-Tenaya
Comprehensive Cancer Centers of Nevada-Summerlin
Cancer and Blood Specialists-Shadow
OptumCare Cancer Care at Charleston
Cancer and Blood Specialists-Henderson
Las Vegas Cancer Center-Henderson
HealthCare Partners Medical Group Oncology/Hematology-San Martin
Comprehensive Cancer Centers of Nevada
GenesisCare USA - Las Vegas
HealthCare Partners Medical Group Oncology/Hematology-Tenaya
OptumCare Cancer Care at MountainView
Comprehensive Cancer Centers of Nevada - Town Center
Carson Tahoe Regional Medical Center
Las Vegas Cancer Center-Medical Center
Comprehensive Cancer Centers of Nevada - Northwest
University Medical Center of Southern Nevada
Comprehensive Cancer Centers of Nevada-Southeast Henderson
Radiation Oncology Centers of Nevada Southeast
OptumCare Cancer Care at Fort Apache
Kingman Regional Medical Center
GenesisCare USA - Vegas Tenaya
Hope Cancer Care of Nevada
Sunrise Hospital and Medical Center
Alliance for Childhood Diseases/Cure 4 the Kids Foundation
Radiation Oncology Centers of Nevada Central
Comprehensive Cancer Centers of Nevada - Henderson
Comprehensive Cancer Centers of Nevada - Central Valley
Renown Regional Medical Center
HealthCare Partners Medical Group Oncology/Hematology-Centennial Hills
Hope Cancer Care of Nevada-Pahrump
HealthCare Partners Medical Group Oncology/Hematology-Maryland Parkway
Summerlin Hospital Medical Center
Saint Mary's Regional Medical Center
GenesisCare USA - Henderson
Urology Specialists of Nevada - Northwest
Las Vegas Urology - Sunset
Las Vegas Urology - Pebble
Las Vegas Urology - Pecos
Urology Specialists of Nevada - Green Valley
Las Vegas Prostate Cancer Center
Las Vegas Urology - Cathedral Rock
Urology Specialists of Nevada - Southwest
Urology Specialists of Nevada - Central
Las Vegas Urology - Green Valley