| Eligibility |
Inclusion Criteria:
1. Male/female participants who are =75 years of age on the day of signing informed
consent with histologically confirmed diagnosis of stage IV (AJCC version 8) NSCLC
with tumor PD-L1 < 50% and negative 'driver' alterations in EGFR, ALK and ROS1 will be
enrolled in this study. Tumor PD-L1 expression should be assessed by FDA approved Dako
22C3 test.
2. Patients should be treatment naïve for stage IV NSCLC. Patients previously treated for
earlier stages of lung cancer are eligible if they have not received systemic therapy
for a minimum of 180 days prior to the start of study therapy.
3. The participant provides written informed consent for the trial.
4. Have measurable disease based on RECIST 1.1 or evaluable disease.
5. Have an Eastern Cooperative Oncology Group (ECOG) performance status of 0,1.
Evaluation of ECOG is to be performed within 7 days prior to the date of start of
therapy.
6. Male participants:
A male participant must agree to use a contraception as detailed in Appendix 3 of this
protocol during the treatment period and for at least 180 days after the last dose of
study treatment and refrain from donating sperm during this period.
7. Have adequate organ function as evidenced by laboratory assessment. Specimens must be
collected within 10 days prior to the start of study treatment.
Exclusion Criteria:
1. Patient could not have received any anti-cancer systemic therapy for a minimum of 180
days prior to the start of study therapy. Patient should not have received prior PD-1
or PD-L1 therapy.
2. Has received prior definitive palliative radiotherapy within 2 weeks or definitive
radiotherapy within 6 months of study intervention. Participants must have recovered
from all radiation-related toxicities, require corticosteroids no more than 10 mg of
prednisone or equivalent dose of other steroids, and not have had clinical radiation
pneumonitis.
3. Has received a live vaccine within 30 days prior to the first dose of study drug.
Examples of live vaccines include, but are not limited to, the following: measles,
mumps, rubella, varicella/zoster (chicken pox), yellow fever, rabies, Bacillus
Calmette-Guérin (BCG), and typhoid vaccine. Seasonal influenza vaccines for injection
are generally killed virus vaccines and are allowed; however, intranasal influenza
vaccines (eg, FluMist®) are live attenuated vaccines and are not allowed.
4. Is currently participating in or has participated in a study of an investigational
agent or has used an investigational device within 4 weeks prior to the first dose of
study intervention.
5. Has a diagnosis of immunodeficiency or is receiving chronic systemic steroid therapy
(in dosing exceeding 10 mg daily of prednisone equivalent) or any other form of
immunosuppressive therapy within 7 days prior to the first dose of study drug.
6. Has a history of a second malignancy, unless potentially curative treatment has been
completed with no evidence of malignancy for 2 years. Patients with cancers such as
PSA only prostate cancer may be considered after discussion with the principal
investigator.
Note: The time requirement does not apply to participants who underwent successful
definitive resection of basal cell carcinoma of the skin, squamous cell carcinoma of
the skin, superficial bladder cancer, in situ cervical cancer, or other in-situ
cancers
7. Has symptomatic CNS metastases and/or carcinomatous meningitis. Subjects with
asymptomatic brain metastases may participate provided they are clinically stable and
are not using steroids equivalent to >10mg of prednisone day prior to trial treatment.
This exception does not include carcinomatous meningitis which is excluded regardless
of whether it is symptomatic or not.
8. Has severe hypersensitivity (=Grade 3) to pembrolizumab and/or any of its excipients.
9. Has active autoimmune disease that has required systemic treatment in the past 2 years
(i.e. with use of disease modifying agents, corticosteroids or immunosuppressive
drugs). Replacement therapy (eg., thyroxine, insulin, or physiologic corticosteroid
replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a
form of systemic treatment and is allowed.
10. Has a history of (non-infectious) pneumonitis that required steroids or has current
pneumonitis.
11. Has an active infection requiring systemic therapy.
12. Has a known history of Human Immunodeficiency Virus (HIV) infection. Note: No HIV
testing is required unless mandated by local health authority.
13. Has a known history of Hepatitis B (defined as Hepatitis B surface antigen [HBsAg]
reactive) or known active Hepatitis C virus (defined as HCV RNA [qualitative] is
detected) infection. Note: no testing for Hepatitis B and Hepatitis C is required
unless mandated by local health authority.
14. Has a known history of active TB (Bacillus Tuberculosis).
15. Has a history or current evidence of any condition, therapy, or laboratory abnormality
that might confound the results of the study, interfere with the subject's
participation for the full duration of the study, or is not in the best interest of
the subject to participate, in the opinion of the treating investigator.
16. Has known psychiatric or substance abuse disorders that would interfere with
cooperation with the requirements of the trial.
17. Has had an allogenic tissue/solid organ transplant.
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