| Eligibility |
Inclusion Criteria:
- Histologically confirmed stage IV NSCLC, with no prior systemic anti-cancer therapy of
any kind (including EGFR and ALK inhibitors). Prior definitive chemoradiation for
locally advanced disease is permitted as long as the last administration of
chemotherapy or radiation (whichever was given last) occurred at least 6 months prior
to enrollment. Prior adjuvant or neoadjuvant chemotherapy for early stage lung cancer
is permitted if completed at least 6 months prior to initiating study treatment.
- Participants must have measurable disease, defined as at least one lesion that can be
accurately measured in at least one dimension (longest diameter to be recorded for
non-nodal lesions and short axis for nodal lesions) as =20 mm with conventional
techniques or as =10 mm with spiral CT scan, MRI, or calipers by clinical exam. See
Section 11 for the evaluation of measurable disease.
- Age = 18 years.
- ECOG performance status = 1 (see Appendix A)
- Participants must have normal organ and marrow function as defined below:
- Absolute neutrophil count = 1,500/mcL
- Platelets = 100,000/mcL
- Total bilirubin = 1.5 × institutional upper limit of normal (ULN)
- AST(SGOT)/ALT(SGPT) = 2.5 × institutional ULN, OR
- AST(SGOT)/ALT(SGPT) = 5 × institutional ULN if liver metastases are present
- Serum creatinine = 1.5 × institutional ULN, OR
- Creatinine clearance = 60 mL/min/1.73 m2 for participants with serum creatinine
levels above 1.5 × institutional ULN.
- Ability to understand and the willingness to sign a written informed consent document.
- Participants must have a tumor tissue sample available (formalin-fixed paraffin
embedded [FFPE] tissue block or unstained slides); may be newly obtained or obtained
within 6 months prior to enrollment (without systemic therapy given after the sample
was obtained). Participants without sufficient archival tissue may be enrolled
following successful completion of the pre-treatment tumor tissue biopsy. Tissue must
be a core needle biopsy, excisional, or incisional biopsy. Fine needle aspirates (FNA)
or malignant effusions are not adequate. Bone biopsies without a soft tissue component
are not adequate.
- The effects of nivolumab and ipilimumab on the developing human fetus are unknown. For
this reason, women of childbearing potential (WOCBP) must agree to follow instructions
for acceptable contraception from the time of signing consent, and for 23 weeks after
their last dose of protocol-indicated treatment. Should a woman become pregnant or
suspect she is pregnant while she or her partner is participating in this study, she
should inform her treating physician immediately. Men treated or enrolled on this
protocol who are not azoospermic who are sexually active with WOCBP must agree to
follow instructions for acceptable contraception from the time of signing consent, and
for 31 weeks after their last dose of protocol-indicated treatment.
- Participants must be able and willing to undergo a pre-treatment tumor tissue biopsy.
Participants must also be willing to undergo an on-treatment tumor tissue biopsy if
clinically feasible.
Exclusion Criteria:
- Participants with known EGFR mutations or ALK rearrangements. All subjects must have
been tested for EGFR mutation and ALK rearrangement prior to study entry, unless they
are known to have a KRAS mutation.
- Participants who have had prior treatment with an anti-PD-1, anti-PD-L1, anti-PD-L2,
anti-CTLA-4 antibody, or any other antibody or drug specifically targeting T-cell
co-stimulation or checkpoint pathways.
- Participants who received prior non-CNS directed palliative radiation therapy within 7
days of the date of study entry.
- Participants who are receiving any other investigational agents.
- Participants with known untreated brain metastases should be excluded from this
clinical trial because of their poor prognosis and because they often develop
progressive neurologic dysfunction that would confound the evaluation of neurologic
and other adverse events. Subjects are eligible if CNS metastases are adequately
treated and subjects are neurologically returned to baseline (except for residual
signs or symptoms related to the CNS treatment) for at least 2 weeks prior to study
entry. Subjects must be either off corticosteroids, or on a stable or decreasing dose
of =10 mg daily prednisone (or equivalent) for at least 2 weeks prior to first study
treatment.
- History of allergic reactions attributed to compounds of similar chemical or biologic
composition to ipilimumab or nivolumab.
- Participants with previous malignancies are excluded unless a complete remission was
achieved at least 2 years prior to first treatment and no additional therapy is
required or anticipated to be required during the study period as judged by the
treating investigator. Exceptions include non-melanoma skin cancers, and in situ
cancers of any type (e.g. bladder, gastric, colon, cervical/dysplasia, melanoma, or
breast carcinoma in situ).
- Participants with any other active malignancy requiring concurrent intervention.
- Participants with an active, known, or suspected autoimmune disease. Subjects with
type I diabetes mellitus, hypothyroidism only requiring hormone replacement, skin
disorders (such as vitiligo, psoriasis, or alopecia) not requiring systemic treatment,
or conditions not expected to recur in the absence of an external trigger are
permitted to enroll.
- Participants with a condition requiring systemic treatment with corticosteroids of >
10 mg daily prednisone (or equivalent), or subjects requiring other immunosuppressive
medications within 14 days of first treatment. Inhaled, topical, ophthalmologic, local
steroid injections, and adrenal replacement steroid > 10 mg daily prednisone or
equivalent are permitted in the absence of active autoimmune disease.
- Participants with interstitial lung disease that is symptomatic or may interfere with
the detection or management of suspected drug-related pulmonary toxicity in the
opinion of the treating investigator.
- Participants with a known history of testing positive for human immunodeficiency virus
(HIV), or known acquired immunodeficiency syndrome (AIDS).
- Participants with known positive test for hepatitis B or C indicating acute or chronic
infection.
- Participants with = Grade 2 peripheral neuropathy.
- Uncontrolled intercurrent illness including, but not limited to, ongoing or active
infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac
arrhythmia, or psychiatric illness/social situations that would limit compliance with
study requirements.
- Pregnant women are excluded from this study because ipilimumab and nivolumab are both
agents with the potential for teratogenic or abortifacient effects. Because there is
an unknown but potential risk for adverse events in nursing infants secondary to
treatment of the mother with ipilimumab or nivolumab, breastfeeding should be
discontinued if the mother is treated with ipilimumab or nivolumab. A negative serum
pregnancy test is required prior to study entry.
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