| Eligibility |
Inclusion Criteria:
- Participants must have histologically confirmed adenoid cystic carcinoma with evidence
of recurrent or metastatic disease not amenable to potentially curative surgery or
radiotherapy.
- Participants must have at least two RECIST v1.1 measurable non-CNS based lesions.
Palliative radiation must be indicated for at least one of these lesions, and this
lesion must be a candidate for radiation to a dose of 30 Gy of radiation over 5
fractions as deemed by a treating radiation oncologist. Documentation of volume and
prescription isodose line will be collected. Re-irradiation of a previously treated
lesion is not allowed. One lesion must be in a location where it will not be
incorporated into the radiation fields so systemic response can be assessed. However,
inclusion of patients with more than 10 measurable lesions is strongly discouraged and
all patients must have life expectancy > 6 months.
- Participants must agree to undergo a research biopsy, if tumor is safely accessible,
at baseline and after 2 cycles of pembrolizumab. Participants can be exempt if
archival tumor tissue has been collected within 12 months of study enrollment that the
Principal Investigator deems it appropriate/sufficient for analysis on this protocol.
Biopsy of a lesion outside of the potential radiation treatment field is preferred to
maintain consistency across cohorts.
- Participants must have archival tissue from the primary tumor or metastases available
for correlative studies. Either a paraffin block or twenty unstained slides are
acceptable. If twenty slides are not available, a lesser amount may be acceptable
after discussion with the Principal Investigator.
- Prior systemic therapy: At least 2 weeks must have elapsed since the end of prior
chemotherapy, biological agents (4 weeks for anti-cancer monoclonal antibody
containing regimens) or any investigational drug product, with adequate recovery of
treatment-related toxicity to NCI CTCAE Version 4.0 grade =1 (or tolerable grade 2) or
back to baseline (except for alopecia or neuropathy). Any number of prior therapies
for recurrent/metastatic ACC are allowed, with the exception of previous treatment
with PD-1 pathway inhibitors.
- Prior radiation therapy: At least 3 weeks must have elapsed from prior radiation
therapy. The prior site of radiotherapy must be documented as reirradiation of the
same site is not allowed in this protocol.
- Be = 18 years of age on day of signing informed consent.
- Have a performance status of 0 or 1 on the ECOG Performance Scale (see Appendix A).
- Participants must have documentation of a new or progressive lesion on a radiologic
imaging study performed within 12 months prior to study enrollment (progression of
disease over any interval is allowed) and/or new/worsening disease related symptoms
within 12 months prior to study enrollment. This assessment is performed by the
treating investigator. Evidence of progression by RECIST criteria is not required.
- Demonstrate adequate organ function as defined in Table 1, all screening labs should
be performed within 10 days of treatment initiation.
Table 1 Adequate Organ Function Laboratory Values System Laboratory Value
- Hematological
- Absolute neutrophil count (ANC) =1,500 /mcL
- Platelets =100,000 / mcL
- Hemoglobin =9 g/dL or =5.6 mmol/L without transfusion or EPO dependency (within 7
days of assessment)
- Renal
- Serum creatinine OR Measured or calculated creatinine clearance (GFR can also be used
in place of creatinine or CrCl) =1.5 X upper limit of normal (ULN) OR =60 mL/min for
subject with creatinine levels > 1.5 X institutional ULN
- Hepatic
- Serum total bilirubin = 1.5 X ULN OR Direct bilirubin = ULN for subjects with
total bilirubin levels > 1.5 ULN
- AST (SGOT) and ALT (SGPT) = 2.5 X ULN OR = 5 X ULN for subjects with liver
metastases
- Albumin >2.5 mg/dL
- Coagulation
- International Normalized Ratio (INR) or Prothrombin Time (PT)
- Activated Partial Thromboplastin Time (aPTT) =1.5 X ULN unless subject is
receiving anticoagulant therapy as long as PT or PTT is within therapeutic range
of intended use of anticoagulants =1.5 X ULN unless subject is receiving
anticoagulant therapy as long as PT or PTT is within therapeutic range of
intended use of anticoagulants
- Creatinine clearance should be calculated per institutional standard.
- Baseline tumor measurements must be documented from tests within 28 days of study
entry. Other non-laboratory tests must be performed within 28 days of study entry.
- Female subjects of childbearing potential should have a negative urine or serum
pregnancy within 7 days prior to receiving the first dose of study medication. If the
urine test is positive or cannot be confirmed as negative, a serum pregnancy test will
be required.
- Female and male subjects of childbearing potential must agree to use an adequate
method of contraception, as outlined in section 5.6, prior to study entry, for the
duration of study participation, and 4 months after completion of pembrolizumab
administration. Contraception is required starting with the first dose of study
medication through 120 days after the last dose of study medication.
- Note: Abstinence is acceptable if this is the usual lifestyle and preferred
contraception for the subject.
- Be willing and able to provide written informed consent for the trial.
Exclusion Criteria:
- Metastatic disease impinging on the spinal cord or threatening spinal cord
compression. Patients that have had previous treatment of disease with impinging on
the cord with either surgery or radiotherapy with clinical or radiographic evidence of
response or stability are eligible.
- Surgical fixation of bone lesion to be irradiated is required and indicated to provide
mechanical stability.
- Participant has known active central nervous system (CNS) metastases and/or
carcinomatous meningitis. Subjects with previously treated brain metastases may
participate provided they are stable (without evidence of progression by imaging for
at least four weeks prior to the first dose of trial treatment), have no evidence of
new or enlarging brain metastases, and are not using steroids for the purposes of
treating brain metastasis induced edema for at least 7 days prior to trial treatment.
This exception does not include carcinomatous meningitis which is excluded regardless
of clinical stability, because of their poor prognosis and because they often develop
progressive neurologic dysfunction that would confound the evaluation of neurologic
and other adverse events.
- Prior treatment with PD-1 or PD-L1 inhibitor
- Concurrent administration of other cancer specific therapy or investigational agents
during the course of this study is not allowed.
- Has a diagnosis of immunodeficiency or is receiving systemic steroid therapy or any
other form of immunosuppressive therapy within 7 days prior to the first dose of trial
treatment.
- Has a known history of active TB (Bacillus Tuberculosis)
- History of allergic reactions or hypersensitivity to pembrolizumab or any of its
excipients.
- 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.
- Has a known additional malignancy that is progressing or requires active treatment.
Exceptions include basal cell carcinoma of the skin or squamous cell carcinoma of the
skin that has undergone potentially curative therapy or in situ cervical cancer.
- Has known history of, or any evidence of active, non-infectious pneumonitis.
- Has an active infection requiring systemic therapy.
- 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 (e.g., thyroxine, insulin, or physiologic corticosteroid
replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a
form of systemic treatment.
- Has a history or current evidence of any condition, therapy, or laboratory abnormality
that might confound the results of the trial, interfere with the subject's
participation for the full duration of the trial, or is not in the best interest of
the subject to participate, in the opinion of the treating investigator.
- Subjects who are pregnant or breastfeeding, or expecting to conceive or father
children within the projected duration of the trial, starting with the pre-screening
or screening visit through 120 days after the last dose of trial treatment. Pregnant
women are excluded from this study because immunotherapy has the potential for
teratogenic or abortifacient effects. Because there is an unknown but potential risk
of adverse events in nursing infants secondary to treatment of the mother with
immunotherapy, breastfeeding should be discontinued if the mother is treated on this
protocol. Women who could potentially become pregnant while undergoing treatment on
this protocol must be willing to use 2 methods of contraception.
- Has a known history of Human Immunodeficiency Virus (HIV) (HIV 1/2 antibodies).
- Has known active Hepatitis B (e.g., HBsAg reactive) or Hepatitis C (e.g., HCV RNA
[qualitative] is detected).
- Has received a live vaccine within 30 days of planned start of study therapy.
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