The co-primary endpoints of the study are to 1) establish the recommended Phase II dose
(RP2D) of pembrolizumab in combination with pemetrexed and oxaliplatin and 2) evaluate the
The secondary aims of the study are to 1) evaluate the clinical benefit rate (CBR) of
pembrolizumab in combination with pemetrexed and with pembrolizumab in combination with
pemetrexed and oxaliplatin in patients with chemo-refractory MSS mCRC and 2) to estimate the
progression free survival (PFS) and 3) overall survival (OS) in patients with MSS mCRC
treated with pembrolizumab and pemetrexed or with pembrolizumab in combination with
pemetrexed and oxaliplatin.
Patients enrolled to Cohort 1 will receive: pembrolizumab 200mg IV and pemetrexed 500 mg/m2
on Day 1 of each 21 day cycle.
Cohort 2 (the dose escalation portion of the study) will be a standard "3+3" design; 2 dose
levels are planned. The first 3 to 6 patients in cohort 2 will be treated at dose level 1 and
will receive pembrolizumab 200 mg IV, pemetrexed 500 mg/m2 IV and oxaliplatin 85 mg/ m2 on
Day 1 of each 21 day cycle. If 1 of 3 patients in this cohort experiences a dose-limiting
toxicity (DLT), see Section 6.4, 3 more patients will be added at the same dose level. If 0
of 3 initial patients or 1 of 6 patients in the cohort experiences a DLT, the dose for the
next cohort will be escalated to dose level 2 and will receive pembrolizumab 200 mg IV,
pemetrexed 500 mg/m2 IV and oxaliplatin 120 mg/ m2 on Day 1 of each 21 day cycle; otherwise,
the combination will be considered too toxic. If ≥ 2 DLTs are experienced at any dose level,
the combination will be considered too toxic and the next lower dose level will be considered
the RP2D. A total of 12 patients will be treated at the RP2D as the expansion portion.
Patients in both cohorts will continue to receive study therapy (maximum of 35 cycles) unless
therapy is discontinued due to patient election, toxicity, or disease progression.
Dose limiting toxicity (DLT) will be monitored during the first 21 days (Cycle 1) of each
dose level in Cohort 2 and will be used for purposes of dose escalation and determination of
RP2D. A DLT is defined as a non-hematologic adverse event (AE) of grade ≥ 3 or a hematologic
toxicity of grade ≥ 4. Toxicity will be graded according to the National Cancer Institute
(NCI) Common Terminology Criteria for Adverse Events version 4.0.
The highest dose level tolerable without dose limiting toxicities (DLTs) in < 2 of 6 patients
will be considered the recommended phase 2 dose (RP2D) and be expanded to 12 patients.
The maximum total enrollment of the study is 33 patients. In Cohort 1, a total of 15 patients
with chemo-refractory MSS mCRC will be treated for further safety assessment and a
preliminary signal. In Cohort 2, 3 to 6 patients will be accrued per dose level. A total of
12 patients with chemo-refractory MSS mCRC will be treated on the RP2D for further safety and
preliminary efficacy signal. Cohort 1 and Cohort 2 will be analyzed separately.
Efficacy will be evaluated as the individual best overall response as defined by a modified
RECIST 1.1 (mRECIST 1.1). The objective response rate (complete response [CR] and partial
response [PR]) will be determined. In either dose level cohort > 3 patients (> 3 of 18) with
objective response (PR or CR) will warrant further investigation.
- The patient must have consented to participate and, prior to beginning specific study
procedures, must have signed and dated an appropriate IRB-approved consent form that
conforms to federal and institutional guidelines for study treatment.
- The ECOG performance status must be 0 or 1.
- There must be histologic or cytologic confirmation of a diagnosis of microsatellite
stable (MSS) colorectal adenocarcinoma using CLIA certified IHC or PCR-based MSI
- Metastatic or locally advanced disease not amenable to curative surgery and/or
- There must be documentation by PET/CT scan, CT scan, or MRI that the patient has
evidence of measurable metastatic disease per RECIST 1.1.
- Patients must have had prior treatment for metastatic or unresectable for cure of
colorectal cancer with standard chemotherapy including fluoropyrimidine-, oxaliplatin-
and irinotecan- based chemotherapy, and if RAS wild-type, an anti-EGFR therapy.
- At the time of study entry, blood counts performed within 2 weeks prior to study entry
must meet the following criteria:
- ANC must be greater than or equal to 1500/mm3;
- Platelet count must be greater than or equal to 100,000/mm3; and
- Hemoglobin must be greater than or equal to 9 g/dL.
- The following criteria for evidence of adequate hepatic function performed within 2
weeks prior to study entry must be met:
- Total bilirubin must be less than or equal to 1.5 x ULN.
- AST and ALT must be less than or equal to 2.5 x ULN for the lab except in the
presence of known hepatic metastasis, wherein transaminases may be up to 5 x ULN.
- Alkaline phosphatase must be less than or equal to 3 x ULN for the lab.
- International normalized ratio of prothrombin time must be less than or equal to 1.5
times the ULN. Patients who are therapeutically treated with an agent such as warfarin
or heparin will be allowed to participate if no underlying abnormality in coagulation
parameters exists per medical history. For laboratories that do not report an ULN for
the INR assay, use less than or equal to 1.2 as the value for the ULN.
- Creatinine must be less than or equal to 1.5 x upper limit of normal (ULN) and
measured or calculated creatinine clearance (CrCl) greater than or equal to 60mL/min.
- All hematologic, gastrointestinal, and genitourinary chemotherapy toxicities must be
less than grade 2 at the time study therapy is to begin. (Note: Transfusions may be
used to correct hemoglobin for patients experiencing anemia from therapy who otherwise
would be eligible for the study.
- Patients must be able to interrupt nonsteroidal anti-inflammatory drugs (NSAIDS) 2
days before (5 days for long acting NSAIDS), the day of and 2 days following
administration of pemetrexed.
- Patients must be able to take folic acid, vitamin B12, and dexamethasone per protocol.
- Female patients of childbearing potential should have a negative urine or serum
pregnancy within 72 hours 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.
- Male and female patients with reproductive potential must agree to use accepted
effective methods of contraception while receiving study therapy and for at least 120
days after the completion of study therapy. Note: Abstinence is acceptable if this is
the usual lifestyle and preferred contraception for the patient.
- Diagnosis of anal or small bowel carcinoma.
- Colorectal cancer other than adenocarcinoma, e.g., sarcoma, lymphoma, carcinoid.
- 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 study
- Use and/or receipt of the last dose of anti-cancer therapy (chemotherapy,
immunotherapy, endocrine therapy, targeted therapy, biologic therapy, tumor
embolization, monoclonal anti-bodies) or radiation therapy within 4 weeks prior to
receiving first dose of study therapy.
- Prior monoclonal antibody therapy within 4 weeks prior to first dose of FC-10 study
therapy or who has not recovered (i.e., less than or equal to grade 1 or at baseline)
from adverse events due to a previously administered agent.
- Neuropathy greater than grade 1.
- Active autoimmune disease requiring systemic treatment within the past 3 months or a
documented history of clinically severe autoimmune disease or a syndrome that requires
systemic steroids or immunosuppressive agents. Note: steroid use is permitted only as
indicated per protocol.
- Receipt of live attenuated vaccination within 30 days prior to study entry or within
- 30 days of receiving study therapy.
- Known history of hepatitis B or hepatitis C.
- Has known active central nervous system (CNS) metastases and/or carcinomatous
meningitis. Patients 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 and any neurologic symptoms have returned
to baseline), have no evidence of new or enlarging brain metastases, and are not using
steroids for at least 14 days prior to trial treatment.
- Active infection or chronic infection requiring systemic therapy.
- Known history of human immunodeficiency virus (HIV) or acquired
immunodeficiency-related (AIDS) illnesses.
- Prior therapy with an anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CD137, or anti-Cytotoxic
T-lymphocyte-associated antigen-4 (CTLA-4) antibody (including ipilimumab or any other
antibody or drug specifically targeting T-cell co-stimulation or checkpoint pathways)
is not allowed.
- History of allogeneic organ transplantation.
- Any of the following cardiac conditions:
- Documented NYHA Class III or IV congestive heart failure,
- Myocardial infarction within 6 months prior to study entry,
- Unstable angina within 6 months prior to study entry,
- Symptomatic arrhythmia.
- Active or prior documented inflammatory bowel disease (e.g., Crohn's disease,
- Ongoing or active gastritis or peptic ulcer disease.
- Presence of third space fluid which cannot be controlled by drainage. Active bleeding
- Known history of previous diagnosis of tuberculosis.
- History of hypersensitivity to pembrolizumab, pemetrexed, or oxaliplatin or any
excipients of these drugs.
- Known history or confirmation of active pneumonia, non-infectious pneumonitis that
requires steroids, current pneumonitis, symptomatic interstitial lung disease, or
definitive evidence of interstitial lung disease described on CT scan, MRI, or chest
x-ray in asymptomatic patients; dyspnea at rest requiring current continuous oxygen
- Major surgical procedure, open biopsy, or significant traumatic injury within 28 days
prior to randomization.
- Other malignancies unless the patient is considered to be disease-free and has
completed therapy for the malignancy greater than or equal to 12 months prior to study
entry. Patients with the following cancers are eligible if diagnosed and treated
within the past 12 months: carcinoma in situ of the cervix, and basal cell and
squamous cell carcinoma of the skin.
- Psychiatric or addictive disorders or other conditions that in the opinion of the
investigator would preclude the patient from meeting the study requirements or
interfere with interpretation of study results.
- Pregnancy or lactation at the time of study entry.
- Use of any investigational agent within 4 weeks prior to the first dose study therapy.