Status and phase
Conditions
Treatments
About
This is a single-arm, interventional, pilot clinical trial. Fifteen evaluable patients will have tumor-informed ctDNA testing at baseline and start botensilimab and balstilimab treatment. They will receive botensilimab and balstilimab in 6-week cycles until progression, after which mFOLFOX6 and bevacizumab or panitumumab will be added to the regimen. Subjects will have safety testing at baseline and every two weeks while on study drug. Study treatment with botensilimab and balstilimab, mFOLFOX6, and bevacizumab or panitumumab will be continued until radiographic or clinical progression, toxicity, or patient withdrawal. Subjects will have one safety follow up visit 30 days after the last treatment and will be followed for survival every 12 weeks for up to 2 years.
Full description
3.1 Study Description
This is a single-arm, interventional, pilot clinical trial. Subjects with newly diagnosed, metastatic or unresectable, microsatellite stable colorectal cancer without liver, bone, or brain metastases will undergo tumor-informed ctDNA collection then start study treatment with botensilimab and balstilimab alone. They will have restaging scans every 12 weeks and will have ctDNA and CEA repeated at every cycle. When the subject experiences radiographic progression per RECIST/iRECIST or clinical progression per investigator's assessment, mFOLFOX6 and either bevacizumab or panitumumab will be added to the study drug regimen. Subject will continue on the new combination until radiographic or clinical progression, intolerable toxicity, or patient withdrawal.
No more than 20 subjects will be enrolled to ensure the trial obtains 15 evaluable subjects. All patients will be enrolled at the Duke Cancer Institute.
Enrolled subjects are defined as subjects who give informed consent.
Screen failures are defined as subjects who give informed consent and do not meet eligibility criteria.
Accrued subjects are defined as subjects who give informed consent and meet eligibility criteria.
Study Treatment Botensilimab 75 mg IV Every 6 weeks for up to 4 doses Balstilimab 240 mg IV Every 2 weeks Oxaliplatin 85 mg/m2 IV Every 2 weeks Leucovorin 400 mg/m2 IV Every 2 weeks Fluorouracil 400 mg/m2 IV bolus Every 2 weeks Fluorouracil 2400 mg/m2 IV Every 2 weeks (over 46 hours) Bevacizumab 5 mg/kg IV Every 2 weeks Panitumumab 6 mg/kg IV Every 2 weeks
5.1 Screening Period
During the screening period, subjects are consented and screened for the study. Informed consent must be obtained before initiation of any screening procedure that is performed solely for the purpose of determining eligibility for this study. Evaluations performed as part of routine care before informed consent can be considered as screening evaluations if done within the defined screening period, and if permitted by the local institutional review board (IRB) policies. Study eligibility is based on meeting all of the inclusion criteria and none of the exclusion criteria before the first dose of study drug on Cycle 1 Day 1.
The following study procedures must be done within 28 days prior to Cycle 1 Day 1:
Inclusion and exclusion criteria
Demographics
Medical and cancer history
Physical examination
Height
Vital signs and weight
Concomitant medications
CT and/or MRI of chest, abdomen, and pelvis
ctDNA
CEA
PT/INR (prior to fresh tissue biopsy)
Fresh tissue biopsy
Archived tissue collection
Tuberculosis (TB) test
The following study procedures must be done or repeated within 7 days prior to Cycle 1 Day 1:
Subject eligibility is determined using lab results obtained up to 7 days prior to Cycle 1 Day 1. Any laboratory assessments repeated on Cycle 1 Day 1 must meet eligibility requirements. The screening period ends upon receipt of the first dose of study drug or final determination that the subject is ineligible for the study.
5.2 Treatment Period
During the treatment period, subjects will receive botensilimab every 6 weeks for up to 4 doses and balstilimab every 2 weeks for up to 2 years. Following progression on the doublet, mFOLFOX6 will be administered every 2 weeks. Investigators will choose between bevacizumab and panitumumab, which will be administered every 2 weeks. Cycle length is every 6 weeks, with study visits occurring every 2 weeks. A treatment window of ± 1 day is allowed for day 1 of cycle 2 and all subsequent cycles. The treatment period lasts until: 1) subject has been receiving balstilimab for 2 years; 2) disease progression; 3) the occurrence of unacceptable treatment-attributed toxicity; or 4) other reasons for subject discontinuation as described in Section 5.7. Toxicity-attributed dose modifications of any of the study drugs may occur during the Treatment Period.
After the completion of the first cycle, laboratory assessments may be obtained up to 1 day prior to treatment. If necessary, the treatment visit may be within ± 1 day of the scheduled day 1 for cycle 2 and all subsequent cycles. If clinically indicated, additional visits and/or safety assessments may be warranted.
The following study procedures must be completed on days 1, 15, and 29 of each cycle:
The following study procedures must be added to the above test/procedures on Day 1 of each cycle:
The following study procedures must be completed every 12 weeks (±1 week):
The following study procedures must be completed at time of progression on doublet therapy (any time prior to the start of chemotherapy administration):
Restaging scans will be performed every 12 weeks and disease response will be assessed using guidelines described in Section 5.6. The treatment period ends when a subject receives his or her last dose of study treatment; the subject then enters the follow-up period.
5.3 Follow-up Period
Subjects should return 30 (±7) days after their last dose of study drug for an end-of-treatment visit to complete the following study procedures:
Subjects will have a telephone visit with the study team at 90 (+/-7) days after the last dose of study drug to complete an AE assessment. Any delayed irAEs must be reported to the principal investigator. Subjects with adverse events (AEs) attributed to study drug that are ongoing at the time of this 90-day safety follow-up visit will continue to be followed unless the AE is deemed unresolvable or the subject has started a new anti-cancer treatment regimen.
For subjects who are discontinued from study treatment for reasons other than disease progression, subjects will have disease status (blood tumor markers and restaging scans per standard of care schedule) followed until disease progression or start of new anti-cancer treatment regimen. Disease status may be collected via personal interviews or review of medical records.
Subjects will be followed for survival up to 2 years after discontinuing the study drug regimen or until the study is closed (whichever comes first). Survival status may be collected by phone call or review of medical or public records every 12 (±2) weeks.
5.4 Laboratory Assessments
Local laboratories will perform all clinical laboratory tests using standard procedures, and results will be provided to the investigator. Abnormalities in clinical laboratory tests that lead to a change in subject management (e.g., dose modification, requirement for additional medication, treatment or monitoring) are considered clinically significant for the purposes of this study and will be recorded on the case report form (CRF). If laboratory values constitute part of an event that meets criteria defining it as serious, the event (and associated laboratory values) must be reported as a serious adverse event (SAE).
5.5 Adverse Event Assessment
AEs will be documented throughout the study. AE seriousness, grade, and relationship to study drug will be assessed by the investigator using NCI-CTCAE version 5.0.
5.6 Tumor Assessments
Tumor response will be assessed using RECIST v.1.1 and iRECIST. Radiographic imaging will be performed with CT scan of chest/abdomen/pelvis with and without contrast and/or MRI scan of abdomen/pelvis every 12 weeks. The same method for tumor assessment should be employed at every assessment.
5.7 Subject Discontinuation
Subjects will receive study treatment until treatment discontinuation for one of the reasons listed below. However, subjects may discontinue study treatment or withdraw their consent to participate in the study at any time without prejudice. All reasons for discontinuation or withdrawal from trial will be recorded.
Subjects who progress on the initial doublet regimen do not have to discontinue study treatment at that time. Rather, they will add mFOLFOX6 and either bevacizumab or panitumumab and continue on study treatment. Patients who have complete response or prolonged stable disease may also elect to end study therapy after a discussion with their treating physician and with approval of the principal investigator. Reasons for subject discontinuation may include, but are not limited to, the following:
Subject has been receiving balstilimab for 2 years
Death
Confirmed radiographic disease progression after switching to the botensilimab and balstilimab plus chemo/bev/pmab
Significant noncompliance by subject or investigator
Investigator or principal investigator determination that it is no longer safe and/or no longer in the subject's best interest to continue participation
Withdrawal of consent
Loss to follow-up
Necessity for treatment with other anticancer treatment prohibited by protocol
Sexually active subjects who refuse to follow the contraceptive guidelines
Women who become pregnant or are breast feeding
Request by regulatory agencies for termination of treatment of an individual subject or all subjects under the protocol
Discontinuation of treatment may be considered for participants who have attained a confirmed complete response (CR)
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Male or female participants who are at least 18 years of age on the day of signing informed consent.
Histologically confirmed metastatic and/or unresectable colorectal cancer without liver metastasis or known or suspected bone or brain metastases.
a. Up to 3 patients with peritoneal carcinomatosis will be included. Other than those three, subjects must only have lung, lymph node, and locoregional sites of disease (primary tumor or serosal implant without carcinomatosis).
Microsatellite stable disease.
Subject must be willing to provide fresh biopsy of tumor lesion. Those who do not have a tumor lesion that is safe and amenable to biopsy may still be enrolled.
ECOG performance status of 0 or 1.
No prior systemic therapy for colon cancer.
a. Subjects who received systemic therapy in the neoadjuvant or adjuvant setting may be eligible with approval from the principal investigator.
Measurable disease per RECIST v1.1.
Female participants must not be pregnant or breastfeeding and meet at least one of the following conditions:
Male participants must practice effective contraceptive methods during the treatment period, unless documentation of infertility exists.
Expected to survive >3 months per investigator assessment.
The participant (or legally acceptable representative if applicable) provides written informed consent for the trial.
Adequate organ function as defined below. Specimens must have been collected within 7 days prior to the start of study treatment:
Exclusion criteria
Prior therapy with an immune checkpoint inhibitor.
A WOCBP who is pregnant or breastfeeding or has a positive pregnancy test within 72 hours prior to receiving study treatment.
Not willing to use an effective method of birth control as defined in the protocol.
Known liver, bone, or CNS metastases and/or carcinomatous meningitis.
Diagnosis of other carcinomas within the last 2 years, except cured non-melanoma skin cancer, treated thyroid cancer, curatively treated in-situ cervical cancer, or localized prostate cancer treated curatively with no evidence of biochemical or imaging recurrence.
Documented history of clinically significant autoimmune disease or syndrome that requires systemic steroids or immunosuppressive agents. Subjects with vitiligo, type 1 diabetes mellitus, psoriasis not requiring systemic treatment, well-controlled hypothyroidism, or conditions not expected to recur in the absence of an external trigger are permitted to enroll.
Any history of chronic or autoimmune pancreatitis.
Known history of or any evidence of active, non-infectious pneumonitis.
Current use of medications specified by the protocol as prohibited for administration in combination with study drug.
Received a live vaccine within 30 days prior to the start of study drug.
Recent or current active infectious disease requiring systemic antivirals, antibiotics, or antifungals, or treatment within 2 weeks prior to the start of study drug.
Concurrent severe and/or uncontrolled medical conditions, which may compromise participation in the study, including impaired heart function or clinically significant heart disease.
Major surgical procedure, open biopsy, or significant traumatic injury within 28 days prior to the start of study drug (56 days for hepatectomy, open thoracotomy, major neurosurgery) or anticipation of need for major surgical procedure during the course of the study.
Serious, non-healing wound, ulcer, or bone fracture.
Patients with a history of organ or allogenic hematopoietic stem cell transplantation.
Partial or complete bowel obstruction within the last 3 months, signs/ symptoms of bowel obstruction, or known radiologic evidence of impeding obstruction.
Refractory ascites defined as requiring 2 or more therapeutic paracenteses within the last 4 weeks or ≥4 times within the last 90 days or ≥1 time within the last 2 weeks prior to study entry or requiring diuretics within 2 weeks of study entry.
Positive tuberculosis test at screening.
Primary purpose
Allocation
Interventional model
Masking
15 participants in 1 patient group
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Central trial contact
Emily Bolch
Data sourced from clinicaltrials.gov
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