Pembrolizumab in Early Stage Colon Cancer

Colon Cancer Clinical Trial

Official title:

A Window of Opportunity Study of Pembrolizumab in Colon Cancer

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04231526
• Other study ID #: IRB19-1411
• Status: Recruiting
• Phase: Phase 2
• Start date: May 20, 2020
• Est. completion date: March 19, 2025

Study information

• Verified date: April 2023
• Source: University of Chicago
• Contact: Daniel Catenacci, MD
• Phone: 773-702-2042
• Email: dcatenacci[@]medicine.bsd.uchicago.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study will gather information on the safety and effectiveness of pembrolizumab, an immunotherapy drug. The purpose of this study is to target early stage colon cancer before it has developed resistance to immunotherapy.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 46
• Est. completion date: March 19, 2025
• Est. primary completion date: March 19, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Patients must have histologically confirmed colon adenocarcinoma.

2. No prior chemotherapy, targeted therapy, or immunotherapy for colon cancer.

3. Deemed to have surgically resectable disease.

4. Archival tissue block containing colon adenocarcinoma must be confirmed available prior to enrollment. MSI testing should be obtained prior to starting therapy.

5. Be willing and able to provide written informed consent/assent for the trial.

6. Be 18 years of age or older on day of signing informed consent.

7. Have a measurable primary lesion by lower endoscopy or CT-imaging with a diameter of 1 or more centimeters.

8. Have a performance status of 0 or 1 on the ECOG Performance Scale.

9. Have no histologically confirmed disseminated disease by CT or PET-CT staging.

10. Male participant must agree to use a contraception as detailed in Appendix 3 of this protocol during the treatment period and for at least 120 days after the last dose of study treatment and refrain from donating sperm during this period.

11. A female participant is eligible to participate if she is not pregnant (see Appendix

3), not breastfeeding, and at least one of the following conditions applies:

1. Not a woman of childbearing potential (WOCBP) as defined in Appendix 3 OR

2. A WOCBP who agrees to follow the contraceptive guidance in Appendix 3 during the treatment period and for at least 90 days after the last dose of study treatment.

12. Demonstrate adequate organ function as defined below. All screening labs should be performed within 14 days of treatment initiation.

• Adequate Organ Function Laboratory Values
• Hematological
• Absolute neutrophil count (ANC) - =1500/µL
• Platelets - =100 000/µL
• Hemoglobin - =7.0 g/dL or =5.6 mmol/La
• Renal
• Creatinine OR measured or calculated creatinine clearance (GFR can also be used in place of creatinine or CrCl) - =1.5 × ULN OR
• 30 mL/min for participant with creatinine levels >1.5 × institutional ULN
• Hepatic
• Total bilirubin - =1.5 ×ULN OR direct bilirubin =ULN for participants with total bilirubin levels >1.5 × ULN
• AST (SGOT) and ALT (SGPT) - =2.5 × ULN (=5 × ULN for participants with liver metastases)
• Coagulation
• International normalized ratio (INR) OR prothrombin time (PT)/ Activated partial thromboplastin time (aPTT) - =1.5 × ULN unless participant is receiving anticoagulant therapy as long as PT or aPTT is within therapeutic range of intended use of anticoagulants
• ALT (SGPT)=alanine aminotransferase (serum glutamic pyruvic transaminase); AST (SGOT)=aspartate aminotransferase (serum glutamic oxaloacetic transaminase); GFR=glomerular filtration rate; ULN=upper limit of normal.
• Criteria must be met without erythropoietin dependency and without packed red blood cell (pRBC) transfusion within last 2 weeks.
• Creatinine clearance (CrCl) should be calculated per institutional standard. Note: This table includes eligibility-defining laboratory value requirements for treatment; laboratory value requirements should be adapted according to local regulations and guidelines for the administration of specific chemotherapies.

Exclusion Criteria:

1. A WOCBP who has a positive urine pregnancy test during screening (see Appendix 3). If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required.

2. Is currently participating and receiving study therapy or has participated in a study of an investigational agent and received study therapy or used an investigational device within 4 weeks of the first dose of treatment.

3. 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.

4. Has a known history of active TB (Bacillus Tuberculosis)

5. Known hypersensitivity to pembrolizumab or any of its excipients.

6. If subject received major surgery, they must have recovered adequately from the toxicity and/or complications from the intervention prior to starting therapy.

7. 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.

8. Has known active central nervous system (CNS) metastases and/or carcinomatous meningitis.

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 (e.g., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a form of systemic treatment.

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 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.

13. Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial.

14. Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent.

15. Has a known history of Human Immunodeficiency Virus (HIV) (HIV 1/2 antibodies).

16. Has known active Hepatitis B (e.g., HBsAg reactive) or Hepatitis C (e.g., HCV RNA [qualitative] is detected).

17. Has received a live vaccine within 30 days of planned start of study therapy.

18. Is pregnant or breastfeeding, or expecting to conceive or father children within the projected duration of the study, starting with the screening visit through 120 days after the last dose of trial treatment.

19. Has complications from colon cancer including but not limited to organ fistulas, bleeding and obstruction.

Related Conditions & MeSH terms

• Colon Cancer
• Colonic Neoplasms

Intervention

Drug:
• Pembrolizumab
2 cycles of neoadjuvant pembrolizumab (200mg IV every 21 days)

Procedure:
• Surgery
Standard of care surgery

Locations

Country	Name	City	State
United States	University Of Chicago Medicine Comprehensive Cancer Center	Chicago	Illinois
United States	Decatur Memorial Hospital	Decatur	Illinois

Sponsors (2)

Lead Sponsor	Collaborator
University of Chicago	Merck Sharp & Dohme LLC

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To measure the feasibility of neoadjuvant pembrolizumab in early stage colon cancer	Measured using RECIST 1.1	14 months
Secondary	Measure the tumor response in early stage colon cancer after neoadjuvant pembrolizumab	Measured using RECIST 1.1	14 months
Secondary	Measure the immune response in early stage colon cancer after neoadjuvant pembrolizumab	Measured using RECIST 1.1	14 months