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Platform Study of Neoadjuvant and Adjuvant Immunotherapy for Patients With Resectable Adenocarcinoma of the Pancreas

A Platform Study of Combination Immunotherapy for the Neoadjuvant and Adjuvant Treatment of Patients With Surgically Resectable Adenocarcinoma of the Pancreas

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02451982
Enrollment
76
Registered
2015-05-22
Start date
2016-03-28
Completion date
2026-05-31
Last updated
2025-12-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pancreatic Cancer

Brief summary

This platform trial will evaluate various immunotherapy combinations given in the neo-adjuvant and adjuvant setting in patients with surgically resectable pancreatic ductal adenocarcinoma.

Detailed description

Immunotherapy is an innovative approach being developed for the treatment of pancreatic cancer, a lethal and relatively chemotherapy-resistant disease. However, the tumor and its environment have developed a number of ways in which they inhibit the function of the immune system preventing it from recognizing and killing the cancer. In addition, the investigators still do not understand how T cells, the cells in the immune system that have the potential to recognize cancer as different and kill cancer cells, traffic into the tumor to accomplish their task. The investigators are currently testing an immune system activating pancreatic cancer vaccine (known as GVAX) in combination with immune boosting doses of the chemotherapy agent, cyclophosphamide, as preoperative and postoperative treatments for pancreatic cancer. The investigators have discovered tertiary lymphoid aggregates, a unique lymph node-like structure formed within resected tumors from the patients who received the vaccine two weeks prior to the surgery. This discovery demonstrates that the immune system can get into the tumor and provides the investigators with the opportunity to better understand how these immune cells traffic into the tumor and function once they arrive. The investigators also found that the vaccine causes an increase in signals that would suppress the immune system's ability to fight off cancer cells, including signals involving PD-1. In this novel study, the investigators will test the effects of blocking PD-1 in combination with the vaccine in patients with pancreatic cancer. The investigators will specifically isolate these immune cells and evaluate at both the genetic and protein level, the types of signals expressed by these aggregates. The investigators will compare aggregates from patients with long term survival versus patients who succumb to their cancer early. In this way, the investigators will be able to determine how safe this novel treatment is, how effective it is at changing the immune system in pancreatic cancer, and how it impacts the health and survival of pancreatic cancer patients who undergo surgery to remove the cancer.

Interventions

DRUGCyclophosphamide

200 mg/m2 IV

BIOLOGICALGVAX pancreatic cancer

5x10\^8 cells intradermal injection

DRUGNivolumab

480 mg IV

8 mg IV

2400 mg IV

Sponsors

National Cancer Institute (NCI)
CollaboratorNIH
Bristol-Myers Squibb
CollaboratorINDUSTRY
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Newly diagnosed or clinically-suspected adenocarcinoma of the head, neck, or uncinate process of the pancreas * Tumor must be surgically resectable * ECOG Performance Status of 0 to 1 * Adequate organ function as defined by study-specified laboratory tests * Must agree to use acceptable form of birth control

Exclusion criteria

* Received any type of anti-cancer treatment or immunotherapy for pancreas cancer * History of autoimmune disease (Graves or Hashimoto's disease, vitiligo, and type I diabetes are allowed) * Systemically steroid use within 14 days * Evidence of active infection * Pregnant or lactating * Diagnosed with another cancer or myeloproliferative disorder (some exceptions) * History of severe hypersensitivity reaction to any monoclonal antibody or known component of the study drugs * Known history of infection with HIV, hepatitis B, or hepatitis C * Oxygen saturation of \<92% on room air by pulse oximetry * On home oxygen

Design outcomes

Primary

MeasureTime frameDescription
Intratumoral CD8+CD137+cells4 yearsFold change of intratumoral CD8+CD137+cells before and after neoadjuvant therapy (Arms B and C only)
IL17A expression4 yearsmedian IL17A expression in lymphoid aggregates from resected tumor (Arms A and B only)
Intratumoral granzyme B+PD-1+CD137+ cells4 yearsPercent change of intratumoral granzyme B+PD-1+CD137+ cells in surgical (post-treatment) tissue compared to baseline (pre-treatment) biopsy (Arm D only)
Pathologic Response4 yearsPercent of patients with a response grade of 0-2 (0=complete response 1=marked response, 2=moderate response) at time of surgery

Secondary

MeasureTime frameDescription
Overall Survival4 yearsOverall Survival is defined as the time from surgery to death from any cause
Disease Free Survival4 yearsDisease Free Survival is defined as the time from surgery until evidence of disease recurrence or death from any cause
Drug-Related Adverse Events4 yearsNumber of participants experiencing study drug-related toxicities

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026