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Intraoperative Radiation Therapy After Stereotactic Body Radiation Therapy and Chemotherapy in Treatment of Pancreatic Adenocarcinoma

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Johns Hopkins Medicine

Status and phase

Enrolling
Phase 1

Conditions

Pancreatic Cancer

Treatments

Radiation: High Dose Rate Brachytherapy (HDR) Intraoperative Radiation Therapy (IORT)

Study type

Interventional

Funder types

Other

Identifiers

NCT05141513
IRB00294801 (Other Identifier)
J21105

Details and patient eligibility

About

This study is designed to investigate the safety of intraoperative radiation therapy (IORT) in patients with localized pancreatic cancer undergoing surgical resection after neoadjuvant chemotherapy and stereotactic body radiation therapy (SBRT).

Full description

Standard of care treatment for patients with non-metastatic pancreatic adenocarcinoma (PDAC) includes chemotherapy and Stereotactic Body Radiation Treatment (SBRT) followed by surgical resection of the tumor with or without Intra-Operative Radiation Therapy (IORT).

There is some evidence from other research studies suggesting that adding radiation treatment during the surgical resection may improve local control of the cancer. The use of IORT plus surgical resection can be used to treat pancreatic cancer and is done on a case by case basis at Johns Hopkins.

The department of Radiation Oncology has developed a program using a High Dose Rate-IORT (HDR-IORT). The HDR-IORT makes it possible to deliver concentrated radiation dose at the surface of the tumor.

Our team has shown in previous studies that the majority of cancer cells that remain after treatment are located around the area of the pancreas called the "Triangle Volume" (TV). This region contains blood vessels, lymphatic vessels, and nerves, and is at high risk of containing cancer cells. This region is difficult to treat with SBRT alone because of being close to normal, healthy organs. Therefore, this study involves using IORT to treat the TV to a therapeutic radiation dose.

The part of the treatment that is considered research is:

  • Giving one dose of 15 Gy during the surgery using IORT to deliver radiation, and
  • Targeting the larger area around the pancreas called the TV

The goal of this study is to determine safety of this added treatment which will be assessed at 3 months after the surgery is completed.

Enrollment

25 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age > 18 years old
  2. Resectable/BRPC/LAPC as defined by NCCN guidelines (Figure 1) as follows confirmed via CT, EUS, or other imaging modalities.
  3. ECOG performance status 0-2
  4. Subject or authorized representative, has been informed of the nature of the study and has provided written informed consent, approved by the appropriate Institutional Review Board (IRB) of the respective clinical site.
  5. Candidate for SBRT at JHU
  6. Upfront treatment with multi-agent chemotherapy
  7. Candidate for surgical exploration at JHU

Exclusion criteria

  1. Previous thoracic/abdominal radiation therapy
  2. Unable to receive SBRT at JHU
  3. Duodenal invasion detected on imaging which would exclude candidacy for SBRT
  4. Tumor located in pancreatic body or tail
  5. Unable to undergo Whipple procedure
  6. Evidence of disease not localized to the pancreas
  7. Any arterial reconstruction during surgery
  8. Currently enrolled in another investigational drug or device trial that clinically interferes with this study
  9. Unable to comply with study requirements or follow-up schedule
  10. Women of child bearing potential or sexually active fertile men with partners who are women of child bearing potenital who are unwilling or unable to use an acceptable method to avoid pregnancy for the entire study

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

25 participants in 1 patient group

Intra Operative Radiation Therapy (IORT) Group
Other group
Description:
The IORT group is the single arm of this study. Enrolled patients who undergo standard of care treatment will also receive a study treatment of High Dose Rate (HDR) Intra Operative Radiation Therapy.
Treatment:
Radiation: High Dose Rate Brachytherapy (HDR) Intraoperative Radiation Therapy (IORT)

Trial contacts and locations

1

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Central trial contact

Amol Narang, MD; Dana B Kaplin, MPH

Data sourced from clinicaltrials.gov

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