Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07407231

Combined Chemotherapy And Ablative Radiotherapy (SBRT) As First-Line Treatment In Locally Advanced Inoperable Pancreatic Cancer (SBRT-PANC)

Led by Institute of Oncology Ljubljana · Updated on 2026-02-17

18

Participants Needed

1

Research Sites

278 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This prospective interventional clinical study evaluates the efficacy and safety of combining systemic chemotherapy followed by ablative stereotactic body radiotherapy (SBRT) as first-line treatment in adult patients with locally advanced, inoperable pancreatic cancer. The study aims to determine the response rate after SBRT delivered following initial chemotherapy, as well as time to disease progression and treatment-related toxicity. Patients receive standard first-line chemotherapy and, in the absence of disease progression, undergo ablative SBRT to the primary tumor, followed by continuation of systemic therapy according to clinical practice. The study is conducted in Slovenia, with patient enrollment expanded to additional participating clinical centers following an approved amendment.

CONDITIONS

Official Title

Combined Chemotherapy And Ablative Radiotherapy (SBRT) As First-Line Treatment In Locally Advanced Inoperable Pancreatic Cancer (SBRT-PANC)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years and older
  • Locally advanced, inoperable pancreatic cancer
  • Treated with first-line systemic chemotherapy followed by stereotactic body radiotherapy (SBRT) at participating centers
  • Ability to provide written informed consent
Not Eligible

You will not qualify if you...

  • Metastatic pancreatic cancer
  • Prior systemic therapy for locally advanced pancreatic cancer (one or more previous lines of systemic treatment)
  • Disease progression after initial chemotherapy prior to SBRT
  • Any condition that would interfere with study participation or evaluation according to the investigator

AI-Screening

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Trial Site Locations

Total: 1 location

1

Institute of Oncology Ljubljana

Ljubljana, Slovenia, 1000

Actively Recruiting

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Research Team

J

Janja Ocvirk, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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