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NCT Number: NCT05424159

Ablative Carbon Ion Radiotherapy With Pencil Beam Scanning for Locally Advanced Unresectable Pancreatic Cancer

The aim of this study is to investigate the clinical efficacy and safety of ablative carbon ion radiotherapy for locally advanced unresectable pancreatic cancer with pencil beam scanning and simultaneous integrated boost (SIB) technology.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

The aim of this study is to investigate the clinical efficacy and safety of ablative carbon ion radiotherapy for locally advanced unresectable pancreatic cancer using pencil beam scanning and simultaneous integrated boost technology with respect to toxicity and tumor control. All enrolled patients will receive carbon ion radiotherapy for the primary pancreatic lesions, positive lymph nodes, and retroperitoneal high-risk recurrence areas. The prescription dose for primary pancreatic lesion, positive lymph node, and retroperitoneal high-risk recurrence area is 67.5 Gy (RBE weighted dose) in 15 fractions for 3 weeks; Pancreatic primary lesion and positive lymph node SIB to 75 Gy (RBE weighted dose) in 15 fractions for 3 weeks. The primary endpoint is 2-year cumulative local regional progression rate (LRP), and the secondary endpoint is to assess the overall survival (OS) and toxicities. Toxicity was assessed using the Common Adverse Event Evaluation Criteria (CTCAE) Version 5.0, and safety and toxicity will be assessed by clinical examination, laboratory examination, and imaging (including CT, MRI, and/or PET/CT).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Have the ability to sign the written informed consent;
  • Ductal adenocarcinoma of the pancreas confirmed by histopathology or cytopathology;
  • Distant metastasis was excluded by imaging assessment (PET-CT, cranial MRI), and was defined as locally advanced unresectable according to NCCN Guidelines Version 2022.1, that is, T4N0-2M0, Stage III (AJCC/UICC Version 8);
  • The maximum diameter of pancreatic primary lesion and positive lymph node ≤7cm;
  • Pancreas primary lesion or positive lymph node did not invade digestive tract (stomach, duodenum and small intestine);
  • Eastern Cooperative Oncology Group (ECOG) performance score 0-1;
  • Adequate bone marrow function (neutrophil count ≥1.5×109/L, platelet count ≥100×109/L, hemoglobin ≥10.0g/dL);
  • Adequate liver function (total bilirubin <1.5 times the upper limit of normal value, aminotransferase <2.5 times the upper limit of normal value);
  • Adequate renal function (serum creatinine <2mg/dL, or creatinine clearance >50mL/min).

Exclusion criteria

  • Multiple primary pancreatic lesions (>1);
  • Tumor invaded the adjacent digestive tract;
  • Radiation therapy history;
  • Other local treatments history for pancreatic cancer, such as HIFU and irreversible electroporation;
  • The irradiation dose of organs at risk cannot reach the dose constraint;
  • Other malignant tumors history;
  • Inability to understand the purpose of treatment or unwillingness/inability to sign informed consent.

Treatment and study plan

Carbon Ion Radiotherapy

Radiation

Patients with locally advanced unresectable pancreatic cancer without invasion of gastrointestinal tract will received ablative carbon ion radiotherapy. The prescription dose for primary pancreatic lesion, positive lymph node, and retroperitoneal high-risk recurrence area is 67.5 Gy (RBE weighted dose) in 15 fractions for 3 weeks; Pancreatic primary lesion and positive lymph node SIB to 75 Gy (RBE weighted dose) in 15 fractions for 3 weeks.

Primary outcomes

  1. 2-year cumulative local regional progression rate (LRP)

    Time frame: From the date of the initiation of radiotherapy until the date of first documented occurrence of local regional progression, assessed up to 24 months.

    LRP was defined as the percentage of patients with local disease progression (within irradiated area) in the intentional population.

Secondary outcomes

  1. 2-year Overall survival (OS)

    Time frame: From the date of diagnosis until the date of death from any cause, assessed up to 24 months.

    OS was defined as the percentage of patients dead in the intentional population.

  2. Acute toxicity

    Time frame: From the date of the initiation of radiotherapy until the date of 3 months after radiotherapy.

    Toxicity was assessed using Common Terminology Criteria for Adverse Events (CTCAE) version 5.0. Safety and toxicity will be assessed by clinical examination, laboratory examination, and imaging (including CT, MRI, and/or PET/CT).

  3. Late toxicity

    Time frame: 3 months after radiotherapy.

    Toxicity was assessed using Common Terminology Criteria for Adverse Events (CTCAE) version 5.0. Safety and toxicity will be assessed by clinical examination, laboratory examination, and imaging (including CT, MRI, and/or PET/CT).

Study contacts

Contact information is provided by the study sponsor or research team.

Guo-Liang Jiang, MD

CONTACT

[email protected]

+86-02138296606

Zheng Wang, MD, PhD

CONTACT

[email protected]

+86-02138296666 ext. 53407

Sponsors and collaborators

Lead sponsor

Shanghai Proton and Heavy Ion Center

Other

Registry information

Official study title

Prospective Phase II Clinical Trial of Ablative Carbon Ion Radiotherapy With Pencil Beam Scanning Using Simultaneous Integrated Boost for Locally Advanced Unresectable Pancreatic Cancer

Important dates

Study start
2022
Primary completion
2025
Study completion
2026
First posted
Jun 21, 2022
Registry last updated
Dec 7, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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