Exploring Photon-Counting CT for Enhanced Target Delineation and Dose Accuracy in Personalized Radiotherapy - ANTHEM

NCT ID: NCT07098247

Last Updated: 2025-08-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

500 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-04-04

Study Completion Date

2027-05-31

Brief Summary

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Radiotherapy remains a cornerstone of oncology care, particularly for rare or orphan cancers and chronic oncologic and rare non oncologic conditions, where precision and individualized treatment planning are necessary. Advances in imaging technologies are crucial to overcome the challenges posed by these cases, especially in achieving accurate tumor delineation and dose delivery. Photon-counting CT (PCCT) represents a transformative step forward in imaging technology. Unlike conventional energy-integrating CT, PCCT offers a) superior spatial resolution, enabling clearer visualization of tumor margins and fine anatomical structures, b) enhanced tissue characterization, allowing better differentiation between tumor tissues and normal tissue; c) spectral imaging capabilities, facilitating improved dose calculations. These attributes are particularly advantageous in high-precision radiotherapy techniques, such as stereotactic body radiotherapy (SBRT) or proton therapy, where small errors in target delineation or dose delivery can significantly impact treatment outcomes. However, very limited data reporting the clinical use of PCCT for RT planning are available.

Detailed Description

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Conditions

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Cancer

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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patient with cancer

500 patients undergoing radiotherapy for orphan cancers, chronic conditions, and anatomically complex regions such as brain, head and neck, thorax, liver, pancreas and pelvis.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* ≥18 years old patients
* tumors located in challenging anatomical regions (brain, head and neck, liver, pancreas prostate), or Cardiac disease requiring RT by photon or proton at our Institution.

Exclusion Criteria

\- 18 years old patients
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Istituto Clinico Humanitas

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Marta Scorsettti, MD, radiation oncologist

Role: PRINCIPAL_INVESTIGATOR

Humanitas University

Locations

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IRCCS Humanitas Research Hospital

Rozzano, Milan, Italy

Site Status RECRUITING

Countries

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Italy

Central Contacts

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Research study coordinator

Role: CONTACT

+39 0282247026

Research nurse

Role: CONTACT

+39 0282248513

Other Identifiers

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RAD4/RT_ANTHEM

Identifier Type: -

Identifier Source: org_study_id

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