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Recruiting

NCT Number: NCT07744074

Phase I Study of Carbon-Ion Lattice Radiotherapy for Large Thoracic Tumors

This is the first prospective clinical study to evaluate the efficacy and safety of induction chemoimmunotherapy followed by carbon ion radiotherapy and consolidation immunotherapy in patients with unresectable locally advanced non-small cell lung cancer (NSCLC). Based on this prospective study, tumor tissue, blood, urine, and stool samples from participants will be collected and analyzed to identify predictive markers of treatment response.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age ≥ 18 years old;
  • Pathologically confirmed thoracic solid malignant tumors;
  • Local recurrence or failure of prior standard therapies (including surgery, radiotherapy, systemic therapy, etc.), deemed unsuitable for or lacking standard treatment options following Multidisciplinary Team (MDT) evaluation, and planned to receive heavy-ion radiotherapy;
  • Maximum diameter of the target lesion ≥ 4.5 cm;
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0-2;
  • Life expectancy ≥ 6 months;
  • Signed informed consent.

Exclusion criteria

  • Tumors adjacent to critical organs at risk (OARs) where dose constraints cannot be met through plan optimization;
  • Prior radiotherapy to the intended treatment area, where re-irradiation would fail to meet normal tissue dose constraints;
  • Presence of recognized standard treatment options for which the patient is eligible (e.g., radical surgery, concurrent chemoradiotherapy, or standard systemic therapy);
  • Primary hematologic malignancies;
  • Uncontrolled severe comorbidities, including active infections, unstable cardiovascular or cerebrovascular diseases, and severe hepatic or renal insufficiency;
  • Other diseases deemed by the investigator to compromise patient safety;
  • Psychiatric disorders or cognitive impairment that would prevent cooperation with treatment;
  • Pregnancy or lactation.

Treatment and study plan

Carbon ion - Lattice radioIon Lattice Radiation Therapy for Thoracic bulky solid tumors

Radiation

Carbon ion - Lattice radioIon Lattice Radiation Therapy for Thoracic bulky solid tumors

Primary outcomes

  1. Dose-Limiting Toxicities

    Time frame: 90 days

    To determine the dose-limiting toxicities (DLTs) of carbon ion - lattice radiotherapy (CI-LRT) in this population.

Study contacts

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

Qingren Lin

CONTACT

[email protected]

0086-571-88122088

Yongling Ji, MD

CONTACT

[email protected]

0086-571-88122088

Sponsors and collaborators

Lead sponsor

Ji Yongling

Other

Registry information

Official study title

A Single-Arm Phase I Clinical Study of Carbon-Ion Lattice Radiotherapy for Large Thoracic Malignant Tumors

Acronym: CILAT-I

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Aug 4, 2026
Registry last updated
Aug 4, 2026

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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