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Retrospective Study of Radio-induced Toxicities in the Treatment of Lung Cancer With Tomotherapy

Retrospective Study of Radio-induced Toxicities in the Treatment of Lung Cancer With Tomotherapy

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05883735
Acronym
ETRICAPT
Enrollment
318
Registered
2023-06-01
Start date
2023-05-01
Completion date
2023-12-01
Last updated
2024-01-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung Cancer

Keywords

Tomotherapy, Toxicity

Brief summary

Lung cancers treated by Tomotherapy represent between 60 and 100 patients per year at the CHR of Metz-Thionville. Some patients were observed to present acute toxicities during treatment such as dysphagia or esophagitis of CTCAE grade \> 2. Beyond well known therapeutic and comorbidities factors, the pathophysiology of these events is largely ruled by a constitutional factor - the enzymatic equipment allowing more or less good repair of the DNA lesions induced by radiotherapy (RT). This equipment is characteristic of each individual, hence the term individual radiosensitivity (IR).The scientific literature is rather poor in data describing the frequency of these toxicities in patients receiving RT for lung cancer. The objective of this study is to describe the frequency of acute and late toxicities after normofractionated radiotherapy of 66 Gy in 33 fractions in patients with small cell or non-small cell lung cancer, stage 2 or 3.

Interventions

None listed

Sponsors

Centre Hospitalier Régional Metz-Thionville
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* stage II-III non-small cell or small cell lung cancer treated with normo-fractionated radiotherapy of 66Gy in 33 fractions using Tomotherapy

Exclusion criteria

* patient who refused to be included in the study.

Design outcomes

Primary

MeasureTime frameDescription
late toxicity of radiotherapyup to 2 years after tomotherapy treatmentaccording to CTCAE v5.0 grading

Secondary

MeasureTime frameDescription
acute toxicity of radiotherapy6 months following tomotherapy treatmentaccording to CTCAE v5.0 grading

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026