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Hemithoracic Arc Radiotherapy Post Pleural Decortication

Hemithoracic Volumetric Modulated Arc Radiotherapy as Part of Lung-Sparing Multimodality Therapy in Patients With Malignant Pleural Mesothelioma Phase II Trial

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06910449
Enrollment
45
Registered
2025-04-04
Start date
2024-11-11
Completion date
2027-02-28
Last updated
2025-04-08

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

Conditions

Malignant Pleural Mesothelioma

Brief summary

Malignant Pleural Mesothelioma is an aggressive and refractory disease , the most aggressive treatment plan offered to these patients include trimodalitiy approach with chemotherapy as the mainstay of treatment . the rationale of post operative Radiotherapy is to sterilize the post operative volume to reduce local failure meanwhile minimizing toxicities in this trial we are going to assess the safety and efficacy of Radiotherapy in Mesothelioma patients poat Pleural decortication

Detailed description

This study will include malignant Pleural Mesothelioma patients treated by trimodalitiy approach starting with neoadjuvant chemotherapy followed by surgery in the form of Pleural decortication then all patients will receive post operative hemithoracic radiation

Interventions

RADIATIONhemithoracic Volumetric Arc Radiotherapy post Pleural decortication

post operative delivery of hemithoracic Volumetric Arc Radiotherapy

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

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

Inclusion criteria

* Evidence of metastatic disease. * Underwent Pleural decortication. * Able to provide informed consent.

Exclusion criteria

* Poor pulmonary function tests. * Recurrent or palliative cases. * Inability to attend full course of Radiotherapy or follow up visits.

Design outcomes

Primary

MeasureTime frameDescription
Acute Radiation Toxicityweekly assessment during radiation course and monthly follow up for the first 6 monthsQuestionnaire based Follow up about acute Radiation toxicity according to RTOG including dysnea , cough , chest pain , dysnea on effort from grade 1-5
late radiation toxicityBi-monthly fashion of minimum 6 months post radiation coursefollow up of patients using both Questionnaire and performing pulmonary function tests and Echo , focusing on DLCO & FEV1

Countries

Egypt

Contacts

Primary ContactGamal
Esraa.gamal@nci.cu.edu.eg01000704731

Outcome results

None listed

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