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CPAP or BiPAP for Motion Mitigation During Radiotherapy

Continuous and Bi-level Positive Airway Pressure for Motion Mitigation of Intra-thoracic Tumors Treated With Radiotherapy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04986293
Acronym
SISTER
Enrollment
31
Registered
2021-08-02
Start date
2021-06-01
Completion date
2027-12-01
Last updated
2026-05-04

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

Conditions

Esophageal Cancer, Malignant Lymphoma, NSCLC, Radiotherapy Side Effect

Keywords

BiPAP, CPAP, Mechanical ventilation

Brief summary

When using highly conformal radiotherapy techniques, such as proton therapy, a controlled breathing pattern and a minimal breathing amplitude could greatly benefit the treatment of mobile tumors. This reduction in tumor motion may be achieved with the use of a ventilator that is able to regulate and modulate the breathing pattern. CPAP provides a constant level of positive airway pressure. Compared to spontaneous breathing, the use of CPAP increased lung volume and can result in a significant decrease in tumor movement and a significant decrease in both mean lung and mean heart radiation dose. These results were found in patients treated for limited stage disease, it is not clear if this approach is feasible for patients with more advanced stage of disease that undergo radiotherapy with curative intent. With Bilevel Positive Airway Pressure (BiPAP), tidal volume excursions are determined by the pressure difference between the set inspiratory positive airway pressure (IPAP) and the set expiratory positive airway pressure (EPAP). This mode of ventilation increases lung volume comparable to CPAP, but also to control tidal volumes and breathing frequency. However, BiPAP has never been studied in the setting of motion mitigation during radiotherapy and BiPAP might be more difficult to adjust to for patients compared to CPAP. Therefore, the current study is proposed to evaluate whether or not CPAP or BiPAP is of benefit in patients that undergo radiotherapy for larger intra-thoracic tumor volumes.

Detailed description

The study will follow a 2-step approach. First (Phase 1, n=10), the feasibility of short-term use of CPAP and BiPAP and its effects on (regional) lung volumes, tidal volumes and breathing frequency will be investigated in patients with intra-thoracic tumors who are planned for radiotherapy. This is necessary to select the best setting of CPAP or BiPAP with which minimal tumor motion is expected (and that is feasible for the patient). In the second phase (n=21), the particular setting found in fase 1 is investigated: weekly repeated radiotherapy planning (4D) CT scans with and without CPAP/BiPAP will be aquired to evaluate the influence on tumor motion and dose to the target and organs at risk. Radiotherapy will be deliverd according to local protocol without the use of CPAP/BiPAP.

Interventions

DEVICECPAP

Different settings of CPAP and BiPAP will be tested using a home mechanical ventilator

Sponsors

University Medical Center Groningen
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

* Age ≥18 years * Stage III/IV (N)SCLC, esophageal cancer or malignant lymphoma that will be treated with curative intent * WHO 0-2. * Written informed consent

Exclusion criteria

* Facial deformations so that facial mask is impossible to fit * Noncompliance with any of the inclusion criteria. * Planned for radiotherapy with fraction dose ≥3 Gy. * Severe heart failure (LVEF\<30%)

Design outcomes

Primary

MeasureTime frameDescription
Lung volume changes induced by the use of mechanical ventilation2-3 hours of measurement (only once)The primary objective is to evaluate the lung volume changes (in cm3) induced by the use of mechanical ventilation

Secondary

MeasureTime frameDescription
Feasibility of mechanical ventilationonce every week up to a maximum of 5 consecutive weeks (depending on the duration of the course of radiotherapy)Feasibility is expressed as a score (using a Visual Analoge Scale)

Countries

Netherlands

Contacts

CONTACTRobin Wijsman
info@rt.umcg.nl+31503612711
CONTACTJ. Elshof
j.elshof@umcg.nl+31503611036
PRINCIPAL_INVESTIGATORRobin Wijsman

University Medical Center Groningen

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 5, 2026