Skip to content

Prospecitve Observational Study on a Risk Adaptive Scheme for SBRT for Thoracic Nodes Metastases

Prospective Observational Study on a Risk Adaptive Scheme for Stereotactic Body Radiation Therapy (SBRT) for Medically Inoperable Thoracic Nodes Metastases

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02970955
Enrollment
32
Registered
2016-11-22
Start date
2017-03-22
Completion date
2022-12-01
Last updated
2023-02-06

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

Conditions

Thoracic Nodes Metastases

Brief summary

Oligometastatic patients with inoperable thoracic nodes metastases from any primary, except for hematologic malignancies, will undergo a risk adaptive scheme of stereotactic body radiation therapy (SBRT).

Detailed description

The observational study is designed to evaluate safety and efficacy of a risk adaptive scheme of stereotactic body radiation therapy (SRT) in oligometastatic patients with thoracic nodes metastases, medically inoperable, using VMAT RapidArc approach. The potential advantage of this technique is the ability to deliver a more selective irradiation to tumour's target while reducing doses to normal tissue, optimizing the therapeutic window.

Interventions

PROCEDUREInoperable thoracic nodes metastases

The radiation treatment will be delivered with three possible schedules, with a risk adaptive scheme according to number, site and size of metastatic nodes and based on the possibility to respect the constraints of healthy tissues

Sponsors

Istituto Clinico Humanitas
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Patients aged \>18 years with ECOG 0-2 * Karnofsky index \> 70% (ECOG \>2) * Any primary, except for hematologic malignancies * DFI (Disease-free interval) from diagnosis \> 6 months * Unresectable lesions or inoperable patients or patients who refused surgery * Less than 3 metastatic thoracic nodes * No extrathoracic disease or other metastatic sites stable or responding after chemotherapy, with less than 5 metastatic sites * No life threatening conditions * Chemotherapy completed at least 1 week before treatment * Chemotherapy started at least 1 week after treatment allowed * Systemic therapies other than chemotherapy allowed (i.e hormonal therapies and/or immunotherapy) * Written informed consent

Exclusion criteria

* Previous RT in the same region * Pregnant women * Patients with inability to consent

Design outcomes

Primary

MeasureTime frameDescription
Local control of disease7 yearsLocal control of the thoracic nodes stereotactic radiation therapy schedules for medically inoperable oligometastatic patients

Secondary

MeasureTime frameDescription
Progression-free survival for patients7 yearsA measure of the activity of the SBRT treatment on the disease by statistical methods
Overall survival for patients7 yearsPercentage of patients who are alive after a length of time
Quality of life evaluated by EORTC QLQ C30 questionnaires7 yearsAt the end of the treatment and during the first follow-up appointment patients will complete the EORTC QLQ C30
Hematologic and non-hematologic toxicities7 yearsHematologic and non-hematologic toxicities will be graded according to Common Terminology Criteria for Adverse Events version 4.0

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026