Bronchial Mapping (GCC 1635)

Thoracic Cancer Clinical Trial

Official title:

Investigating Radiation-Induced Injury to Airways and Pulmonary Vasculature in Lung Stereotactic Ablative Body Radiotherapy (SAbR)

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02745548
• Other study ID #: HP-00069334
• Status: Recruiting
• Start date: June 1, 2017
• Est. completion date: December 2027

Study information

• Verified date: May 2023
• Source: University of Maryland, Baltimore
• Contact: Amit Sawant, PhD
• Phone: 410-706-5517
• Email: asawant[@]som.umaryland.edu
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

In order to better understand radiation-induced lung toxicity, the investigator proposes a novel functional avoidance approach that incorporates central as well as peripheral BSS segments in the treatment planning process in order to quantify and account for their respective radiosensitivities. Specifically, the investigator proposes a systematic study that involves acquiring pre- and post-SAbR high-resolution CT and SPECT V/Q scans from lung cancer patients who receive radiotherapy, followed by auto-segmentation of the BSS elements using virtual bronchoscopy.

Description:

Very few recent lung cancer therapies have had as positive an impact on public health as lung SAbR. Lung SAbR involves the precise administration of very high, biologically potent doses (54-70 Gy) in 3-5 fractions. The most recent update of the Radiation Therapy Oncology Group (RTOG) 0236 Phase II multi-center lung SAbR trial showed 5-year primary tumor control >90% in inoperable Stage I NSCLC patients with tumors ≤ 5cm. However, the use of such highly potent doses puts patients at risk for collateral toxicity including radiation pneumonitis and radiation injury to airways, causing stenosis, atelectasis and ultimately fibrosis. A review of 35 early-stage NSCLC SAbR clinical studies found that the reported maximum values of Grade ≥3 toxicities were between 10-28%. In the RTOG 0236 trial, 17% patients presented Grade ≥3 toxicities. Furthermore, toxicity has been shown to increase dramatically for centrally-located and/or larger (> 5cm) early-stage tumors. Due to these concerns, in current clinical practice, the use of high-dose-per-fraction lung SAbR is routinely indicated only for a small percentage (~3 - 4%) of the NSCLC population - inoperable, early-stage patients with small, peripheral lesions. Inoperable patients with early-stage central and/or larger tumors, higher stage and/or multiple lesions, and pulmonary oligometastases (metastatic disease that is limited in number of lesions and sites) are either treated with conventional radiotherapy and/or chemotherapy (~30 - 40% 5-year survival), or not treated (median survival ~1 year). The segmented structures will be imported into a clinical radiotherapy treatment planning system in order to calculate dose to individual BSS elements. Follow-up CT images and follow-up SPECT V/Q scans will be used to characterize the radiosensitivity of these structures and spatially map the potential radiation-induced loss of lung function. Eventually, using this information, the investigator will investigate treatment planning strategies that help limit radiation dose and consequent damage to BSS elements, thereby reducing lung toxicity. The investigator hypothesizes that - Anatomically variable radiation injury to the bronchial tree and pulmonary vasculature is an important determinant of post-SAbR pulmonary toxicity and residual pulmonary function.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 40
• Est. completion date: December 2027
• Est. primary completion date: December 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

• Patients with primary or metastatic lung lesions to be treated using stereotactic ablative radiotherapy (There is no limitation on the location or number of lesions for this study) OR Conventionally fractionated RT patients with primary or metastatic lung lesions
• Age = 18 years. No gender or ethnic restrictions.
• Performance status ECOG = 3
• Ability to hold breath for ~20 seconds
• Ability to understand and the willingness to sign a written informed consent.
• Any types and amounts of prior therapy will be allowed for this study.
• Maximum PTV dimension = 70 mm

Exclusion Criteria:

• Children (age <18 years).
• Women who are pregnant, nursing, or trying to get pregnant.
• ECOG performance status < 3

Related Conditions & MeSH terms

• Thoracic Cancer

Locations

Country	Name	City	State
United States	Ummc Msgcc	Baltimore	Maryland

Sponsors (1)

Lead Sponsor	Collaborator
University of Maryland, Baltimore

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of patients that show an association between radiation-induced collapse of branching serial structures elements and localized change in pulmonary function	Evaluating the association of RT and how branching structures change in lung function	3 years
Primary	Radiosensitivity of peripheral BSS segments in terms of dose dependent probability of collapse.	Evaluating the difference between dose and segmental collapse with pre- and post treatment MRI's	3 years
Secondary	Number of patients analyzed for creation of intensity modulated radiotherapy treatment plans that incorporate radiation dose thresholds for BSS elements	Evaluating IMRT plans incorporated radiation dose thresholds for BSS elements	3 years