Stereotactic body radiotherapy for centrally located early-stage non-small cell lung cancer or lung metastases from the RSSearch® patient registry
Creators
- 1. The Radiosurgery Society, 1350 Dell, Suite 105, Campbell, CA 95008 (United States)
- 2. Department of Radiation Oncology, St. Anthony Hospital, Oklahoma City, OK (United States)
- 3. Department of Radiation Oncology, St. Mary's Medical Center, Huntington, WV (United States)
- 4. Department of Radiation Oncology, St. Joseph/Candler Hospital, Savannah, GA (United States)
- 5. Department of Radiation Oncology, Erlanger Health System, Chattanooga, TN (United States)
- 6. Department of Radiation Oncology, Medstar Franklin Square Medical Center, Baltimore, MD (United States)
- 7. European CyberKnife Center Munich-Grosshadern and Munich University, Munich (Germany)
- 8. Department of Radiation Oncology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA (United States)
Description
The purpose of this study was to evaluate treatment patterns and outcomes of stereotactic body radiotherapy (SBRT) for centrally located primary non-small cell lung cancer (NSCLC) or lung metastases from the RSSearch® Patient Registry, an international, multi-center patient registry dedicated to radiosurgery and SBRT. Eligible patients included those with centrally located lung tumors clinically staged T1-T2 N0, M0, biopsy-confirmed NSCLC or lung metastases treated with SBRT between November 2004 and January 2014. Descriptive analysis was used to report patient demographics and treatment patterns. Overall survival (OS) and local control (LC) were determined using Kaplan-Meier method. Toxicity was reported using the Common Terminology Criteria for Adverse Events version 3.0. In total, 111 patients with 114 centrally located lung tumors (48 T1-T2,N0,M0 NSCLC and 66 lung metastases) were treated with SBRT at 19 academic and community-based radiotherapy centers in the US and Germany. Median follow-up was 17 months (range, 1–72). Median age was 74 years for primary NSCLC patients and 65 years for lung metastases patients (p < 0.001). SBRT dose varied from 16 – 60 Gy (median 48 Gy) delivered in 1–5 fractions (median 4 fractions). Median dose to centrally located primary NSCLC was 48 Gy compared to 37.5 Gy for lung metastases (p = 0.0001) and median BED10 was 105.6 Gy for primary NSCLC and 93.6 Gy for lung metastases (p = 0.0005). Two-year OS for T1N0M0 and T2N0M0 NSCLC was 79 and 32.1 %, respectively (p = 0.009) and 2-year OS for lung metastases was 49.6 %. Two-year LC was 76.4 and 69.8 % for primary NSCLC and lung metastases, respectively. Toxicity was low with no Grade 3 or higher acute or late toxicities. Overall, patients with centrally located primary NSCLC were older and received higher doses of SBRT than those with lung metastases. Despite these differences, LC and OS was favorable for patients with central lung tumors treated with SBRT. Reported toxicity was low, although low grade toxicities were observed in patients where dose tolerances approached or exceeded published guidelines. Prospective studies are needed to further define the optimal SBRT dose for this cohort of patients
Availability note (English)
Available from http://dx.doi.org/10.1186/s13014-015-0417-5; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4443630Additional details
Identifiers
Publishing Information
- Journal Title
- Radiation Oncology (Online)
- Journal Volume
- 10
- Journal Page Range
- vp.
- ISSN
- 1748-717X
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 47069983
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- GY RANGE 100-1000; GY RANGE 10-100; LUNGS; METASTASES; NEOPLASMS; PATIENTS; RADIATION DOSES; RADIOTHERAPY; TOXICITY
- Descriptors DEC
- ABSORBED DOSE RANGE; BODY; DISEASES; DOSES; GY RANGE; MEDICINE; NUCLEAR MEDICINE; ORGANS; RADIATION DOSE RANGES; RADIOLOGY; RESPIRATORY SYSTEM; THERAPY
Optional Information
- Copyright
- Copyright (c) Davis et al.
- Notes
- PMCID: PMC4443630; PMID: 25975848; PUBLISHER-ID: 417; OAI: oai:pubmedcentral.nih.gov:4443630; licensee BioMed Central. 2015