Copenhagen, Denmark
Onsite/Online

ESTRO 2022

Session Item

Lung
6008
Poster (digital)
Clinical
Is SBRT an effective treatment in metastatic lung cancer with oligoprogressive disease?
Michele Aquilano, Italy
PO-1261

Abstract

Is SBRT an effective treatment in metastatic lung cancer with oligoprogressive disease?
Authors:

Michele Aquilano1, Mauro Loi2, Lorenzo Livi3, Joost Nuyttens4

1University of Florence, Department of Biomedical, Experimental and Clinical Sciences "Mario Serio" University of Florence, Florence, Italy; 2Azienda Ospedaliero-Universitaria Careggi, Department of Radiation Oncology , Florence, Italy; 3University of Florence, Department of Biomedical, Experimental and Clinical Sciences "Mario Serio" , Florence, Italy; 4Erasmus MC Cancer Institute, Department of Radiation Oncology, Rotterdam, The Netherlands

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Purpose or Objective

Oligoprogression (OPD) is defined as a disease’ state where limited progression (1-3 metastases) is observed in patients undergoing systemic treatment. Local treatment of OPD may enable to postpone systemic therapy switch, in particular in patients undergoing novel targeted or immune therapies. In this study we investigated the outcome after stereotactic body radiotherapy (SBRT) in patients with metastatic lung cancer treated with chemo-immunotherapy who were diagnosed with oligoprogression. 

Material and Methods

Thirty-seven patients, 21 female and 16 male, with metastatic lung cancer and diagnosis of oligoprogression were included and were treated with Cyberknife and Linac SBRT between June 2015 and August 2021. SBRT was delivered to lung (n=18), mediastinal node (n=8), bone (n=5), adrenal gland (n=5) and kidney (n=1). Dose regimens consisted of 30-51 Gy in 3 fractions, 30-55 Gy in 5 fractions, 52.5 Gy in 7 fractions and 44-56 Gy in 8 fractions, resulting in a median BED of 115.5 (range 48-138) Gy10. Dose was expressed as Biological Effective Dose for α/β=10 (BED10). Kaplan-Meyer method was used to calculate Overall Survival (OS), Local Control (LC) and Disease Progression-free Survival (DPFS) from the start date of SBRT to event.

Results

After a median follow up of 20 months (range 1-48), median overall survival  was  26 months (figure 1), and median DPFS was 6 months. LC was 82% at 1 year and 74% at 2 years. Median age was 66 years (range 25–82). All patients were treated with systemic treatment before the start of the SBRT: 9 chemotherapy (CT) alone (24%), 14 CT plus immunotherapy (IT) or plus Tyrosin kinase inhibitors (TKI) (38%) and 14 IT/TKI alone (38%). At univariate analysis, age, type of systemic treatment, and number of chemotherapy lines were not significant prognostic factors for overall survival. 

Conclusion

SBRT in lung cancer patients for oligoprogression resulted in a long median overall survival of 26 months. Local control  at 1 year was 82%. The median DFS was 6 months as other metastases grow slowely. SBRT could be a valid alternative to postpone the change of chemotherapy and/or immunotherapy. More research is needed to address the gain of the SBRT in patients with oligoprogressive disease.