SBRT WITH CDK4/6 INHIBITORS FOR OLIGORECURRENT/OLIGOPROGRESSIVE BREAST CANCER PATIENTS
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Abstract
SBRT WITH CDK4/6 INHIBITORS FOR OLIGORECURRENT/OLIGOPROGRESSIVE BREAST CANCER PATIENTS
Authors: Edy Ippolito1, Elena Onorati2, Carlo Greco1, Michele Fiore1, Sonia Silipigni2, Paolo Matteucci2, Laura Cerasani2, Sofia Carrafiello2, Vincenzo Palumbo2, Sara Ramella1
1Università Campus Biomedico, Fondazione Policlinico Campus Biomedico, Radiation Oncology, Rome, Italy; 2Fondazione Policlinico Campus Biomedico, Radiation Oncology, Rome, Italy
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Purpose or Objective
Stereotactic body radiotherapy (SBRT) for oligoprogressive/oligorecurrent metastases can delay next line systemic therapy. We evaluated safety and efficacy of concurrent SBRT with CDK4/6 inhibitors in stage IV breast cancer patients.
Material and Methods
The clinical records of metastatic breast cancer patients treated with SBRT to oligoprogressive/oligorecurrent lesions concurrently with anti-CDK4/6 inhibitors were reviewed. Toxicities were measured according to CTCAE 4.0. Response was evaluated according to RECIST/PERCIST criteria. PFS was evaluated from SBRT to local/systemic failure.
Results
Twenty-three patients treated to a total of 50 lesions were included in the analysis. Median age was 62 years (range 38-86 years). Mean Biological Effective Dose (BED) delivered (alpha/beta=4 Gy) was 89.3 (SD = 45). SBRT was delivered to bone metastases (58%), brain metastases (16%) and visceral metastases (26%).
10 patients were treated with concurrent Palbociclib (43.5%), 9 with concurrent Ribociclib (39.1%) and 4 with concurrent Abemaciclib (17.4%).
Median FUP was 15 months (range 2-65 months). All lesions were evaluable for response: no patients experienced local failure on sites treated with SBRT. Response was evaluated on a per lesion basis. Complete response was achieved in 19 sites (38%), partial response in 17 sites (34%).
After SBRT, 1-year and 3-year PFS were 16.8% and 30.5 % respectively. Mean duration of anti-CDK4/6 therapy after SBRT was 17.6 13.9 months.
Only two toxicities were observed: a G1 dysphagia developed in a patient treated to a cervical spine lesion and a G3 neutropenia developed in a patient treated to a central lung lesion in 8 fractions.
Conclusion
SBRT for oligoprogressive/oligorecurrent breast cancer metastases delivered concurrently with CDK4/6 inhibitors seems safe and effective and should be tested in prospective studies.