1. Toxicity and time lapse between immunotherapy and stereotactic radiotherapy of brain metastases
- Author
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Michel Lapeyre, S. Mansard, Ioana Molnar, Pierre Verrelle, Julian Biau, T. Khalil, Xavier Durando, V. Chassin, G. Dupic, C. Cabanie, Imagerie Moléculaire et Stratégies Théranostiques (IMoST), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Clermont Auvergne (UCA), Centre Jean Perrin [Clermont-Ferrand] (UNICANCER/CJP), and UNICANCER
- Subjects
Male ,Oncology ,medicine.medical_specialty ,Lung Neoplasms ,Skin Neoplasms ,medicine.medical_treatment ,[SDV]Life Sciences [q-bio] ,Radiosurgery ,Group B ,Time-to-Treatment ,030218 nuclear medicine & medical imaging ,03 medical and health sciences ,Antineoplastic Agents, Immunological ,0302 clinical medicine ,Carcinoma, Non-Small-Cell Lung ,Internal medicine ,Humans ,Medicine ,Radiology, Nuclear Medicine and imaging ,Lung cancer ,Melanoma ,ComputingMilieux_MISCELLANEOUS ,Aged ,Retrospective Studies ,Brain Neoplasms ,business.industry ,Standard treatment ,Radiotherapy Dosage ,Histology ,Immunotherapy ,Middle Aged ,medicine.disease ,Tumor Burden ,3. Good health ,030220 oncology & carcinogenesis ,Concomitant ,Toxicity ,Female ,business ,Follow-Up Studies - Abstract
Stereotactic radiotherapy (SRT) is the standard treatment for brain metastases of non-small-cell lung cancer (NSCLC) and melanoma, mostly in combination with immunotherapy. The objective was to retrospectively evaluate the influence of the time-lapse between immunotherapy and stereotactic radiotherapy on toxicity.From 2016 to 2019, 59 patients treated with SRT for 103 brain metastases of NSCLC (60%) and melanoma (40%) in combination with concomitant immunotherapy (≤30 days) were included. The prescribed dose was 20Gy/1f or 33Gy/3f at the isocentre and 14Gy or 23.1Gy (70%) respectively at the PTV envelope (PTV=GTV+2mm). The mean tumour diameter was 14mm (4-52mm). The immunotherapies used were anti-PD1 and anti-PDL1. The 103 metastases were classified into 3 groups according to the time-lapse between instatement of immunotherapy and instatement of SRT for the patient concerned: 7 (7%) in group A (≤7 days), 38 (37%) in group B (7 to 14 days) and 58 (56%) in group C (14 to 30 days).The mean follow-up was 10.1 months. The median overall survival was 11.5 months for NSCLC and 12.5 months for melanoma. The percentage of local control (LC) at one year was 65.1% (93.6% for NSCLC and 26.5% for melanoma). The time-lapse between immunotherapy and SRT was not a significant predictor of LC (P=0.86), while the histology was (P0.001). The proportion of grade≥3 toxicities was 5.1%, and that of radionecrosis was 9.7% (among these patients, 80% were non-symptomatic): 0%, 13.1% and 8.6% for groups A, B and C respectively. The time-lapse between immunotherapy and SRT was not a significant predictor of toxicity. Only tumour volume was a significant predictive factor (P=0.03).The time lapse between immunotherapy and SRT does not influence brain toxicity. The tumour volume remains the main factor.
- Published
- 2021
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