Stereotactic radiation therapy in oligometastatic colorectal cancer: outcome of 102 patients and 150 lesions

Springer Science and Business Media LLC - Tập 36 - Trang 331-342 - 2019
V. Dell’Acqua1, A. Surgo1, F. Kraja2, J. Kobiela3, Maria Alessia Zerella1,4, P. Spychalski3, S. Gandini5, C. M. Francia6, D. Ciardo1, C. Fodor1, A. M. Ferrari1, G. Piperno1, F. Cattani7, S. Vigorito7, F. Pansini7, W. Petz8, R. Orecchia9, M. C. Leonardi1, B. A. Jereczek-Fossa1,4
1Division of Radiotherapy, IEO European Institute of Oncology, IRCCS, Milan, Italy
2Division of Oncology, University Hospital Centre “Mother Theresa”, Tirana, Albania
3Department of General, Endocrine and Transplant Surgery, Medical University of Gdansk, Gdańsk, Poland
4Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy
5Group Leader Department of Experimental Oncology, European Institute of Oncology, IRCCS, Milan, Italy
6Palliative Care and Pain Therapy Unit, European Institute of Oncology, IRCCS, Milan, Italy
7Unit of Medical Physics, European Institute of Oncology, IRCCS, Milan, Italy
8Division of Gastrointestinal Surgery, European Institute of Oncology, Milan, Italy
9Scientific Directorate, European Institute of Oncology, IRCCS, Milan, Italy

Tóm tắt

To evaluate the local control (LC), progression free survival (PFS), out-field PFS, overall survival (OS), toxicity and failure predictors of SRT in a series of various sites oligometastatic CRC patients. Patients with oligometastatic CRC disease were analyzed retrospectively. The SRT prescribed dose was dependent on the lesion volume and its location. 102 consecutive oligometastatic CRC patients (150 lesions) were included. They underwent SRT between 2012 and 2015. Median prescription dose was 45 Gy (median dose/fraction was 15 Gy/3 fractions biological equivalent dose (BED10) 112.5 Gy). Median follow-up was 11.4 months. No patients experienced G3 and G4 toxicity. No progression was found in 82% (radiological response at 3 months) and 85% (best radiological response) out of 150 evaluable lesions. At 1 and 2 years: LC was 70% and 55%; OS was 90% and 90%; PFS was 37% and 27%; out-field PFS was 37% and 23% respectively. Progressive disease was correlated with BED10 (better LC when BED10 was ≥ 75 Gy (p < 0.0001)). In multivariate analysis, LC was higher in lesions with a Plpnning target volume (PTV) volume < 42 cm3 and BED10 ≥ 75 Gy. Patients with Karnofsky performance status < 90 showed higher out-field progression. SRT is an effective treatment for patients with oligometastases from CRC. Its low treatment-associated morbidity and acceptable LC make of SRT an option not only in selected cases. Further studies should be focused to clarify which patient subgroup will benefit most from this treatment modality and to define the optimal dose to improve LC while maintaining low toxicity profile.

Tài liệu tham khảo

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