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  •   University of Thessaly Institutional Repository
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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  •   University of Thessaly Institutional Repository
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • View Item
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Stereotactic body radiotherapy (SBRT) can delay polymetastatic conversion in patients affected by liver oligometastases

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Author
Nicosia L., Cuccia F., Mazzola R., Figlia V., Giaj-Levra N., Ricchetti F., Rigo M., Bonù M., Corradini S., Tolia M., Alongi F.
Date
2020
Language
en
DOI
10.1007/s00432-020-03223-9
Keyword
adult
aged
Article
cancer control
cancer specific survival
disease exacerbation
female
follow up
human
liver metastasis
liver oligometastasis
major clinical study
male
multivariate analysis
overall survival
predictive value
priority journal
progression free survival
relapse
stereotactic body radiation therapy
liver tumor
metastasis
middle aged
pathology
procedures
prognosis
radiosurgery
tumor recurrence
very elderly
Adult
Aged
Aged, 80 and over
Female
Humans
Liver Neoplasms
Male
Middle Aged
Neoplasm Metastasis
Neoplasm Recurrence, Local
Prognosis
Radiosurgery
Springer
Metadata display
Abstract
Purpose: SBRT demonstrated to increase survival in oligometastatic patients. Nevertheless, little is known regarding the natural history of oligometastatic disease (OMD) and how SBRT may impact the transition to the polymetastatic disease (PMD). Methods: 97 liver metastases in 61 oligometastatic patients were treated with SBRT. Twenty patients (33%) had synchronous oligometastases, 41 (67%) presented with metachronous oligometastases. Median number of treated metastases was 2 (range 1–5). Results: Median follow-up was 24 months. Median tPMC was 11 months (range 4–17 months). Median overall survival (OS) was 23 months (range 16–29 months). Cancer-specific survival predictive factors were having further OMD after SBRT (21 months versus 15 months; p = 0.00), and local control of treated metastases (27 months versus 18 months; p = 0.031). Median PFS was 7 months (range 4–12 months). Patients with 1 metastasis had longer median PFS as compared to those with 2–3 and 4–5 metastases (14.7 months versus 5.3 months versus 6.5 months; p = 0.041). At the last follow-up, 50/61 patients (82%) progressed, 16 of which (26.6%) again as oligometastatic and 34 (56%) as polymetastatic. Conclusion: In the setting of oligometastatic disease, SBRT is able to delay the transition to the PMD. A proportion of patients relapse as oligometastatic and can be eventually evaluated for a further SBRT course. Interestingly, those patients retain a survival benefit as compared to those who had PMD. Further studies are needed to explore the role of SBRT in OMD and to identify treatment strategies able to maintain the oligometastatic state. © 2020, Springer-Verlag GmbH Germany, part of Springer Nature.
URI
http://hdl.handle.net/11615/77170
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  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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