TY - JOUR
T1 - Stereotactic radiation therapy in the strategy of treatment of metastatic renal cell carcinoma
T2 - A study of the Getug group
AU - Meyer, Emmanuel
AU - Pasquier, David
AU - Bernadou, Guillemette
AU - Calais, Gilles
AU - Maroun, Pierre
AU - Bossi, Alberto
AU - Theodore, Christine
AU - Albiges, Laurence
AU - Stefan, Dinu
AU - Crevoisier, Renaud D.E.
AU - Hennequin, Christophe
AU - Lagrange, Jean Léon
AU - Grellard, Jean Michel
AU - Clarisse, Bénédicte
AU - Licaj, Idlir
AU - Habrand, Jean Louis
AU - Carrie, Christian
AU - Joly, Florence
N1 - Publisher Copyright:
© 2018 Elsevier Ltd
PY - 2018/7/1
Y1 - 2018/7/1
N2 - Background: Renal cell carcinoma (RCC) is usually considered radioresistant, but stereotactic radiation therapy (SRT) may increase local disease control. This study aimed to assess the benefit of SRT in the management of metastatic RCC patients. Methods: Data of all RCC patients who received SRT between 2008 and 2015 with curative intent were retrospectively collected in six French referral centres. Local control (LC), progression-free survival (PFS), local recurrence-free survival (LRFS), time to systemic therapy (TTS) and overall survival (OS) were assessed. Results: One hundred and eighty-eight patients treated with SRT for 252 RCC metastases (brain [n = 120]; spine [n = 75]; and others [n = 57]) were recensed. SRT was performed for oligoprogressive disease (101 patients), oligometastatic disease (80 patients) or residual tumour after a partial response to systemic treatment (7 patients). The median biologically effective dose was 78 Gy. For the whole population, local control rates at 6, 12 and 24 months were 87.5%, 82.9% and 77.6%, respectively; median PFS, LRFS, TTS and OS were 8.5, 23.2, 13.2 and 29.2 months, respectively. Among patients treated for oligoprogressive/oligometastatic disease, the median PFS, TTS, and OS were 8.6/7.6, 10.5/14.2 and 23.2/33.9 months, respectively. Among the 7 patients treated with SRT after partial response to systemic treatment, no relapse occurred for 3 of them after a median follow-up of 22 months. Acute and late severe toxicities were noted in 5 (2.6%) patients. Conclusions: SRT is effective and safe for oligometastatic and oligoprogressive RCC patients and may delay introduction or change of systemic therapy.
AB - Background: Renal cell carcinoma (RCC) is usually considered radioresistant, but stereotactic radiation therapy (SRT) may increase local disease control. This study aimed to assess the benefit of SRT in the management of metastatic RCC patients. Methods: Data of all RCC patients who received SRT between 2008 and 2015 with curative intent were retrospectively collected in six French referral centres. Local control (LC), progression-free survival (PFS), local recurrence-free survival (LRFS), time to systemic therapy (TTS) and overall survival (OS) were assessed. Results: One hundred and eighty-eight patients treated with SRT for 252 RCC metastases (brain [n = 120]; spine [n = 75]; and others [n = 57]) were recensed. SRT was performed for oligoprogressive disease (101 patients), oligometastatic disease (80 patients) or residual tumour after a partial response to systemic treatment (7 patients). The median biologically effective dose was 78 Gy. For the whole population, local control rates at 6, 12 and 24 months were 87.5%, 82.9% and 77.6%, respectively; median PFS, LRFS, TTS and OS were 8.5, 23.2, 13.2 and 29.2 months, respectively. Among patients treated for oligoprogressive/oligometastatic disease, the median PFS, TTS, and OS were 8.6/7.6, 10.5/14.2 and 23.2/33.9 months, respectively. Among the 7 patients treated with SRT after partial response to systemic treatment, no relapse occurred for 3 of them after a median follow-up of 22 months. Acute and late severe toxicities were noted in 5 (2.6%) patients. Conclusions: SRT is effective and safe for oligometastatic and oligoprogressive RCC patients and may delay introduction or change of systemic therapy.
KW - Oligometastatic disease
KW - Oligoprogressive disease
KW - Renal cell carcinoma
KW - Stereotactic radiation therapy
UR - http://www.scopus.com/inward/record.url?scp=85048486047&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2018.04.008
DO - 10.1016/j.ejca.2018.04.008
M3 - Article
C2 - 29864737
AN - SCOPUS:85048486047
SN - 0959-8049
VL - 98
SP - 38
EP - 47
JO - European Journal of Cancer
JF - European Journal of Cancer
ER -