TY - JOUR
T1 - Stereotactic radiosurgery (SRS) in high-grade glioma
T2 - judicious selection of small target volumes improves results
AU - Bokstein, Felix
AU - Blumenthal, Deborah T.
AU - Corn, Benjamin W.
AU - Gez, Eliahu
AU - Matceyevsky, Diana
AU - Shtraus, Natan
AU - Ram, Zvi
AU - Kanner, Andrew A.
N1 - Publisher Copyright:
© 2015, Springer Science+Business Media New York.
PY - 2016/2/1
Y1 - 2016/2/1
N2 - We present a retrospective review of 55 Stereotactic Radiosurgery (SRS) procedures performed in 47 consecutive patients with high-grade glioma (HGG). Thirty-three (70.2 %) patients were diagnosed with glioblastoma and 14 (29.8 %) with grade III glioma. The indications for SRS were small (up to 30 mm in diameter) locally progressing lesions in 32/47 (68 %) or new distant lesions in 15/47 (32 %) patients. The median target volume was 2.2 cc (0.2–9.5 cc) and the median prescription dose was 18 Gy (14–24 Gy). Three patients (5.5 % incidence in 55 treatments) developed radiation necrosis. In eight cases (17 %) patients received a second salvage SRS treatment to nine new lesions detected during follow-up. In 22/55 SRS treatments (40.0 %) patients received concurrent chemo- or biological therapy, including temozolamide (TMZ) (15 patients), bevacizumab (BVZ) (6 patients) and carboplatin in one patient. Median time to progression after SRS was 5.0 months (1.0–96.4). Median survival time after SRS was 15.9 months (2.3–109.3) overall median survival (since diagnosis) was 37.4 months (9.6–193.6 months). Long-lasting responses (>12 months) after SRS were observed in 25/46 (54.3 %) patients. We compared a matched (histology, age, KPS) cohort of patients with recurrent HGG treated with BVZ alone with the current study group. Median survival was significantly longer for SRS treated patients compared to the BVZ only cohort (12.6 vs. 7.3 months, p = 0.0102). SRS may be considered an effective salvage procedure for selected patients with small volume, recurrent high-grade gliomas. Long-term radiological control was observed in more than 50 % of the patients.
AB - We present a retrospective review of 55 Stereotactic Radiosurgery (SRS) procedures performed in 47 consecutive patients with high-grade glioma (HGG). Thirty-three (70.2 %) patients were diagnosed with glioblastoma and 14 (29.8 %) with grade III glioma. The indications for SRS were small (up to 30 mm in diameter) locally progressing lesions in 32/47 (68 %) or new distant lesions in 15/47 (32 %) patients. The median target volume was 2.2 cc (0.2–9.5 cc) and the median prescription dose was 18 Gy (14–24 Gy). Three patients (5.5 % incidence in 55 treatments) developed radiation necrosis. In eight cases (17 %) patients received a second salvage SRS treatment to nine new lesions detected during follow-up. In 22/55 SRS treatments (40.0 %) patients received concurrent chemo- or biological therapy, including temozolamide (TMZ) (15 patients), bevacizumab (BVZ) (6 patients) and carboplatin in one patient. Median time to progression after SRS was 5.0 months (1.0–96.4). Median survival time after SRS was 15.9 months (2.3–109.3) overall median survival (since diagnosis) was 37.4 months (9.6–193.6 months). Long-lasting responses (>12 months) after SRS were observed in 25/46 (54.3 %) patients. We compared a matched (histology, age, KPS) cohort of patients with recurrent HGG treated with BVZ alone with the current study group. Median survival was significantly longer for SRS treated patients compared to the BVZ only cohort (12.6 vs. 7.3 months, p = 0.0102). SRS may be considered an effective salvage procedure for selected patients with small volume, recurrent high-grade gliomas. Long-term radiological control was observed in more than 50 % of the patients.
KW - Glioblastoma multiforme
KW - High grade glioma
KW - Stereotactic radiosurgery
KW - Temozolamide
UR - http://www.scopus.com/inward/record.url?scp=84956663315&partnerID=8YFLogxK
U2 - 10.1007/s11060-015-1997-5
DO - 10.1007/s11060-015-1997-5
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C2 - 26603164
AN - SCOPUS:84956663315
SN - 0167-594X
VL - 126
SP - 551
EP - 557
JO - Journal of Neuro-Oncology
JF - Journal of Neuro-Oncology
IS - 3
ER -