| Literature DB >> 28534151 |
Yukihiko Sonoda1, Ichiyo Shibahara2, Ken-Ichiro Matsuda3, Ryuta Saito4, Tomoyuki Kawataki5, Masaya Oda6, Yuichi Sato7, Hirokazu Sadahiro8, Sadahiro Nomura8, Toshio Sasajima6, Takaaki Beppu7, Masayuki Kanamori4, Kaori Sakurada3, Toshihiro Kumabe2, Teiji Tominaga4, Hiroyuki Kinouchi5, Hiroaki Shimizu6, Kuniaki Ogasawara7, Michiyasu Suzuki8.
Abstract
Carmustine wafers (CW) were approved in Japan for newly diagnosed and recurrent malignant gliomas during 2013. The ventricle is often opened during surgery to achieve maximum resection. While not generally recommended in such situations, CW might be safely achieved by occluding an opened ventricle using gelform or collagen sheets. However, whether CW implantation actually confers a survival benefit for patients who undergo surgery with an open ventricle to treat glioblastoma remains unclear. Clinical, imaging, and survival data were collected in this multicenter retrospective study of 122 consecutive patients with newly diagnosed glioblastoma to determine adverse events and efficacy. Overall, 54 adverse events of all grades developed in 35 (28.6%) patients, with the most common being new seizures (16%). Adverse events did not significantly differ between patients with opened and closed ventricles during surgery. The 10- and 21.7-month, median, progression-free (PFS) and overall survival (OS), respectively did not significantly differ according to resection rates. However, median PFS and OS were significantly longer among patients with closed, than open ventricles (12.8 vs. 7.4 months; p = 0.0039 and 26.9 vs. 18.6 months; p = 0.011, respectively). Implanting CW into the resection cavity during concomitant radiochemotherapy with temozolomide seems to yield better survival rates without increased adverse events. Occlusion of the ventricular opening during surgery might be safe for CW implantation, but less so for treating patients with newly diagnosed glioblastoma.Entities:
Keywords: Carmustine wafers; Glioblastoma; Ventricle
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Year: 2017 PMID: 28534151 DOI: 10.1007/s11060-017-2488-7
Source DB: PubMed Journal: J Neurooncol ISSN: 0167-594X Impact factor: 4.130