Evidence map›Paper›PMID 39527165›Full record

Trial reportInternational journal of clinical oncology2025

Efficacy and safety of carmustine wafers, followed by radiation, temozolomide, and bevacizumab therapy, for newly diagnosed glioblastoma with maximal resection.

Masayuki Kanamori, Ichiyo Shibahara, Yoshiteru Shimoda, Yukinori Akiyama, Takaaki Beppu, Shigeo Ohba, Toshiyuki Enomoto, Takahiro Ono, Yuta Mitobe, Mitsuto Hanihara and 22 more

Abstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in International journal of clinical oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Advancements in Drug Delivery Systems in Glioblastoma Therapy.International journal of molecular sciences · 2026
    Review
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

32 authors.

Masayuki KanamoriDepartment of Neurosurgery, Tohoku University Graduate School of Medicine, Sendai, Japan. mkanamori@med.tohoku.ac.jp.ORCID http://orcid.org/0000-0002-3380-1192
Ichiyo ShibaharaDepartment of Neurosurgery, Kitasato University School of Medicine, Sagamihara, Japan.
Yoshiteru ShimodaDepartment of Neurosurgery, Tohoku University Graduate School of Medicine, Sendai, Japan.
Yukinori AkiyamaDepartment of Neurosurgery, Sapporo Medical University School of Medicine, Sapporo, Japan.
Takaaki BeppuDepartment of Neurosurgery, Iwate Medical University, Shiwa, Japan.
Shigeo OhbaDepartment of Neurosurgery, Fujita Health University, Toyoake, Japan.
Toshiyuki EnomotoDepartment of Neurosurgery, Fukuoka University, Fukuoka, Japan.
Takahiro OnoDepartment of Neurosurgery, Akita University Graduate School of Medicine, Akita, Japan.
Yuta MitobeDepartment of Neurosurgery, Faculty of Medicine, Yamagata University, Yamagata, Japan.
Mitsuto HaniharaDepartment of Neurosurgery, Graduate School of Medicine, University of Yamanashi, Yamanashi, Japan.
Yohei MineharuDepartment of Neurosurgery, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Joji IshidaDepartment of Neurological Surgery, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama, Japan.
Kenichiro AsanoDepartment of Neurosurgery, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Yasuyuki YoshidaDepartment of Neurosurgery, St. Marianna University School of Medicine, Kawasaki, Japan.
Manabu NatsumedaDepartment of Neurosurgery, Niigata University Brain Research Institute, Niigata, Japan.
Sadahiro NomuraDepartment of Neurosurgery, Yamaguchi University School of Medicine, Ube, Japan.
Tatsuya AbeDepartment of Neurosurgery, Faculty of Medicine, Saga University, Saga, Japan.
Hajime YonezawaDepartment of Neurosurgery, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan.
Ryuichi KatakuraDepartment of Neurosurgery, Miyagi Cancer Center, Natori, Japan.
Soichiro ShibuiDepartment of Neurosurgery, Teikyo University Hospital, Kawasaki, Japan.
Toshihiko KuroiwaDepartment of Neurosurgery, Osaka Medical and Pharmaceutical University, Takatsuki, Japan.
Hiroyoshi SuzukiDepartment of Pathology and Laboratory Medicine, National Hospital Organization Sendai Medical Center, Miyagi, Japan.
Hidehiro TakeiDepartment of Pathology and Laboratory Medicine, University of Texas, Houston, USA.
Haruo MatsushitaDepartment of Radiation Oncology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Ryuta SaitoDepartment of Neurosurgery, Tohoku University Graduate School of Medicine, Sendai, Japan.
Yoshiki ArakawaDepartment of Neurosurgery, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Yukihiko SonodaDepartment of Neurosurgery, Faculty of Medicine, Yamagata University, Yamagata, Japan.
Yuichi HiroseDepartment of Neurosurgery, Fujita Health University, Toyoake, Japan.
Toshihiro KumabeDepartment of Neurosurgery, Kitasato University School of Medicine, Sagamihara, Japan.
Takuhiro YamaguchiDivision of Biostatistics, Tohoku University Graduate School of Medicine, Sendai, Japan.
Hidenori EndoDepartment of Neurosurgery, Tohoku University Graduate School of Medicine, Sendai, Japan.
Teiji TominagaDepartment of Neurosurgery, Tohoku University Graduate School of Medicine, Sendai, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo improve the outcome in newly diagnosed glioblastoma patients with maximal resection, we aimed to evaluate the efficacy and safety of implantation of carmustine wafers (CWs), radiation concomitant with temozolomide and bevacizumab, and maintenance chemotherapy with six cycles of temozolomide and bevacizumab.

methodThis prospective phase II study enrolled glioblastoma patients considered candidates for complete resection (> 90%) of a contrast-enhanced lesion. The CWs were intraoperatively implanted into the resection cavity after achieving maximal resection. Patients without a measurable contrast-enhanced lesion on magnetic resonance imaging within 48 h after resection received concomitant radiotherapy and chemotherapy with temozolomide and bevacizumab, followed by maintenance treatment with up to six cycles of temozolomide and bevacizumab. The primary endpoint was the 2-year overall survival rate in glioblastoma patients with protocol treatment.

resultsFrom October 2015 to April 2018, we obtained consent for the first registration from 70 patients across 17 institutions in Japan, and 49 patients were treated according to the protocol. We evaluated the safety in 49 patients who were part of the second registration and the efficacy in 45 glioblastoma patients treated according to the protocol. The profile of hematological and most of the non-hematological adverse effects was similar to that in previous studies, but stroke occurred in 12% of cases (6/49 patients). The estimated 2-year overall survival rate was 51.3%.

conclusionImplantation of CWs, followed by concomitant radiation, temozolomide, and bevacizumab, and six cycles of temozolomide and bevacizumab may offer some benefit to survival in Japanese glioblastoma patients with maximal resection. TRIAL ID: jRCTs021180007.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBevacizumabBrain NeoplasmsCarmustineChemoradiotherapyGlioblastomaTemozolomideAdultAgedFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedProspective StudiesSurvival RateBevacizumabCarmustineTemozolomideBevacizumabCarmustine wafersGlioblastomaMaximal resectionTemozolomide

Identifiers

PMID39527165
PMCPMC11700082

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.