Evidence map›Paper›PMID 30715997›Full record

Trial reportJournal of clinical oncology : official journal of the American Society of Clinical Oncology2019

Buparlisib in Patients With Recurrent Glioblastoma Harboring Phosphatidylinositol 3-Kinase Pathway Activation: An Open-Label, Multicenter, Multi-Arm, Phase II Trial.

Patrick Y Wen, Mehdi Touat, Brian M Alexander, Ingo K Mellinghoff, Shakti Ramkissoon, Christine S McCluskey, Kristine Pelton, Sam Haidar, Sankha S Basu, Sarah C Gaffey and 34 more

Open access · greenAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 113 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
113citing papers in PubMed, 3 pooled it
10.7field-weighted citation impact, top 1% of its field
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

113 citing papers in PubMed, 3 syntheses or guidelines pooled it, 150 citations in OpenAlex.

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  17. Recent Advances in Targeted Therapies for Adult Gliomas.Current neurology and neuroscience reports · 2026
    Review
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53 more citing papers are in PubMed but not listed here.

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

44 authors at 12 institutions in 1 country.

Patrick Y Wen1 Dana-Farber Cancer Institute, Boston, MA.
Mehdi Touat1 Dana-Farber Cancer Institute, Boston, MA.
Brian M Alexander1 Dana-Farber Cancer Institute, Boston, MA.
Ingo K Mellinghoff3 Memorial Sloan Kettering Cancer Center, New York, NY.
Shakti Ramkissoon1 Dana-Farber Cancer Institute, Boston, MA.
Christine S McCluskey1 Dana-Farber Cancer Institute, Boston, MA.
Kristine Pelton1 Dana-Farber Cancer Institute, Boston, MA.
Sam Haidar1 Dana-Farber Cancer Institute, Boston, MA.
Sankha S Basu1 Dana-Farber Cancer Institute, Boston, MA.
Sarah C Gaffey1 Dana-Farber Cancer Institute, Boston, MA.
Loreal E Brown1 Dana-Farber Cancer Institute, Boston, MA.
Juan Emmanuel Martinez-Ledesma4 The University of Texas M.D. Anderson Cancer Center, Houston, TX.
Shaofang Wu4 The University of Texas M.D. Anderson Cancer Center, Houston, TX.
Jungwoo Kim5 California Institute of Technology, Pasadena, CA.
Wei Wei6 David Geffen School of Medicine at University of California, Los Angeles, Los Angeles, CA.
Mi-Ae Park1 Dana-Farber Cancer Institute, Boston, MA.
Jason T Huse4 The University of Texas M.D. Anderson Cancer Center, Houston, TX.
John G Kuhn7 The University of Texas, San Antonio, San Antonio, TX.
Mikael L Rinne1 Dana-Farber Cancer Institute, Boston, MA.
Howard Colman8 Huntsman Cancer Institute and University of Utah, Salt Lake City, UT.
Nathalie Y R Agar1 Dana-Farber Cancer Institute, Boston, MA.
Antonio M Omuro3 Memorial Sloan Kettering Cancer Center, New York, NY.
Lisa M DeAngelis3 Memorial Sloan Kettering Cancer Center, New York, NY.
Mark R Gilbert4 The University of Texas M.D. Anderson Cancer Center, Houston, TX.
John F de Groot4 The University of Texas M.D. Anderson Cancer Center, Houston, TX.
Timothy F Cloughesy6 David Geffen School of Medicine at University of California, Los Angeles, Los Angeles, CA.
Andrew S Chi9 New York University School of Medicine, New York, NY.
Thomas M Roberts1 Dana-Farber Cancer Institute, Boston, MA.
Jean J Zhao1 Dana-Farber Cancer Institute, Boston, MA.
Eudocia Q Lee1 Dana-Farber Cancer Institute, Boston, MA.
Lakshmi Nayak1 Dana-Farber Cancer Institute, Boston, MA.
James R Heath10 Institute for Systems Biology, Seattle, WA.
Laura L Horky1 Dana-Farber Cancer Institute, Boston, MA.
Tracy T Batchelor11 Massachusetts General Hospital, Boston, MA.
Rameen Beroukhim1 Dana-Farber Cancer Institute, Boston, MA.
Susan M Chang12 University of California, San Francisco, San Francisco, CA.
Azra H Ligon2 Brigham and Women's Hospital, Boston, MA.
Ian F Dunn2 Brigham and Women's Hospital, Boston, MA.
Dimpy Koul4 The University of Texas M.D. Anderson Cancer Center, Houston, TX.
Geoffrey S Young2 Brigham and Women's Hospital, Boston, MA.
Michael D Prados12 University of California, San Francisco, San Francisco, CA.
David A Reardon1 Dana-Farber Cancer Institute, Boston, MA.
W K Alfred Yung4 The University of Texas M.D. Anderson Cancer Center, Houston, TX.
Keith L Ligon1 Dana-Farber Cancer Institute, Boston, MA.
Dana-Farber Cancer Institute · USBrigham and Women's Hospital · USThe University of Texas MD Anderson Cancer Center · USMemorial Sloan Kettering Cancer Center · USUniversity of California, Los Angeles · USUniversity of California, San Francisco · USCalifornia Institute of Technology · USHuntsman Cancer Institute · USInstitute for Systems Biology · USMassachusetts General Hospital · USNew York University · USThe University of Texas at San Antonio · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
Targeting the Vasular SystemP50CA165962 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI WENDY Beth LONDON · 2013 to 2026
$33.5M
Tissue and Pathology CoreP50CA168504 · NCI · DANA-FARBER CANCER INST · PI Nabihah Tayob · 2013 to 2026
$30.1M
UCLA SPORE in Brain CancerP50CA211015 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Yvonne Yu-Hsuan Chen · 2017 to 2026
$25.2M
Brain Tumor Clinical and Clinical Research Program (Clinical Support Services)ZIDBC011642 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI OZER, BYRAM · 2015 to 2025
$23.4M
Repurposing of cancer therapeutics for treatment of patients with COVID-19 diseaseU54CA199090 · NCI · INSTITUTE FOR SYSTEMS BIOLOGY · PI HEATH, JAMES R., RIBAS, ANTONI · 2015 to 2020
$11.4M
Integrating targeted therapy and immunotherapy to break through cancerR35CA210057 · NCI · DANA-FARBER CANCER INST · PI Jean Zhao · 2016 to 2026
$10.8M
Genetic evolution of glioblastomas during radiation and temozolomide therapyR01CA188228 · NCI · DANA-FARBER CANCER INST · PI BEROUKHIM, RAMEEN, CHAKRAVARTI, ARNAB · 2015 to 2025
$6.9M
Characterizing TP53 and PPM1D mutations as resistance drivers to radiation therapy in Diffuse Intrinsic Pontine GliomasR01CA219943 · NCI · BROAD INSTITUTE, INC. · PI BEROUKHIM, RAMEEN, LIGON, KEITH LLOYD · 2017 to 2021
$2.5M
NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA165962NCI NIH HHS P50 CA168504NCI NIH HHS P50 CA211015NCI NIH HHS R01 CA188228NCI NIH HHS R01 CA219943NCI NIH HHS R35 CA210057NCI NIH HHS U54 CA199090
6 · The paper itself

Abstract

purposePhosphatidylinositol 3-kinase (PI3K) signaling is highly active in glioblastomas. We assessed pharmacokinetics, pharmacodynamics, and efficacy of the pan-PI3K inhibitor buparlisib in patients with recurrent glioblastoma with PI3K pathway activation.

methodsThis study was a multicenter, open-label, multi-arm, phase II trial in patients with PI3K pathway-activated glioblastoma at first or second recurrence. In cohort 1, patients scheduled for re-operation after progression received buparlisib for 7 to 13 days before surgery to evaluate brain penetration and modulation of the PI3K pathway in resected tumor tissue. In cohort 2, patients not eligible for re-operation received buparlisib until progression or unacceptable toxicity. Once daily oral buparlisib 100 mg was administered on a continuous 28-day schedule. Primary end points were PI3K pathway inhibition in tumor tissue and buparlisib pharmacokinetics in cohort 1 and 6-month progression-free survival (PFS6) in cohort 2.

resultsSixty-five patients were treated (cohort 1, n = 15; cohort 2, n = 50). In cohort 1, reduction of phosphorylated AKT

conclusionBuparlisib had minimal single-agent efficacy in patients with PI3K-activated recurrent glioblastoma. Although buparlisib achieved significant brain penetration, the lack of clinical efficacy was explained by incomplete blockade of the PI3K pathway in tumor tissue. Integrative results suggest that additional study of PI3K inhibitors that achieve more-complete pathway inhibition may still be warranted.

Indexed as

Neoadjuvant TherapyNeoplasm Recurrence, LocalAdultAgedAged, 80 and overAminopyridinesAntineoplastic AgentsBrain NeoplasmsChemotherapy, AdjuvantDisease ProgressionEnzyme ActivationFemaleGlioblastomaHumansMaleMiddle AgedAminopyridinesAntineoplastic AgentsMorpholinesNVP-BKM120Phosphatidylinositol 3-KinasePhosphoinositide-3 Kinase Inhibitors

Identifiers

PMID30715997
PMCPMC6553812
OpenAlexW2913589503

What OpenQuestion holds

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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.