Evidence map›Paper›PMID 30266892›Full record

Trial reportThe oncologist2019

A Randomized Phase II Trial (TAMIGA) Evaluating the Efficacy and Safety of Continuous Bevacizumab Through Multiple Lines of Treatment for Recurrent Glioblastoma.

Alba A Brandes, Miguel Gil-Gil, Frank Saran, Antoine F Carpentier, Anna K Nowak, Warren Mason, Vittorina Zagonel, François Dubois, Gaetano Finocchiaro, George Fountzilas and 11 more

Registry-linked trialOpen access · bronzeAbstract readClinical Trial, Phase IIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in The oncologist, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01860638 (A Double-Blind, Placebo-Controlled, Randomised, Phase II Study Evaluating the Efficacy and Safety of Addition of Continuous Multiple Line Bevacizumab Treatment to Lomustine in Second), which is not on this map. Cited by 41 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 8 pooled it
3.8field-weighted citation impact, top 6% 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.

NCT01860638 phase2completednot on this map

A Double-Blind, Placebo-Controlled, Randomised, Phase II Study Evaluating the Efficacy and Safety of Addition of Continuous Multiple Line Bevacizumab Treatment to Lomustine in Second (2nd)-Line Followed by Standard of Care (SOC) in Third (3rd)-Line and Beyond Compared to Addition of Placebo, Following First Progression of Disease (PD1) in Patients With Glioblastoma (GBM) After First (1st)-Line Treatment With Radiotherapy, Temozolomide and Bevacizumab

TypeinterventionalSponsorHoffmann-La RocheRan2013 to 2017Enrolled296ConditionsGlioblastomaArmsBevacizumab, Lomustine, Placebo, Radiotherapy, Temozolomide
3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 8 syntheses or guidelines pooled it, 68 citations in OpenAlex.

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  19. Glioblastoma Therapy: Past, Present and Future.International journal of molecular sciences · 2024
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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

21 authors at 16 institutions in 10 countries.

Alba A BrandesDepartment of Medical Oncology, AUSL, Bologna, Italy alba.brandes@yahoo.it.
Miguel Gil-GilInstitut Catala d'Oncologia, L'Hospitalet, Institut d'Investigació Biomédica de Bellvitge (IDIBELL), Barcelona, Spain.
Frank SaranRoyal Marsden National Health Service Foundation Trust, Sutton, United Kingdom.
Antoine F CarpentierParis 7 University, Assistance publique - Hôpitaux de Paris (AP-HP), Paris, France.
Anna K NowakSchool of Medicine, University of Western Australia, Crawley, Australia.
Warren MasonCancer Clinical Research Unit, Princess Margaret Cancer Centre, Toronto, Canada.
Vittorina ZagonelDepartment of Clinical and Experimental Oncology, Medical Oncology Unit 1, Veneto Institute of Oncology-IRCCS, Padua, Italy.
François DuboisCentre Hospitalier Régional et Universitaire de Lille, Lille, France.
Gaetano FinocchiaroIstituto Neurologico Carlo Besta, Milan, Italy.
George FountzilasAristotle University of Thessaloniki, Thessaloniki, Greece.
Dana Michaela CerneaThe Oncology Institute "Prof. Dr. Ion Chiricuta," Cluj-Napoca, Romania.
Oliver ChinotAix-Marseille University, Assistance publique - Hôpitaux de Marseille (AP-HM), CHU Timone, Marseille, France.
Rodica AnghelAlexandru Trestioreanu Bucharest Institute of Oncology, Bucharest, Romania.
Francois GhiringhelliCentre Georges Francois Leclerc, Dijon, France.
Patrick BeauchesneDépartement de Neuro-Oncologie, Hôpital Central, Nancy, France.
Giuseppe LombardiDepartment of Clinical and Experimental Oncology, Medical Oncology Unit 1, Veneto Institute of Oncology-IRCCS, Padua, Italy.
Enrico FranceschiDepartment of Medical Oncology, AUSL, Bologna, Italy.
Martina MakrutzkiF. Hoffmann-La Roche Ltd., Basel, Switzerland.
Chiedzo MpofuF. Hoffmann-La Roche Ltd., Basel, Switzerland.
Hans-Joerg UrbanF. Hoffmann-La Roche Ltd., Basel, Switzerland.
Josef PichlerInstitut für Innere Medizin mit Neuroonkologie, Linz, Austria.
Roche (Switzerland) · CHAzienda USL di Bologna · ITIstituto Oncologico Veneto · ITAix-Marseille Université · FRAristotle University of Thessaloniki · GRCarol Davila University of Medicine and Pharmacy · ROCentre Georges François Leclerc · FRCentre Hospitalier Universitaire de Lille · FRFondazione IRCCS Istituto Neurologico Carlo Besta · ITInstitut d'Investigació Biomédica de Bellvitge · ESInstitute of Oncology Prof. Dr. Ion Chiricuta · ROMedical University of Vienna · ATNational Health Service · GBPrincess Margaret Cancer Centre · CAUniversité Paris Cité · FRUniversity of Western Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe assessed the efficacy and safety of bevacizumab (BEV) through multiple lines in patients with recurrent glioblastoma who had progressed after first-line treatment with radiotherapy, temozolomide, and BEV. PATIENTS AND

methodsTAMIGA (NCT01860638) was a phase II, randomized, double-blind, placebo-controlled, multicenter trial in adult patients with glioblastoma. Following surgery, patients with newly diagnosed glioblastoma received first-line treatment consisting of radiotherapy plus temozolomide and BEV, followed by six cycles of temozolomide and BEV, then BEV monotherapy until disease progression (PD1). Randomization occurred at PD1 (second line), and patients received lomustine (CCNU) plus BEV (CCNU + BEV) or CCNU plus placebo (CCNU + placebo) until further disease progression (PD2). At PD2 (third line), patients continued BEV or placebo with chemotherapy (investigator's choice). The primary endpoint was survival from randomization. Secondary endpoints were progression-free survival in the second and third lines (PFS2 and PFS3) and safety.

resultsOf the 296 patients enrolled, 123 were randomized at PD1 (CCNU + BEV,

conclusionThere was no survival benefit and no detriment observed with continuing BEV through multiple lines in patients with recurrent glioblastoma. IMPLICATIONS FOR PRACTICE: Previous research suggested that there may be value in continuing bevacizumab (BEV) beyond progression through multiple lines of therapy. No survival benefit was observed with the use of BEV through multiple lines in patients with glioblastoma who had progressed after first-line treatment (radiotherapy + temozolomide + BEV). No new safety concerns arose from the use of BEV through multiple lines of therapy.

Indexed as

AdultAgedAntineoplastic Agents, ImmunologicalBevacizumabBrain NeoplasmsDouble-Blind MethodFemaleFollow-Up StudiesGlioblastomaHumansMaleMiddle AgedNeoplasm Recurrence, LocalPrognosisSurvival RateAntineoplastic Agents, ImmunologicalBevacizumabClinical trialContinuous bevacizumabOverall survivalRecurrent glioblastoma

Identifiers

PMID30266892
PMCPMC6459244
OpenAlexW2892927588

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.