Evidence map›Paper›PMID 41248393›Full record

ArticleBMJ open2025

LSTA1-GBM-2A: study protocol for an exploratory phase 2a randomised controlled trial evaluating tumour-homing peptide certepetide with temozolomide in glioblastoma multiforme.

Johannes Pärtel Truusalu, Kersti Oselin, Jana Lass, Kristen K Buck, William Sietsema, Hiie Soeorg, Kadri Toome, Katrin Kaarna, Tambet Teesalu, Lenne-Triin Kõrgvee

Abstract readClinical Trial Protocol
In one paragraph

Article in BMJ open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Johannes Pärtel TruusaluTartu University Hospital, Tartu, Estonia johannes.partel.truusalu@ut.ee.ORCID http://orcid.org/0009-0003-0323-913X
Kersti OselinNorth Estonia Medical Centre, Tallinn, Estonia.
Jana LassTartu University Hospital, Tartu, Estonia.
Kristen K BuckLisata Therapeutics Inc, Basking Ridge, New Jersey, USA.ORCID http://orcid.org/0000-0001-8364-3578
William SietsemaLisata Therapeutics Inc, Basking Ridge, New Jersey, USA.ORCID http://orcid.org/0000-0003-1950-1692
Hiie SoeorgUniversity of Tartu, Tartu, Estonia.
Kadri ToomeTartu University Hospital, Tartu, Estonia.
Katrin KaarnaTartu University Hospital, Tartu, Estonia.
Tambet TeesaluUniversity of Tartu, Tartu, Estonia.
Lenne-Triin KõrgveeTartu University Hospital, Tartu, Estonia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionGlioblastoma multiforme (GBM) is an aggressive primary brain tumour associated with a poor prognosis despite standard-of-care treatment, including surgical resection, radiotherapy and temozolomide (TMZ) chemotherapy. Certepetide (also known as LSTA1, CEND-1) is an investigational tumour-penetrating peptide that facilitates the extravascular delivery and intratumoural penetration of co-administered immune/chemotherapeutics; however, it has not yet been evaluated in clinical trials for the treatment of intracranial malignancies. METHODS AND ANALYSIS: LSTA1-GBM-2A is an exploratory phase 2a, double-blind, placebo-controlled, randomised, proof-of-concept investigator-initiated trial assessing the safety, tolerability and preliminary efficacy of certepetide in combination with standard-of-care TMZ, compared with TMZ with a matching placebo, in subjects with newly diagnosed GBM.The trial is funded by Lisata Therapeutics, sponsored by Tartu University Hospital and conducted at hospitals in Estonia and Latvia. Subjects are randomised in a 2:1 ratio. Following initial surgery and radiotherapy with concurrent TMZ, the subjects receive intravenous certepetide or placebo alongside six cycles of adjuvant TMZ treatment. The primary endpoint is overall survival. The target number of subjects is 30. The first subject was recruited in January 2024, and accrual is ongoing. ETHICS AND DISSEMINATION: This study was approved by the Republic of Estonia State Agency of Medicines (17 October 2023) and the State Agency of Medicines of the Republic of Latvia (1 February 2024). The results of this study will be published in peer-reviewed journals and reported at academic conferences. TRIAL REGISTRATION NUMBER: 2023-506813-23-00.

Indexed as

Antineoplastic Agents, AlkylatingAntineoplastic Combined Chemotherapy ProtocolsBrain NeoplasmsGlioblastomaTemozolomideAdultClinical Trials, Phase II as TopicDouble-Blind MethodFemaleHumansMaleMiddle AgedRandomized Controlled Trials as TopicAntineoplastic Agents, AlkylatingTemozolomideCHEMOTHERAPYClinical TrialONCOLOGY

Identifiers

PMID41248393
PMCPMC12625905

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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.