Evidence map›Paper›PMID 42254833›Full record

ArticleNeuro-oncology advances

Combining the KRAS

Consuelo Torrini, Naema Nayyar, Gregory R Wojtkiewicz, Anita Giobbie-Hurder, Magali A de Sauvage, Christian Migliarese, Elizabeth J Summers, Nazanin Ijad, Erika Yamazawa, Britney S Zhang and 7 more

Abstract read
In one paragraph

Article in Neuro-oncology advances. 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

17 authors.

Consuelo TorriniKrantz Center for Cancer Research, Massachusetts General Hospital, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0003-2743-0839
Naema NayyarKrantz Center for Cancer Research, Massachusetts General Hospital, Boston, Massachusetts, USA.
Gregory R WojtkiewiczKrantz Center for Cancer Research, Massachusetts General Hospital, Boston, Massachusetts, USA.
Anita Giobbie-HurderKrantz Center for Cancer Research, Massachusetts General Hospital, Boston, Massachusetts, USA.
Magali A de SauvageKrantz Center for Cancer Research, Massachusetts General Hospital, Boston, Massachusetts, USA.
Christian MigliareseDepartment of Neurosurgery, Massachusetts General Hospital, Boston, Massachusetts, USA.
Elizabeth J SummersKrantz Center for Cancer Research, Massachusetts General Hospital, Boston, Massachusetts, USA.
Nazanin IjadKrantz Center for Cancer Research, Massachusetts General Hospital, Boston, Massachusetts, USA.
Erika Yamazawa
Britney S Zhang
Emily M SullivanKrantz Center for Cancer Research, Massachusetts General Hospital, Boston, Massachusetts, USA.
Varun Sasisekharan
Leland G RichardsonDepartment of Neurosurgery, Massachusetts General Hospital, Boston, Massachusetts, USA.
Braxton M MarionKrantz Center for Cancer Research, Massachusetts General Hospital, Boston, Massachusetts, USA.
Peter OlsonMirati Therapeutics, Inc., A Bristol Myers Squibb Company, San Diego, California, USA.
Hiroaki WakimotoDepartment of Neurosurgery, Massachusetts General Hospital, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0001-8225-241X
Priscilla K BrastianosKrantz Center for Cancer Research, Massachusetts General Hospital, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0003-4470-8425

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Despite advances in treatment, brain metastasis (BM) management remains a significant challenge. Adagrasib is a brain-penetrant KRAS Methods: We tested the in vitro efficacy of adagrasib on two Kras Results: Three-week adagrasib monotherapy and combination therapy with ICI demonstrated benefit in colorectal and lung cancer BM models. Adagrasib alone and in combination demonstrated similarly potent anti-tumor effects against extracranial tumors. While monotherapies reduced intracranial tumor growth, adagrasib with ICI showed the most favorable outcome. Although both adagrasib monotherapy and combination therapy extended survival, long-term intracranial disease control after rechallenge was the greatest with combination therapy. Conclusions: Adagrasib with ICI improved long-term survival and blocked CNS progression in dual extra- and intracranial BM models.  These findings support investigation of adagrasib with ICI in patients with KRASG12C-mutant BM.

Indexed as

anti-PD-1brain metastasesimmunotherapyKRAS inhibitortargeted therapy

Identifiers

PMID42254833
PMCPMC13242296

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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.