Evidence map›Paper›PMID 34158340›Full record

ArticleMolecular cancer therapeutics2021

TPX-0131, a Potent CNS-penetrant, Next-generation Inhibitor of Wild-type ALK and ALK-resistant Mutations.

Brion W Murray, Dayong Zhai, Wei Deng, Xin Zhang, Jane Ung, Vivian Nguyen, Han Zhang, Maria Barrera, Ana Parra, Jessica Cowell and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed, 1 pooled it
9.7field-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

48 citing papers in PubMed, 1 synthesis or guideline pooled it, 86 citations in OpenAlex.

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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

13 authors at 1 institution in 1 country.

Brion W MurrayTurning Point Therapeutics, San Diego, California. brion.murray@tptherapeutics.com.ORCID 0000-0003-1591-2566
Dayong ZhaiTurning Point Therapeutics, San Diego, California.
Wei DengTurning Point Therapeutics, San Diego, California.
Xin ZhangTurning Point Therapeutics, San Diego, California.
Jane UngTurning Point Therapeutics, San Diego, California.
Vivian NguyenTurning Point Therapeutics, San Diego, California.ORCID 0000-0002-6139-9743
Han ZhangTurning Point Therapeutics, San Diego, California.ORCID 0000-0003-3074-0563
Maria BarreraTurning Point Therapeutics, San Diego, California.
Ana ParraTurning Point Therapeutics, San Diego, California.
Jessica CowellTurning Point Therapeutics, San Diego, California.
Dong J LeeTurning Point Therapeutics, San Diego, California.
Herve AloysiusTurning Point Therapeutics, San Diego, California.
Evan RogersTurning Point Therapeutics, San Diego, California.
Cidara Therapeutics (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since 2011, with the approval of crizotinib and subsequent approval of four additional targeted therapies, anaplastic lymphoma kinase (ALK) inhibitors have become important treatments for a subset of patients with lung cancer. Each generation of ALK inhibitor showed improvements in terms of central nervous system (CNS) penetration and potency against wild-type (WT) ALK, yet a key continued limitation is their susceptibility to resistance from ALK active-site mutations. The solvent front mutation (G1202R) and gatekeeper mutation (L1196M) are major resistance mechanisms to the first two generations of inhibitors while patients treated with the third-generation ALK inhibitor lorlatinib often experience progressive disease with multiple mutations on the same allele (mutations

Indexed as

Anaplastic Lymphoma KinaseAntineoplastic AgentsCell Transformation, NeoplasticDrug Resistance, NeoplasmMacrocyclic CompoundsMutationProtein Kinase InhibitorsAnimalsApoptosisB-LymphocytesCell ProliferationFemaleHumansMiceMice, NudeRatsALK protein, humanAnaplastic Lymphoma KinaseAntineoplastic AgentsMacrocyclic CompoundsProtein Kinase InhibitorsTPX-0131

Identifiers

PMID34158340
PMCPMC9398166
OpenAlexW3173160576

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.