Evidence map›Paper›PMID 39198692›Full record

ArticleNPJ precision oncology2024

Pharmacogenomic discovery of genetically targeted cancer therapies optimized against clinical outcomes.

Peter Truesdell, Jessica Chang, Doris Coto Villa, Meiou Dai, Yulei Zhao, Robin McIlwain, Stephanie Young, Shawna Hiley, Andrew W Craig, Tomas Babak

Abstract read
In one paragraph

Article in NPJ precision oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. A functional map of mNature cancer · 2026
    Article
  2. Article
  3. Article
  4. Review
  5. Review
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.

Peter TruesdellLeapfrog Bio, San Mateo, USA.
Jessica ChangLeapfrog Bio, San Mateo, USA.
Doris Coto VillaLeapfrog Bio, San Mateo, USA.
Meiou DaiLeapfrog Bio, San Mateo, USA.
Yulei ZhaoCancer Biology & Genetics, Queen's Cancer Research Institute; Queen's University, Kingston, Canada.ORCID http://orcid.org/0000-0002-2242-3843
Robin McIlwainLeapfrog Bio, San Mateo, USA.
Stephanie YoungCancer Biology & Genetics, Queen's Cancer Research Institute; Queen's University, Kingston, Canada.
Shawna HileyThird Degree Science Communication, Edmonton, Canada.
Andrew W CraigCancer Biology & Genetics, Queen's Cancer Research Institute; Queen's University, Kingston, Canada.
Tomas BabakLeapfrog Bio, San Mateo, USA. tomas@leapfrog.bio.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the clinical success of dozens of genetically targeted cancer therapies, the vast majority of patients with tumors caused by loss-of-function (LoF) mutations do not have access to these treatments. This is primarily due to the challenge of developing a drug that treats a disease caused by the absence of a protein target. The success of PARP inhibitors has solidified synthetic lethality (SL) as a means to overcome this obstacle. Recent mapping of SL networks using pooled CRISPR-Cas9 screens is a promising approach for expanding this concept to treating cancers driven by additional LoF drivers. In practice, however, translating signals from cell lines, where these screens are typically conducted, to patient outcomes remains a challenge. We developed a pharmacogenomic (PGx) approach called "Clinically Optimized Driver Associated-PGx" (CODA-PGX) that accurately predicts genetically targeted therapies with clinical-stage efficacy in specific LoF driver contexts. Using approved targeted therapies and cancer drugs with available real-world evidence and molecular data from hundreds of patients, we discovered and optimized the key screening principles predictive of efficacy and overall patient survival. In addition to establishing basic technical conventions, such as drug concentration and screening kinetics, we found that replicating the driver perturbation in the right context, as well as selecting patients where those drivers are genuine founder mutations, were key to accurate translation. We used CODA-PGX to screen a diverse collection of clinical stage drugs and report dozens of novel LoF genetically targeted opportunities; many validated in xenografts and by real-world evidence. Notable examples include treating STAG2-mutant tumors with Carboplatin, SMARCB1-mutant tumors with Oxaliplatin, and TP53BP1-mutant tumors with Etoposide or Bleomycin.

Identifiers

PMID39198692
PMCPMC11358483

What Socratic 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 Socratic graph.