Evidence map›Paper›PMID 25801821›Full record

ArticleThe Journal of molecular diagnostics : JMD2015

Memorial Sloan Kettering-Integrated Mutation Profiling of Actionable Cancer Targets (MSK-IMPACT): A Hybridization Capture-Based Next-Generation Sequencing Clinical Assay for Solid Tumor Molecular Oncology.

Donavan T Cheng, Talia N Mitchell, Ahmet Zehir, Ronak H Shah, Ryma Benayed, Aijazuddin Syed, Raghu Chandramohan, Zhen Yu Liu, Helen H Won, Sasinya N Scott and 17 more

Abstract readEvaluation Study
In one paragraph

Article in The Journal of molecular diagnostics : JMD, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1,588 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1,588citing papers in PubMed, 2 pooled it
50.4field-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

1,588 citing papers in PubMed, 2 syntheses or guidelines pooled it, 2,114 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. A Phase II Trial of Olaparib plus Pembrolizumab in Patients with Recurrent Copy Number-High/p53-Abnormal Endometrial Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Trial
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  8. Accelerating Drug Development in Hormone-Naïve Prostate Cancer through Multimodal Therapy Strategies: The MetaCURE Phase 2 Randomized Clinical Trial.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Trial
  9. Trial
  10. Trial
  11. Immune Checkpoint Inhibitor Therapy for Aggressive Pituitary Neuroendocrine Tumors.The Journal of clinical endocrinology and metabolism · 2025
    Trial
  12. ctDNA as a Molecular Biomarker in the Phase II Trial of Imatinib plus Binimetinib in Patients with Advanced Gastrointestinal Stromal Tumor.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Trial
  13. Article
  14. Review
  15. Article
  16. Brief Report: Proposed Clinical Trial Guidelines Based on Clinicopathologic Heterogeneity of Metastatic Pulmonary Large Cell Neuroendocrine Carcinoma.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2026
    Article
  17. Article
  18. Article
  19. Article
  20. Molecular and Clinical Determinants of Targeted Therapy Treatment in Biliary Tract Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Article

1,528 more citing papers are in PubMed but not listed here.

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

27 authors at 1 institution in 1 country.

Donavan T ChengDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Talia N MitchellDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Ahmet ZehirDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Ronak H ShahDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Ryma BenayedDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Aijazuddin SyedDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Raghu ChandramohanDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Zhen Yu LiuDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Helen H WonDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Sasinya N ScottDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
A Rose BrannonDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Catherine O'ReillyDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Justyna SadowskaDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Jacklyn CasanovaDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Angela YannesDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Jaclyn F HechtmanDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Jinjuan YaoDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Wei SongDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Dara S RossDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Alifya OultacheDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Snjezana DoganDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Laetitia BorsuDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Meera HameedDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Khedoudja NafaDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Maria E ArcilaDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Marc LadanyiDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York; Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York.
Michael F BergerDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York; Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York. Electronic address: bergerm1@mskcc.org.
Memorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
The Role of Focal Oncogene Amplifications in Lung CancerP01CA129243 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Marc Ladanyi · 2007 to 2026
$31.2M
NCI NIH HHS P01 CA129243NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

The identification of specific genetic alterations as key oncogenic drivers and the development of targeted therapies are together transforming clinical oncology and creating a pressing need for increased breadth and throughput of clinical genotyping. Next-generation sequencing assays allow the efficient and unbiased detection of clinically actionable mutations. To enable precision oncology in patients with solid tumors, we developed Memorial Sloan Kettering-Integrated Mutation Profiling of Actionable Cancer Targets (MSK-IMPACT), a hybridization capture-based next-generation sequencing assay for targeted deep sequencing of all exons and selected introns of 341 key cancer genes in formalin-fixed, paraffin-embedded tumors. Barcoded libraries from patient-matched tumor and normal samples were captured, sequenced, and subjected to a custom analysis pipeline to identify somatic mutations. Sensitivity, specificity, reproducibility of MSK-IMPACT were assessed through extensive analytical validation. We tested 284 tumor samples with previously known point mutations and insertions/deletions in 47 exons of 19 cancer genes. All known variants were accurately detected, and there was high reproducibility of inter- and intrarun replicates. The detection limit for low-frequency variants was approximately 2% for hotspot mutations and 5% for nonhotspot mutations. Copy number alterations and structural rearrangements were also reliably detected. MSK-IMPACT profiles oncogenic DNA alterations in clinical solid tumor samples with high accuracy and sensitivity. Paired analysis of tumors and patient-matched normal samples enables unambiguous detection of somatic mutations to guide treatment decisions.

Indexed as

DNADNA Mutational AnalysisGenotypeHigh-Throughput Nucleotide SequencingHumansMutationNeoplasmsParaffin EmbeddingReproducibility of ResultsDNA

Identifiers

PMID25801821
PMCPMC5808190
OpenAlexW223909586

What OpenQuestion holds

Textmetadata
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.