Evidence map›Paper›PMID 34476329›Full record

Observational studyJCO precision oncology2021

Real-World Performance of a Comprehensive Genomic Profiling Test Optimized for Small Tumor Samples.

Scott A Tomlins, Daniel H Hovelson, Jennifer M Suga, Daniel M Anderson, Han A Koh, Elizabeth C Dees, Brendan McNulty, Mark E Burkard, Michael Guarino, Jamil Khatri and 34 more

Registry-linked trialAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in JCO precision oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03061305 (An Observational Trial Assessing the Clinical Benefit of Molecular Profiling in Patients With Solid Tumors), which is not on this map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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.

NCT03061305 terminatednot on this map

An Observational Trial Assessing the Clinical Benefit of Molecular Profiling in Patients With Solid Tumors

Typeobservational_patient_registrySponsorStrata OncologyRan2016 to 2024Enrolled58,213ConditionsCancer, Adult Solid Tumor, Lymphoma, Multiple Myeloma
3 · Its place in the literature

Who cites it

20 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Observational
  5. Article
  6. Article
  7. Observational
  8. Article
  9. Molecular Biological Determination ofInternational journal of molecular sciences · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

44 authors.

Scott A TomlinsStrata Oncology, Ann Arbor, MI.
Daniel H HovelsonStrata Oncology, Ann Arbor, MI.
Jennifer M SugaKaiser Permanente, Dept of Medical Oncology, Vallejo, CA.
Daniel M AndersonMetro-Minnesota Community Oncology Research Consortium (MMCORC), St Louis Park, MN.
Han A KohKaiser Permanente, Bellflower, CA.
Elizabeth C DeesThe University of North Carolina Lineberger Comprehensive Cancer Center, Chapel Hill, NC.
Brendan McNultyUNC Rex Healthcare, Raleigh, NC.
Mark E BurkardUniversity of Wisconsin Carbone Cancer Center, Madison, WI.
Michael GuarinoChristianaCare's Helen F. Graham Cancer Center & Research Institute, Newark, DE.
Jamil KhatriChristianaCare's Helen F. Graham Cancer Center & Research Institute, Newark, DE.
Malek M SafaKettering Cancer Center, Kettering, OH.
Marc R MatranaOchsner Cancer Institute, New Orleans, LA.
Eddy S YangUniversity of Alabama at Birmingham, Birmingham, AL.
Alex R MenterKaiser Permanente Medical Group, Denver, CO.
Benjamin M ParsonsGundersen Health System, La Crosse, WI.
Jennifer N SlimMultiCare, Auburn, WA.
Michael A ThompsonAdvocate Aurora Health Care, Milwaukee, WI.
Leon HwangKaiser Permanente Mid Atlantic, Rockville, MD.
William J EdenfieldPrisma Health Cancer Institute, Greenville, SC.
Suresh NairLehigh Valley Health Network, Allentown, PA.
Adedayo OnitiloMarshfield Clinic, Marshfield WI.
Robert SiegelBon Secours St Francis Cancer Center, Greenville, SC.
Alan MillerSCL Health Colorado, Broomfield, CO.
Timothy WassenaarProHealth Care, Waukesha, WI.
William J IrvinBon Secours St Francis Medical Center Midlothian, Midlothian, VA.
William SchulzSwedish American, Rockford, IL.
Arvinda PadmanabhanBaptist Health, Lexington, KY.
Vallathucherry HarishHigh Point Medical Center, High Point, NC.
Anneliese GonzalezUT Health-Memorial Hermann Cancer Institute, Houston, TX.
Abdul Hai MansoorKaiser Permanente Northwest, Portland, OR.
Andrew KellumNorth Mississippi Medical Center, Tupelo, MS.
Paul HarmsUniversity of Michigan Health Systems, Ann Arbor, MI.
Stephanie DreweryStrata Oncology, Ann Arbor, MI.
Jayson FalknerStrata Oncology, Ann Arbor, MI.
Andrew FischerStrata Oncology, Ann Arbor, MI.
Jennifer HippStrata Oncology, Ann Arbor, MI.
Kat KwiatkowskiStrata Oncology, Ann Arbor, MI.
Lorena Lazo de la VegaStrata Oncology, Ann Arbor, MI.
Khalis MitchellStrata Oncology, Ann Arbor, MI.
Travis ReederStrata Oncology, Ann Arbor, MI.
Javed SiddiquiStrata Oncology, Ann Arbor, MI.
Hana VakilStrata Oncology, Ann Arbor, MI.
D Bryan JohnsonStrata Oncology, Ann Arbor, MI.
Daniel R RhodesStrata Oncology, Ann Arbor, MI.

Funding

Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Christopher K Laubenthal · 2000 to 2026
$70.0M
NCI NIH HHS P30 CA086862
6 · The paper itself

Abstract

purposeTissue-based comprehensive genomic profiling (CGP) is increasingly used for treatment selection in patients with advanced cancer; however, tissue availability may limit widespread implementation. Here, we established real-world CGP tissue availability and assessed CGP performance on consecutively received samples. MATERIALS AND

methodsWe conducted a post hoc, nonprespecified analysis of 32,048 consecutive tumor tissue samples received for StrataNGS, a multiplex polymerase chain reaction (PCR)-based comprehensive genomic profiling (PCR-CGP) test, as part of an ongoing observational trial (NCT03061305). Sample characteristics and PCR-CGP performance were assessed across all tested samples, including exception samples not meeting minimum input quality control (QC) requirements (< 20% tumor content [TC], < 2 mm

resultsAmong 31,165 (97.2%) samples where PCR-CGP was attempted, 10.7% had < 20% TC and 59.2% were small (< 25 mm

conclusionMost real-world tissue samples from patients with advanced cancer desiring CGP are limited, requiring optimized CGP approaches to produce meaningful results. An optimized PCR-CGP test, coupled with an inclusive exception testing policy, delivered reportable results for > 94% of samples, potentially expanding the proportion of CGP-testable patients and impact of biomarker-guided therapies.

Indexed as

Genome, HumanBiomarkers, TumorGenomicsHigh-Throughput Nucleotide SequencingHumansMultiplex Polymerase Chain ReactionNeoplasmsProspective StudiesBiomarkers, Tumor

Identifiers

PMID34476329
PMCPMC8384401

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Registered trials

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.