Evidence map›Paper›PMID 36480779›Full record

ArticleJCO precision oncology2022

Analysis of Circulating Tumor DNA to Predict Risk of Recurrence in Patients With Esophageal and Gastric Cancers.

Brandon M Huffman, Vasily N Aushev, Griffin L Budde, Joseph Chao, Farshid Dayyani, Diana Hanna, Gregory P Botta, Daniel V T Catenacci, Steven B Maron, Shifra Krinshpun and 8 more

Open access · hybridAbstract read
In one paragraph

Article in JCO precision oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 2 pooled it
5.7field-weighted citation impact, top 3% 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

61 citing papers in PubMed, 2 syntheses or guidelines pooled it, 65 citations in OpenAlex.

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 9 institutions in 1 country.

Brandon M HuffmanDepartment of Medicine, Division of Hematology-Oncology, Massachusetts General Hospital Cancer Center, Boston, MA.ORCID 0000-0002-0768-3145
Vasily N AushevNatera, Inc, Austin, TX.ORCID 0000-0001-8003-358X
Griffin L BuddeNatera, Inc, Austin, TX.
Joseph ChaoCity of Hope Comprehensive Cancer Center, Duarte, CA.ORCID 0000-0002-1809-504X
Farshid DayyaniUniversity of California Irvine Chao Family Comprehensive Cancer Center, Orange, CA.ORCID 0000-0002-4970-5189
Diana HannaKeck Hospital of USC, Los Angeles, CA.
Gregory P BottaUCSD Moores Cancer Center, La Jolla, CA.ORCID 0000-0001-9606-4508
Daniel V T CatenacciUniversity of Chicago, Chicago, IL.ORCID 0000-0001-7517-8020
Steven B MaronMemorial Sloan Kettering Cancer Center, New York City, NY.ORCID 0000-0002-8794-130X
Shifra KrinshpunNatera, Inc, Austin, TX.
Shruti SharmaNatera, Inc, Austin, TX.
Giby V GeorgeNatera, Inc, Austin, TX.
Meenakshi MalhotraNatera, Inc, Austin, TX.ORCID 0000-0002-9731-5628
Adham JurdiNatera, Inc, Austin, TX.
Solomon MoshkevichNatera, Inc, Austin, TX.
Alexey AleshinNatera, Inc, Austin, TX.ORCID 0000-0002-0425-0301
Pashtoon M KasiWeill Cornell Medicine, Englander Institute of Precision Medicine, New York Presbyterian Hospital, New York, NY.ORCID 0000-0002-5169-7085
Samuel J KlempnerDepartment of Medicine, Division of Hematology-Oncology, Massachusetts General Hospital Cancer Center, Boston, MA.ORCID 0000-0002-4062-0808
Natera (United States) · USMassachusetts General Hospital · USCity of Hope · USKeck Hospital of USC · USMemorial Sloan Kettering Cancer Center · USMoores Cancer CenterNewYork–Presbyterian Hospital · USUniversity of California, Irvine · USUniversity of Chicago · US

Funding

VIRAL MALIGNANCYP30CA023100 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Jesse Nodora · 1985 to 2026
$124.9M
Tumor Microenvironment and Cancer ImmunologyP30CA030199 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI ELENA B PASQUALE · 1985 to 2026
$107.2M
NCI NIH HHS P30 CA023100NCI NIH HHS P30 CA030199
6 · The paper itself

Abstract

purposeCirculating tumor DNA (ctDNA) analyses allow for postoperative risk stratification in patients with curatively treated colon and breast cancers. Use of ctDNA in esophagogastric cancers (EGC) is less characterized and could identify high-risk patients who have been treated with curative intent.

methodsIn this retrospective analysis of real-world data, ctDNA levels were analyzed in the preoperative, postoperative, and surveillance settings in patients with EGC using a personalized multiplex polymerase chain reaction-based next-generation sequencing assay. Plasma samples (n = 943) from 295 patients at > 70 institutions were collected before surgery, postoperatively, and/or serially during routine clinical follow-up from September 19, 2019, to February 21, 2022. ctDNA detection was annotated to clinicopathologic features and recurrence-free survival.

resultsA total of 295 patients with EGC were analyzed, and 212 patients with stages I-III disease were further explored. Pretreatment ctDNA was detected in 96% (23/24) of patients with preoperative time points. Postoperative ctDNA was detected in 23.5% (16/68) of patients with stage I-III EGC within 16 weeks (molecular residual disease window) after surgery without receiving systemic therapy. ctDNA detection at any time point after surgery (hazard ratio [HR], 23.6; 95% CI, 10.2 to 66.0;

conclusionUsing real-world data, we demonstrate that postoperative tumor-informed ctDNA detection in EGC is feasible and allows for enhanced patient risk stratification and prognostication during curative-intent therapy.

Indexed as

Circulating Tumor DNAEsophageal NeoplasmsStomach NeoplasmsHumansRetrospective StudiesCirculating Tumor DNA

Identifiers

PMID36480779
PMCPMC10530958
OpenAlexW4310887597

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.