Evidence map›Paper›PMID 39074345›Full record

ArticleJCO precision oncology2024

TOWARDS Study: Patient-Derived Xenograft Engraftment Predicts Poor Survival in Patients With Newly Diagnosed Triple-Negative Breast Cancer.

Christos Vaklavas, Cindy B Matsen, Zhengtao Chu, Kenneth M Boucher, Sandra D Scherer, Satya Pathi, Anna Beck, Kirstyn E Brownson, Saundra S Buys, Namita Chittoria and 10 more

Abstract read
In one paragraph

Article in JCO precision oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Trial
  2. The functional imperative in high-grade glioma.Experimental & molecular medicine · 2026
    Review
  3. Resistance to neoadjuvant chemotherapy in breast cancers: a metabolic perspective.Journal of experimental & clinical cancer research : CR · 2025
    Review
  4. Article
  5. Review
  6. Article
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

20 authors.

Christos VaklavasDepartment of Internal Medicine, Division of Oncology, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT.ORCID 0000-0002-9919-2748
Cindy B MatsenDepartment of Surgery, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT.ORCID 0000-0003-0179-5311
Zhengtao ChuDepartment of Oncological Sciences, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT.
Kenneth M BoucherDepartment of Internal Medicine, Division of Epidemiology, Salt Lake City, UT.ORCID 0000-0003-2833-0127
Sandra D SchererDepartment of Oncological Sciences, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT.ORCID 0000-0002-7943-8595
Satya PathiDepartment of Oncological Sciences, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT.
Anna BeckDepartment of Internal Medicine, Division of Oncology, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT.
Kirstyn E BrownsonDepartment of Surgery, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT.ORCID 0000-0001-6060-9625
Saundra S BuysDepartment of Internal Medicine, Division of Oncology, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT.ORCID 0000-0003-4120-5697
Namita ChittoriaDepartment of Internal Medicine, Division of Oncology, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT.
Elyse D'AstousHuntsman Cancer Institute Clinical Trials Office, Salt Lake City, UT.
H Evin GulbahceDepartment of Pathology, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT.ORCID 0000-0003-1869-0268
N Lynn HenryDepartment of Internal Medicine, Division of Oncology, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT.
Stephen KimaniDepartment of Internal Medicine, Division of Oncology, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT.ORCID 0000-0003-0403-1296
Jane PorrettaDepartment of Surgery, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT.
Regina RosenthalDepartment of Surgery, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT.
John WardDepartment of Internal Medicine, Division of Oncology, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT.
Mei WeiDepartment of Internal Medicine, Division of Oncology, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT.
Bryan E WelmDepartment of Surgery, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT.ORCID 0000-0002-1879-6612
Alana L WelmDepartment of Oncological Sciences, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT.ORCID 0000-0002-1412-1351

Funding

UTAH REGIONAL CANCER CENTERP30CA042014 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Jared P Rutter · 1986 to 2026
$72.6M
CTSA UM1 Program at University of UtahUM1TR004409 · NCATS · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI RACHEL HESS, Jennifer Juhl Majersik · 2023 to 2026
$21.9M
NCATS NIH HHS UM1 TR004409NCI NIH HHS P30 CA042014
6 · The paper itself

Abstract

purposeAssessing risk of recurrence for nonmetastatic triple-negative breast cancer (TNBC) is a key determinant of therapeutic strategy. The best predictor of recurrence risk is failure to achieve a pathologic complete response after preoperative chemotherapy, but it imperfectly correlates with the definitive end points of relapse-free and overall survival (OS). The inability to accurately predict recurrence has led to increasingly toxic treatment regimens for patients with early-stage TNBC. Better assays for recurrence risk are needed to tailor aggressive therapy for patients who need it and avoid overtreatment and unnecessary toxicity for those at low risk. The purpose of this study was to determine if patient-derived xenograft (PDX) engraftment of newly diagnosed breast tumors can serve as an accurate predictor of recurrence and death from breast cancer.

methodsThis study was a blinded noninterventional trial comprising 80 patients with newly diagnosed, nonmetastatic, estrogen receptor (ER)-negative or ER-low breast cancer.

resultsPDX engraftment was strongly associated with relapse in 1 year: 8 of 18 (44.4%) patients whose tumors engrafted relapsed versus 1 of 62 (1.6%) patients whose tumors did not engraft (

conclusionWe report that the ability of a tumor to engraft as a PDX predicts early recurrence by serving as a functional readout of aggressiveness and prospectively identifies the most devastating tumors. This provides new opportunity to develop surrogate assays, such as biomarkers of engraftment, which will extend the clinical feasibility of this finding.

Indexed as

Triple Negative Breast NeoplasmsAdultAgedAnimalsFemaleHeterograftsHumansMiceMiddle AgedNeoplasm Recurrence, Local

Identifiers

PMID39074345
PMCPMC11371112

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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.