Evidence map›Paper›PMID 34117261›Full record

ArticleNPJ breast cancer2021

Circulating tumor cell number and endocrine therapy index in ER positive metastatic breast cancer patients.

Costanza Paoletti, Meredith M Regan, Samuel M Niman, Emily M Dolce, Elizabeth P Darga, Minetta C Liu, P Kelly Marcom, Lowell L Hart, John W Smith, Karen L Tedesco and 9 more

Open access · goldAbstract read
In one paragraph

Article in NPJ breast cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.0field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 26 citations in OpenAlex.

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  14. Circulating tumor cells: biology and clinical significance.Signal transduction and targeted therapy · 2021
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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

19 authors at 12 institutions in 2 countries.

Costanza PaolettiDepartment of Internal Medicine, Division of Hematology/Oncology, University of Michigan Rogel Cancer Center, Ann Arbor, MI, USA.ORCID http://orcid.org/0000-0003-0162-2453
Meredith M ReganDivision of Biostatistics, Dana-Farber Cancer Institute, Boston, MA, USA.
Samuel M NimanDivision of Biostatistics, Dana-Farber Cancer Institute, Boston, MA, USA.
Emily M DolceDepartment of Internal Medicine, Division of Hematology/Oncology, University of Michigan Rogel Cancer Center, Ann Arbor, MI, USA.
Elizabeth P DargaDepartment of Internal Medicine, Division of Hematology/Oncology, University of Michigan Rogel Cancer Center, Ann Arbor, MI, USA.ORCID http://orcid.org/0000-0001-7728-9162
Minetta C LiuDepartment of Oncology, Division of Medical Oncology, and Department of Laboratory Medicine and Pathology, Division of Anatomic Pathology, Mayo Clinic, Rochester, MN, USA.ORCID http://orcid.org/0000-0002-8206-5232
P Kelly MarcomDepartment of Medicine, Division of Medical Oncology, Duke Cancer Institute, Durham, NC, USA.
Lowell L HartFlorida Cancer Specialists/Wake Forest School of Medicine, Fort Myers, FL, USA.
John W SmithUS Oncology Research, Compass Oncology, Portland, OR, USA.
Karen L TedescoNew York Oncology Hematology, US Oncology Network, Albany, NY, USA.
Eitan AmirDivision of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, ON, Canada.ORCID http://orcid.org/0000-0002-3706-525X
Ian E KropDepartment of Medical Oncology, Division of Breast Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.ORCID http://orcid.org/0000-0002-6380-5944
Angela M DeMicheleDepartment of Medicine, Division of Hematology/Oncology, University of Pennsylvania, Philadelphia, PA, USA.ORCID http://orcid.org/0000-0003-1297-4251
Pamela J GoodwinDepartment of Medicine, Sinai Health System, University of Toronto, Toronto, ON, Canada.
Margaret BlockNebraska Cancer Specialists, Omaha, NE, USA.
Kimberly AungDepartment of Internal Medicine, Division of Hematology/Oncology, University of Michigan Rogel Cancer Center, Ann Arbor, MI, USA.
Martha E BrownDepartment of Internal Medicine, Division of Hematology/Oncology, University of Michigan Rogel Cancer Center, Ann Arbor, MI, USA.
Robert T McCormackJanssen Pharmaceuticals, Inc., Raritan, NJ, USA.
Daniel F HayesDepartment of Internal Medicine, Division of Hematology/Oncology, University of Michigan Rogel Cancer Center, Ann Arbor, MI, USA. hayesdf@umich.edu.
University of Michigan · USDana-Farber Cancer Institute · USCompass Oncology · USDuke Medical Center · USFlorida Cancer Specialists & Research Institute · USJanssen (United States) · USMayo Clinic in Arizona · USNebraska Cancer Specialists · USNew York Oncology Hematology · USPrincess Margaret Cancer Centre · CAUniversity of Pennsylvania · USUniversity of Toronto · CA

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI THEODORE S LAWRENCE · 1988 to 2026
$178.2M
Secondary Prevention through Surveillance and InterventionR01CA208273 · NCI · UNIVERSITY OF PENNSYLVANIA · PI CHODOSH, LEWIS A, DEMICHELE, ANGELA · 2017 to 2021
$3.2M
NCI NIH HHS P30 CA046592NCI NIH HHS R01 CA208273
6 · The paper itself

Abstract

Circulating tumor cells (CTC) are prognostic in metastatic breast cancer (MBC). The CTC-endocrine therapy index (CTC-ETI), consisting of CTC-ER (estrogen receptor), BCL2, human epidermal growth factor receptor (HER2), and Ki67 expression, might predict resistance to endocrine therapy (ET) in patients with ER-positive MBC. One hundred twenty-one patients with ER-positive/HER2-negative MBC initiating a new ET after ≥1 lines of ET were enrolled in a prospective, multi-institutional clinical trial. CTC-ETI and clinical/imaging follow-up were performed at baseline and serial time points. Progression-free survival (PFS) and rapid progression (RP; determined at the 3-month time point) were primary endpoints. Associations with clinical outcomes used logrank and Fisher's exact tests. At baseline, 36% (38/107) of patients had ≥5 CTC/7.5 ml whole blood (WB). Patients with ≥5 vs. <5 CTC/7.5 ml WB had significantly worse PFS (median 3.3 vs. 5.9 months, P = 0.03). Elevated CTC at 1 month was associated with even worse PFS (1.9 vs. 5.0 months from the 1-month sample, P < 0.001). Low, intermediate, and high CTC-ETI were observed in 71 (66%), 8 (8%), and 28 (26%) patients, with median PFS of 6.9, 8.5, and 2.8 months, respectively (P = 0.008). Patients with high vs. low CTC and CTC-ETI more frequently experienced RP (CTC: 66% vs. 41%; P = 0.03; CTC-ETI: 79% vs. 40%; P = 0.002). In conclusion, CTC enumeration and the CTC-ETI assay are prognostic at baseline and follow-up in patients with ER-positive/HER2-negative MBC starting new ET. CTC at first follow-up might identify a group of patients with ER-positive MBC that could forego ET, but CTC-ETI did not contribute further.

Identifiers

PMID34117261
PMCPMC8196036
OpenAlexW3169325545

What OpenQuestion holds

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Registered trials

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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.