Evidence map›Paper›PMID 28986743›Full record

Trial reportBreast cancer research and treatment2018

Monosomy 17 in potentially curable HER2-amplified breast cancer: prognostic and predictive impact.

David B Page, Hannah Wen, Edi Brogi, Dana Dure, Dara Ross, Kateri J Spinelli, Sujata Patil, Larry Norton, Clifford Hudis, Heather L McArthur

Open access · greenAbstract readClinical Trial, Phase III
In one paragraph

Trial report in Breast cancer research and treatment, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 19% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
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  7. Review
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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

10 authors at 3 institutions in 1 country.

David B PageProvidence Cancer Center, Earle A. Chiles Research Institute, 4805 NE Glisan St., Suite 6N40, Portland, OR, 97213, USA. David.Page2@providence.org.
Hannah WenMemorial Sloan Kettering Cancer Center, 300 E 66th Street, New York, NY, 10065, USA.
Edi BrogiMemorial Sloan Kettering Cancer Center, 300 E 66th Street, New York, NY, 10065, USA.
Dana DureMemorial Sloan Kettering Cancer Center, 300 E 66th Street, New York, NY, 10065, USA.
Dara RossMemorial Sloan Kettering Cancer Center, 300 E 66th Street, New York, NY, 10065, USA.
Kateri J SpinelliProvidence Cancer Center, Earle A. Chiles Research Institute, 4805 NE Glisan St., Suite 6N40, Portland, OR, 97213, USA.
Sujata PatilMemorial Sloan Kettering Cancer Center, 300 E 66th Street, New York, NY, 10065, USA.
Larry NortonMemorial Sloan Kettering Cancer Center, 300 E 66th Street, New York, NY, 10065, USA.
Clifford HudisMemorial Sloan Kettering Cancer Center, 300 E 66th Street, New York, NY, 10065, USA.
Heather L McArthurCedars-Sinai Medical Center, 8700 Beverly Blvd, AC 1042B, Los Angeles, CA, 90048, USA. heather.mcarthur@cshs.org.
Memorial Sloan Kettering Cancer Center · USProvidence Portland Medical Center · USCedars-Sinai Medical Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Cancer Center Support National Institutes of Health/National Cancer Institute P30CA008748NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

purposeHER2 copy number by fluorescence in situ hybridization (FISH) is typically reported relative to the centromere enumeration probe 17 (CEP17). HER2/CEP17 ratio could be impacted by alterations in the number of chromosome 17 copies. Monosomy of chromosome 17 (m17) is found in ~ 1900 cases of early-stage HER2-positive breast cancer annually in the United States; however, the efficacy of HER2-directed trastuzumab therapy in these patients is not well characterized. Here, we retrospectively identified HER2-amplified, stage I-III breast cancers with m17 and characterized the impact of trastuzumab treatment.

methodsFrom January 1, 2000 to June 1, 2011, we identified 99 women with HER2-amplified m17 breast cancers, as defined by a CEP17 signal of < 1.5 per nucleus and a HER2/CEP17 ratio of ≥ 2.0.

resultsMost HER2-amplified m17 patients were treated with trastuzumab plus chemotherapy (51%, n = 50), whereas 31% (n = 31) received chemotherapy alone and 18% (n = 18) received no chemotherapy. The 4-year overall survival (OS) was superior with trastuzumab compared to chemotherapy alone or no chemotherapy (100 vs. 93 vs. 81%, respectively; p = 0.005). OS was not influenced by estrogen/progesterone-receptor (ER/PR) status, tumor stage, or degree of FISH positivity. A proportion of patients who would be considered HER2-negative by standard immunohistochemistry staging criteria (0-1+) were HER2 amplified by FISH.

conclusionsIn the largest series reported to date, patients with HER2-amplified m17 cancers treated with trastuzumab have outcomes comparable to patients from the large phase III adjuvant trastuzumab trials who were HER2-positive, supporting the critical role of HER2-directed therapy in this patient population.

Indexed as

PrognosisAdultAgedBreast NeoplasmsChromosomes, Human, Pair 17Erb-b2 Receptor Tyrosine KinasesFemaleGene AmplificationHumansIn Situ Hybridization, FluorescenceMiddle AgedMonosomyTrastuzumabERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesTrastuzumabAneusomy 17CEP17Chromosome 17FISHHER2HER2-amplifiedMonosomy 17Polysomy 17Trastuzumab

Identifiers

PMID28986743
PMCPMC7405897
OpenAlexW2764083324

What OpenQuestion holds

Textmetadata
LicenceTDM
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.