Evidence map›Paper›PMID 37643636›Full record

ArticleJournal of the National Comprehensive Cancer Network : JNCCN2023

Hormone Receptor-Positive Breast Cancer Sensitive to Pembrolizumab: Evidence of the Pathogenicity of the MLH1 Variant 1835del3.

Henry G Kaplan, Jeffrey R Whiteaker, Brianna Nelson, Richard G Ivey, Travis D Lorentzen, Uliana Voytovich, Lei Zhao, David J Corwin, Robert Resta, Amanda G Paulovich

Open access · bronzeAbstract readCase Reports
In one paragraph

Article in Journal of the National Comprehensive Cancer Network : JNCCN, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 31% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

10 authors at 2 institutions in 1 country.

Henry G KaplanSwedish Cancer Institute, Seattle, Washington.
Jeffrey R WhiteakerFred Hutchinson Cancer Center, Seattle, Washington.
Brianna NelsonSwedish Cancer Institute, Seattle, Washington.
Richard G IveyFred Hutchinson Cancer Center, Seattle, Washington.
Travis D LorentzenFred Hutchinson Cancer Center, Seattle, Washington.
Uliana VoytovichFred Hutchinson Cancer Center, Seattle, Washington.
Lei ZhaoFred Hutchinson Cancer Center, Seattle, Washington.
David J CorwinCellNetix, Tukwila, Washington.
Robert RestaSwedish Cancer Institute, Seattle, Washington.
Amanda G PaulovichFred Hutchinson Cancer Center, Seattle, Washington.
Fred Hutch Cancer Center · USSwedish Medical Center · US

Funding

Proteogenomic Studies aimed at understanding ovarian tumor responses to agents targeting the DNA damage response and translating this knowledge into clinical benefitU01CA214114 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI BIRRER, MICHAEL, PAULOVICH, AMANDA G · 2017 to 2021
$8.4M
Proteogenomic studies to understand mechanisms and drivers of resistance to immunotherapiesU01CA271407 · NCI · FRED HUTCHINSON CANCER CENTER · PI Diwakar Davar, AMANDA G PAULOVICH · 2022 to 2026
$5.6M
A proteomics research specialist in developing targeted mass spectrometry methods for quantifying proteins important in cancerR50CA211499 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Jeff Whiteaker · 2016 to 2026
$2.8M
NCI NIH HHS HHSN261201500003CNCI NIH HHS HHSN261201500003INCI NIH HHS R50 CA211499NCI NIH HHS U01 CA214114NCI NIH HHS U01 CA271407
6 · The paper itself

Abstract

A woman with estrogen/progesterone receptor-positive, ERBB2-negative metastatic breast cancer developed progressive disease despite treatment with multiple hormonal and chemotherapeutic modalities. She carried a germline variant of MLH1 (1835del3), also known as c.1835_1837del and v612del, the pathogenicity of which has not been conclusively determined. MLH1 staining was not seen on immunohistochemical staining of her tumor tissue. The patient experienced a >5-year dramatic response to 4 doses of pembrolizumab. Family studies revealed multiple other relatives with the MLH1 1835del3 variant, as well as multiple relatives with colon cancer. The one relative with colon cancer who underwent genetic testing demonstrated the same variant. Laboratory studies revealed that the patient's tumor showed loss of heterozygosity (LOH) in the MLH1 region, high levels of microsatellite instability, and a high tumor mutational burden. LOH in the MLH1 region, along with the remarkable clinical response to pembrolizumab treatment and the presence of the same MLH1 variant in affected relatives, supports the hypothesis that the MLH1 1835del3 variant is pathogenic. Given the patient's family history, this likely represents an uncommon presentation of Lynch syndrome. Physicians should be alert to evaluate patients for targetable genetic variants even in unlikely clinical situations such as the one described here.

Indexed as

Breast NeoplasmsColonic NeoplasmsColorectal Neoplasms, Hereditary NonpolyposisAntibodies, Monoclonal, HumanizedFemaleGerm-Line MutationHumansMutL Protein Homolog 1VirulenceAntibodies, Monoclonal, HumanizedMLH1 protein, humanMutL Protein Homolog 1pembrolizumabbreast cancerLynch SyndromeMLH1

Identifiers

PMID37643636
PMCPMC11051703
OpenAlexW4386241615

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.