Evidence map›Paper›PMID 37835414›Full record

ArticleCancers2023

Comprehensive Clinical Characterization of Decade-Long Survivors of Metastatic Breast Cancer.

Junghoon Shin, Ji-Yeon Kim, Jung Min Oh, Jeong Eon Lee, Seok Won Kim, Seok Jin Nam, Won Park, Yeon Hee Park, Jin Seok Ahn, Young-Hyuck Im

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 23% 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

4 citing papers in PubMed, 3 citations in OpenAlex.

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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 1 institution in 1 country.

Junghoon ShinDivision of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Seoul 06351, Republic of Korea.ORCID 0000-0002-6834-7217
Ji-Yeon KimDivision of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Seoul 06351, Republic of Korea.ORCID 0000-0002-4223-1929
Jung Min OhBiomedical Research Institute, Samsung Medical Center, Seoul 06351, Republic of Korea.
Jeong Eon LeeSchool of Medicine, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Seok Won KimSchool of Medicine, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Seok Jin NamSchool of Medicine, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Won ParkSchool of Medicine, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Yeon Hee ParkDivision of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Seoul 06351, Republic of Korea.ORCID 0000-0003-4156-9212
Jin Seok AhnDivision of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Seoul 06351, Republic of Korea.
Young-Hyuck ImDivision of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Seoul 06351, Republic of Korea.ORCID 0000-0001-6459-8118
Samsung Medical Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundElucidating the clinical features of metastatic breast cancer (MBC) patients with an exceptionally favorable prognosis may offer insights to improve the survival of more typical patients.

methodsWe collected comprehensive real-world data on clinicopathologic characteristics, treatments, and outcomes of 110 consecutive MBC patients who survived for over ten years from the clinical data warehouse of Samsung Medical Center.

resultsThe cohort included 54 hormone receptor (HR)-positive/HER2-negative (HR+/HER2-), 21 HR+/HER2+, 16 HR-/HER2+, and 14 triple-negative breast cancer (TNBC) patients. The median age at MBC diagnosis was 48.5 years. Approximately 70% of patients initially had a single-organ metastasis. The most common site of metastasis was the lung (46.4%), followed by distant lymph nodes (37.3%). During a median follow-up of 14.6 years, the median duration of systemic therapy was 11, 8.4, 7.3, and 0.8 years in the HR+/HER2-, HR+/HER2+, HR-/HER2+, and TNBC subgroups, respectively. Seven HER2+ and ten TNBC patients received systemic treatment for less than two years and remained treatment-free for most of the follow-up period, suggesting a potential chance of cure. The TNBC subtype (

conclusionsA small subset of patients with HER2+ MBC and metastatic TNBC may be curable with multimodality therapy. Prospective studies integrating clinical and genomic data may identify unique clinicogenomic features of MBC patients who can achieve durable disease control without prolonged chemotherapy.

Indexed as

chemotherapyendocrine therapyHER2hormone receptormetastatic breast cancersurvivaltriple-negative breast cancer

Identifiers

PMID37835414
PMCPMC10571750
OpenAlexW4387048579

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.