Evidence map›Paper›PMID 33692409›Full record

Trial reportScientific reports2021

Mutation analysis using cell-free DNA for endocrine therapy in patients with HR+ metastatic breast cancer.

Sung Hoon Sim, Han Na Yang, Su Yeon Jeon, Keun Seok Lee, In Hae Park

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in Scientific reports, 2021. 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
0.5field-weighted citation impact, top 44% 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, 11 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. The Combined Assessment of CTC andInternational journal of molecular sciences · 2025
    Article
  7. Serial analysis ofFrontiers in oncology · 2025
    Article
  8. Review
  9. Review
  10. 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

5 authors at 1 institution in 1 country.

Sung Hoon SimTranslational Cancer Research Branch, Research Institute, National Cancer Center, Goyang, Republic of Korea.
Han Na YangTranslational Cancer Research Branch, Research Institute, National Cancer Center, Goyang, Republic of Korea.
Su Yeon JeonTranslational Cancer Research Branch, Research Institute, National Cancer Center, Goyang, Republic of Korea.
Keun Seok LeeCenter for Breast Cancer, National Cancer Center Hospital, National Cancer Center, Goyang, Republic of Korea.
In Hae ParkTranslational Cancer Research Branch, Research Institute, National Cancer Center, Goyang, Republic of Korea. parkih@korea.ac.kr.
National Cancer Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We prospectively evaluated the utility of ESR1 and PIK3CA mutation analysis with cell-free DNA (cfDNA) using droplet digital PCR (ddPCR) for the efficacy of endocrine therapy (ET) in hormone receptive positive (HR+) metastatic breast cancer (MBC) patients. CfDNA was analyzed just before the start of ET for MBC. E380Q, Y537N, Y537S, and D538G were assessed for ESR1 mutations and H1047R, E545K, and E542K were assessed for PIK3CA mutations. A total of 75 patients were enrolled. Of those, 31 (41.3%) received letrozole with palbociclib, and 28 (37.3%) received exemestane and everolimus (EverX). ESR1 mutations were found in 36 (48.0%) patients, of which 16 (21.3%) had more than one variant. Seventeen (23.6%) patients had one PIK3CA mutation and 8 (11.1%) had two. In the total population, time to progression of the first ET after enrollment (TTP1) decreased significantly as the number of ESR1 mutations increased (p < 0.001). PIK3CA mutations were also significantly associated with shorter TTP1 (median TTP1: 16.2 months vs. 10.9 months, p = 0.03). In contrast, PIK3CA mutations were significantly associated with longer TTP in patients receiving EverX treatment (median TTP of EverX: 15.9 months vs. 5.2 months, p = 0.01) and remained a significant factor in multivariable analysis for TTP of EverX in this subgroup (hazard ratio = 0.2, 95% CI = 0.1- 0.8, p = 0.03). ESR1 and PIK3CA mutations in cfDNA were associated with clinical efficacies of ET in HR+ MBC patients.

Indexed as

Breast NeoplasmsMutationAdultAgedAged, 80 and overAndrostadienesAntineoplastic Combined Chemotherapy ProtocolsCirculating Tumor DNADNA Mutational AnalysisEverolimusFemaleHumansLetrozoleMiddle AgedNeoplasm ProteinsPiperazinesAndrostadienesCirculating Tumor DNAEverolimusexemestaneLetrozoleNeoplasm ProteinspalbociclibPiperazinesPyridines

Identifiers

PMID33692409
PMCPMC7946916
OpenAlexW3133701816

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.