Evidence map›Paper›PMID 39742376›Full record

ArticleThe breast journal2024

Associations between PIK3CA Mutations and Disease Free Survival in Patients with HR+, HER2- Tumors Treated with Adjuvant Hormonal Therapy: A Real-World Study in Croatia.

Dora Čerina Pavlinović, Natalija Dedić Plavetić, Ingrid Belac Lovasić, Robert Šeparović, Josipa Flam, Marija Pancirov, Žarko Bajić, Snježana Tomić, Eduard Vrdoljak

Abstract readMulticenter Study
In one paragraph

Article in The breast journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Review
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

9 authors.

Dora Čerina PavlinovićDepartment of Oncology University Hospital Center Split School of Medicine University of Split, Split, Croatia.ORCID 0000-0002-1116-0136
Natalija Dedić PlavetićDepartment of Oncology University Hospital Center Zagreb School of Medicine University of Zagreb, Zagreb, Croatia.ORCID 0000-0003-0505-4756
Ingrid Belac LovasićSchool of Medicine University of Rijeka, Rijeka, Croatia.ORCID 0000-0001-5653-9070
Robert ŠeparovićDepartment of Medical Oncology Sestre Milosrdnice University Hospital Centre University Hospital for Tumors, Zagreb, Croatia.ORCID 0000-0002-4002-2699
Josipa FlamDepartment of Radiotherapy and Oncology University Hospital Center Osijek School of Medicine University of Osijek, Osijek, Croatia.ORCID 0000-0003-1351-7511
Marija PancirovDepartment of Oncology University Hospital Center Split School of Medicine University of Split, Split, Croatia.ORCID 0000-0003-0487-893X
Žarko BajićResearch Unit "Dr. Mirko Grmek" Psychiatric Clinic "Sveti Ivan", Zagreb, Croatia.ORCID 0000-0002-7983-6892
Snježana TomićDepartment of Pathology University Hospital Center Split School of Medicine University of Split, Split, Croatia.ORCID 0000-0003-4297-069X
Eduard VrdoljakDepartment of Oncology University Hospital Center Split School of Medicine University of Split, Split, Croatia.ORCID 0000-0001-8739-5946

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Disease recurrence in patients with the early hormone receptor-positive (HR+), human epidermal growth factor receptor 2-negative (HER2-) breast tumor subtype is particularly challenging to manage due to its complex and very heterogeneous biological nature. Namely, due to primary and secondary resistance, one-quarter of patients with early-stage disease will experience disease recurrence. This variability in the timing of recurrence highlights the need to better identify key biomarkers that could predict therapeutic outcomes and guide personalized treatment strategies for these patients. Mutations in the phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA) gene are highly prevalent (30-40%) in HR+/HER2- advanced breast cancer. They lead to activation of the PI3K/AKT/mTOR pathway, promoting cell growth, and proliferation, and are associated with poor prognosis in advanced breast cancer. Our aim was to examine the association between and impact of PIK3CA mutation status on disease-free survival (DFS) in HR+/HER2- early breast cancer patients. Methods: This cohort study was multicentric and retrospective in nature and was conducted at five Croatian institutions from July 2020 to December 2021. The study included initially early and locally advanced operable HR+/HER2- breast cancer patients who were diagnosed with disease recurrence during adjuvant hormonal treatment or within the first six years of follow-up. Results: A total of 186 patients were included, 40.9% of whom tested positive for the PIK3CA mutation. Primary and adjuvant treatment, particularly adjuvant endocrine treatment, were similar between the two groups. After adjustment for 14 relevant covariates, we found that patients with a positive PIK3CA status and the H1047 PIK3CA mutation had a significantly lower hazard of disease recurrence than patients with no PIK3CA mutation (HR 0.65; 95% CI 0.45; 0.95; Conclusions: This study highlights the potential impact of PIK3CA mutations on disease recurrence during or following adjuvant endocrine therapy and potentially opens the door for further investigation of possibly more personalized treatment strategies.

Indexed as

Breast NeoplasmsClass I Phosphatidylinositol 3-KinasesErb-b2 Receptor Tyrosine KinasesMutationAdultAgedAntineoplastic Agents, HormonalBiomarkers, TumorChemotherapy, AdjuvantCroatiaDisease-Free SurvivalFemaleHumansMiddle AgedNeoplasm Recurrence, LocalReceptors, EstrogenAntineoplastic Agents, HormonalBiomarkers, TumorClass I Phosphatidylinositol 3-KinasesERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesPIK3CA protein, humanReceptors, EstrogenReceptors, Progesterone

Identifiers

PMID39742376
PMCPMC11416163

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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.