Evidence map›Paper›PMID 42265489›Full record

ArticleDiscover oncology2026

Long-term outcomes of rare pure histological subtypes of breast cancer in a tertiary single-center retrospective cohort.

Mehmet Cem Fidan, Murad Guliyev, Murat Günaltılı, Zeliha Birsin, Ebru Çiçek, Hamza Abbasov, Emir Çerme, Selin Cebeci, Vali Aliyev, Berrin Papila and 6 more

Abstract read
In one paragraph

Article in Discover oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

16 authors.

Mehmet Cem FidanDivision of Medical Oncology, Department of Internal Medicine, Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, 34098, Istanbul, Turkey. mcemfidan@hotmail.com.
Murad GuliyevDivision of Medical Oncology, Department of Internal Medicine, Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, 34098, Istanbul, Turkey.
Murat GünaltılıDivision of Medical Oncology, Department of Internal Medicine, Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, 34098, Istanbul, Turkey.
Zeliha BirsinDivision of Medical Oncology, Department of Internal Medicine, Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, 34098, Istanbul, Turkey.
Ebru ÇiçekDivision of Medical Oncology, Department of Internal Medicine, Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, 34098, Istanbul, Turkey.
Hamza AbbasovDivision of Medical Oncology, Department of Internal Medicine, Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, 34098, Istanbul, Turkey.
Emir ÇermeDivision of Medical Oncology, Department of Internal Medicine, Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, 34098, Istanbul, Turkey.
Selin CebeciDivision of Medical Oncology, Department of Internal Medicine, Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, 34098, Istanbul, Turkey.
Vali AliyevDivision of Medical Oncology, Department of Internal Medicine, Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, 34098, Istanbul, Turkey.
Berrin PapilaDepartment of General Surgery, Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, 34098, Istanbul, Turkey.
İpek SertbudakDepartment of Pathology, Cerrahpasa Faculty of Medicine, Istanbul University- Cerrahpasa, 34098, Istanbul, Turkey.
Tülin ÖztürkDepartment of Pathology, Cerrahpasa Faculty of Medicine, Istanbul University- Cerrahpasa, 34098, Istanbul, Turkey.
Gökmen Umut ErdemDepartment of Medical Oncology, Basaksehir Cam and Sakura City Hospital, 34480, Istanbul, Turkey.
Özkan AlanDivision of Medical Oncology, Department of Internal Medicine, Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, 34098, Istanbul, Turkey.
Nebi Serkan DemirciDivision of Medical Oncology, Department of Internal Medicine, Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, 34098, Istanbul, Turkey.
Çiğdem PapilaDivision of Medical Oncology, Department of Internal Medicine, Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, 34098, Istanbul, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRare pure histological breast cancer subtypes represent a clinically heterogeneous group of tumors with diverse biological behaviours and prognostic profiles. Due to their rarity, data, particularly regarding long-term survival outcomes, are limited and controversial. This study aimed to evaluate the clinicopathological features and long-term survival outcomes of patients diagnosed with rare pure histological breast cancer subtypes in a single tertiary center.

methodsThis retrospective single-center study included 117 patients diagnosed with pure rare breast cancer histologies between November 2000 and February 2024. These included mucinous, metaplastic, micropapillary, and tubular carcinomas, as well as malignant phyllodes tumors. Clinicopathological features, treatment methods, recurrence risks, and survival outcomes were analyzed. 5-year and 10-year overall survival (OS) rates were calculated.

resultsThe most common subtype was mucinous carcinoma (41.9%), followed by metaplastic (25.6%), micropapillary (14.5%), tubular carcinoma (10.2%), and malignant phyllodes tumor (7.7%). Favourable biological features such as low grade, low Ki-67 proliferation index, and high hormone receptor expression were dominant in mucinous and tubular carcinomas, while metaplastic and micropapillary carcinomas frequently exhibited aggressive biological features such as high grade, high Ki-67, and more frequent lymph node involvement. In long-term follow-up, recurrence was most common in malignant phyllodes tumors, micropapillary carcinomas, and metaplastic carcinomas. Five- and ten-year overall survival rates differed significantly among subtypes, with the most favourable outcomes observed in tubular and mucinous carcinomas and relatively lower long-term survival observed in metaplastic and malignant phyllodes tumors.

conclusionsPure rare histological breast cancer subtypes appear to show heterogeneity in clinicopathological features and long-term survival outcomes. Due to the small number of patients in individual subgroups, these findings should be interpreted with caution. Our descriptive data suggest a potential prognostic role for histological subtype and highlight the importance of accurate pathological classification. Long-term follow-up data from tertiary care centers may provide useful descriptive information about the natural history and survival patterns of these rare breast cancer subtypes.

Indexed as

Clinicopathological characteristicsLong-term survivalPure histological subtypesRare breast cancerSingle-centre study

Identifiers

PMID42265489
PMCPMC13473031

What Socratic holds

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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 Socratic graph.