Evidence map›Paper›PMID 42163875›Full record

ArticleAmerican journal of cancer research2026

Low dose abemaciclib in heavily treated hormone receptor-positive/human epidermal growth factor receptor 2-negative advanced breast cancer.

Yi-Ru Lu, Chien-Ting Liu, Shih-Chung Wu, Chia-Che Wu, Shih-Yu Huang, Ching-Hua Tsai, Yen-Hao Chen

Abstract read
In one paragraph

Article in American journal of cancer research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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

7 authors.

Yi-Ru LuDivision of Hematology-Oncology, Department of Internal Medicine, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine Kaohsiung 833, Taiwan.
Chien-Ting LiuDivision of Hematology-Oncology, Department of Internal Medicine, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine Kaohsiung 833, Taiwan.
Shih-Chung WuDivision of General Surgery, Department of Surgery, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine Kaohsiung 833, Taiwan.
Chia-Che WuDivision of Hematology-Oncology, Department of Internal Medicine, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine Kaohsiung 833, Taiwan.
Shih-Yu HuangDivision of Hematology-Oncology, Department of Internal Medicine, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine Kaohsiung 833, Taiwan.
Ching-Hua TsaiDivision of Trauma Surgery, Department of Surgery, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine Kaohsiung 833, Taiwan.
Yen-Hao ChenDivision of Hematology-Oncology, Department of Internal Medicine, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine Kaohsiung 833, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cyclin-dependent kinase 4/6 (CDK4/6) inhibitors combined with endocrine therapy are the standard first-line treatment for hormone receptor-positive/human epidermal growth factor receptor 2-negative (HR+/HER2-) metastatic breast cancer, yet therapeutic options after progression are limited, particularly in heavily pretreated patients with tolerability concerns. We performed a retrospective real-world analysis of 17 patients with advanced HR+/HER2- breast cancer treated with low-dose abemaciclib at Kaohsiung Chang Gung Memorial Hospital between January 2023 and April 2025, of whom 41.2% had prior CDK4/6 inhibitor exposure and 47.1% had received more than four prior systemic therapy lines. Abemaciclib was administered at 200 mg once daily, with responses assessed by RECIST version 1.1. Partial response and stable disease were each observed in 29.4% of patients, yielding a disease control rate of 58.8%, including activity in patients with brain metastases. Median progression-free survival and overall survival were 10.3 months and 18.8 months, respectively, with numerically better outcomes in CDK4/6 inhibitor-naïve patients. Treatment was well tolerated, with low rates of gastrointestinal toxicity and only one grade 3-4 adverse event, and no treatment interruptions or further dose reductions. These findings suggest that low-dose abemaciclib may retain clinical activity with improved tolerability and represent a feasible option for selected heavily pretreated patients with HR+/HER2- metastatic breast cancer, warranting prospective validation.

Indexed as

abemaciclibHR+/HER2- breast cancerlow-dosesafety

Identifiers

PMID42163875
PMCPMC13184746

What OpenQuestion holds

Textmetadata
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.