Evidence map›Paper›PMID 40129925›Full record

ReviewFrontiers in oncology2025

Real-world effectiveness of CDK4/6i in first-line treatment of HR+/HER2- advanced/metastatic breast cancer: updated systematic review.

Nadia Harbeck, Adam Brufsky, Chloe Grace Rose, Beata Korytowsky, Connie Chen, Krista Tantakoun, Endri Jazexhi, Do Hoang Vien Nguyen, Meaghan Bartlett, Imtiaz A Samjoo and 1 more

Abstract readReview
In one paragraph

Review in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Real-world efficacy and prognostic factors of CDK4/6 inhibitors in HRTranslational breast cancer research : a journal focusing on translational research in breast cancer · 2026
    Article
  10. Article
  11. Genomic Predictive Biomarkers in Breast Cancer: TheInternational journal of molecular sciences · 2025
    Review
  12. Article
  13. Article
  14. 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

11 authors.

Nadia HarbeckBreast Center, Department of Gynecology and Obstetrics and Comprehensive Cancer Center Munich, LMU University Hospital, Munich, Germany.
Adam BrufskyUPMC Hillman Cancer Center, University of Pittsburgh Medical Center, Pittsburgh, PA, United States.
Chloe Grace RosePfizer, Inc., New York, NY, United States.
Beata KorytowskyPfizer, Inc., New York, NY, United States.
Connie ChenPfizer, Inc., New York, NY, United States.
Krista TantakounValue & Evidence, EVERSANATM, Burlington, ON, Canada.
Endri JazexhiValue & Evidence, EVERSANATM, Burlington, ON, Canada.
Do Hoang Vien NguyenValue & Evidence, EVERSANATM, Burlington, ON, Canada.
Meaghan BartlettValue & Evidence, EVERSANATM, Burlington, ON, Canada.
Imtiaz A SamjooValue & Evidence, EVERSANATM, Burlington, ON, Canada.
Timothy PluardHematology and Medical Oncology, St. Luke's Cancer Institute, Kansas City, MO, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aim: Since 2021, additional real-world evidence (RWE) has emerged on the effectiveness of cyclin-dependent kinase 4/6 inhibitors (CDK4/6i) as first-line treatment of HR-positive/HER2-negative (HR+/HER2-) advanced/metastatic breast cancer (A/MBC), necessitating this updated review. Methods: MEDLINE Results: This update included 82 unique studies, 42.7% for palbociclib, 7.3% for ribociclib, and 3.7% for abemaciclib; 46.3% assessed multiple CDK4/6i. In studies including multiple CDK4/6is, median PFS was 23.4-31.0 months for palbociclib, 19.8-44.0 for ribociclib, and 14.0-39.5 for abemaciclib. When reached, median OS was 38.0-58.0 months, 40.4-52.0 months, and 34.4 months, respectively. These real-world PFS and OS results were within the range of single-arm and CDK4/6i versus endocrine therapy (ET) studies, where CDK4/6i demonstrated greater benefits than ET alone. Conclusion: First-line CDK4/6i RWE demonstrates significant clinical benefits in HR+/HER2- A/MBC. These data are important to guide clinical decision-making, as they include patients who are not adequately represented in clinical trials. Studies with longer follow-up are needed to assess long-term benefits of all three CDK4/6i therapies in HR+/HER2- A/MBC.

Indexed as

breastCDK4/6 inhibitorsHR+/HER2−metastasisquality assessmentreal-world evidencesystematic literature review

Identifiers

PMID40129925
PMCPMC11931418

What Socratic 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 Socratic graph.