Evidence map›Paper›PMID 36132153›Full record

ArticleFrontiers in oncology2022

Cost-effectiveness of palbociclib in early breast cancer patients with a high risk of relapse: Results from the PENELOPE-B trial.

Katya Galactionova, Sibylle Loibl, Paola Salari, Frederik Marmé, Miguel Martin, Michael Untch, Hervé R Bonnefoi, Sung-Bae Kim, Harry D Bear, Nicole McCarthy and 10 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2022. 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
0.5field-weighted citation impact, top 35% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Economic assessment of abemaciclib for the adjuvant treatment of luminal HER2- breast cancer from the perspective of the Spanish health system.The European journal of health economics : HEPAC : health economics in prevention and care · 2025
    Article
  2. 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

20 authors at 15 institutions in 11 countries.

Katya GalactionovaInstitute of Pharmaceutical Medicine (ECPM), University of Basel, Basel, Switzerland.
Sibylle LoiblGerman Breast Group, Neu-Isenburg, Germany.
Paola SalariInstitute of Pharmaceutical Medicine (ECPM), University of Basel, Basel, Switzerland.
Frederik MarméMedical Faculty Mannheim, Heidelberg University, University Hospital Mannheim, Mannheim, Germany.
Miguel MartinInstituto de Investigacion Sanitaria Gregorio Marañon, Centro de Investigación Biomédica en Red Cáncer (CIBERONC), Universidad Complutense, Madrid, Spain.
Michael UntchDepartment of Obstetrics and Gynaecology, Helios Kliniken Berlin-Buch, Berlin, Germany.
Hervé R BonnefoiDepartment of Medical Oncology, Institut Bergonié and Université de Bordeaux Institut National de la Santé et de la Recherche Médicale (INSERM) U916, Bordeaux, France.
Sung-Bae KimAsan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.
Harry D BearDivision of Surgical Oncology, Massey Cancer Center, Virginia Commonwealth University, Virginia Commonwealth University (VCU) Health, Richmond, VA, United States.
Nicole McCarthyAustralia and New Zealand Breast Cancer Trials Group, Newcastle, NSW, Australia.
Karen A GelmonBC Cancer, Vancouver, BC, Canada.
José A García-SáenzInstituto de Investigación Sanitaria del Hospital Clinico San Carlos (IdISSC), Madrid, Spain.
Catherine M KellyMater Private Hospital, Cancer Trials Ireland, Dublin, Ireland.
Toralf ReimerDepartment of Obstetrics and Gynecology, University of Rostock, Rostock, Germany.
Masakazu ToiBreast Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Hope S RugoUniversity of California San Francisco Comprehensive Cancer Center, San Francisco, CA, United States.
Michael GnantComprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Andreas MakrisInstitute of Cancer Research, London, United Kingdom.
Nicole BurchardiGerman Breast Group, Neu-Isenburg, Germany.
Matthias SchwenkglenksInstitute of Pharmaceutical Medicine (ECPM), University of Basel, Basel, Switzerland.
University of Basel · CHGEICAM – Spanish Breast Cancer Group · ESGerman Breast group · DEAsan Medical Center · KRBreast Cancer Trials · AUCancer Trials Ireland · IEComprehensive Cancer Center Vienna · ATHelios Kliniken · DEInstitute of Cancer Research · GBKyoto University · JPUCSF Helen Diller Family Comprehensive Cancer Center · USUniversité de Bordeaux · FRUniversity Medical Centre Mannheim · DEUniversity of Rostock · DEVirginia Commonwealth University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Patients with hormone receptor-positive, HER2-negative breast cancer who have residual invasive disease after neoadjuvant chemotherapy (NACT) are at a high risk of relapse. PENELOPE-B was a double-blind, placebo-controlled, phase III trial that investigated adding palbociclib (PAL) for thirteen 28-day cycles to adjuvant endocrine therapy (ET) in these patients. Clinical results showed no significant improvement in invasive disease-free survival with PAL. Methods: We performed a pre-planned cost-effectiveness analysis of PAL within PENELOPE-B from the perspective of the German statutory health insurance. Health-related quality of life scores, collected in the trial using the EQ-5D-3L instrument, were converted to utilities based on the German valuation algorithm. Resource use was valued using German price weights. Outcomes were discounted at 3% and modeled with mixed-level linear models to adjust for attrition, repeated measurements, and residual baseline imbalances. Subgroup analyses were performed for key prognostic risk factors. Scenario analyses addressed data limitations and evaluated the robustness of the estimated cost-effectiveness of PAL to methodological choices. Results: The effects of PAL on quality-adjusted life years (QALYs) were marginal during the active treatment phase, increasing thereafter to 0.088 (95% confidence interval: -0.001; 0.177) QALYs gained over the 4 years of follow-up. The incremental costs were dominated by PAL averaging EUR 33,000 per patient; costs were higher in the PAL arm but not significantly different after the second year. At an incremental cost-effectiveness ratio of EUR 380,000 per QALY gained, PAL was not cost-effective compared to the standard-of-care ET. Analyses restricted to Germany and other subgroups were consistent with the main results. Findings were robust in the scenarios evaluated. Conclusions: One year of PAL added to ET is not cost-effective in women with residual invasive disease after NACT in Germany.

Indexed as

CDKicost-effectivenessearly breast cancerGermanyPalbociclibPenelope-B(postneo)adjuvant

Identifiers

PMID36132153
PMCPMC9484462
OpenAlexW4294681412

What OpenQuestion 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 OpenQuestion graph.