Evidence map›Paper›PMID 38381274›Full record

ArticleBreast cancer research and treatment2024

Time trends in real-world treatment patterns and survival in patients diagnosed with de novo HER2+ metastatic breast cancer: an analysis of the SONABRE registry.

Sandra M E Geurts, Khava I E Ibragimova, Nan Ding, Marissa Meegdes, Frans Erdkamp, Joan B Heijns, Jolien Tol, Birgit E P J Vriens, Marcus W Dercksen, Kirsten N A Aaldering and 9 more

Registry-linked trialAbstract read
In one paragraph

Article in Breast cancer research and treatment, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03577197 (Southeast Netherlands Advanced Breast Cancer Registry), which is not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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.

NCT03577197 recruitingnot on this map

Southeast Netherlands Advanced Breast Cancer Registry

Typeobservational_patient_registrySponsorAcademisch Ziekenhuis MaastrichtRan2007 to 2027Enrolled7,000ConditionsAdvanced Breast Cancer, Metastatic Breast Cancer
3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Observational
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

19 authors.

Sandra M E GeurtsDepartment of Medical Oncology, GROW- School for Oncology and Reproduction, Maastricht University Medical Center, PO BOX 5800, 6202 AZ, Maastricht, The Netherlands. sandra.geurts@mumc.nl.ORCID http://orcid.org/0000-0002-4265-9968
Khava I E IbragimovaDepartment of Medical Oncology, GROW- School for Oncology and Reproduction, Maastricht University Medical Center, PO BOX 5800, 6202 AZ, Maastricht, The Netherlands.
Nan DingDepartment of Medical Oncology, GROW- School for Oncology and Reproduction, Maastricht University Medical Center, PO BOX 5800, 6202 AZ, Maastricht, The Netherlands.
Marissa MeegdesDepartment of Medical Oncology, GROW- School for Oncology and Reproduction, Maastricht University Medical Center, PO BOX 5800, 6202 AZ, Maastricht, The Netherlands.
Frans ErdkampDepartment of Internal Medicine, Zuyderland Medical Center, Sittard-Geleen, The Netherlands.
Joan B HeijnsDepartment of Medical Oncology, Amphia, Breda, The Netherlands.
Jolien TolDepartment of Medical Oncology, Jeroen Bosch Hospital, Den Bosch, The Netherlands.
Birgit E P J VriensDepartment of Internal Medicine, Catharina Hospital, Eindhoven, The Netherlands.
Marcus W DercksenDepartment of Medical Oncology, Máxima Medical Center, Eindhoven, The Netherlands.
Kirsten N A AalderingDepartment of Internal Medicine, Laurentius Hospital, Roermond, The Netherlands.
Manon J A E PepelsDepartment of Internal Medicine, Elkerliek Hospital, Helmond, The Netherlands.
Linda van de WinkelDepartment of Internal Medicine, St Anna Hospital, Geldrop, The Netherlands.
Natascha A J B PetersDepartment of Internal Medicine, Sint Jans Gasthuis Hospital, Weert, Netherlands.
Agnes J van de WouwDepartment of Internal Medicine, Viecuri Medical Centre, Venlo, The Netherlands.
Sabrina A J G MaaskantDepartment of Surgery, Máxima Medical Center, Eindhoven, The Netherlands.
Nathalie J A Teeuwen-DedroogDepartment of Medical Oncology, GROW- School for Oncology and Reproduction, Maastricht University Medical Center, PO BOX 5800, 6202 AZ, Maastricht, The Netherlands.
Thiemo J A van NijnattenDepartment of Radiology and Nuclear Medicine, GROW, Maastricht University Medical Center, Maastricht, The Netherlands.
Maaike de BoerDepartment of Medical Oncology, GROW- School for Oncology and Reproduction, Maastricht University Medical Center, PO BOX 5800, 6202 AZ, Maastricht, The Netherlands.
Vivianne C G Tjan-HeijnenDepartment of Medical Oncology, GROW- School for Oncology and Reproduction, Maastricht University Medical Center, PO BOX 5800, 6202 AZ, Maastricht, The Netherlands.

Funding

Netherlands Organization for Health Research and Development 80-82500-98-8003
6 · The paper itself

Abstract

purposeThe aim was to determine whether the real-world first-line progression-free survival (PFS) of patients diagnosed with de novo human epidermal growth factor receptor 2 positive (HER2+) advanced breast cancer (ABC) has improved since the introduction of pertuzumab in 2013. In addition to PFS, we aimed to determine differences in overall survival (OS) and the use of systemic and locoregional therapies.

methodsIncluded were patients systemically treated for de novo HER2+ ABC in ten hospitals in 2008-2017 from the SONABRE Registry (NCT-03577197). First-line PFS and OS in 2013-2017 versus 2008-2012 was determined using Kaplan-Meier analyses and multivariable Cox proportional hazards modelling. First-given systemic therapy and the use of locoregional therapy within the first year following diagnosis were determined per period of diagnosis.

resultsMedian and five-year PFS were 26.6 months and 24% in 2013-2017 (n = 85) versus 14.5 months and 10% in 2008-2012 (n = 81) (adjusted HR = 0.65, 95%CI:0.45-0.94). Median and five-year OS were 61.2 months and 51% in 2013-2017 versus 26.1 months and 28% in 2008-2012 (adjusted HR = 0.55, 95%CI:0.37-0.81). Of patients diagnosed in 2013-2017 versus 2008-2012, 84% versus 60% received HER2-targeted therapy and 59% versus 0% pertuzumab-based therapy as first-given therapy. Respectively, 27% and 23% of patients underwent locoregional breast surgery, and 6% and 7% surgery of a metastatic site during the first year following diagnosis.

conclusionThe prognosis of patients with de novo HER2 + ABC has improved considerably. Since 2013 one in four patients were alive and free from progression on first-given therapy for at least five years.

Indexed as

Breast NeoplasmsErb-b2 Receptor Tyrosine KinasesRegistriesAdultAgedAged, 80 and overAntibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsFemaleHumansKaplan-Meier EstimateMiddle AgedNeoplasm MetastasisAntibodies, Monoclonal, HumanizedERBB2 protein, humanErb-b2 Receptor Tyrosine KinasespertuzumabBreast neoplasmsERBB2 protein, humanNeoplasm metastasisPertuzumabRegistriesSurvival

Identifiers

PMID38381274
PMCPMC11101547

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Registered trials

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.