Evidence map›Paper›PMID 36130155›Full record

ArticleJCO global oncology2022

Clinical Profile and Outcome of Patients With Human Epidermal Growth Factor Receptor 2-Positive Breast Cancer With Brain Metastases: Real-World Experience.

Prabhat Bhargava, Narmadha Rathnasamy, Ramnath Shenoy, Seema Gulia, Jyoti Bajpai, Jaya Ghosh, Sushmita Rath, Ashwini Budrukkar, Tanuja Shet, Asawari Patil and 10 more

Open access · goldAbstract read
In one paragraph

Article in JCO global oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 45% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. IRX4204 Induces Senescence and Cell Death in HER2-positive Breast Cancer and Synergizes with Anti-HER2 Therapy.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Article
  3. 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 1 institution in 1 country.

Prabhat BhargavaDepartment of Medical Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.ORCID 0000-0002-6440-2186
Narmadha RathnasamyDepartment of Medical Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.ORCID 0000-0001-8176-5854
Ramnath ShenoyDepartment of Medical Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
Seema GuliaDepartment of Medical Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
Jyoti BajpaiDepartment of Medical Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.ORCID 0000-0001-7657-3460
Jaya GhoshDepartment of Medical Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.ORCID 0000-0001-6670-1772
Sushmita RathDepartment of Medical Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
Ashwini BudrukkarDepartment of Radiation Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
Tanuja ShetDepartment of Pathology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
Asawari PatilDepartment of Pathology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.ORCID 0000-0002-8203-986X
Sangeeta DesaiDepartment of Pathology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.ORCID 0000-0002-3588-9888
Nita NairDepartment of Surgical Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.ORCID 0000-0001-5481-7292
Shalaka JoshiDepartment of Surgical Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.ORCID 0000-0003-3813-4680
Palak PopatDepartment of Biostatistics, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.ORCID 0000-0002-6495-0721
Tabassum WadasadawalaDepartment of Radiation Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.ORCID 0000-0003-2167-420X
Rima PathakDepartment of Radiation Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.ORCID 0000-0002-4887-7130
Rajiv SarinDepartment of Radiation Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.ORCID 0000-0002-6405-8282
Sadhana KannanDepartment of Biostatistics, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.
Rajendra BadweDepartment of Surgical Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.ORCID 0000-0002-0480-2831
Sudeep GuptaDepartment of Medical Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, India.ORCID 0000-0002-6742-6378
Homi Bhabha National Institute · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThere are sparse data in patients with human epidermal growth factor receptor 2 (HER2)-positive breast cancer with brain metastases from real-world settings, especially where access to newer targeted therapies is limited.

methodsThis was a single institution, retrospective cohort study of patients with HER2-positive breast cancer diagnosed between January 2013 and December 2017 to have brain metastases and treated with any HER2-targeted therapy. The main objectives were to estimate progression-free survival (PFS) and overall survival (OS) from the time of brain metastases.

resultsA total of 102 patients with a median age of 52 (interquartile range, 45-57) years were included, of whom 63 (61.8%) had received one line and 14 (13.7%) had received two lines of HER2-targeted therapies before brain metastasis, 98 (96.1%) were symptomatic at presentation, 22 (25.3%) had solitary brain lesion, 22 (25.3%) had 2-5 lesions, and 43 (49.4%) had ≥ 5 lesions. Local treatment included surgical resection in nine (8.9%) and radiotherapy in all (100%) patients. The first HER2-targeted therapy after brain metastasis was lapatinib in 71 (68.6%), trastuzumab in 19 (18.6%), lapatinib and trastuzumab in three (2.9%), trastuzumab emtansine in four (3.9%), and intrathecal trastuzumab in five (4.9%) patients. At a median follow-up of 13.9 months, the median PFS and OS were 8 (95% CI, 6.2 to 9.8) months and 14 (95% CI, 10.8 to 17.2) months, respectively, with a 2-year OS of 25% (95% CI, 16.7 to 34.4). The median PFS in patients who received lapatinib-capecitabine regimen (n = 62) was 9.0 (95% CI, 7.3 to 10.7) months.

conclusionThere was a substantial clinical benefit of local and systemic therapy in patients with brain metastases and HER2-positive disease in a real-world setting with limited access to newer HER2-targeted drugs.

Indexed as

Brain NeoplasmsBreast NeoplasmsAdo-Trastuzumab EmtansineAntineoplastic Combined Chemotherapy ProtocolsCapecitabineErb-b2 Receptor Tyrosine KinasesFemaleHumansLapatinibMiddle AgedQuinazolinesRetrospective StudiesTrastuzumabAdo-Trastuzumab EmtansineCapecitabineERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesLapatinibQuinazolinesTrastuzumab

Identifiers

PMID36130155
PMCPMC9812453
OpenAlexW4296710212

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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 OpenQuestion graph.