Evidence map›Paper›PMID 34351544›Full record

ArticleJournal of neuro-oncology2021

Incidence and characteristics of metastatic intracranial lesions in stage III and IV melanoma: a single institute retrospective analysis.

Mani Ratnesh S Sandhu, Veronica L Chiang, Thuy Tran, James B Yu, Sarah A Weiss, Sarah B Goldberg, Mariam S Aboian, Harriet M Kluger, Amit Mahajan

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Journal of neuro-oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
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  4. Molecular Underpinnings of Brain Metastases.International journal of molecular sciences · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Mani Ratnesh S SandhuLaboratory Medicine, Yale School of Medicine, New Haven, CT, USA.ORCID http://orcid.org/0000-0002-5361-0414
Veronica L ChiangNeurosurgery, Yale School of Medicine, New Haven, CT, USA.
Thuy TranInternal Medicine (Medical Oncology), Yale School of Medicine, New Haven, CT, USA.
James B YuTherapeutic Radiology, Yale School of Medicine, New Haven, CT, USA.
Sarah A WeissInternal Medicine (Medical Oncology), Yale School of Medicine, New Haven, CT, USA.
Sarah B GoldbergInternal Medicine (Medical Oncology), Yale School of Medicine, New Haven, CT, USA.
Mariam S AboianRadiology and Biomedical Imaging, Yale School of Medicine, New Haven, CT, USA.
Harriet M KlugerInternal Medicine (Medical Oncology), Yale School of Medicine, New Haven, CT, USA.
Amit MahajanRadiology and Biomedical Imaging, Yale School of Medicine, New Haven, CT, USA. amit.mahajan@yale.edu.ORCID http://orcid.org/0000-0002-6532-2209
Yale University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe study aimed to describe the brain metastases (BM) incidence, at diagnosis and follow-up, in patients initially presenting with stage III or IV melanoma and characterize their metastatic brain lesions. We also sought to describe the association of common genetic mutations and immunotherapy with BM development in advanced melanoma.

methodsUsing our institution's tumor registry, we identified patients with initial diagnoses of stage III and stage IV melanoma. In this cohort, we obtained BM incidence at diagnosis and follow-up, characterized the metastatic brain lesions and primary tumor's genetic profile.

resultsDuring the follow-up period, 22.9% of patients with an initial diagnosis of stage III developed BM. In this cohort, the median time for BM occurrence was 20 months; [95% CI (14-29)]. Likewise, 37.7% of patients with Stage IV melanoma presented with BM at the time of diagnosis, and 22.7% of remaining patients developed BM at follow-up over a median duration of 6 months [95% CI (4-11)]. Therefore, suggesting an overall incidence of 51.9% in stage IV melanoma. Next, we observed that the incidence of BM development during the follow-up period significantly decreased from 2012 to 2017 (p < 0.001). Lastly, we found a significantly higher frequency of mutational BRAF in the primary tumor of patients with BM (68.7% vs. 31.2%; p = 0.02).

conclusionsWhile the overall incidence of BM remains high, the decreasing incidence of BM over the follow-up period is promising. Similar BM incidence in patients with an initial diagnosis of stage III or stage IV warrants appropriate imaging surveillance regimen for stage III patients.

Indexed as

Brain NeoplasmsMelanomaTesticular NeoplasmsHumansIncidenceMalePrognosisRetrospective StudiesBRAFBrain metastasisImaging surveillanceMelanoma

Identifiers

PMID34351544
OpenAlexW3192212518

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.