Evidence map›Paper›PMID 38083908›Full record

ArticleCancer medicine2023

A single-center retrospective analysis of prognoses in patients with melanoma brain metastases and effectiveness of treatment in Japan.

Shogo Wada, Dai Ogata, Tairo Kashihara, Kae Okuma, Hirofumi Eto, Eiji Nakano, Akira Takahashi, Kenjiro Namikawa, Hiroshi Igaki, Naoya Yamazaki

Abstract read
In one paragraph

Article in Cancer medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

10 authors.

Shogo WadaDepartment of Dermatologic Oncology, National Cancer Center Hospital, Tokyo, Japan.ORCID 0000-0002-0153-1773
Dai OgataDepartment of Dermatologic Oncology, National Cancer Center Hospital, Tokyo, Japan.
Tairo KashiharaDepartment of Radiation Oncology, National Cancer Center Hospital, Tokyo, Japan.ORCID 0000-0002-2471-605X
Kae OkumaDepartment of Radiation Oncology, National Cancer Center Hospital, Tokyo, Japan.
Hirofumi EtoDepartment of Dermatologic Oncology, National Cancer Center Hospital, Tokyo, Japan.
Eiji NakanoDepartment of Dermatologic Oncology, National Cancer Center Hospital, Tokyo, Japan.
Akira TakahashiDepartment of Dermatologic Oncology, National Cancer Center Hospital, Tokyo, Japan.
Kenjiro NamikawaDepartment of Dermatologic Oncology, National Cancer Center Hospital, Tokyo, Japan.ORCID 0000-0003-2763-7346
Hiroshi IgakiDepartment of Radiation Oncology, National Cancer Center Hospital, Tokyo, Japan.ORCID 0000-0001-7817-624X
Naoya YamazakiDepartment of Dermatologic Oncology, National Cancer Center Hospital, Tokyo, Japan.

Funding

National Cancer Center Research and Development Fund 2023-J-3
6 · The paper itself

Abstract

backgroundMelanoma brain metastasis (MBM) has a poor prognosis, although recent treatments, including immune checkpoint inhibitors and targeted therapy, have improved the prognosis. However, these systemic therapies have been reported to be less efficient for Asian patients. We investigated the survival of Asian patients with MBM and the effectiveness of systemic therapies.

methodsWe retrospectively reviewed the survival rates of patients diagnosed with MBM between January 2011 and December 2021 at the National Cancer Center Hospital in Tokyo, Japan. In addition, we identified factors associated with survival using Cox regression analysis.

resultsA total of 135 patients were included. The median overall survival (OS) after an MBM diagnosis was 7.8 months (95% confidence interval [CI] 6.1-9.6). The 6-month and 1-year survival rates were 60.7% and 34.8%, respectively. We identified the prognostic factors of MBM, including non-acral primary location, low serum LDH levels, systemic therapy of single-agent immune checkpoint inhibitors (ICIs) or targeted therapies (TTs), and radiotherapy of stereotactic irradiation (STI). We found no significant difference in effectiveness between single-agent ICIs, the combination of Nivolumab and Ipilimumab (COMBI-ICI), and TTs (COMBI-ICI vs. single-agent ICI, hazard ratio 0.71, 95% confidence interval 0.27-1.88, p = 0.49; COMBI-ICI vs. TT: hazard ratio 0.46, 95% confidence interval 0.14-1.55, p = 0.21).

conclusionsSystemic therapy and radiotherapy have improved the survival of MBM patients, but the survival of Asian patients remains poor. Our findings suggest that COMBI-ICIs are not significantly more effective than single-agent ICI or TT in treating MBM.

Indexed as

Brain NeoplasmsMelanomaHumansImmune Checkpoint InhibitorsJapanPrognosisRetrospective StudiesImmune Checkpoint Inhibitorsbrain metastasisimmunotherapymelanomaprognostic factors

Identifiers

PMID38083908
PMCPMC10757137

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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.