Evidence map›Paper›PMID 39001417›Full record

ArticleCancers2024

Primary Tumor Characteristics as Biomarkers of Immunotherapy Response in Advanced Melanoma: A Retrospective Cohort Study.

Rachel S Goodman, Seungyeon Jung, Kylie Fletcher, Hannah Burnette, Ismail Mohyuddin, Rebecca Irlmeier, Fei Ye, Douglas B Johnson

Abstract read
In one paragraph

Article in Cancers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Rachel S GoodmanVanderbilt University School of Medicine, Nashville, TN 37240, USA.ORCID 0000-0001-7992-8108
Seungyeon JungVanderbilt University School of Medicine, Nashville, TN 37240, USA.
Kylie FletcherVanderbilt University School of Medicine, Nashville, TN 37240, USA.ORCID 0000-0003-0723-9236
Hannah BurnetteDepartment of Hematology/Oncology, Vanderbilt University Medical Center, Nashville, TN 37240, USA.ORCID 0009-0009-7784-634X
Ismail MohyuddinVanderbilt University, Nashville, TN 37240, USA.
Rebecca IrlmeierVanderbilt University School of Medicine, Nashville, TN 37240, USA.
Fei YeVanderbilt University School of Medicine, Nashville, TN 37240, USA.ORCID 0000-0001-6472-5076
Douglas B JohnsonDepartment of Hematology/Oncology, Vanderbilt University Medical Center, Nashville, TN 37240, USA.

Funding

(PQ8) Patient- and tumor-specific biomarkers and mechanisms that predict irAEs resulting from checkpoint inhibitionR01CA227481 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BALKO, JUSTIN M, JOHNSON, DOUGLAS B · 2019 to 2023
$2.6M
Burroughs Wellcome Fund. NAJames C. Bradford Melanoma Fund NAMedical Scholars, Vanderbilt University Medical Center NANCI NIH HHS R01CA227481SCRIPS Foundation NASusan and Luke Simons Directorship for Melanoma NAVan Stephenson Melanoma Fund NA
6 · The paper itself

Abstract

Identifying patients likely to benefit from immune checkpoint inhibitor (ICI) treatment remains a crucial goal for melanoma. The objective of this study is to assess the association between primary tumor features and immunotherapy response and survival in advanced melanoma patients. In this single-center retrospective cohort study, disease characteristics, response to immunotherapy, PFS, and OS were assessed among melanoma patients (excluding mucosal and uveal primaries) treated with ICI. Among 447 patients, 300 (67.1%) received anti-PD-1 monotherapy and 147 (32.9%) received ipilimumab/nivolumab. A total of 338 (75.6%) had cutaneous melanoma, 29 (6.5%) had acral melanoma, and 80 (17.9%) had melanoma of unknown primary. Ulceration and stage at initial presentation were associated with inferior outcomes on univariate analysis. However, on multivariate analysis, this result was not observed, but cutaneous melanoma and each of its subtypes (superficial spreading, nodular, other, unknown) were positively associated with response, longer PFS, and longer OS. Metastatic stage (M1c, M1d) at presentation (OR = 1.8,

Indexed as

biomarkersimmunotherapymelanoma

Identifiers

PMID39001417
PMCPMC11240575

What OpenQuestion holds

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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.