Evidence map›Paper›PMID 30769874›Full record

ArticleCancers2019

Combination of Baseline LDH, Performance Status and Age as Integrated Algorithm to Identify Solid Tumor Patients with Higher Probability of Response to Anti PD-1 and PD-L1 Monoclonal Antibodies.

Maria Silvia Cona, Mara Lecchi, Sara Cresta, Silvia Damian, Michele Del Vecchio, Andrea Necchi, Marta Maria Poggi, Daniele Raggi, Giovanni Randon, Raffaele Ratta and 5 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 2 pooled it
1.7field-weighted citation impact, top 14% 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

19 citing papers in PubMed, 2 syntheses or guidelines pooled it, 28 citations in OpenAlex.

  1. Pooled it
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  11. Exploring immunotherapy in colorectal cancer.Journal of hematology & oncology · 2022
    Review
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  18. An overview of immune checkpoint inhibitors in breast cancer.Exploration of targeted anti-tumor therapy · 2020
    Review
  19. Review
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

15 authors at 3 institutions in 1 country.

Maria Silvia ConaMedical Oncology Unit, Fondazione IRCCS, Istituto Nazionale dei Tumori di Milano, Via Giacomo Venezian 1, 20133 Milan, Italy. mariasilvia.cona@istitutotumori.mi.it.
Mara LecchiBioinformatics and Biostatistics Unit, Fondazione IRCCS, Istituto Nazionale dei Tumori di Milano, Via Giacomo Venezian 1, 20133 Milan, Italy. mara.lecchi@istitutotumori.mi.it.
Sara CrestaMedical Oncology Unit, Fondazione IRCCS, Istituto Nazionale dei Tumori di Milano, Via Giacomo Venezian 1, 20133 Milan, Italy. sara.cresta@istitutotumori.mi.it.
Silvia DamianMedical Oncology Unit, Fondazione IRCCS, Istituto Nazionale dei Tumori di Milano, Via Giacomo Venezian 1, 20133 Milan, Italy. silvia.damian@istitutotumori.mi.it.
Michele Del VecchioMedical Oncology Unit, Fondazione IRCCS, Istituto Nazionale dei Tumori di Milano, Via Giacomo Venezian 1, 20133 Milan, Italy. michele.delvecchio@istitutotumori.mi.it.
Andrea NecchiMedical Oncology Unit, Fondazione IRCCS, Istituto Nazionale dei Tumori di Milano, Via Giacomo Venezian 1, 20133 Milan, Italy. andrea.necchi@istitutotumori.mi.it.
Marta Maria PoggiMedical Oncology Unit, Fondazione IRCCS, Istituto Nazionale dei Tumori di Milano, Via Giacomo Venezian 1, 20133 Milan, Italy. martamariapoggi@gmail.com.
Daniele RaggiMedical Oncology Unit, Fondazione IRCCS, Istituto Nazionale dei Tumori di Milano, Via Giacomo Venezian 1, 20133 Milan, Italy. daniele.raggi@istitutotumori.mi.it.
Giovanni RandonMedical Oncology Unit, Fondazione IRCCS, Istituto Nazionale dei Tumori di Milano, Via Giacomo Venezian 1, 20133 Milan, Italy. giovanni.randon@istitutotumori.mi.it.
Raffaele RattaMedical Oncology Unit, Fondazione IRCCS, Istituto Nazionale dei Tumori di Milano, Via Giacomo Venezian 1, 20133 Milan, Italy. raffaele.ratta@istitutotumori.mi.it.
Diego SignorelliMedical Oncology Unit, Fondazione IRCCS, Istituto Nazionale dei Tumori di Milano, Via Giacomo Venezian 1, 20133 Milan, Italy. diego.signorelli@istitutotumori.mi.it.
Claudio VernieriMedical Oncology Unit, Fondazione IRCCS, Istituto Nazionale dei Tumori di Milano, Via Giacomo Venezian 1, 20133 Milan, Italy. claudio.vernieri@istitutotumori.mi.it.
Filippo de BraudMedical Oncology Unit, Fondazione IRCCS, Istituto Nazionale dei Tumori di Milano, Via Giacomo Venezian 1, 20133 Milan, Italy. filippo.debraud@istitutotumori.mi.it.
Paolo VerderioBioinformatics and Biostatistics Unit, Fondazione IRCCS, Istituto Nazionale dei Tumori di Milano, Via Giacomo Venezian 1, 20133 Milan, Italy. paolo.verderio@istitutotumori.mi.it.
Massimo Di NicolaMedical Oncology Unit, Fondazione IRCCS, Istituto Nazionale dei Tumori di Milano, Via Giacomo Venezian 1, 20133 Milan, Italy. massimo.dinicola@istitutotumori.mi.it.
Fondazione IRCCS Istituto Nazionale dei Tumori · ITIFOM · ITUniversity of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Predictive biomarkers of response to immune-checkpoint inhibitors (ICIs) are an urgent clinical need. The aim of this study is to identify manageable parameters to use in clinical practice to select patients with higher probability of response to ICIs. Two-hundred-and-seventy-one consecutive metastatic solid tumor patients, treated from 2013 until 2017 with anti- Programmed death-ligand 1 (PD-L1)/programmed cell death protein 1 (PD-1) ICIs, were evaluated for baseline lactate dehydrogenase (LDH) serum level, performance status (PS), age, neutrophil-lymphocyte ratio, type of immunotherapy, number of metastatic sites, histology, and sex. A training and validation set were used to build and test models, respectively. The variables' effects were assessed through odds ratio estimates (OR) and area under the receive operating characteristic curves (AUC), from univariate and multivariate logistic regression models. A final multivariate model with LDH, age and PS showed significant ORs and an AUC of 0.771. Results were statistically validated and used to devise an Excel algorithm to calculate the patient's response probabilities. We implemented an interactive Excel algorithm based on three variables (baseline LDH serum level, age and PS) which is able to provide a higher performance in response prediction to ICIs compared with LDH alone. This tool could be used in a real-life setting to identify ICIs in responding patients.

Indexed as

biomarkersimmune-checkpoint inhibitorsLDH

Identifiers

PMID30769874
PMCPMC6406250
OpenAlexW2914935470

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.