Evidence map›Paper›PMID 38672547›Full record

ArticleCancers2024

Development and Validation of an Inflammatory Prognostic Index to Predict Outcomes in Advanced/Metastatic Urothelial Cancer Patients Receiving Immune Checkpoint Inhibitors.

Sara Mokbel, Giuilia Baciarello, Pernelle Lavaud, Aurelius Omlin, Fabio Calabrò, Richard Cathomas, Stefanie Aeppli, Pauline Parent, Patrizia Giannatempo, Kira-Lee Koster and 12 more

Open access · goldAbstract 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. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.3field-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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
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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

22 authors at 12 institutions in 4 countries.

Sara MokbelFaculty of Medicine, UCL-University College London, London WC1H 0AP, UK.ORCID 0009-0004-7805-1606
Giuilia BaciarelloMedical Oncology Department, Azienda Ospedaliera San Camillo Forlanini, 00152 Roma, Italy.
Pernelle LavaudMedical Oncology Department, Gustave Roussy Cancer Campus, 94805 Villejuif, France.
Aurelius OmlinMedical Oncology and Haematology Department, OnkoZentrum Zürich, 8038 Zurich, Switzerland.
Fabio CalabròMedical Oncology 1, IRCCS National Cancer Institute Regina Elena, 00144 Rome, Italy.ORCID 0000-0002-7863-3540
Richard CathomasMedical Oncology 1, IRCCS National Cancer Institute Regina Elena, 00144 Rome, Italy.ORCID 0000-0002-9677-9885
Stefanie AeppliDepartment of Medical Oncology and Haematology, Cantonal Hospital St.Gallen, 9000 St. Gallen, Switzerland.
Pauline ParentMedical Oncology Departement, CHU Lille-Centre Hospitalier Régional Universitaire de Lille, 59000 Lille, France.ORCID 0000-0001-6072-7357
Patrizia GiannatempoMedical Oncology Department, Fondazione IRCCS-Istituto Nazionale dei Tumori, 20133 Milan, Italy.
Kira-Lee KosterDepartment of Medical Oncology and Haematology, Cantonal Hospital St.Gallen, 9000 St. Gallen, Switzerland.ORCID 0000-0002-6549-8124
Naara AppelMedical Oncology Departement, HUG-Hopitaux Universitaires Geneve, 1205 Geneva, Switzerland.
Philippe GonnetMedical Oncology Departement, HUG-Hopitaux Universitaires Geneve, 1205 Geneva, Switzerland.
Gesuino AngiusMedical Oncology Department, Azienda Ospedaliera San Camillo Forlanini, 00152 Roma, Italy.
Petros TsantoulisMedical Oncology Departement, HUG-Hopitaux Universitaires Geneve, 1205 Geneva, Switzerland.ORCID 0000-0003-3613-6682
Hendrick-Tobias ArkenauSCRI, London W1G 6AD, UK.
Carlo CattriniMaggiore della Carità University Hospital, 28100 Novara, Italy.ORCID 0000-0003-4785-9480
Carlo MessinaOspedale A.R.N.A.S Civico, 90127 Palermo, Italy.ORCID 0000-0002-7934-1419
Jean ZeghondyMedical Oncology Department, Gustave Roussy Cancer Campus, 94805 Villejuif, France.ORCID 0000-0001-8811-4085
Cristina MorelliMedical Oncology Unit, Policlinico Tor Vergata, 00133 Rome, Italy.
Yohann LoriotMedical Oncology Department, Gustave Roussy Cancer Campus, 94805 Villejuif, France.
Vincenzo FormicaMedical Oncology Unit, Policlinico Tor Vergata, 00133 Rome, Italy.ORCID 0000-0002-5380-3144
Anna PatrikidouMedical Oncology Department, Gustave Roussy Cancer Campus, 94805 Villejuif, France.
Institut Gustave Roussy · FRHôpital Beau-Séjour · CHAzienda Ospedaliera San Camillo-Forlanini · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITPoliclinico Tor Vergata · ITUniversity of St.Gallen · CHAzienda di Rilievo Nazionale ed Alta Specializzazione · ITCentre Hospitalier Universitaire de Lille · FRFondazione IRCCS Istituto Nazionale dei Tumori · ITSarah Cannon Research Institute · GBUniversità degli Studi del Piemonte Orientale “Amedeo Avogadro” · ITUniversity College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmune checkpoint inhibitors (ICIs) improve overall survival (OS) in advanced/metastatic urothelial cancer (a/mUC) patients. Preliminary evidence suggests a prognostic role of inflammatory biomarkers in this setting. We aimed to develop a disease-specific prognostic inflammatory index for a/mUC patients on ICIs.

methodsFifteen variables were retrospectively correlated with OS and progression-free survival (PFS) in a development (D, n = 264) and a validation (V, n = 132) cohort of platinum-pretreated a/mUC pts receiving ICIs at L2 or further line. A nomogram and inflammatory prognostic index (U-IPI) were developed. The index was also tested in a control cohort of patients treated with chemotherapy only (C, n = 114).

resultsThe strongest predictors of OS were baseline platelet/lymphocyte (PLR) and neutrophil/lymphocyte (NLR) ratios, and lactate dehydrogenase (LDH), NLR, and albumin changes at 4 weeks. These were used to build the U-IPI, which can distinctly classify patients into good or poor response groups. The nomogram scoring is significant for PFS and OS (

conclusionsThe lack of a baseline systemic inflammatory profile and the absence of early serum inflammatory biomarker changes are associated with significantly better outcomes on ICIs in a/mUC pts. The U-IPI is an easily applicable dynamic prognostic tool for PFS and OS, allowing for the early identification of a sub-group with dismal outcomes that would not benefit from ICIs, while distinguishing another that draws an important benefit.

Indexed as

advanced/metastatic urothelial cancerimmune checkpoint inhibitorsinflammatory markers

Identifiers

PMID38672547
PMCPMC11048042
OpenAlexW4394717134

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.