Evidence map›Paper›PMID 39195335›Full record

SynthesisCurrent oncology (Toronto, Ont.)2024

Immunotherapy-Based Combinations in First-Line Urothelial Cancer: A Systematic Review and Individual Patient Data (IPD) Meta-Analysis.

Mattia Alberto Di Civita, Andrea Torchia, Daniele Santini, Daniele Marinelli, Virginia Magro, Marianna Cerro, Laura Pappalardo, Giulia Maltese, Fiorenza Santamaria, Luca Zacco and 6 more

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in Current oncology (Toronto, Ont.), 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

16 authors.

Mattia Alberto Di CivitaDepartment of Experimental Medicine, Sapienza University, 00161 Rome, Italy.ORCID 0009-0009-3013-2622
Andrea TorchiaClinical and Molecular Medicine, Sapienza University of Rome, 00185 Rome, Italy.ORCID 0000-0002-4020-6893
Daniele SantiniDivision of Medical Oncology A, Policlinico Umberto I, 00161 Rome, Italy.
Daniele MarinelliDepartment of Experimental Medicine, Sapienza University, 00161 Rome, Italy.ORCID 0000-0002-6002-363X
Virginia MagroFaculty of Medicine and Surgery, Sapienza University, 00161 Rome, Italy.
Marianna CerroClinical and Molecular Medicine, Sapienza University of Rome, 00185 Rome, Italy.ORCID 0009-0009-9017-1383
Laura PappalardoDepartment of Radiological Sciences, Oncology and Pathology, Sapienza University of Rome, 00185 Rome, Italy.
Giulia MalteseDepartment of Radiological Sciences, Oncology and Pathology, Sapienza University of Rome, 00185 Rome, Italy.
Fiorenza SantamariaDepartment of Experimental Medicine, Sapienza University, 00161 Rome, Italy.ORCID 0000-0002-1214-9342
Luca ZaccoDepartment of Radiological Sciences, Oncology and Pathology, Sapienza University of Rome, 00185 Rome, Italy.
Dorelsa BuccilliDepartment of Radiological Sciences, Oncology and Pathology, Sapienza University of Rome, 00185 Rome, Italy.
Ailin DehghanpourDepartment of Radiological Sciences, Oncology and Pathology, Sapienza University of Rome, 00185 Rome, Italy.
Iolanda SperanzaDivision of Medical Oncology A, Policlinico Umberto I, 00161 Rome, Italy.
Alessandro SciarraDepartment of Urology, Sapienza Rome University, Policlinico Umberto I, 00161 Rome, Italy.ORCID 0000-0002-7899-8056
Valeria PanebiancoDepartment of Radiological Sciences, Oncology and Pathology, Sapienza University of Rome, 00185 Rome, Italy.
Michela RobertoDivision of Medical Oncology A, Policlinico Umberto I, 00161 Rome, Italy.ORCID 0000-0001-5339-8348

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPlatinum-based chemotherapy represents the standard of care (SoC) for the first-line treatment of advanced urothelial carcinoma (mUC). The benefit of adding immune checkpoint inhibitors (ICIs) to platinum-based chemotherapy was recently investigated. We performed an individual patient data (IPD) meta-analysis of phase 3 clinical trials comparing ICI-based treatments.

methodsA systematic literature search was conducted on the MEDLINE and CENTRAL databases. The results were filtered by including only reports on clinical trials or randomized clinical trials from 2018 to 2023, including 3047 patients from four clinical trials (EV302, CHECKMATE-901, IMVIGOR130, KEYNOTE-361). An IPD meta-analysis was performed by reconstructing IPD from Kaplan-Meier curves. The primary endpoints were overall survival (OS) and progression-free survival (PFS) of Pembrolizumab + EV compared to experimental arms of the other trials of immunotherapy + chemotherapy.

resultsThe OS analysis showed an advantage of IPD from EV302 vs. all the other trials. For EV302 vs. KEYNOTE-361, the HR was 0.51; for EV302 vs. IMVIGOR130, the HR was 0.47; and for EV302 vs. CHECKMATE-901, the HR was 0.66 (CI 95% 0.51-0.85). In the PFS analysis, the EV302 arm showed a statistically significant advantage compared to CHECKMATE-901 (HR 0.66) and versus IMVIGOR130 (HR 0.51). LIMITATIONS: By using reconstructed IPD curves, it was not possible to adjust patient-level covariates, and the heterogeneity of the included population may have affected the pooled results.

conclusionsThe EV302 experimental arm showed better OS and PFS when compared to the other immunochemotherapy combinations. An immunochemotherapy combination strategy at the beginning of treatment in mUC seems to be superior in terms of OS and PFS compared to platinum-based chemotherapy alone. EV-Pembrolizumab resulted to have better outcomes compared to avelumab, rather than other immunochemotherapy combinations. However, given the heterogeneity of these studies, a longer follow up and prospective trials are needed to confirm these data.

Indexed as

Immune Checkpoint InhibitorsImmunotherapyAntibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsCarcinoma, Transitional CellHumansProgression-Free SurvivalUrologic NeoplasmsAntibodies, Monoclonal, HumanizedImmune Checkpoint Inhibitorsantibody–drug conjugateatezolizumabenfortumab vedotinnivolumabpembrolizumab

Identifiers

PMID39195335
PMCPMC11352654

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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.