Evidence map›Paper›PMID 38031003›Full record

SynthesisBMC cancer2023

PD-1/PD-L1 inhibitors plus carboplatin and paclitaxel compared with carboplatin and paclitaxel in primary advanced or recurrent endometrial cancer: a systematic review and meta-analysis of randomized clinical trials.

Francisco Cezar Aquino de Moraes, Eric Pasqualotto, Lucca Moreira Lopes, Maria Eduarda Cavalcanti Souza, Anna Luíza Soares de Oliveira Rodrigues, Artur Menegaz de Almeida, Carlos Stecca, Marianne Rodrigues Fernandes, Ney Pereira Carneiro Dos Santos

Open access · goldAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in BMC cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 10 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 10 pooled it
7.4field-weighted citation impact, top 2% 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

12 citing papers in PubMed, 10 syntheses or guidelines pooled it, 25 citations in OpenAlex.

  1. Impact of TP53 somatic mutations on prognosis in endometrial cancer: a systematic review and meta-analysis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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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

9 authors at 6 institutions in 1 country.

Francisco Cezar Aquino de MoraesOncology Research Center, Federal University of Pará, University Hospital João de Barros de Barreto, Rua dos Mundurucus, nº4487, Belém, 66073-000, PA, Brazil. francisco.cezar2205@gmail.com.ORCID http://orcid.org/0000-0003-0623-8135
Eric PasqualottoFederal University of Santa Catarina, Florianópolis, 88040-900, Santa Catarina, Brazil.ORCID http://orcid.org/0000-0002-6484-1162
Lucca Moreira LopesSciences Medical School of Santos, Santos, São Paulo, 11045-101, Brazil.ORCID http://orcid.org/0000-0002-2770-2198
Maria Eduarda Cavalcanti SouzaUniversity of Pernambuco, Recife, 50670-901, Pernambuco, Brazil.ORCID http://orcid.org/0000-0002-7244-6461
Anna Luíza Soares de Oliveira RodriguesUniversity Center of João Pessoa, João Pessoa, Paraíba, 58053-000, Brazil.ORCID http://orcid.org/0000-0001-7213-2350
Artur Menegaz de AlmeidaFederal University of Mato Grosso, Sinop, 78550-704, Mato Grosso, Brazil.ORCID http://orcid.org/0009-0004-3869-7373
Carlos SteccaMackenzie Evangelical University Hospital, Curitiba, 80730-150, Paraná, Brazil.ORCID http://orcid.org/0000-0001-9103-9119
Marianne Rodrigues FernandesOncology Research Center, Federal University of Pará, University Hospital João de Barros de Barreto, Rua dos Mundurucus, nº4487, Belém, 66073-000, PA, Brazil.ORCID http://orcid.org/0000-0002-1396-3442
Ney Pereira Carneiro Dos SantosOncology Research Center, Federal University of Pará, University Hospital João de Barros de Barreto, Rua dos Mundurucus, nº4487, Belém, 66073-000, PA, Brazil.ORCID http://orcid.org/0000-0001-8087-7037
Universidade Federal do Pará · BRCentro Universitário de João Pessoa · BRHospital Universitário Evangélico de Curitiba · BRUniversidade de Pernambuco · BRUniversidade Federal de Mato Grosso · BRUniversidade Federal de Santa Catarina · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPaclitaxel and carboplatin is the standard chemotherapy for the treatment of advanced or recurrent endometrial cancer. However, the benefit of adding programmed cell death 1 (PD-1)/programmed death ligand 1 (PD-L1) inhibitors to chemotherapy is still unclear.

methodWe searched PubMed, Scopus, Cochrane, and Web of Science databases for randomized controlled trials that investigated PD-1/PD-L1 inhibitors plus carboplatin and paclitaxel compared with carboplatin and paclitaxel in primary advanced or recurrent endometrial cancer. We computed hazard ratios (HRs) or risk ratios (RRs) for binary endpoints, with 95% confidence intervals (CIs). We used DerSimonian and Laird random-effect models for all endpoints. Heterogeneity was assessed using I

resultsA total of three studies and 1,431 patients were included. Compared with carboplatin plus paclitaxel-based chemotherapy, progression-free survival (PFS) rate (HR 0.32; 95% CI 0.23-0.44; p < 0.001) and overall survival (OS) at 30 months (RR 3.13; 95% CI 1.26-7.78; p = 0.01) were significant in favor of the PD-1/PD-L1 inhibitors plus carboplatin and paclitaxel group in the mismatch repair-deficient subgroup. However, there were no significant differences in the mismatch repair-proficient subgroup for PFS (HR 0.74; 95% CI 0.50-1.08; p = 0.117) or OS at 30 months (RR 2.24; 95% CI 0.79-6.39; p = 0.13).

conclusionImmunotherapy plus carboplatin-paclitaxel increased significantly PFS and OS among patients with advanced or recurrent endometrial cancer, with a significant benefit in the mismatch repair-deficient and high microsatellite instability population.

Indexed as

Endometrial NeoplasmsLung NeoplasmsB7-H1 AntigenCarboplatinFemaleHumansImmune Checkpoint InhibitorsPaclitaxelProgrammed Cell Death 1 ReceptorRandomized Controlled Trials as TopicB7-H1 AntigenCarboplatinImmune Checkpoint InhibitorsPaclitaxelProgrammed Cell Death 1 ReceptorChemotherapyEndometrial cancerImmune Checkpoint inhibitorsMismatch repair–deficient

Identifiers

PMID38031003
PMCPMC10688003
OpenAlexW4389135759

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.