Evidence map›Paper›PMID 40078182›Full record

ArticleFrontiers in oncology2025

Brazilian real-world data of immunotherapy in extensive stage small cell lung cancer.

Flavia A Duarte, Rodrigo Dienstmann, Paulo H C Diniz, Matheus C E Silva, Gilson G V Veloso, Georgia S Arcanjo, Rafael Paes, Tatiane C Montella, Helena F C A Lima, Bruno L Ferrari and 2 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

12 authors.

Flavia A DuarteOncoclinicas&Co - Medica Scientia Innovation Research (MEDSIR), Sao Paulo, SP, Brazil.
Rodrigo DienstmannOncoclinicas&Co - Medica Scientia Innovation Research (MEDSIR), Sao Paulo, SP, Brazil.
Paulo H C DinizDepartamento de Clínica Médica, Faculdade de Medicina, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Matheus C E SilvaOncoclinicas&Co - Medica Scientia Innovation Research (MEDSIR), Sao Paulo, SP, Brazil.
Gilson G V VelosoOncoclinicas&Co - Medica Scientia Innovation Research (MEDSIR), Sao Paulo, SP, Brazil.
Georgia S ArcanjoOncoclinicas&Co - Medica Scientia Innovation Research (MEDSIR), Sao Paulo, SP, Brazil.
Rafael PaesOncoclinicas&Co - Medica Scientia Innovation Research (MEDSIR), Sao Paulo, SP, Brazil.
Tatiane C MontellaOncoclinicas&Co - Medica Scientia Innovation Research (MEDSIR), Sao Paulo, SP, Brazil.
Helena F C A LimaOncoclinicas&Co - Medica Scientia Innovation Research (MEDSIR), Sao Paulo, SP, Brazil.
Bruno L FerrariOncoclinicas&Co - Medica Scientia Innovation Research (MEDSIR), Sao Paulo, SP, Brazil.
Eliane V MacuzoDepartamento de Clínica Médica, Faculdade de Medicina, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Carlos G FerreiraOncoclinicas&Co - Medica Scientia Innovation Research (MEDSIR), Sao Paulo, SP, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The landmarks of Thoracic Oncology in the last two decades have been accompanied by exponential growth in costs, making it imperative to assess the real benefit of incorporating new technologies. Combining immunotherapy (IO) with platinum-etoposide chemotherapy has become the standard of care in first-line treatment of extensive-stage small cell lung cancer (ES-SCLC). However, the absolute difference in overall survival (OS) has reached three months. This study aimed to investigate the impact of this intervention in a real-world cohort. Material and methods: We retrospectively analyzed data from ES-SCLC patients (pts) from a Brazilian Oncology Group, diagnosed and treated between January 2018 and June 2022. The primary objectives were median OS (mOS) and median time to subsequent treatment (mTST) according to IO exposure in the first-line setting. Secondarily, we intend to compare these results with the literature data and with an internal and contemporary cohort of patients treated with chemotherapy alone. Results: In total, 85 SCLC patients were included in this analysis. The median follow-up was nine months. First line regimens were atezolizumab + platinum-etoposide in 53%, platinum-etoposide in 36% and platinum-irinotecan in 11%. Among ES-SCLC pts who received IO in their first-line treatment, the mOS was 15.0 months (95% CI: 11.20; 18.80) and the mTST was 8.0 months (95% CI: 6.25; 9.75). As a reference, our internal and contemporary control presented numerically lower mOS and mTST: 9.0 months (95% CI: 2.08; 19.92) and 7.0 months (95% CI: 5.88; 8.12), respectively. Discussion: Few real-world cohorts are evaluating the impact of IO in ES-SCLC, limited to high-income countries. Our data suggest that IO has a meaningful impact on the outcome of ES-SCLC in daily clinical practice, confirming previous trial results.

Indexed as

Brazilian dataextensive diseaseimmunotherapylong-term outcomesreal-world datasmall cell lung cacer

Identifiers

PMID40078182
PMCPMC11897917

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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.