Evidence map›Paper›PMID 41494223›Full record

Observational studyESMO open2026

Real-world outcomes versus clinical trial results of first-line immunotherapy with or without chemotherapy in patients with metastatic non-small-cell lung cancer: the CORRELATE study.

S Peters, R J-B Salomonsen, I Diaz Perez, T Shcherbakova, A Wang, L Cai, S Sadow, S V Liu

Abstract readObservational Study
In one paragraph

Observational study in ESMO open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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

8 authors.

S PetersCentre Hospitalier Universitaire Vaudois, Lausanne University, Lausanne, Switzerland. Electronic address: Solange.Peters@chuv.ch.
R J-B SalomonsenAstraZeneca, Gaithersburg, USA.
I Diaz PerezAstraZeneca, Gaithersburg, USA.
T ShcherbakovaAstraZeneca, Cambridge, UK.
A WangAstraZeneca, Gaithersburg, USA.
L CaiAstraZeneca, Gaithersburg, USA.
S SadowAstraZeneca, Gaithersburg, USA.
S V LiuDivision of Hematology and Oncology, Georgetown University, Washington, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecent data suggest that real-world overall survival (rwOS) and progression-free survival (rwPFS) in patients with metastatic non-small-cell lung cancer (mNSCLC) receiving first-line immunotherapy-based regimens are shorter than reported in randomized controlled trials (RCTs). This retrospective, observational study compared rwOS and rwPFS with outcomes observed in RCTs in patients with mNSCLC who received immunotherapy. PATIENTS AND

methodsEligible real-world (RW) patients from the United States Flatiron Enhanced Datamart had mNSCLC, started first-line treatment with an immunotherapy-based regimen between November 2016 and May 2021, and met key eligibility criteria per the registration RCTs for approved anti-programmed cell death (ligand) 1 [PD-(L)1]-based regimens: KEYNOTE-024, KEYNOTE-189, KEYNOTE-407, IMpower150, CheckMate 9LA, and CheckMate 227. rwOS and rwPFS were analyzed using the Kaplan-Meier method, per regimen/study cohort in subgroups by Eastern Cooperative Oncology Group (ECOG) performance status (PS; 0-1 or 2) and PD-L1 expression level (<1% or ≥1%). Efficacy-effectiveness factors (EEFs) quantified the gaps between RW and RCT outcomes.

resultsThe analysis included 2705 and 661 patients with ECOG PS 0-1 and 2, respectively. Patients in the RW cohorts were older with a greater proportion of females compared with the corresponding RCTs. Among patients with PS 0-1, EEFs showed that median rwOS was 36%-61% shorter and median rwPFS was 21%-60% shorter compared with the reference RCTs. For the RW cohorts with sufficient sample size to permit analysis in patients with PS 2, this subgroup showed even greater differences in outcomes versus RCTs. In the RW KEYNOTE-189 and KEYNOTE-407 PS 0-1 cohorts, the PD-L1 ≥1% subgroup had numerically higher median rwOS and rwPFS than the PD-L1 <1% subgroup.

conclusionsPD-(L)1 inhibitors have been established as the standard-of-care first-line therapy in mNSCLC; however, in this study, RW survival outcomes were considerably shorter than those reported in RCTs. These findings highlight a potential unmet need for more effective treatment options for patients with mNSCLC in RW practice.

Indexed as

Carcinoma, Non-Small-Cell LungImmunotherapyLung NeoplasmsAgedFemaleHumansMaleMiddle AgedNeoplasm MetastasisRandomized Controlled Trials as TopicRetrospective StudiesTreatment Outcomeefficacy–effectiveness gapimmunotherapymetastatic NSCLCPD-L1real-world outcomes

Identifiers

PMID41494223
PMCPMC12810545

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.