Evidence map›Paper›PMID 30515719›Full record

ArticlePharmacoEconomics2019

Q-TWiST Analysis to Assess Benefit-Risk of Pembrolizumab in Patients with PD-L1-Positive Advanced or Metastatic Non-small Cell Lung Cancer.

Min Huang, M Catherine Pietanza, Ayman Samkari, James Pellissier, Thomas Burke, Sheenu Chandwani, Fansen Kong, A Simon Pickard

Open access · hybridAbstract read
In one paragraph

Article in PharmacoEconomics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 2 pooled it
6.8field-weighted citation impact, top 3% 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

10 citing papers in PubMed, 2 syntheses or guidelines pooled it, 23 citations in OpenAlex.

  1. Pooled it
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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

8 authors at 2 institutions in 1 country.

Min HuangCentre for Observational and Real-world Evidence, Merck & Co., Inc., 2000 Galloping Hill Road, Kenilworth, NJ, USA. Min_Huang@merck.com.ORCID 0000-0003-1960-4552
M Catherine PietanzaCentre for Observational and Real-world Evidence, Merck & Co., Inc., 2000 Galloping Hill Road, Kenilworth, NJ, USA.
Ayman SamkariCentre for Observational and Real-world Evidence, Merck & Co., Inc., 2000 Galloping Hill Road, Kenilworth, NJ, USA.
James PellissierCentre for Observational and Real-world Evidence, Merck & Co., Inc., 2000 Galloping Hill Road, Kenilworth, NJ, USA.
Thomas BurkeCentre for Observational and Real-world Evidence, Merck & Co., Inc., 2000 Galloping Hill Road, Kenilworth, NJ, USA.
Sheenu ChandwaniCentre for Observational and Real-world Evidence, Merck & Co., Inc., 2000 Galloping Hill Road, Kenilworth, NJ, USA.
Fansen KongCentre for Observational and Real-world Evidence, Merck & Co., Inc., 2000 Galloping Hill Road, Kenilworth, NJ, USA.
A Simon PickardSecond City Outcomes Research, 414 North Richland Ave., Oak Park, IL, USA.
Merck & Co., Inc., Rahway, NJ, USA (United States) · USHealth Outcomes Solutions (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesPembrolizumab monotherapy showed significantly longer overall survival and fewer treatment-related adverse events compared to chemotherapy in patients with advanced or metastatic non-small cell lung cancer (NSCLC) with programmed death ligand-1 (PD-L1)-positive tumors in the first-line setting in KEYNOTE (KN)-024 and in those previously treated in KN010. The objective of this analysis was to assess the benefit-risk of pembrolizumab in terms of quality-adjusted survival amongst patients in these trials.

methodsThe Quality-adjusted Time Without Symptoms of disease progression or Toxicity of treatment (Q-TWiST) analysis was used to compare treatments. Survival time was partitioned into three health states: with toxicity before disease progression, without toxicity before disease progression, and disease progression until death. Health state utilities were estimated using EuroQol-5 Dimensions, 3 Levels (EQ-5D-3L) data collected in the trials. Q-TWiST was calculated as the utility-weighted sum of the mean health state durations. Trial data analyzed included the primary analysis and subsequent data cutoffs. The base-case analysis was based on the most recent analysis of the trials.

resultsPatients randomized to pembrolizumab had 2.49 months greater Q-TWiST (P value < 0.001) compared to those randomized to platinum-based chemotherapy at a follow-up of 24 months in KN024, and 2.29 months greater Q-TWiST (P value < 0.001) compared to docetaxel over 30 months follow-up in KN010. Results across the trial analyses showed an increase in trend for the Q-TWiST improvement of pembrolizumab over time.

conclusionsPembrolizumab showed significant improvement in Q-TWiST compared to chemotherapy in advanced or metastatic NSCLC in both previously untreated and treated patients. The benefits of pembrolizumab continued to accrue with longer follow-ups.

Indexed as

Quality-Adjusted Life YearsAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalB7-H1 AntigenCarcinoma, Non-Small-Cell LungClinical Trials, Phase III as TopicHumansLung NeoplasmsNeoplasm StagingProgression-Free SurvivalRandomized Controlled Trials as TopicTreatment OutcomeAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalB7-H1 Antigenpembrolizumab

Identifiers

PMID30515719
PMCPMC6323104
OpenAlexW2902869461

What OpenQuestion holds

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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.