Evidence map›Paper›PMID 34382361›Full record

ArticleCancer medicine2021

Determining the optimal PD-1/PD-L1 inhibitors for the first-line treatment of non-small-cell lung cancer with high-level PD-L1 expression in China.

Meng-Meng Teng, Si-Ying Chen, Bo Yang, Yan Wang, Rui-Ying Han, Meng-Na An, Ya-Lin Dong, Hai-Sheng You

Open access · goldAbstract readNetwork Meta-Analysis
In one paragraph

Article in Cancer medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

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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.

Meng-Meng TengDepartment of Pharmacy, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Si-Ying ChenDepartment of Pharmacy, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Bo YangDepartment of Pharmacy, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Yan WangDepartment of Pharmacy, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Rui-Ying HanDepartment of Pharmacy, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Meng-Na AnDepartment of Pharmacy, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Ya-Lin DongDepartment of Pharmacy, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Hai-Sheng YouDepartment of Pharmacy, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.ORCID 0000-0002-2685-3613
First Affiliated Hospital of Xi'an Jiaotong University · CNSecond Affiliated Hospital of Xi'an Jiaotong University · CN

Funding

Clinical Research Award of the First Affiliated Hospital of Xi'an Jiaotong University, China XJTU1AF-CRF-2019-006Institutional Foundation of the First Affiliated Hospital of Xi'an Jiaotong University, China 2019QN-25Science and Technology Development of Shaanxi Province, China 2020SF-210
6 · The paper itself

Abstract

BACKGROUND AND

objectiveThe programmed death 1 and ligand (PD-1/PD-L1) inhibitors have significantly altered therapeutic perspectives on non-small-cell lung cancer (NSCLC). However, their efficacy and safety are unknown since direct clinical trials have not yet been performed on them. It is also necessary to determine the economics of PD-1/PD-L1 inhibitors due to their high cost. The aim was to evaluate the efficacy, safety, and cost-effectiveness of PD-1/PD-L1 inhibitor monotherapy for advanced NSCLC patients in China with high PD-L1 expression as first-line treatment.

methodsFrom the PubMed, Cochrane, and Web of Science databases, we retrieved survival, progression, and safety data on PD-1/PD-L1 inhibitor monotherapy for advanced NSCLC patients. A network meta-analysis (NMA) was performed to consider PD-1/PD-L1 inhibitors in efficacy and safety. A Markov model with a full-lifetime horizon was adopted. Clinical and utility data were collected through the trial. The cost per quality-adjusted life year (QALY) was as incremental cost-effectiveness ratio (ICER). Sensitivity analyses were performed.

resultsThis study included five phase III clinical trials using four drugs: nivolumab, pembrolizumab, atezolizumab, and durvalumab. The NMA demonstrated that the four drugs had similar efficacy and safety, while pembrolizumab and atezolizumab were better for than for nivolumab (hazard ratio (HR) = 0.66, 95% confidence intervals (CIs): 0.46-0.95 and HR = 0.59, 95%CI: 0.37-0.94) in progression-free survival (PFS), and the risk of a severe adverse event was higher for atezolizumab than for nivolumab and pembrolizumab. Compared with nivolumab, durvalumab, pembrolizumab, and atezolizumab had QALY of 0.19, 0.38, and 0.53, respectively, which induced ICERs of $ 197,028.8/QALY, $ 111,859.0/QALY, and $ 76,182.3/QALY, respectively.

conclusionThe efficacy and safety are similar among types of PD-1/PD-L1-inhibitor monotherapy. The cost-effectiveness of nivolumab appears optimal, but the other PD-1/PD-L1 inhibitors are not as cost-effective for the first-line treatment of advanced NSCLC in China.

Indexed as

AdultB7-H1 AntigenCarcinoma, Non-Small-Cell LungChinaClinical Trials, Phase III as TopicCost-Benefit AnalysisDrug CostsFemaleHumansImmune Checkpoint InhibitorsKaplan-Meier EstimateLung NeoplasmsMaleMarkov ChainsModels, EconomicProgrammed Cell Death 1 ReceptorB7-H1 AntigenCD274 protein, humanImmune Checkpoint InhibitorsPDCD1 protein, humanProgrammed Cell Death 1 Receptorcost-effectivenessefficacynon-small lung cancer (NSCLC)PD-1/PD-L1 inhibitorssafety

Identifiers

PMID34382361
PMCPMC8446572
OpenAlexW3189034905

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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.