Evidence map›Paper›PMID 31995619›Full record

ArticlePloS one2020

Cost-effectiveness of pembrolizumab for advanced non-small cell lung cancer patients with varying comorbidity burden.

Steven D Criss, Lauren Palazzo, Tina R Watson, Adelle M Paquette, Keith Sigel, Juan Wisnivesky, Chung Yin Kong

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 2 pooled it
0.8field-weighted citation impact, top 25% 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

11 citing papers in PubMed, 2 syntheses or guidelines pooled it, 17 citations in OpenAlex.

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  11. Prognostication Based on Texture Analysis of BaselineIndian journal of nuclear medicine : IJNM : the official journal of the Society of Nuclear Medicine, India
    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

7 authors at 3 institutions in 1 country.

Steven D CrissInstitute for Technology Assessment, Massachusetts General Hospital, Boston, MA, United States of America.
Lauren PalazzoInstitute for Technology Assessment, Massachusetts General Hospital, Boston, MA, United States of America.
Tina R WatsonInstitute for Technology Assessment, Massachusetts General Hospital, Boston, MA, United States of America.
Adelle M PaquetteInstitute for Technology Assessment, Massachusetts General Hospital, Boston, MA, United States of America.
Keith SigelDivision of General Internal Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, United States of America.
Juan WisniveskyDivision of General Internal Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, United States of America.
Chung Yin KongInstitute for Technology Assessment, Massachusetts General Hospital, Boston, MA, United States of America.ORCID 0000-0001-6431-7830
Massachusetts General Hospital · USIcahn School of Medicine at Mount Sinai · USHarvard University · US

Funding

Comparative Modeling of Lung Cancer Prevention and Control PoliciesU01CA199284 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DE KONING, HARRY J, HOLFORD, THEODORE R · 2015 to 2019
$8.4M
Optimizing Treatment of Lung Cancer Patients with ComorbiditiesR01CA202956 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI KONG, CHUNG YIN, WISNIVESKY, JUAN P · 2016 to 2019
$2.9M
NCI NIH HHS R01 CA202956NCI NIH HHS U01 CA199284
6 · The paper itself

Abstract

objectivesWhile previous cost-effectiveness studies on pembrolizumab in stage IV non-small cell lung cancer (NSCLC) have found these regimens to be cost-effective, their reliance on randomized controlled trial (RCT) data with strict inclusion criteria limits generalizability to patients with comorbidities. We estimated the cost-effectiveness of first-line pembrolizumab for patients with various comorbidities. MATERIALS AND

methodsIn our base case analysis, we studied pembrolizumab plus chemotherapy (pembrolizumab combination therapy) versus chemotherapy alone. In a secondary analysis, we considered only patients with PD-L1 expression of at least 50% (PD-L1-high) and evaluated pembrolizumab monotherapy, pembrolizumab combination therapy, and chemotherapy alone. Microsimulation models were developed for the base case and the PD-L1-high analyses. To estimate outcomes of patients with differing comorbidities, we combined survival data from patients with few or no comorbidities from the RCTs with estimates from the general population obtained from the Surveillance, Epidemiology, and End Results (SEER)-Medicare database. Comorbidity burden level was divided into three groups based on the Charlson score (equal to 0, 1, or 2+); patients with various other specific comorbidities were also analyzed. Incremental cost-effectiveness ratios (ICER) were compared to a willingness-to-pay (WTP) threshold of $100,000/quality-adjusted life-year (QALY).

resultsIn the Charlson 0, Charlson 1, and Charlson 2+ patient populations, estimated ICERs for pembrolizumab combination therapy in the base case model were $173,919/QALY, $175,165/QALY, and $181,777/QALY, respectively, compared to chemotherapy. In the PD-L1-high model, the Charlson 0, Charlson 1, and Charlson 2+ patients had ICERs of $147,406/QALY, $149,026/QALY, and $154,521/QALY with pembrolizumab combination therapy versus chemotherapy. Pembrolizumab monotherapy was weakly dominated for each comorbidity group in the PD-L1-high model.

conclusionFor patients with stage IV NSCLC and varying comorbidity burden, first-line treatment with pembrolizumab does not represent a cost-effective strategy compared to chemotherapy. Resources should be focused on collecting immunotherapy survival data for more representative NSCLC patient populations.

Indexed as

AgedAged, 80 and overAntibodies, Monoclonal, HumanizedAntineoplastic AgentsAntineoplastic Agents, ImmunologicalAntineoplastic Combined Chemotherapy ProtocolsCarcinoma, Non-Small-Cell LungComorbidityCost-Benefit AnalysisDrug CostsHealth Care CostsHumansLung NeoplasmsMaleModels, StatisticalQuality-Adjusted Life YearsAntibodies, Monoclonal, HumanizedAntineoplastic AgentsAntineoplastic Agents, Immunologicalpembrolizumab

Identifiers

PMID31995619
PMCPMC6988966
OpenAlexW3003532911

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.