Evidence map›Paper›PMID 32148492›Full record

ArticleJournal of oncology2020

Cost-Effectiveness Analysis of Biomarker-Guided Treatment for Metastatic Gastric Cancer in the Second-Line Setting.

Brianna Lauren, Sassan Ostvar, Elisabeth Silver, Myles Ingram, Aaron Oh, Lindsay Kumble, Monika Laszkowska, Jacqueline N Chu, Dawn L Hershman, Gulam Manji and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 17% 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, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Biomaterials for biomarker imaging and detection.Journal of advanced research · 2026
    Review
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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

12 authors at 3 institutions in 1 country.

Brianna LaurenColumbia University Medical Center, New York, NY, USA.ORCID https://orcid.org/0000-0003-3608-6777
Sassan OstvarColumbia University Medical Center, New York, NY, USA.ORCID https://orcid.org/0000-0002-7034-9625
Elisabeth SilverColumbia University Medical Center, New York, NY, USA.
Myles IngramColumbia University Medical Center, New York, NY, USA.
Aaron OhColumbia University Medical Center, New York, NY, USA.
Lindsay KumbleColumbia University Medical Center, New York, NY, USA.
Monika LaszkowskaColumbia University Medical Center, New York, NY, USA.
Jacqueline N ChuMassachusetts General Hospital, Boston, MA, USA.
Dawn L HershmanColumbia University Medical Center, New York, NY, USA.
Gulam ManjiColumbia University Medical Center, New York, NY, USA.
Alfred I NeugutColumbia University Irving Cancer Research Center, New York, NY, USA.
Chin HurColumbia University Medical Center, New York, NY, USA.ORCID https://orcid.org/0000-0002-2819-7576
Columbia University Irving Medical Center · USCancer Research Center · USMassachusetts General Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe 5-year survival rate of patients with metastatic gastric cancer (GC) is only 5%. However, trials have demonstrated promising antitumor activity for targeted therapies/immunotherapies among chemorefractory metastatic GC patients. Pembrolizumab has shown particular efficacy among patients with programmed death ligand-1 (PD-L1) expression and high microsatellite instability (MSI-H). The aim of this study was to assess the effectiveness and cost-effectiveness of biomarker-guided second-line GC treatment.

methodsWe constructed a Markov decision-analytic model using clinical trial data. Our model compared pembrolizumab monotherapy and ramucirumab/paclitaxel combination therapy for all patients and pembrolizumab for patients based on MSI status or PD-L1 expression. Paclitaxel monotherapy and best supportive care for all patients were additional comparators. Costs of drugs, treatment administration, follow-up, and management of adverse events were estimated from a US payer perspective. The primary outcomes were quality-adjusted life years (QALYs) and incremental cost-effectiveness ratios (ICERs) with a willingness-to-pay threshold of $100,000/QALY over 60 months. Secondary outcomes were unadjusted life years (survival) and costs. Deterministic and probabilistic sensitivity analyses were performed to evaluate model uncertainty.

resultsThe most effective strategy was pembrolizumab for MSI-H patients and ramucirumab/paclitaxel for all other patients, adding 3.8 months or 2.0 quality-adjusted months compared to paclitaxel. However, this strategy resulted in a prohibitively high ICER of $1,074,620/QALY. The only cost-effective strategy was paclitaxel monotherapy for all patients, with an ICER of $53,705/QALY.

conclusionBiomarker-based treatments with targeted therapies/immunotherapies for second-line metastatic GC patients substantially improve unadjusted and quality-adjusted survival but are not cost-effective at current drug prices.

Identifiers

PMID32148492
PMCPMC7048937
OpenAlexW3005813230

What OpenQuestion holds

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LicenceCC BY
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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.