Evidence map›Paper›PMID 39499492›Full record

ArticleOncology and therapy2025

Cost-Effectiveness of Pembrolizumab as First-Line Treatment in Patients with Persistent, Recurrent, or Metastatic Cervical Cancer in the United States.

Bradley J Monk, Sophie van Mens, Oliver Hale, Jennifer Boer, Frank van Hees, Shilpi Swami, Dominic Muston, Cumhur Tekin, Steve Keefe, Matthew Monberg

Registry-linked trialAbstract read
In one paragraph

Article in Oncology and therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03635567 (A Phase 3 Randomized, Double-Blind, Placebo-Controlled Trial of Pembrolizumab), which is not on this map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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.

NCT03635567 phase3completednot on this map

A Phase 3 Randomized, Double-Blind, Placebo-Controlled Trial of Pembrolizumab (MK-3475) Plus Chemotherapy Versus Chemotherapy Plus Placebo for the First-Line Treatment of Persistent, Recurrent, or Metastatic Cervical Cancer (KEYNOTE-826)

TypeinterventionalSponsorMerck Sharp & Dohme LLCRan2018 to 2024Enrolled617ConditionsCervical CancerArmsPembrolizumab, Paclitaxel, Cisplatin, Carboplatin, Bevacizumab
3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. 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

10 authors.

Bradley J MonkHonorHealth Research and Innovation Institute, University of Arizona, Creighton University Phoenix, 10510 N 92nd St #200, Scottsdale, AZ, 85258, USA.ORCID http://orcid.org/0000-0001-6985-0159
Sophie van MensLumanity, Arthur van Schendelstraat 650, 3511 MJ, Utrecht, The Netherlands.
Oliver HaleLumanity, Steel City House West Street, Sheffield, S1 2GQ, UK.ORCID http://orcid.org/0000-0001-9025-751X
Jennifer BoerLumanity, Arthur van Schendelstraat 650, 3511 MJ, Utrecht, The Netherlands.ORCID http://orcid.org/0009-0006-9389-813X
Frank van HeesLumanity, Arthur van Schendelstraat 650, 3511 MJ, Utrecht, The Netherlands.ORCID http://orcid.org/0009-0005-6156-2378
Shilpi SwamiMSD (UK) Limited, 2 Pancras Sq, London, N1C 4AG, UK.ORCID http://orcid.org/0000-0002-7537-8636
Dominic MustonMerck & Co., Inc., 2025 E Scott Ave, Rahway, NJ, 07065, USA. dominic.muston@merck.com.ORCID http://orcid.org/0000-0003-4876-7940
Cumhur TekinMerck & Co., Inc., 2025 E Scott Ave, Rahway, NJ, 07065, USA.ORCID http://orcid.org/0009-0003-9579-2935
Steve KeefeMerck & Co., Inc., 2025 E Scott Ave, Rahway, NJ, 07065, USA.
Matthew MonbergMerck & Co., Inc., 2025 E Scott Ave, Rahway, NJ, 07065, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionFirst-line treatment of persistent, recurrent, or metastatic (advanced) cervical cancer in patients who have a combined positive score (CPS) ≥ 1 with pembrolizumab + chemotherapy versus standard-of-care chemotherapy provides meaningful improvements in overall survival. We conducted a cost-effectiveness analysis from a US payer perspective. A societal perspective scenario was also considered, including productivity gains.

methodsThe cost-effectiveness of pembrolizumab + chemotherapy versus chemotherapy was assessed using a state-transition model comprising the health states "pre-progression," "post-progression," and "death," with a 1-week cycle length and 50-year time horizon. Patient-level KEYNOTE-826 data informed the efficacy, safety, and health-related quality of life of pembrolizumab + chemotherapy versus chemotherapy at first-line and subsequent treatments. Real-world data were sought to cost subsequent treatments according to US clinical practice. Transition probabilities were derived from parametric survival models fit to time-to-progression, progression-free survival, and post-progression survival patient-level KEYNOTE-826 data. Sensitivity analyses explored the impact on outcomes from variables such as bevacizumab use.

resultsAccording to the state-transition model, pembrolizumab + chemotherapy extended mean life expectancy versus chemotherapy from 1.8 to 6.7 life-years. The mean gain of 4.9 life-years/patient was mostly caused by pembrolizumab delaying progression. Total discounted quality-adjusted life-years (QALY) were 5.0 and 1.3 per patient for pembrolizumab + chemotherapy and chemotherapy, respectively (mean gain: 3.7 QALY/patient). Pembrolizumab + chemotherapy had comparable safety outcomes to chemotherapy alone. Total costs incurred were US $320,247 (pembrolizumab + chemotherapy) versus US $105,446 (chemotherapy; mean incremental costs: US $214,801/patient). The incremental cost-effectiveness ratio of pembrolizumab + chemotherapy versus chemotherapy was US $58,446/QALY. Sensitivity analyses showed results were insensitive to bevacizumab use. Including productivity gains led to an incremental cost-effectiveness ratio of US $58,385 per QALY.

conclusionsOur model-based analysis suggests that first-line treatment of pembrolizumab + chemotherapy in advanced cervical cancer with a CPS ≥ 1 offers a substantial clinical benefit over standard-of-care chemotherapy alone and is cost-effective at a willingness-to-pay threshold of US $150,000. The approximate doubling of life-years and QALYs associated with pembrolizumab + chemotherapy represents a step improvement in the treatment of advanced cervical cancer.

trial registrationClinicalTrials.gov Identification Number: NCT03635567.

Indexed as

Cost–benefit analysisCosts and cost analysisImmunotherapyPembrolizumabQuality of lifeUterine cervical neoplasms

Identifiers

PMID39499492
PMCPMC11880493

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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.