Evidence map›Paper›PMID 29041898›Full record

ArticleBMC cancer2017

Societal preferences for adjuvant melanoma health states: UK and Australia.

Mark R Middleton, Michael B Atkins, Kaitlan Amos, Peter Feng Wang, Srividya Kotapati, Javier Sabater, Kathleen Beusterien

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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 6 institutions in 6 countries.

Mark R MiddletonUniversity of Oxford Department of Oncology, Roosevelt Drive, Oxford, OX3 7DQ, UK.
Michael B AtkinsGeorgetown-Lombardi Comprehensive Cancer Ctr, 3970 Reservoir Road, NW Research Building, Room E501, Washington, DC, 20057, USA.
Kaitlan AmosOutcomes Research Strategies in Health, Washington, DC, 20008, USA.
Peter Feng WangBristol-Myers Squibb Co, 3401 Princeton Pike, Lawrenceville, NJ, 08648, USA.
Srividya KotapatiBristol-Myers Squibb Co, 3401 Princeton Pike, Lawrenceville, NJ, 08648, USA.
Javier SabaterBristol-Myers Squibb S.A. Quintanavides, 15, 28050, Madrid, Spain.
Kathleen BeusterienOutcomes Research Strategies in Health, Washington, DC, 20008, USA. Kathy.beusterien@orshealth.com.
Bristol-Myers Squibb (Belgium) · BEBristol-Myers Squibb (Germany) · DEBristol-Myers Squibb (United States) · USCRUK/MRC Oxford Institute for Radiation Oncology · GBGeorgetown University Medical Center · USHealth Strat (Kenya) · KE

Funding

Cancer Research UK 8466
6 · The paper itself

Abstract

backgroundNo studies have measured preference-based utility weights for specific toxicities and outcomes associated with approved and investigational adjuvant treatments for patients with resected high-risk melanoma.

methodsA cross-sectional study was conducted in the United Kingdom and Australia to obtain utilities for 14 adjuvant melanoma health states. One-on-one interviews were conducted using standard gamble; utility weights range from 0.0, dead, to 1.0, full health. Supplemental risk questions also were asked.

resultsAmong 155 participants (52% male; mean age, 46 years) "adjuvant treatment no toxicities" (0.89) was most preferred, followed by "induction treatment" (0.88), and "no treatment" (0.86). Participants least preferred "cancer recurrence" (0.62); the utility for "cancer recurrence and 10-year survival with treatment" was 0.70. Disutilities for grade 2 toxicities ranged from -0.06 for fatigue to -0.13 for hypophysitis. The mean maximum acceptable risk of a life-threatening event ranged from 30% for a 6% increase in the chance of remaining cancer free over 3 years to 40% for an 18% increase; Australian respondents were willing to take higher risks.

conclusionReproducible health utilities for adjuvant melanoma health states were obtained from the general population in two countries. These utilities can be incorporated into treatment-specific cost-effectiveness evaluations.

Indexed as

Adjuvants, ImmunologicAdultAntineoplastic Agents, ImmunologicalAustraliaCross-Sectional StudiesFemaleHumansInterferon Type IIpilimumabMaleMelanomaMiddle AgedTreatment OutcomeUnited KingdomAdjuvants, ImmunologicAntineoplastic Agents, ImmunologicalInterferon Type IIpilimumab

Identifiers

PMID29041898
PMCPMC5646133
OpenAlexW2766564946

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.