Evidence map›Paper›PMID 41215753›Full record

ArticleFuture oncology (London, England)2025

Oncologists' preferences for first-line treatment of ALK-positive metastatic NSCLC in the United States: a discrete choice experiment.

Kathryn F Mileham, Laura Panattoni, Grace Gahlon, Pedro Labisa, Nicole Bariahtaris, Marlon Graf, Christopher Danes, Luis Hernandez

Abstract read
In one paragraph

Article in Future oncology (London, England), 2025. 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
–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.

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.

  1. Observational
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.

Kathryn F MilehamAtrium Health Levine Cancer Institute, Wake Forest University School of Medicine, Charlotte, NC, USA.
Laura PanattoniPrecision AQ, New York, NY, USA.
Grace GahlonPrecision AQ, New York, NY, USA.
Pedro LabisaTakeda Farmacêuticos Portugal, Lisbon, Portugal.
Nicole BariahtarisPrecision AQ, New York, NY, USA.
Marlon GrafPrecision AQ, New York, NY, USA.
Christopher DanesTakeda Pharmaceuticals America, Inc., Lexington, MA, USA.
Luis HernandezTakeda Pharmaceuticals America, Inc., Lexington, MA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTradeoffs between efficacy, safety, and administration may influence decision-making for first-line (1L) treatments for ALK+ mNSCLC. This study explored heterogeneity in provider preferences.

methodsA survey of US oncologists treating ≥1 ALK+ mNSCLC patient was conducted June-August 2024. Participants answered 12 questions comparing 1 L profiles characterized by eight treatment attributes for patients without brain metastases. Attributes included 3-year PFS, intracranial duration of response (iDOR), 16-month risk of edema, myalgia, or cognitive effects, grade ≥3 interstitial lung disease/pneumonitis, 2 L+ treatment options, and administration. Relative attribute importance (RAI) (0-100%) was calculated for aggregate efficacy and safety attributes. Latent class analysis (LCA) explored preference heterogeneity and differences in respondent characteristics.

resultsIn total, 201 oncologists completed the discrete choice experiment. Oncologists emphasized the efficacy over safety (RAI = 47.0% vs 39.0%). LCA identified two classes, placing similar importance on efficacy (RAI = 44.5% vs 48.2%) and safety (RAI = 39% vs 41.2%), but preferring different levels in five attributes. Class 1 oncologists (61%) preferred 3-year PFS of 64% over 43-46%, while Class 2 oncologists (39%) did not differentiate. Conversely, Class 2 focused on iDOR.

conclusionWe identified two oncologist groups with distinct preferences for treatment attributes. Given various 1 L ALK+ mNSCLC treatments, clinical decision-making balances multiple objectives.

Indexed as

Anaplastic Lymphoma KinaseCarcinoma, Non-Small-Cell LungLung NeoplasmsOncologistsPractice Patterns, Physicians'AdultAgedChoice BehaviorClinical Decision-MakingFemaleHumansMaleMiddle AgedSurveys and QuestionnairesUnited StatesALK protein, humanAnaplastic Lymphoma KinaseALK+ metastatic non-small-cell lung cancerdecision making, treatment attributesdiscrete choice experimentpatient outcomesprovider preferencetyrosine kinase inhibitors

Identifiers

PMID41215753
PMCPMC12688241

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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.