Evidence map›Paper›PMID 38916812›Full record

ArticleAdvances in therapy2024

Real-World Treatment Patterns and Outcomes Across Three Lines of Therapy in Patients with ALK+ NSCLC.

Konstantinos Arnaoutakis, Yin Wan, Jennifer Elliott, Matt Young, Yu Yin, Konstantinos Leventakos, Huamao M Lin, Anastasios Dimou

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Article in Advances in therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

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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

8 authors.

Konstantinos ArnaoutakisUniversity of Arkansas for Medical Sciences, Little Rock, AR, USA.
Yin WanTakeda Development Center Americas, Inc., 500 Kendall Street, Cambridge, MA, 02142, USA.
Jennifer ElliottTakeda Pharmaceuticals USA, Inc., Lexington, MA, USA.
Matt YoungTakeda Pharmaceuticals America, Inc., Lexington, MA, USA.
Yu YinTakeda Development Center Americas, Inc., 500 Kendall Street, Cambridge, MA, 02142, USA.
Konstantinos LeventakosMayo Clinic, Rochester, MN, USA.
Huamao M LinGlobal Evidence and Outcomes Research, Takeda Development Center Americas, Inc., 500 Kendall Street, Cambridge, MA, 02142, USA. mark.lin@takeda.com.
Anastasios DimouMayo Clinic, Rochester, MN, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAnaplastic lymphoma kinase (ALK) tyrosine kinase inhibitors (TKIs) are standard first- and second-line treatment for advanced ALK+ non-small cell lung cancer (NSCLC). We evaluated outcomes in patients with ALK+ NSCLC receiving third-line ALK TKI versus non-ALK-directed therapy.

methodsFlatiron Health OncoEMR data were extracted for patients with ALK+ NSCLC initiating first-line ALK TKI between January 2015 and March 2022 followed by second-line ALK TKI and third-line ALK TKI (group A) or non-TKI therapy (group B). Time-to-treatment discontinuation (TTD) and overall survival (OS) were analyzed using multivariate modelling.

resultsAmong patients receiving third-line ALK TKI (A, n = 85) or non-TKI therapy (B, n = 43), most received first-line crizotinib (A/B: 64%/60%) and second-line alectinib (36%/30%), ceritinib (24%/19%), or lorlatinib (15%/30%). Common third-line treatments were lorlatinib/alectinib (41%/33%) in A and immunotherapy, chemotherapy, or chemotherapy + immunotherapy (30%/28%/21%) in B. Group A versus B had longer TTD of first-line treatment (hazard ratio [HR] 0.62, 95% confidence interval [CI] 0.41-0.93; p = 0.020) and second-line treatment (HR 0.50, 95% CI 0.33-0.75; p < 0.001) and longer OS from start of first-line treatment (HR 0.32, 95% CI 0.19-0.54; p < 0.001) and second-line treatment (HR 0.40, 95% CI 0.24-0.66; p < 0.001). For third-line treatment, median TTD (A/B) was 6.2/2.4 months (HR 0.61, 95% CI 0.37-1.00; p = 0.049) and OS was 17.6/6.5 months (HR 0.57, 95% CI 0.33-0.98; p = 0.042).

conclusionsPatients receiving third-line non-ALK-directed therapy had suboptimal outcomes on prior TKIs. Patients with longer duration of prior ALK TKI treatment appeared to benefit from third-line ALK TKIs.

Indexed as

Anaplastic Lymphoma KinaseCarcinoma, Non-Small-Cell LungCrizotinibLung NeoplasmsPiperidinesProtein Kinase InhibitorsAdultAgedAminopyridinesAntineoplastic AgentsCarbazolesFemaleHumansLactamsMaleMiddle AgedalectinibALK protein, humanAminopyridinesAnaplastic Lymphoma KinaseAntineoplastic AgentsCarbazolesceritinibCrizotinibLactamslorlatinibPiperidinesProtein Kinase InhibitorsPyrazolesPyrimidinesSulfonesAnaplastic lymphoma kinaseChemotherapyImmunotherapyNon-small cell lung cancerTreatment efficacyTreatment sequencingTyrosine kinase inhibitor

Identifiers

PMID38916812
PMCPMC11263478

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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.