Evidence map›Paper›PMID 32665165›Full record

ArticleClinical lung cancer2020

Duration of Targeted Therapy in Patients With Advanced Non-small-cell Lung Cancer Identified by Circulating Tumor DNA Analysis.

Karen L Reckamp, Tejas Patil, Kedar Kirtane, Thereasa A Rich, Carin R Espenschied, Caroline M Weipert, Victoria M Raymond, Rafael Santana-Davila, Robert C Doebele, Christina S Baik

Abstract readMulticenter Study
In one paragraph

Article in Clinical lung cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 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

10 authors.

Karen L ReckampDepartment of Medical Oncology, City of Hope, Duarte, CA.
Tejas PatilDivision of Medical Oncology, University of Colorado Anschutz Medical Campus, Aurora, CO.
Kedar KirtaneDivision of Medical Oncology, University of Washington, Seattle Cancer Care Alliance, Seattle, WA.
Thereasa A RichGuardant Health, Redwood City, CA.
Carin R EspenschiedGuardant Health, Redwood City, CA.
Caroline M WeipertGuardant Health, Redwood City, CA.
Victoria M RaymondGuardant Health, Redwood City, CA.
Rafael Santana-DavilaDivision of Medical Oncology, University of Washington, Seattle Cancer Care Alliance, Seattle, WA.
Robert C DoebeleDivision of Medical Oncology, University of Colorado Anschutz Medical Campus, Aurora, CO.
Christina S BaikDivision of Medical Oncology, University of Washington, Seattle Cancer Care Alliance, Seattle, WA. Electronic address: cbaik2@uw.edu.

Funding

Transgenic Mouse FacilityP30CA033572 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI STANLEY R. HAMILTON · 1985 to 2026
$86.3M
TRAINING IN CANCER BIOLOGY &TRANSPLANTATIONT32CA009515 · NCI · UNIVERSITY OF WASHINGTON · PI NANCY ELLEN DAVIDSON, Effie W Petersdorf · 1985 to 2026
$16.2M
NCI NIH HHS P30 CA033572NCI NIH HHS T32 CA009515
6 · The paper itself

Abstract

backgroundOutcomes of therapy targeting molecular driver alterations detected in advanced non-small-cell lung (NSCLC) using circulating tumor DNA (ctDNA) have not been widely reported in patients who are targeted therapy-naive. PATIENTS AND

methodsWe performed a multicenter retrospective review of patients with unresectable stage IIIB to IV NSCLC who received matched therapy after a targetable driver alteration was identified using a commercial ctDNA assay through usual clinical care. Eligible patients must not have received targeted therapy prior to ctDNA testing (prior chemotherapy or immunotherapy was permitted). Kaplan-Meier analysis was used to estimate the median duration of targeted therapy. Patients still on targeted therapy were censored at last follow-up.

resultsSeventy-six patients met inclusion criteria. The median age of diagnosis of NSCLC was 64.5 years (range, 31-87 years), 67% were female, 74% were never-smokers, and 97% had adenocarcinoma histology. Twenty-one (28%) patients received systemic treatment prior to targeted therapy, including chemotherapy (n = 17), immunotherapy (n = 5), and/or a biologic (n = 4). Thirty-three (43%) patients remain on targeted therapy at the time of data analysis. The median time on targeted therapy was similar to what has been reported for tissue-detected oncogenic driver mutations in the targeted therapy-naive setting.

conclusionsPatients with ctDNA-detected drivers had durable time on targeted therapy. These treatment outcomes data compliment previous studies that have shown enhanced targetable biomarker discovery rates and high tissue concordance of ctDNA testing when incorporated at initial diagnosis of NSCLC. Identification of NSCLC driver mutations using well-validated ctDNA assays can be used for clinical decision-making and targeted therapy assignment.

Indexed as

Molecular Targeted TherapyAdenocarcinoma of LungAdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorCarcinoma, Non-Small-Cell LungCarcinoma, Squamous CellCirculating Tumor DNAFemaleFollow-Up StudiesHumansLung NeoplasmsMaleMiddle AgedBiomarkers, TumorCirculating Tumor DNAGenotype directed therapyLiquid biopsyLung cancerOncogene

Identifiers

PMID32665165
PMCPMC9227978

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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.