Evidence map›Paper›PMID 32558067›Full record

ArticleThe oncologist2020

ALK-Rearranged Non-Small Cell Lung Cancer in 2020: Real-World Triumphs in an Era of Multigeneration ALK-Inhibitor Sequencing Informed by Drug Resistance Profiling.

Malinda Itchins, Brandon Lau, Amanda L Hudson, Helen Westman, Cathy Yi Xia, Sarah A Hayes, Viive M Howell, Michael Rodriguez, Wendy A Cooper, Heng Wei and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in The oncologist, 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
1.4field-weighted citation impact, top 16% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

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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

19 authors at 6 institutions in 2 countries.

Malinda ItchinsDepartment of Medical Oncology, Royal North Shore Hospital, St Leonards, New South Wales, Australia.
Brandon LauChris O'Brien Lifehouse, Camperdown, New South Wales, Australia.
Amanda L HudsonBill Walsh Translational Research Laboratory, Kolling Institute, St Leonards, New South Wales, Australia.
Helen WestmanDepartment of Medical Oncology, Royal North Shore Hospital, St Leonards, New South Wales, Australia.
Cathy Yi XiaDepartment of Medical Oncology, Royal North Shore Hospital, St Leonards, New South Wales, Australia.
Sarah A HayesBill Walsh Translational Research Laboratory, Kolling Institute, St Leonards, New South Wales, Australia.
Viive M HowellBill Walsh Translational Research Laboratory, Kolling Institute, St Leonards, New South Wales, Australia.
Michael RodriguezBill Walsh Translational Research Laboratory, Kolling Institute, St Leonards, New South Wales, Australia.
Wendy A CooperCentral Clinical School, School of Medicine, University of Sydney, St Leonards, New South Wales, Australia.
Heng WeiBrain and Mind Centre, University of Sydney, St Leonards, New South Wales, Australia.
Michael BucklandBrain and Mind Centre, University of Sydney, St Leonards, New South Wales, Australia.
Bob T LiNorthern Clinical School, Faculty of Medicine and Health, University of Sydney, St Leonards, New South Wales, Australia.
Mark LiResolution Bioscience, Redmond, Washington, USA.
Vivek RathiDepartment of Anatomical Pathology, St Vincent's, Victoria Parade, Fitzroy, Victoria, Australia.
Stephen B FoxDepartment of Pathology, Peter MacCallum Cancer Centre, and University of Melbourne, Victoria, Australia.
Anthony J GillDepartment of Anatomical Pathology, Royal North Shore Hospital, St Leonards, New South Wales, Australia.
Stephen J ClarkeDepartment of Medical Oncology, Royal North Shore Hospital, St Leonards, New South Wales, Australia.
Michael J BoyerChris O'Brien Lifehouse, Camperdown, New South Wales, Australia.
Nick PavlakisDepartment of Medical Oncology, Royal North Shore Hospital, St Leonards, New South Wales, Australia.
University of Sydney · AUNorthern Sydney Local Health District · AUPeter MacCallum Cancer Centre · AURoyal North Shore Hospital · AUChris O’Brien Lifehouse · AURoyal Prince Alfred Hospital · AU

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Since its discovery in 2007, we have seen the lives of patients diagnosed with advanced anaplastic lymphoma kinase (ALK)-rearranged non-small cell lung cancers (NSCLC) transform with the advent of molecular therapies with first-, second-, and third-generation ALK inhibitors now available in the clinic. Despite great gains in patient survival now measured in years and preserved quality of life with targeted therapies, drug resistance is unfortunately inevitably encountered in this rare and unique molecular subset of lung cancer, and patients will eventually succumb to the disease. As these patients are often young, fit, and never smokers, the clinical and scientific communities have aligned to expedite drug development and access. Drug resistance profiling and further strategies are being explored through clinical trials, including the evaluation of specific drug sequencing and combinations to overcome such resistance and promote patient longevity. The cases of this report focus on precision medicine and aim to portray the pertinent aspects to consider when treating ALK-rearranged NSCLC in 2020, an ever-shifting space. By way of case examples, this report offers valuable information to the treating clinician, including the evolution of systemic treatments and the management of oligo-progression and multisite drug resistance. With the maturation of real-world data, we are fortunate to be experiencing quality and length of life for patients with this disease surpassing prior expectations in advanced lung cancer. KEY POINTS: This report focuses on the importance of genetic analysis of serial biopsies to capture the dynamic therapeutic vulnerabilities of a patient's tumor, providing a perspective on the complexity of ALK tyrosine kinase inhibitor (ALKi) treatment sequencing. These case examples contribute to the literature on ALK-rearranged and oncogene addicted non-small cell lung cancer (NSCLC), providing a framework for care in the clinic. In oligo-progressive disease, local ablative therapy and continuation of ALKi postprogression should be considered with potential for sustained disease control. ALK G1202R kinase domain mutations (KDM), highly prevalent at resistance to second-generation ALKi resistances, may emerge in non-EML4-ALK variant 3 cases and is sensitive to third-generation lorlatinib. When in compound with one or more ALK KDMs, resistance to lorlatinib is expected. In the case of rampantly progressive disease, rebiopsy and redefining biology in a timely manner may be informative.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsAnaplastic Lymphoma KinaseDrug Resistance, NeoplasmHumansProtein Kinase InhibitorsQuality of LifeAnaplastic Lymphoma KinaseProtein Kinase Inhibitors

Identifiers

PMID32558067
PMCPMC7418351
OpenAlexW3036665789

What OpenQuestion holds

Textmetadata
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.