Evidence map›Paper›PMID 37999149›Full record

ReviewCurrent oncology (Toronto, Ont.)2023

Sharing Experience with Anaplastic Lymphoma Kinase Tyrosine Kinase Inhibitors in Lung Cancer: An Italian Expert Panel Discussion.

Cesare Gridelli, Marcello Tiseo, Diego Luigi Cortinovis, Maria Rita Migliorino, Vito Barbieri, Paolo Bironzo, Alessandra Bearz, Ilaria Attili, Filippo de Marinis

Abstract readReview
In one paragraph

Review in Current oncology (Toronto, Ont.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
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

9 authors.

Cesare GridelliDivision of Medical Oncology, "S.G. Moscati" Hospital, 83100 Avellino, Italy.
Marcello TiseoDepartment of Medicine and Surgery, University of Parma, 43126 Parma, Italy.ORCID 0000-0002-9553-8465
Diego Luigi CortinovisSC Medical Oncology, Fondazione IRCCS San Gerardo dei Tintori, 20900 Monza, Italy.ORCID 0000-0001-7611-7369
Maria Rita MigliorinoDepartment of Oncology, San Camillo-Forlanini Hospital, 00152 Rome, Italy.
Vito BarbieriMedical Oncology Unit, AOU Renato Dulbecco, 88100 Catanzaro, Italy.
Paolo BironzoDepartment of Oncology, University of Turin, 10124 Turin, Italy.
Alessandra BearzDepartment of Medical Oncology, Centro di Riferimento Oncologico di Aviano (CRO), IRCCS, 33081 Aviano, Italy.
Ilaria AttiliDivision of Thoracic Oncology, European Institute of Oncology, IRCCS, 20141 Milan, Italy.ORCID 0000-0003-1333-6622
Filippo de MarinisDivision of Thoracic Oncology, European Institute of Oncology, IRCCS, 20141 Milan, Italy.

Funding

Associazione Italiana di Oncologia Toracica (AIOT) no grant number
6 · The paper itself

Abstract

backgroundALK tyrosine kinase inhibitors (TKIs) have revolutionized the treatment and largely improved the survival outcomes of patients with NSCLC harboring

methodsA virtual webinar was held on July 2023 to discuss the state of the art and future perspectives in the treatment of

resultsAlectinib and brigatinib are the preferred front-line treatment options in Italy, pending approval of the front-line medicine lorlatinib, which would be considered among the choices. Due to a local regulatory limitation of second-line lorlatinib, which is not allowed after front-line brigatinib, alectinib is commonly the preferred front-line choice to follow a sequence of alectinib, followed by lorlatinib, followed by platinum plus pemetrexed chemotherapy. Age and performance status were not considered per se as clinical features influencing treatment choice. However, treatment compliance is deemed a relevant factor in decision making with regard to the number of pills to be administered. In general, given the availability of alternative choices, the spectrum of patients' comorbidities and polypharmacotherapy interactions should be taken into account in treatment selection according to the toxicity profile of each compound. In addition, several issues were debated with regard to improving treatment outcomes, including testing, brain metastases, and management of an oligoprogressive disease.

conclusionsThe treatment scenario of ALK-positive disease is dynamically evolving. Furthermore, not all FDA- and EMA-approved compounds are approved in Italy with the same indications. This influences therapeutic opportunities and increases the need for greater clinical expertise to help and guide treatment selection.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsAminopyridinesAnaplastic Lymphoma KinaseHumansLactamsLactams, MacrocyclicOrganophosphorus CompoundsProtein Kinase InhibitorsProtein-Tyrosine KinasesPyrazolesPyrimidinesTyrosine Kinase InhibitorsAminopyridinesAnaplastic Lymphoma KinasebrigatinibLactamsLactams, MacrocycliclorlatinibOrganophosphorus CompoundsProtein Kinase InhibitorsProtein-Tyrosine KinasesPyrazolesPyrimidinesTyrosine Kinase InhibitorsalectinibALKbrigatiniblorlatiniblung cancer

Identifiers

PMID37999149
PMCPMC10670405

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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.