Evidence map›Paper›PMID 42003979›Full record

ArticleExploration of targeted anti-tumor therapy2026

Lorlatinib in advanced ALK-positive NSCLC after prior progression on ALK inhibitors: real-world experience in Russia.

Sergey V Orlov, Konstantin K Laktionov, Aram A Musaelyan, Elena V Reutova, Svetlana V Odintsova, Magaripa A Urtenova, Valeria A Kuzmina, Vladislav I Tiurin, Alexandra E Lomakova, Evgeny N Imyanitov

Abstract read
In one paragraph

Article in Exploration of targeted anti-tumor therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Sergey V OrlovDepartment of Clinical Oncology, Pavlov First Saint Petersburg State Medical University, St. Petersburg 197022, Russia.ORCID https://orcid.org/0000-0001-6080-8042
Konstantin K LaktionovN.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of the Russian Federation, Moscow 115522, Russia.
Aram A MusaelyanDepartment of Clinical Oncology, Pavlov First Saint Petersburg State Medical University, St. Petersburg 197022, Russia.ORCID https://orcid.org/0000-0002-7570-2256
Elena V ReutovaN.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of the Russian Federation, Moscow 115522, Russia.
Svetlana V OdintsovaDepartment of Clinical Oncology, Pavlov First Saint Petersburg State Medical University, St. Petersburg 197022, Russia.ORCID https://orcid.org/0000-0001-5591-7746
Magaripa A UrtenovaDepartment of Clinical Oncology, Pavlov First Saint Petersburg State Medical University, St. Petersburg 197022, Russia.
Valeria A KuzminaN.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of the Russian Federation, Moscow 115522, Russia.
Vladislav I TiurinDepartment of Tumor Growth Biology, N.N. Petrov National Medical Research Center of Oncology, Ministry of Health of the Russian Federation, St. Petersburg 197758, Russia.ORCID https://orcid.org/0000-0002-0157-5952
Alexandra E LomakovaDepartment of Tumor Growth Biology, N.N. Petrov National Medical Research Center of Oncology, Ministry of Health of the Russian Federation, St. Petersburg 197758, Russia.
Evgeny N ImyanitovI.V. Kurchatov Complex for Medical Primatology, National Research Centre "Kurchatov Institute", Sochi 354376, Russia.ORCID https://orcid.org/0000-0003-4529-7891

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aim: This study aimed to evaluate the real-world efficacy and safety of lorlatinib in patients with anaplastic lymphoma kinase (ALK)-rearranged metastatic non-small cell lung cancer (NSCLC) after the failure of at least one prior ALK tyrosine kinase inhibitor (TKI). Methods: The dataset included 82 subjects with metastatic NSCLC, who received lorlatinib upon compassionate use program or routine treatment between January 2017 and May 2025. All patients involved in this study responded to a prior ALK inhibitor for at least 4 months and switched to the above drug due to disease progression. Results: The overall objective response rate (ORR) was 64.6%, with the disease control rate (DCR) of 96.3%. Among 65 patients with brain metastases, the intracranial ORR and DCR were 66.2% and 96.9%, respectively. After a median follow-up of 82.7 months, the median progression-free survival (PFS) was 66.7 months (95% CI, 40.5-75.0 months), while the median overall survival (OS) was not reached (NR) (95% CI, NR-NR). Patients who had benefited from prior ALK TKI for more than 12 months achieved significantly longer PFS (NR vs. 34.0 months; Conclusions: This real-world dataset demonstrates an unusually pronounced benefit from lorlatinib in selected patients who progressed on early-generation TKIs, especially in long-term responders to prior therapy. However, the observed outcomes should be interpreted within the context of patient selection. The enrichment for prior responders limits the generalizability to unselected post-TKI populations, including those with primary resistance.

Indexed as

ALKefficacylorlatinibNSCLCreal-world evidencesafetytyrosine kinase inhibitor

Identifiers

PMID42003979
PMCPMC13087447

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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.