Evidence map›Paper›PMID 35720977›Full record

Observational studyOncotarget2022

Alectinib after failure to crizotinib in patients with ALK-positive non-small cell lung cancer: results from the Spanish early access program.

Reyes Bernabé-Caro, Pilar Garrido, Rosario García-Campelo, Ramón Palmero, Ángel Artal, Cristina Bayona, Delvys Rodríguez-Abreu, Marta López-Brea, Alfredo Paredes, David Vicente and 6 more

Abstract readObservational Study
In one paragraph

Observational study in Oncotarget, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

16 authors.

Reyes Bernabé-CaroDepartment of Medical Oncology, Hospital Virgen del Rocío, Sevilla, Spain.
Pilar GarridoDepartment of Medical Oncology, Hospital Universitario Ramon y Cajal, Madrid, Spain.
Rosario García-CampeloDepartment of Medical Oncology, Hospital Universitario A Coruña, A Coruña, Spain.
Ramón PalmeroDepartment of Medical Oncology, ICO Bellvitge, Hospitalet Llobregat, Barcelona, Spain.
Ángel ArtalDepartment of Medical Oncology, Hospital Universitario Miguel Servet, Zaragoza, Spain.
Cristina BayonaDepartment of Medical Oncology, Hospital General Yague, Burgos, Spain.
Delvys Rodríguez-AbreuDepartment of Medical Oncology, Hospital Insular de Gran Canaria, Las Palmas de Gran Canaria, Spain.
Marta López-BreaDepartment of Medical Oncology, Hospital Marqués de Valdecilla, Santander, Spain.
Alfredo ParedesDepartment of Medical Oncology, Hospital Universitario Donostia, Donostia-San Sebastián, Spain.
David VicenteDepartment of Medical Oncology, Hospital Universitario Virgen Macarena, Sevilla, Spain.
José Miguel Sánchez TorresDepartment of Medical Oncology, Hospital Universitario La Princesa, Madrid, Spain.
Margarita MajemDepartment of Medical Oncology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Pilar DizDepartment of Medical Oncology, Complejo Asistencial Universitario de León, León, Spain.
Rocío GordoRoche Farma, S.A., Madrid, Spain.
Margarita CocaRoche Farma, S.A., Madrid, Spain.
Javier de CastroDepartment of Medical Oncology, Hospital Universitario La Paz, Madrid, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This retrospective observational study analyzed the clinical characteristics, treatment patterns and outcomes of 120 patients with advanced ALK-positive non-small-cell lung cancer (ALK+ NSCLC) according to data collected between November 2019 and October 2020 in 38 Spanish hospitals. Patients had progressed after 1-5 prior treatment lines (which included crizotinib in any prior line) and received subsequent therapy with alectinib in a local expanded access program. Median age was 58.7 years, 50% of patients were female, 64.1% had ECOG PS of 0-1, 85% presented stage IV, 95% had adenocarcinoma histology and 20.8% had brain metastases. After a median 9.6 months of alectinib treatment, objective response rate (ORR) was 54.5%, disease control rate (DCR) was 80%, median progression-free survival (PFS) was 9.4 months and median overall survival (OS) was 24.1 months. Patients with brain metastases achieved an intracranial DCR of 71.4%. Adverse events (AEs) were reported in 35.8% of patients (14.2% of AEs were grade ≥3). Over 40% of patients received some treatment after alectinib, most frequently lorlatinib (65.2%) and brigatinib (32.6%). This study provides information on real-world treatment patterns and confirms the tolerability and prolonged PFS and OS observed with alectinib in clinical trials, in unselected pretreated patients with advanced ALK+ NSCLC.

Indexed as

Brain NeoplasmsCarcinoma, Non-Small-Cell LungLung NeoplasmsAnaplastic Lymphoma KinaseCarbazolesCrizotinibFemaleHumansMaleMiddle AgedPiperidinesProtein Kinase InhibitorsalectinibAnaplastic Lymphoma KinaseCarbazolesCrizotinibPiperidinesProtein Kinase InhibitorsalectinibALK inhibitorALK-positive NSCLCcrizotinibunselected patient

Identifiers

PMID35720977
PMCPMC9200434

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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.