Impact of lorlatinib on patient-reported outcomes in patients with advanced ALK-positive or ROS1-positive non-small cell lung cancer.


Journal

Lung cancer (Amsterdam, Netherlands)
ISSN: 1872-8332
Titre abrégé: Lung Cancer
Pays: Ireland
ID NLM: 8800805

Informations de publication

Date de publication:
06 2020
Historique:
received: 14 11 2019
revised: 12 02 2020
accepted: 18 02 2020
pubmed: 29 4 2020
medline: 22 6 2021
entrez: 29 4 2020
Statut: ppublish

Résumé

To evaluate patient-reported outcomes (PROs) from a phase 1/2 study (NCT01970865) in patients with anaplastic lymphoma kinase (ALK)- or ROS1-positive advanced non-small cell lung cancer (NSCLC) treated with lorlatinib 100 mg once daily. PRO measures, including global quality of life (QoL), functioning domains and symptoms, were assessed by the European Organisation for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire Core 30 (QLQ-C30) and the 13-item Lung Cancer (QLQ-LC13) module. Mean changes of absolute scores from baseline were assessed. Percentages of patients showing improvement, stability or worsening on each scale were reported, with a change of ≥10 points considered clinically meaningful (CM). 255 patients completed baseline and ≥1 post-baseline PRO assessment. Most patients had CM improvement (42.4 %) or stable (38.0 %) scores for global QoL. Functioning domains with the greatest proportion of patients with improved scores were role (37.6 %) and emotional (36.9 %); only one domain had more patients showing worsening than improving function (cognitive [24.3 % vs 22.4 %]). Most patients showed improved or stable scores for disease-related symptoms. No QLQ-C30 symptom domains had more patients worsening than improving. Symptoms on the QLQ-C30 scale with the greatest proportion of patients with improved scores were fatigue (49.4 %) and insomnia (46.3 %). Four QLQ-LC13 domains had more patients worsening than improving (two most affected were peripheral neuropathy [37.3 % vs 13.7 %] and alopecia [19.2 % vs 13.3 %]). Symptoms on the QLQ-LC13 scale with the greatest proportion of patients with improved scores were cough (42.7 %) and pain in other parts (32.9 %). Lorlatinib treatment showed CM improvement from baseline in global QOL that was maintained over time. Additionally, there were improvements in physical, emotional, social, and role functioning. Improvements were shown in appetite loss and key symptoms such as pain, dyspnea, cough and fatigue; a worsening in peripheral neuropathy was noted.

Identifiants

pubmed: 32344248
pii: S0169-5002(20)30308-1
doi: 10.1016/j.lungcan.2020.02.011
pii:
doi:

Substances chimiques

Aminopyridines 0
Lactams 0
Lactams, Macrocyclic 0
Proto-Oncogene Proteins 0
Pyrazoles 0
Protein-Tyrosine Kinases EC 2.7.10.1
ROS1 protein, human EC 2.7.10.1
lorlatinib OSP71S83EU

Banques de données

ClinicalTrials.gov
['NCT01970865']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

10-19

Informations de copyright

Copyright © 2020. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest None.

Auteurs

Solange Peters (S)

Centre Hospitalier Universitaire Vaudois, Lausanne University, Lausanne, Switzerland. Electronic address: Solange.Peters@chuv.ch.

Alice T Shaw (AT)

Massachusetts General Hospital, Boston, MA, USA. Electronic address: ashaw1@mgh.harvard.edu.

Benjamin Besse (B)

Gustave Roussy Cancer Campus, Villejuif, France; Paris-Sud University, Orsay, France. Electronic address: Benjamin.BESSE@gustaveroussy.fr.

Enriqueta Felip (E)

Vall d'Hebron University Hospital and Vall d'Hebron Institute of Oncology, Barcelona, Spain. Electronic address: efelip@vhio.net.

Benjamin J Solomon (BJ)

Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia. Electronic address: Ben.Solomon@petermac.org.

Ross A Soo (RA)

National University Cancer Institute, Singapore. Electronic address: ross_soo@nuhs.edu.sg.

Alessandra Bearz (A)

National Cancer Institute, Aviano, Italy. Electronic address: abearz@cro.it.

Shirish M Gadgeel (SM)

University of Michigan/Rogel Cancer Center, Ann Arbor, MI, USA. Electronic address: sgadgeel@med.umich.edu.

Chia-Chi Lin (CC)

National Taiwan University Hospital, Taipei, Taiwan. Electronic address: cclin1@ntu.edu.tw.

Steven Kao (S)

Chris O'Brien Lifehouse, Camperdown, New South Wales, Australia. Electronic address: Steven.Kao@lh.org.au.

Takashi Seto (T)

National Hospital Organization Kyushu Cancer Center, Fukuoka, Japan. Electronic address: setocruise@gmail.com.

Elizabeth T Masters (ET)

Pfizer Oncology, New York, NY, USA. Electronic address: elizabeth.masters@pfizer.com.

Antonello Abbattista (A)

Pfizer Oncology, Milan, Italy. Electronic address: antonello.abbattista@pfizer.com.

Jill S Clancy (JS)

Pfizer Oncology, Cambridge, MA, USA. Electronic address: Jill.S.Clancy@pfizer.com.

Holger Thurm (H)

Pfizer Oncology, La Jolla, CA, USA. Electronic address: holger.thurm@pfizer.com.

Arlene Reisman (A)

Pfizer Global Product Development, New York, NY, USA. Electronic address: Arlene.Reisman@pfizer.com.

Gerson Peltz (G)

Pfizer Oncology, Groton, CT, USA. Electronic address: Gerson.Peltz@pfizer.com.

D Ross Camidge (D)

University of Colorado, Aurora, CO, USA. Electronic address: Ross.Camidge@ucdenver.edu.

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Classifications MeSH