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Impact of lorlatinib on patient-reported outcomes in patients with advanced ALK-positive or ROS1-positive non-small cell lung cancer.
Peters, Solange; Shaw, Alice T; Besse, Benjamin; Felip, Enriqueta; Solomon, Benjamin J; Soo, Ross A; Bearz, Alessandra; Gadgeel, Shirish M; Lin, Chia-Chi; Kao, Steven; Seto, Takashi; Masters, Elizabeth T; Abbattista, Antonello; Clancy, Jill S; Thurm, Holger; Reisman, Arlene; Peltz, Gerson; Ross Camidge, D.
Afiliação
  • Peters S; Centre Hospitalier Universitaire Vaudois, Lausanne University, Lausanne, Switzerland. Electronic address: Solange.Peters@chuv.ch.
  • Shaw AT; Massachusetts General Hospital, Boston, MA, USA. Electronic address: ashaw1@mgh.harvard.edu.
  • Besse B; Gustave Roussy Cancer Campus, Villejuif, France; Paris-Sud University, Orsay, France. Electronic address: Benjamin.BESSE@gustaveroussy.fr.
  • Felip E; Vall d'Hebron University Hospital and Vall d'Hebron Institute of Oncology, Barcelona, Spain. Electronic address: efelip@vhio.net.
  • Solomon BJ; Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia. Electronic address: Ben.Solomon@petermac.org.
  • Soo RA; National University Cancer Institute, Singapore. Electronic address: ross_soo@nuhs.edu.sg.
  • Bearz A; National Cancer Institute, Aviano, Italy. Electronic address: abearz@cro.it.
  • Gadgeel SM; University of Michigan/Rogel Cancer Center, Ann Arbor, MI, USA. Electronic address: sgadgeel@med.umich.edu.
  • Lin CC; National Taiwan University Hospital, Taipei, Taiwan. Electronic address: cclin1@ntu.edu.tw.
  • Kao S; Chris O'Brien Lifehouse, Camperdown, New South Wales, Australia. Electronic address: Steven.Kao@lh.org.au.
  • Seto T; National Hospital Organization Kyushu Cancer Center, Fukuoka, Japan. Electronic address: setocruise@gmail.com.
  • Masters ET; Pfizer Oncology, New York, NY, USA. Electronic address: elizabeth.masters@pfizer.com.
  • Abbattista A; Pfizer Oncology, Milan, Italy. Electronic address: antonello.abbattista@pfizer.com.
  • Clancy JS; Pfizer Oncology, Cambridge, MA, USA. Electronic address: Jill.S.Clancy@pfizer.com.
  • Thurm H; Pfizer Oncology, La Jolla, CA, USA. Electronic address: holger.thurm@pfizer.com.
  • Reisman A; Pfizer Global Product Development, New York, NY, USA. Electronic address: Arlene.Reisman@pfizer.com.
  • Peltz G; Pfizer Oncology, Groton, CT, USA. Electronic address: Gerson.Peltz@pfizer.com.
  • Ross Camidge D; University of Colorado, Aurora, CO, USA. Electronic address: Ross.Camidge@ucdenver.edu.
Lung Cancer ; 144: 10-19, 2020 06.
Article em En | MEDLINE | ID: mdl-32344248
ABSTRACT

OBJECTIVES:

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. MATERIALS AND

METHODS:

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).

RESULTS:

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 %).

CONCLUSIONS:

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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article