dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
dc.contributor.author | Moy, Beverly |
dc.contributor.author | Antunes de Melo Oliveira, Ana Mafalda |
dc.contributor.author | Saura Manich, Cristina |
dc.contributor.author | Gradishar, William |
dc.contributor.author | Kim, Sung‑Bae |
dc.contributor.author | Brufsky, Adam |
dc.date.accessioned | 2022-06-15T10:54:34Z |
dc.date.available | 2022-06-15T10:54:34Z |
dc.date.issued | 2021-07 |
dc.identifier.citation | Moy B, Oliveira M, Saura C, Gradishar W, Kim SB, Brufsky A, et al. Neratinib + capecitabine sustains health-related quality of life in patients with HER2-positive metastatic breast cancer and ≥ 2 prior HER2-directed regimens. Breast Cancer Res Treat. 2021 Jul;188:449–458. |
dc.identifier.issn | 1460-2156 |
dc.identifier.uri | http://hdl.handle.net/11351/7682 |
dc.description | Health-related quality of life; Metastatic breast cancer; Neratinib |
dc.description.abstract | Purpose
To characterize health-related quality of life (HRQoL) in patients with human epidermal growth factor receptor 2 (HER2)-positive metastatic breast cancer (MBC) from the NALA phase 3 study.
Methods
In NALA (NCT01808573), patients were randomized 1:1 to neratinib + capecitabine (N + C) or lapatinib + capecitabine (L + C). HRQoL was assessed using seven prespecified scores from the European Organisation for Research and Treatment of Cancer Quality Of Life Questionnaire core module (QLQ-C30) and breast cancer-specific questionnaire (QLQ-BR23) at baseline and every 6 weeks. Descriptive statistics summarized scores over time, mixed models evaluated differences between treatment arms, and Kaplan–Meier methods were used to assess time to deterioration in HRQoL scores of ≥ 10 points.
Results
Of the 621 patients randomized in NALA, patients were included in the HRQoL analysis if they completed baseline and at least one follow-up questionnaire. The summary, global health status, physical functioning, fatigue, constipation, and systemic therapy side effects scores were stable over time with no persistent differences between treatment groups. There were no differences in time to deterioration (TTD) for the QLQ-C30 summary score between treatment arms; the hazard ratio (HR) for N + C vs. L + C was 0.94 (95% CI 0.63–1.40). Only the diarrhea score worsened significantly more in the N + C arm as compared to the L + C arm, and this remained over time (HR for TTD for N + C vs. L + C was 1.71 [95% CI 1.32–2.23]).
Conclusion
In NALA, patients treated with N + C maintained their global HRQoL over time, despite a worsening of the diarrhea-related scores. These results may help guide optimal treatment selection for HER2-positive MBC. |
dc.language.iso | eng |
dc.publisher | Oxford University Press |
dc.relation.ispartofseries | Breast Cancer Research and Treatment;188 |
dc.rights | Attribution 4.0 International |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ |
dc.source | Scientia |
dc.subject | Mama - Càncer - Tractament |
dc.subject | Medicaments antineoplàstics - Ús terapèutic |
dc.subject | Qualitat de vida - Avaluació |
dc.subject.mesh | Breast Neoplasms |
dc.subject.mesh | /drug therapy |
dc.subject.mesh | Antineoplastic Combined Chemotherapy Protocols |
dc.title | Neratinib + capecitabine sustains health-related quality of life in patients with HER2-positive metastatic breast cancer and ≥ 2 prior HER2-directed regimens |
dc.type | info:eu-repo/semantics/article |
dc.identifier.doi | 10.1007/s10549-021-06217-4 |
dc.subject.decs | neoplasias de la mama |
dc.subject.decs | /farmacoterapia |
dc.subject.decs | protocolos de quimioterapia antineoplásica combinada |
dc.relation.publishversion | https://doi.org/10.1007/s10549-021-06217-4 |
dc.type.version | info:eu-repo/semantics/publishedVersion |
dc.audience | Professionals |
dc.contributor.organismes | Institut Català de la Salut |
dc.contributor.authoraffiliation | [Moy B] Massachusetts General Hospital Cancer Center, 55 Fruit Street, Boston, MA 02114, USA. [Oliveira M, Saura C] Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. [Gradishar W] Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL, USA. [Kim SB] Asan Medical Center, University of Ulsan College of Medicine, Seoul, Kore. [Brufsky A] Magee-Womens Hospital of UPMC, Pittsburgh, PA, USA |
dc.identifier.pmid | 33909203 |
dc.identifier.wos | 000710927500019 |
dc.rights.accessrights | info:eu-repo/semantics/openAccess |