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Health-Related Quality of Life in MONARCH 2: Abemaciclib plus Fulvestrant in Hormone Receptor-Positive, HER2-Negative Advanced Breast Cancer After Endocrine Therapy.
Kaufman, Peter A; Toi, Masakazu; Neven, Patrick; Sohn, Joohyuk; Grischke, Eva-Maria; Andre, Valerie; Stoffregen, Clemens; Shekarriz, Sarah; Price, Gregory L; Carter, Gebra Cuyun; Sledge, George W.
Afiliação
  • Kaufman PA; University of Vermont Cancer Center, University of Vermont Medical Center, Burlington, Vermont, USA.
  • Toi M; Department of Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Neven P; University Hospitals Leuven, Leuven, Belgium.
  • Sohn J; Yonsei Cancer Center, Seoul, Republic of Korea.
  • Grischke EM; Department of Women's Health, University Hospital Tübingen, Tübingen, Germany.
  • Andre V; Eli Lilly and Company, Paris, France.
  • Stoffregen C; Eli Lilly and Company, Bad Homburg, Germany.
  • Shekarriz S; Eli Lilly and Company, Bad Homburg, Germany.
  • Price GL; Eli Lilly and Company, Indianapolis, Indiana, USA.
  • Carter GC; Eli Lilly and Company, Indianapolis, Indiana, USA.
  • Sledge GW; Stanford University School of Medicine, Stanford, California, USA.
Oncologist ; 25(2): e243-e251, 2020 02.
Article em En | MEDLINE | ID: mdl-32043763
ABSTRACT

BACKGROUND:

In the phase III MONARCH 2 study (NCT02107703), abemaciclib plus fulvestrant significantly improved progression-free survival (PFS) versus placebo plus fulvestrant in patients with hormone receptor-positive (HR+), HER2-negative advanced breast cancer (ABC). This study assessed patient-reported pain, global health-related quality of life (HRQoL), functioning, and symptoms. MATERIALS AND

METHODS:

Abemaciclib or placebo (150 p.o. mg twice daily) plus fulvestrant (500 mg, per label) were randomly assigned (21). The modified Brief Pain Inventory, Short Form (mBPI-sf); European Organization for Research and Treatment of Cancer (EORTC) QoL Core 30 (QLQ-C30); and Breast Cancer Questionnaire (QLQ-BR23) assessed outcomes. Data were collected at baseline, cycle 2, every two cycles 3-13, thereafter at every three cycles, and 30 days postdiscontinuation. Longitudinal mixed regression and Cox proportional hazards models assessed postbaseline change and time to sustained deterioration (TTSD) by study arm.

RESULTS:

On-treatment HRQoL scores were consistently maintained from baseline and similar between arms. Patients in the abemaciclib arm (n = 446) experienced a 4.9-month delay in pain deterioration (mBPI-sf), compared with the control arm (n = 223), and significantly greater TTSD on the mBPI-sf and analgesic use (hazard ratio, 0.76; 95% CI, 0.59-0.98) and QLQ-C30 pain item (hazard ratio, 0.62; 95% CI, 0.48-0.79). TTSD for functioning and most symptoms significantly favored the abemaciclib arm, including fatigue, nausea and vomiting, and cognitive and social functioning. Only diarrhea significantly favored the control arm (hazard ratio, 1.60; 95% CI, 1.20-2.10).

CONCLUSION:

HRQoL was maintained on abemaciclib plus fulvestrant. Alongside superior PFS and manageable safety profile, results support treatment with abemaciclib plus fulvestrant in a population of patients with endocrine-resistant HR+, HER2-negative ABC. IMPLICATIONS FOR PRACTICE In MONARCH 2, abemaciclib plus fulvestrant demonstrated superior efficacy and a manageable safety profile for patients with in hormone receptor-positive (HR+), HER2-negative (-) advanced breast cancer (ABC). Impact on health-related quality of life (HRQoL) is important to consider, given the palliative nature of ABC treatment. In this study, abemaciclib plus fulvestrant, compared with placebo plus fulvestrant, significantly delayed sustained deterioration of pain and other patient-reported symptoms (including fatigue, nausea, vomiting), and social and cognitive functioning. Combined with demonstrated clinical benefit and tolerability, the stabilization of patient-reported symptoms and HRQoL further supports abemaciclib plus fulvestrant as a desirable treatment option in endocrine resistant, HR+, HER2- ABC.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Neoplasias da Mama Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Female / Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Neoplasias da Mama Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Female / Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article