Quality-of-life and quality-adjusted survival (Q-TWiST) in patients receiving lapatinib in combination with paclitaxel as first-line treatment for metastatic breast cancer

被引:15
|
作者
Sherrill, Beth
Di Leo, Angelo [2 ]
Amonkar, Mayur M. [3 ]
Wu, Yun [1 ]
Zvirbule, Zanete [4 ]
Aziz, Zeba [5 ]
Bines, Jose [6 ]
Gomez, Henry L. [7 ]
机构
[1] RTI Hlth Solut, MStat, Res Triangle Pk, NC USA
[2] Sandro Pitigliani Med Oncol Unit, Prato, Italy
[3] GSK Oncol, Collegeville, PA USA
[4] Riga Eastern Univ Hosp, Latvian Oncol Ctr, Riga, Latvia
[5] Allama Iqbal Med Coll, Lahore, Pakistan
[6] Natl Canc Inst, Rio De Janeiro, Brazil
[7] Inst Nacl Enfermedades Neoplas, Lima, Peru
关键词
Cancer; metastatic breast; ErbB2+; HER2; Lapatinib; Paclitaxel; Q-TWiST; Quality-of-life; MONOCLONAL-ANTIBODY; TRASTUZUMAB; THERAPY; SAFETY; TRIAL; PLUS;
D O I
10.1185/03007991003590860
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In a phase 3 randomized, multicenter, double-blind, placebo-controlled study, first-line therapy with lapatinib plus paclitaxel significantly improved clinical outcomes based on a pre-planned analysis of ErbB2+ metastatic breast cancer patients (GSK Study #EGF30001; ClinicalTrials.gov identifier: NCT00075270). Patients with ErbB2- or untested did not significantly benefit. This article focuses on the quality of life (QOL) and quality-adjusted survival outcomes (Q-TWiST) in the study. QOL was assessed using the Functional Assessment of Cancer Therapy-Breast (FACT-B). Changes from baseline were analyzed using ANCOVAs, repeated measures and pattern mixture modeling. The Q-TWiST method was used to examine the trade-off between toxicities and delayed progression. The study included 579 subjects, of whom 86 were ErbB2+. In the ITT population, no significant differences in QOL or Q-TWiST scores were observed. In the ErbB2+ subgroup, the lapatinib plus paclitaxel (L + P) arm demonstrated stable FACT-B scores over the first year, while average scores for patients on P + placebo (P + pla) monotherapy decreased (change from baseline: L + P, p = 0.99; P + pla, p = 0.01). Clinically meaningful differences were observed between treatment arms on the FACT-B, Trial Outcome Index and breast cancer subscale scores. Pattern mixture models suggested more QOL differentiation between treatments among patients who progressed or withdrew early. Q-TWiST differences between the arms in the ErbB2+ subgroup ranged from 2 to 15 weeks with an L + P advantage across all utility weight combinations. In the ITT population, results provide no evidence of QOL differences between treatment groups. In a small, prospectively-defined subgroup of ErbB2+ patients, L + P resulted in more stable QOL and more quality-adjusted survival than paclitaxel monotherapy, representing clinically important differences between treatments.
引用
收藏
页码:767 / 775
页数:9
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