Abstract
Background: With recent FDA approvals of inhibitors of Cyclin Dependent Kinases 4 and 6 (CDK 4/6) in combination with endocrine therapy for the treatment of postmenopausal women with hormone-receptor positive metastatic breast cancer (MBC), an increasing number of older adults will be treated with this class of agents. An improved understanding of the safety and efficacy of CDK 4/6 inhibitors in this population is important to inform clinical decision making for the treatment of older patients.
Methods: Data from two prospective randomized controlled studies (n=1334) of different CDK 4/6 inhibitors in combination with an aromatase inhibitor for the initial treatment of postmenopausal patients with hormone-receptor positive MBC were pooled and analyzed. The effect of age on progression free survival (PFS) was explored using Kaplan Meier (KM) estimates and a Cox-proportional hazard model. Safety analysis included adverse events up to 30 days after last administration of drug based on standardized adverse event datasets.
Results: Age was balanced between the two studies, and between treatment arms within each study. The median age of women was 62 (range 23-91). Of the 1334 total patients, 42% were ≥65, and 24% were ≥ 70. For patients ≥70 who were treated with a CDK4/6 inhibitor in combination with an aromatase inhibitor, the estimated PFS was not reached (95% CI: 25.1months, NR) vs an estimated 18 months (95% CI: 13.8, 31.3) for those treated only with an aromatase inhibitor. For patients <70 treated with a CDK4/6 inhibitor, the estimated PFS was 23.5 months (95% CI: 21.4, 25.7) vs an estimated 13.8 months (95% CI: 12.9, 16.5) for those treated only with an aromatase inhibitor.
Safety was evaluated in the 778 patients who received at least one dose of CDK4/6 inhibitor.
Patients < 65 years | Patients≥65 years | Patients≥70 years | |
N=447 | N=331 | N=187 | |
n (%) | n (%) | n (%) | |
Grade 1-2 Adverse Events | 437 (98) | 324 (98) | 185 (99) |
Grade 3-4 Adverse Events | 340 (76) | 276 (83) | 159 (85) |
Serious Adverse Events | 72 (16) | 88 (27) | 50 (27) |
Adverse Events Leading to Discontinuation | 35 (8) | 56 (17) | 38 (20) |
Adverse Events leading to dose reduction and/or interruption | 323 (72) | 253 (76) | 147 (79) |
Selected Adverse Events | |||
Neutropenia (all grades) | 341 (76) | 256 (77) | 150 (80) |
Grade 3-4 neutropenia | 292 (65) | 228 (69) | 134 (72) |
Infections (all grades) | 190 (43) | 165 (50) | 100 (53) |
Hepatotoxicty (all grades) | 79 (18) | 51 (15) | 34 (18) |
Grade 3-4 hepatotoxicity | 32 (7) | 16 (5) | 12 (6) |
Fatigue (all grades) | 195 (44) | 153 (46) | 89 (48) |
Grade 3 fatigue | 11 (2) | 11 (3) | 7 (4) |
Patients < 65 years | Patients≥65 years | Patients≥70 years | |
N=447 | N=331 | N=187 | |
n (%) | n (%) | n (%) | |
Grade 1-2 Adverse Events | 437 (98) | 324 (98) | 185 (99) |
Grade 3-4 Adverse Events | 340 (76) | 276 (83) | 159 (85) |
Serious Adverse Events | 72 (16) | 88 (27) | 50 (27) |
Adverse Events Leading to Discontinuation | 35 (8) | 56 (17) | 38 (20) |
Adverse Events leading to dose reduction and/or interruption | 323 (72) | 253 (76) | 147 (79) |
Selected Adverse Events | |||
Neutropenia (all grades) | 341 (76) | 256 (77) | 150 (80) |
Grade 3-4 neutropenia | 292 (65) | 228 (69) | 134 (72) |
Infections (all grades) | 190 (43) | 165 (50) | 100 (53) |
Hepatotoxicty (all grades) | 79 (18) | 51 (15) | 34 (18) |
Grade 3-4 hepatotoxicity | 32 (7) | 16 (5) | 12 (6) |
Fatigue (all grades) | 195 (44) | 153 (46) | 89 (48) |
Grade 3 fatigue | 11 (2) | 11 (3) | 7 (4) |
Conclusions: This exploratory analysis suggests the use of a CDK4/6 inhibitor in combination with an aromatase inhibitor for the first line treatment of HR+ MBC in older women results in similar efficacy benefit as seen in younger women. Although incidence and severity of Grade 1-4 adverse reactions appeared similar between age groups, greater serious adverse events and discontinuations occurred in patients ≥65. The inclusion of greater numbers of patients ≥70, in clinical trials will further inform clinicians about the safety and efficacy of CDK4/6 inhibitors in older adults.
Citation Format: Singh H, Howie LJ, Bloomquist E, Wedam S, Amiri-Kordestani L, Tang S, Sridhara R, Ibrahim A, Goldberg K, McKee A, Beaver JA, Pazdur R. A U.S. food and drug administration pooled analysis of outcomes of older women with hormone-receptor positive metastatic breast cancer treated with a CDK4/6 inhibitor as initial endocrine based therapy [abstract]. In: Proceedings of the 2017 San Antonio Breast Cancer Symposium; 2017 Dec 5-9; San Antonio, TX. Philadelphia (PA): AACR; Cancer Res 2018;78(4 Suppl):Abstract nr GS5-06.