Session Information
Date: Monday, November 6, 2017
Title: ACR/ARHP Combined: Epidemiology and Public Health: Prevention, Recognition, and Treatment
Session Type: ACR Concurrent Abstract Session
Session Time: 4:30PM-6:00PM
Background/Purpose: Asian women accounted for more than 40% of incident breast cancer (BC) worldwide. While aromatase inhibitors (AIs) significantly reduce recurrence of breast cancer (BC) and improve disease-free survival in post-menopausal women with hormone receptor-presenting BC, over one-third of AI users in randomized controlled trials developed arthralgia. Little is known about the risk of AI-induced arthralgia among Asian women with BC in real-world settings. Our objective was to compare the risk of AI-induced arthritis/musculoskeletal problems (A/MSK) between use of AIs vs. tamoxifen in a large Taiwan administrative claims dataset having >99% national coverage and ~23 million enrollees. Methods: In a retrospective cohort study using Taiwan Catastrophic Illness Patient Datasets and Taiwan National Health Insurance Research Datasets, we identified BC women (ICD-9 code: 174) that newly initiated AIs (anatrazole, exemestane and letrozole) or tamoxifen (TAM) from 2007 to 2012. We examined three A/MSK -related outcomes of interest within a year after therapy initiation, including women having 1) prescription pain relievers (i.e., non-steroidal anti-inflammatory drugs [NSAIDs], acetaminophen and opioids), 2) diagnosis of any type of arthritis (ICD-9: 710-719), or 3) carpal tunnel syndrome (CTS) or trigger fingers (TF; ICD-9: 354.0, 727.03). Individuals having outcome episodes that occurred within 3 months prior to AI/TAM initiation were excluded. We applied Greedy methods to match AI users with up to 5 TAM users on age and prior use of taxane therapy. To ensure the robustness of our results, we estimated the association between A/MSK risk and AI use compared to TAM use using conditional logistic regression, cause-specific Cox regression and competing risk regression models. Results: Among 40,761 BC women initiating endocrine therapy from 2007 to 2012, 15.5% were AI users and 84.5% were TAM users. The mean age was 54.1 (SD±12.1) years and 19.6% had history of taxane exposure prior to AI/TAM initiation. There were significant differences (p <0.0001) in the crude rates of pain reliever use (68.7% vs. 65.0%), diagnosed arthritis (16.8% vs. 11.7%) and CTS/TF (2.6% vs. 1.1%) within a year after AIs or TAM initiation. After matching, AI users had higher odds of receiving pain relievers (OR: 1.13, 95%CI: 1.02-1.24), having a diagnosis of arthritis (OR: 1.09, 95%CI: 1.00-1.18) and a diagnosis of CTS/TF (OR: 2.19, 95%CI: 1.76-2.74) compared to TAM users (Table 1). Similar findings were seen using cause-specific Cox regression and competing risk regression (Table 1). Conclusion: We found that AI users have a higher risk of A/MSK within the first year of treatment compared with TAM users among Taiwanese BC women. Timely pain management and close follow-up for AI-induced A/MSK is suggested to prevent poor adherence or discontinuation of AI therapy.
Table 1. Crude incidence and the risk of arthralgia among Taiwanese women with breast cancer that received aromatase inhibitor vs. tamoxifen therapy. |
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Outcomes of interest |
Using pain relievers |
Arthritis |
CTS/TF |
|||
|
AI users |
TAM users |
AI users |
TAM users |
AI users |
TAM users |
Unmatched cohort |
|
|
|
|
|
|
No. for eligible patients for each outcome |
2,967 |
16,329 |
5,845 |
32,710 |
6,298 |
34,336 |
Event No. |
2,039 |
10,619 |
983 |
3,823 |
164 |
379 |
Crude Incidence (%) |
68.7 |
65.0 |
16.8 |
11.7 |
2.6 |
1.1 |
Matched cohort |
|
|
|
|
|
|
No. for eligible patients |
2,727 |
8,743 |
5,365 |
18,133 |
5,779 |
19,427 |
Event No. |
1,869 |
5,764 |
891 |
2,723 |
148 |
216 |
OR (95% CI) |
1.13 (1.02-1.24) |
1.09 (1.00-1.18) |
2.19 (1.76-2.74) |
|||
HR (95% CI) |
1.13 (1.06-1.20) |
1.11 (1.02-1.20) |
2.20 (1.76-2.75) |
|||
sHR (95% CI) |
1.11 (1.05-1.16) |
1.08 (1.01-1.15) |
2.15 (1.80-2.57) |
|||
Abbreviations: AIs: aromatase inhibitors; CTS: carpal tunnel syndrome; HR: hazard ratio, estimated by Cox regression; sHR: subdistributional hazard ratio, estimated by competing risk regression model; TF: trigger fingers, OR: odds ratio, estimated by conditional logistic regression. |
To cite this abstract in AMA style:
Chien HC, Lo-Ciganic WH, Kwoh CK, Kao Yang YH. Use of Aromatase Inhibitors and Risk of Arthritis and Musculoskeletal Problems Among Taiwanese Women with Breast Cancer: A Nationwide Claims Analysis [abstract]. Arthritis Rheumatol. 2017; 69 (suppl 10). https://acrabstracts.org/abstract/use-of-aromatase-inhibitors-and-risk-of-arthritis-and-musculoskeletal-problems-among-taiwanese-women-with-breast-cancer-a-nationwide-claims-analysis/. Accessed .« Back to 2017 ACR/ARHP Annual Meeting
ACR Meeting Abstracts - https://acrabstracts.org/abstract/use-of-aromatase-inhibitors-and-risk-of-arthritis-and-musculoskeletal-problems-among-taiwanese-women-with-breast-cancer-a-nationwide-claims-analysis/