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.
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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 |
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|
AI users |
TAM users |
AI users |
TAM users |
AI users |
TAM users |
|
Unmatched cohort |
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|
|
|
|
|
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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 |
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Matched cohort |
|
|
|
|
|
|
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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 |
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OR (95% CI) |
1.13 (1.02-1.24) |
1.09 (1.00-1.18) |
2.19 (1.76-2.74) |
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HR (95% CI) |
1.13 (1.06-1.20) |
1.11 (1.02-1.20) |
2.20 (1.76-2.75) |
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sHR (95% CI) |
1.11 (1.05-1.16) |
1.08 (1.01-1.15) |
2.15 (1.80-2.57) |
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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. |
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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/
