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  | 
 
  | 
 
  | 
 
  | 
 
  | 
 
  | 
 
  | 
| 
 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)  | 
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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/
