Endocrine therapy initiation among women diagnosed with ductal carcinoma in situ breast cancer from 2001-2016.

Authors

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Erin Aiello Bowles

Kaiser Permanente Washington Health Research Institute, Seattle, WA

Erin Aiello Bowles, Cody Ramin, Heather S. Feigelson, Jennifer C Gander, Lene H. S. Veiga, Clara Bodelon, Rochelle E. Curtis, Carolyn Brandt, Jacqueline B Vo, Amy Berrington de González, Gretchen Gierach

Organizations

Kaiser Permanente Washington Health Research Institute, Seattle, WA, Cedars-Sinai Medical Center, Los Angeles, CA, Kaiser Permanente Colorado, Aurora, CO, Kaiser Permanente Georgia, Atlanta, GA, National Cancer Institute, Bethesda, MD, Institute of Cancer Research, London, United Kingdom

Research Funding

U.S. National Institutes of Health
U.S. National Institutes of Health

Background: Endocrine therapy (ET) initiation in people within 1 year of diagnosis of estrogen-receptor-positive (ER+) ductal carcinoma in situ (DCIS) has ranged from 21-45% in prior studies; however, these studies did not evaluate initiation post-2011 and may not reflect current patterns of use. ET use following ER+ DCIS diagnosis can reduce the relative risks of recurrence and contralateral breast cancer by 30-50%. We evaluated ET initiation over time and by demographic, tumor, and treatment characteristics in the Kaiser Permanente Breast Cancer Survivors Study between 2001-2016. Methods: We included people aged 20+ years diagnosed with unilateral DCIS with at least 1 year of cancer-free follow-up from three U.S. integrated health systems. We excluded people with ER-negative disease, no surgery, and those who received chemotherapy or unknown radiation therapy. ET dispensings (tamoxifen and aromatase inhibitors) were extracted from electronic pharmacy records within 1 year of a person’s initial DCIS breast cancer diagnosis. Using generalized linear models with a log link and Poisson distribution, we estimated relative rates (RRs) of ET use (vs none) over time and by demographic, tumor, and other treatment characteristics. Results: Among 1,782 pre- and postmenopausal people, 577 (32%) initiated ET within 1 year of diagnosis. From 2001-2016, ET use did not change over time (34% vs 36%), tamoxifen use declined slightly (34% vs 29%), and aromatase inhibitor use increased slightly (0% vs 7%). People were less likely to initiate ET if they were ≥65 years, Black, had borderline or unknown ER status, were not tested for ER, had breast conserving surgery (BCS) without radiation, or had a unilateral mastectomy. Conclusions: Only one-third of people with DCIS diagnosed in a community healthcare setting and potentially eligible for ET, initiated treatment within 1 year of their diagnosis. Previous studies have shown long-term benefits of ET use in people with DCIS; however, we saw no increase in use over time. Concerns about side-effects, overdiagnosis and overtreatment of DCIS, and confusion about treatment guidelines may explain relatively low ET initiation.

Adjusted ET Initiation Within 1 Year of DCIS vs None1Adjusted ET Initiation Within 1 Year of DCIS vs None2
CharacteristicRR (95% CI)RR (95% CI)
Diagnosis age: 65-<75y (reference 55-<65y)0.77 (0.64-0.93)0.76 (0.63-0.92)
Diagnosis age: ≥75y (reference 55-<65y)0.52 (0.36-0.74)0.53 (0.37-0.76)
Race: Black (reference White)0.79 (0.63-1.00)0.79 (0.63-0.98)
ER status: Borderline/Unknown (reference ER positive)0.48 (0.38-0.63)0.51 (0.40-0.66)
ER status: No test (reference positive)0.58 (0.45-0.76)0.61 (0.47-0.80)
BCS alone (reference BCS + radiotherapy)0.59 (0.48-0.74)--
Unilateral mastectomy (reference BCS + radiotherapy)0.59 (0.49-0.71)--

1Adjusted for diagnosis age and year, ER status, and study site; 2Also adjusted for surgery.

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Abstract Details

Meeting

2023 ASCO Quality Care Symposium

Session Type

Poster Session

Session Title

Poster Session A

Track

Quality, Safety, and Implementation Science,Cost, Value, and Policy,Patient Experience,Survivorship

Sub Track

Chronic Anticancer Therapy

Citation

JCO Oncol Pract 19, 2023 (suppl 11; abstr 487)

DOI

10.1200/OP.2023.19.11_suppl.487

Abstract #

487

Poster Bd #

L13

Abstract Disclosures