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e19065 Background: ESAs are used in first-line treatment for symptomatic or transfusion-dependent anemia in patients (pts) with LR-MDS. Ultimately, the majority of pts with LR-MDS who receive an ESA will experience ESA treatment failure. This real-world (RW) study aims to describe pt characteristics, treatment patterns including ESA use, and outcomes in pts with LR-MDS. Methods: A retrospective, observational, US multisite, cohort chart review of adult pts diagnosed with LR-MDS between January 1, 2015 and June 24, 2020 was conducted. Eligible pts had not received luspatercept or participated in a clinical trial and had ≥ 1 year of follow-up after LR-MDS diagnosis, unless follow-up was < 1 year due to death during this interval. Demographics, clinical characteristics, treatment patterns, and outcomes were summarized using descriptive statistics. Median duration of therapy (DOT) was estimated using the Kaplan-Meier method. Results: Among 338 eligible pts, median age at LR-MDS diagnosis was 70 years (range: 19–100), 55% were female, 71% were White, 17% had known detection of del(5q), and ring sideroblast status was known to be positive for 7%. Transfusion independence within the 8 weeks prior to diagnosis (TI8) was reported for 48% of eligible pts and 17% had intermediate-1/ intermediate disease risk by IPSS/ IPSS-R risk classification. Within the study follow-up time (median of 28.3 months from diagnosis), 76% of pts had received systemic therapy for MDS (median DOT: 29.2 months). An ESA was used in 56% (n = 190) of pts, of whom 38% received red blood cell (RBC) transfusions during ESA treatment. Of those receiving systemic treatment for LR-MDS, 11% were hospitalized for reasons that physicians reported were related to MDS treatment complications. At the time of data collection, 30% of pts had died. Among 38 pts determined to have failed ESA treatment by abstracting physicians, 11% had TI8, 34% had intermediate-1/ intermediate disease risk, 82% received RBC transfusions during ESA treatment, 26% required hospitalization that abstracting physicians reported was related to MDS treatment complications, 32% continued to receive ESA post-failure, and 53% were deceased at data collection. Conclusions: Results from this RW study indicate that a higher proportion of pts with LR-MDS who experienced ESA treatment failure according to abstracting physicians had intermediate-1/ intermediate disease risk at diagnosis, were transfusion dependent at diagnosis, required RBC transfusions during ESA treatment, were hospitalized for reasons related to MDS treatment complications, and had poor short-term survival. Nearly a third of pts who experienced ESA treatment failure still received an ESA after initial failure. In summary, findings from this study indicate that pts with LR-MDS who experience ESA treatment failure are likely to have worse outcomes.

1036 Background: Trastuzumab Deruxtecan (T-DXd) was associated with an increased risk of interstitial lung disease (ILD)/pneumonitis (P) in metastatic breast cancer (mBC) patients (pts) in clinical trials, leading to ILD/P monitoring and management guidelines in the product label. This study aims to describe the monitoring and management of ILD/P during T-DXd therapy among US community oncology practices. Methods: Oncologists in the Cardinal Health Oncology Provider Extended Network (OPEN) participated in a cross-sectional survey on monitoring approaches for ILD/P among mBC pts. Participating physicians provided data from medical charts of up to 10 pts who were treated with T-DXd regarding presence of ILD/P symptoms, management, and outcomes of ILD/P symptoms. Results: Twenty-eight physicians from across the U.S participated and provided data on 149 T-DXd pts. Nearly all physicians reported they were monitoring ILD/P after T-DXd initiation by physical examination (n = 27), symptoms checklist (n = 25) and pulse oximetry (n = 23) at every visit, whereas fewer reported performing lung CT scan (n = 18), echocardiogram (n = 13), chest X-ray (n = 12), lung PET scan (n = 10), pulmonary function tests (n = 8) and diffusion testing (n = 7) on a less frequent basis. Among 149 T-DXd pts, 4 pts were diagnosed with ILD/P over an average T-DXd treatment duration of 5.5 months. All 4 cases initiated T-DXd treatment at 5.4mg/kg every 3 weeks, experienced ILD/P within the first 5 cycles of T-DXd, were diagnosed with lung CT scan and initially presented with Grade 2 symptomology (2 cases progressed to Grade 3). For both cases that remained as Grade 2, ILD/P completely resolved within 23 days. One case received IV methylprednisolone (1000mg daily; duration of therapy (DOT): 3 days) during hospitalization, oxygen therapy and T-DXd was permanently discontinued; whereas the other one received oral prednisone (started at 40mg daily and tapered to 5mg daily; DOT: 7 days) and T-DXd dose was held. For the two grade 3 cases, one received IV methylprednisolone (125mg daily; DOT: 7 days) during hospitalization, T-DXd dose was held, and ILD/P completely resolved within 11 days; whereas the other case received oral prednisone (started at 80mg daily and tapered to 5mg daily; DOT: 63 days), oxygen therapy, T-DXd was permanently discontinued, and ILD/P resolved with sequela within 46 days. Conclusions: ILD/P incidence in this small study sample of patients receiving T-DXd treatment was 2.7%. Although general awareness of ILD and routine screening by pulse oximetry and physical exam were common, management approaches for ILD/P were not always consistent with T-DXd prescribing information. Further physician education may be needed to improve appropriate management of ILD/P and outcomes for T-DXd pts.

6550 Background: Despite similar incidence rates of uterine cancer (UC) in Black and White women, the former have worse prognosis and survival. Absence of denominator correction for UC hysterectomy (prevalence varies within the United States [US] by race/region) may underestimate incidence. The objective of this study is to compare treatment and survival of patients with UC by race in a large, contemporary, population-based study with at least 5 years of follow-up. Methods: With the latest available data from the Surveillance, Epidemiology, and End Results database, comparisons between Black and White patients were made using chi-square and Mann-Whitney tests. Cox proportional hazards regression estimated the adjusted risk of mortality by including age at diagnosis, race, US region, tumor histology/stage/grade, and receipt of hysterectomy as covariates. Results: A total of 105,036 women (11,028 Black and 94,008 White) newly diagnosed with UC in 2000-2013 and followed through 2018 were identified. Median age at diagnosis was 62 years, and more patients in the South were Black (41% vs 17%, P