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Abstracts presented Saturday at the American Society of Hematology in San Diego, California, included studies on access to care and an analysis of young physicians' relocation patterns as they transition to fellowship and attending positions.
Beyond the clinical findings presented at the 66th American Society of Hematology (ASH) Annual Meeting & Exposition, sessions on multiple myeloma; diversity, equity, and inclusion; and outcomes research highlighted abstracts focused on key topics in managed care, from factors that affect access to treatment to those that impact where clinicians set up practice.
HRQOL Results in PERSEUS Support Quadruplet as Standard
Pieter Sonneveld, MD, of the Erasmus MC Cancer Institute in Rotterdam, the Netherlands, last year presented the main findings of the PERSEUS trial (NCT03710603) at ASH; the results showed that adding subcutaneous daratumumab (Darzalex Faspro, Johnson & Johnson) to bortezomib, lenalidomide, and dexamethasone (VRd) was associated with a significantly higher rate of progression-free survival (PFS) in transplant-eligible patients newly diagnosed with multiple myeloma (HR, 0.42; 95% CI, 0.30–0.59; P < .001).
On Saturday, Sonneveld presented results from questionnaires completed by patients in the phase 3 trial, which aimed to measure health-related quality of life (HRQOL), a secondary end point in PERSEUS. Patients completed 2 questionnaires on quality of life, the 30-question EORTC Core Quality of Life questionnaire (EORTC QLQ-C30) and the EuroQoL EQ-5D descriptive system and the EQ visual analogue scale (EQ VAS). They also completed 1 questionnaire on myeloma-specific symptoms, EORTC-MY-20.1
Baseline characteristics were well-balanced between the 2 arms of PERSEUS. At the time of clinical cutoff, follow-up was 47.5 months. At maintenance cycle 34, there were 254 patients in the daratumumab group and 164 in the control arm on study. Results showed the following1:
“Together with favorable efficacy outcomes data,” the authors wrote, the HRQOL data support the addition of daratumumab to a VRd triplet “as a new standard of care for [transplant-eligible] newly diagnosed multiple myeloma.”1
As Training Progresses, Cancer Doctors Move Away From Black Patients
Researchers from Georgia, located at Wellstar Spalding Medical Center in Griffin and the Medical College of Georgia in Augusta, have created data to support a pattern observed anecdotally: As trainees in hematology and oncology progress through residency, fellowship, and their first attending positions, they migrate away from areas that serve high numbers of non-Hispanic Black patients. Among the factors that contribute to health care disparities are shortages of oncologists, particularly in areas that serve high numbers of Black patients.2
As the authors note, “geographical distribution of hematology/oncology fellowship graduates is crucial for shaping health care delivery and highlighting regional health disparities in cancer care.”
Presented by Vishwanath Anil, MD, of Wellstar, the study digs into patterns of movement of these young physicians and identifies the career pivot points where many opt to move to less diverse locations.2
For this study, the investigators analyzed transitions of 703 graduates of 65 accredited hematology and oncology fellowship programs for the period 2019 to 2022 that featured alumni data on their websites. The study team labeled 3 key transitions in medical training:
They measured geographic relocation by straight-line distance and used US Census and zip code data to evaluate retention, as well as racial and socioeconomic data for locations. They divided the country into 4 regions to assess retention. Results showed the following2:
The authors concluded that trainees may seek to diversify their educational experiences early in their training, but as time moves on, their preferences shift to “establishing roots,” possibly influenced by professional, personal, or network connections.
They pattern of moving away from and then back to rural areas likely reflects a similar dynamic, they wrote, where “early training is sought in urban centers with more resources, but eventual practice might be to areas with lower cost of living, higher physician demand and higher salaries which are classified as more rural areas.”
The patterns tracked call for policy solutions to address a workforce that is not moving to the areas of greatest need. “These findings underscore the need for targeted policies to mitigate geographic, socioeconomic, and racial inequality, ensuring equitable access to quality cancer care across all regions,” they write.
Mental Health Issues, Financial Limits Are Barriers to Transplant
Mental health challenges, financial pressures, and not having a caregiver at home are among the reasons patients delayed allogeneic hematopoietic cell transplantation (HCT) when diagnosed with acute myeloid leukemia (AML), according to a study conducted by Knight Cancer Institute, Oregon Health & Science University (OHSU) in Portland, Oregon.
Although being referred early for HCT is linked to improved survival for adults with intermediate and high-risk AML, many patients have delays in accessing this curative therapy for reasons unrelated to their disease. For this reason, investigators at OHSU sought to gain a deeper understanding of what keeps patients with AML who are clinically eligible from progressing to transplant.
The analysis involved 369 patients with HCT delays from 2019 through 2022. Through evaluations by social workers, the team was able to uncover multiple reasons, with many patients affected by more than 1 factor. Results showed the following3:
Investigators reported that referral for human leukocyte antigen (HLA) typing was completed for 42% of the patients. The median time was 46 days from diagnosis, with a range of 0 to 280 days; 21% of the patients had HLA completed within 6 weeks of diagnosis.
HCT consults were completed for 45% of patients; the median time to HCT consultation was 58 days, with a range of 0 to 483 days; of those who completed consults, 73% proceeded to HCT with a median of 154 days from diagnosis, and a range of 64 to 1030 days.
The documented reasons for not having HLA typing or HCT consults were disease progression (37%), oncologist determined not indicated (32%), comorbidities (16%), patient wishes (8%), and advanced age (4%). Nondisease related factors that were associated with reduced likelihood of proceeding to HCT were being older than 70 years and not having private insurance, while factors such as gender, race/ethnicity, living in a nonmetropolitan or poverty area, being a long distance to the transplant center, and SDOH were not statistically significant.
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