Abstract

Background Multiple myeloma (MM) patients (pts) are older and have poorer quality of life (QOL) compared to pts with other hematologic malignancies (Nielsen et al, Eur J Haematol 2017). Autologous hematopoietic stem cell transplantation (HCT) acutely exacerbates psychosocial distress & insomnia. These symptoms are often treated with benzodiazepines and zolpidem-class drugs (B/Z Rx) that come with serious toxicities in older adults. B/Z Rx patterns in HCT recipients, particularly among MM patients who tend to be older with more co-morbidities, are unknown. Methods We conducted a retrospective cohort study including all pts with MM or light-chain amyloidosis who underwent autologous HCT at our institution from 1/1/17-12/31/18. We identified B/Z Rx at 3 timepoints: (1) pre-HCT baseline; (2) discharge, or D+14 for outpatient HCT; and (3) D+100 follow-up. Results 205 pts (43% female) underwent HCT, 184 (90%) as inpatient (inpt) and 21 (10%) as outpatient (outpt). The median age was 61; 27 pts (13%) were ≥ 70. 174 pts (85%) had received melphalan 200 mg/m2 conditioning; the remainder received 140 mg/m2. 28% of pts (n=58) had ≥ 1 B/Z Rx at all timepoints, while 38% (n=77) had no Rx at any timepoint. As shown in Figures 1 & 2: 33% of pts (n=67) had B/Z Rx at baseline, 57% (n=116) at discharge, and 51% (n=104) at D+100. Among B/Z-naive pts at baseline (n=138), the D+100 B/Z Rx rate was significantly higher among those with any B/Z Rx at discharge than those without (34% vs. 11%, p The most common B/Z Rx's were lorazepam (55% of pts, n=113) and zolpidem (12%, n=24). Of the 113 pts with lorazepam Rx, 35% (n=40) had a specific indication (2nd-line management of nausea/vomiting) without listing a distress-related symptom (e.g., anxiety). After excluding these 40 pts, overall rates of B/Z Rx fell to: 33% (54/165) at baseline, 47% (77/165) at discharge, and 48% (79/165) at D+100. Conclusions 62% of MM pts undergoing HCT received ≥ 1 B/Z Rx peri-HCT, a substantially higher rate than the 13% prevalence in the US population. ∼1/4 of pts experienced escalation of B/Z Rx therapy. Among B/Z-naive pts at baseline, pts prescribed B/Z Rx at discharge were 3x as likely to have continued B/Z Rx at D+100. These findings demonstrate the prevalence and persistence of B/Z Rx use despite their known toxicities. Limitations of our single-center study include an inability to assess how frequently prn Rx were actually taken or prescribed by local oncologists. Nevertheless, we are now investigating non-pharmacologic interventions to improve distress & insomnia in HCT recipients with the eventual goal of lowering B/Z Rx usage.

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