Balancing Treatment Intervals and Quality of Life in Multiple Myeloma Patients: Patient Perspectives and Recommendations

• Published in: Blood 2024-11, Vol.144 (Supplement 1), p.284-284
• Main Authors: Fleischer, Anna, Barakat, Mohammad, Kadel, Sofie-Katrin, Mersi, Julia, Waldschmidt, Johannes, Einsele, Hermann, Kortüm, K. Martin, Maatouk, Imad, Rasche, Leo
• Format: Article
• Language: English
• ISSN: 0006-4971; 1528-0020
• DOI: 10.1182/blood-2024-205037

Background: According to guidelines, patients with symptomatic multiple myeloma (MM) require continuous long-term treatment, starting at diagnosis and stopping in the refractory palliative setting. Although in the real world the onset of serious adverse events such as infectious complications or high-grade polyneuropathy, or simply a strong patient preference, often leads to some treatment-free intervals (TFIs), systematic studies or recommendations on de-escalation and treatment holidays are largely lacking. The advent of novel T-cell redirection therapies such as CAR-T and bispecific antibodies has brought this issue back to the table, as CAR-T offers for the first time a relevant treatment-free interval of up to several years, whereas bispecific antibodies represent a continuous treatment modality given until progression. Understanding patients' preferences regarding TFIs is crucial for tailoring treatment plans that align with their desires and needs, potentially enhancing adherence and overall outcomes. This study aimed to explore MM patients' preferences for TFIs, identify barriers to attending frequent hospital appointments, and determine the most significant stressors during inpatient stays. By assessing these factors, the study seeks to inform patient-centered care approaches that could improve the overall treatment experience and quality of life for MM patients. Methods: A mixed-methods survey was conducted over twelve months, involving 100 patients with MM at the University Hospital Würzburg. Data collection included both demographic and clinical information, alongside open questions and validated questionnaires to assess various biopsychosocial parameters influencing the perceived significance of TFIs. The assessment tools utilized were the Somatic Symptom Scale (SSS-8) for physical symptom burden, Distress-Thermometer (DT) for psychological distress, Patient Health Questionnaire 4 (PHQ-4) for depression and anxiety screening, EORTC QLQ-C30 for health-related quality of life, SSUK-8 for perceived social support, UCLA 3-item Loneliness Scale (UCLA 3) for perceived loneliness and social isolation, and the Questionnaire on Fear of Progression (PA-F-KF) for fear of disease progression. Results: The survey revealed that a significant 49% of MM patients place an extremely high value (10/10 points on a rating scale) on having extended TFIs, especially between inpatient hospital stays, while only 9.1% rated them “not important” (0/10). No differences i