Abstract
BackgroundFor patients with multiple myeloma (MM), each additional line of therapy (LOT) is associated with lower response rates, shorter treatment duration and treatment-free intervals, and increased rates of toxicities and comorbidities. Here, we examine frontline treatment patterns, and attrition rates by LOT among newly diagnosed MM (NDMM) patients in the United States who were eligible or ineligible for autologous stem cell transplant (ASCT).MethodsData were identified from three US patient-level databases collectively covering the period January 2000 to September 2018. Patients had an index diagnosis of MM on or after January 1, 2007, medical and prescription insurance coverage at diagnosis, a 1-year look-back period prior to the index diagnosis, no prior malignancies in the 1-year period before index diagnosis, and had received ≥1 LOT.ResultsAmong patients who did not receive ASCT (non-transplant; n = 22,062), 12,557 (57%) received only 1 LOT and 9505 (43%) received > 1 LOT. Patients receiving only 1 LOT were significantly older, had higher mean Charlson Comorbidity Index (CCI) scores, and higher incidences of comorbidities. Among the 2763 patients receiving ASCT, 2184 received > 1 LOT, and 579 (21%) received only 1 LOT (ie, ASCT was the last treatment). 1682 (61%) patients received induction therapy as frontline treatment, of whom 187 (11%) also received consolidation therapy. The latter group was younger than those who received only induction therapy, had lower mean CCI scores, and comparable or lower incidences of selected comorbidities. The most common frontline therapy for non-transplant and transplant-eligible patients was bortezomib/dexamethasone and bortezomib/lenalidomide/dexamethasone, respectively. Attrition rates across all LOTs were high for non-transplant patients (range, 43–57%) and transplant patients (range, 21–37%). Treatment duration decreased by LOT for non-transplant patients and was consistent across LOTs for transplant patients.ConclusionsIn this analysis, a substantial proportion of patients with NDMM who received frontline therapy did not appear to receive a subsequent LOT. These high attrition rates underscore the need to use the most optimal treatment regimens upfront rather than reserving them for later LOTs in which the clinical benefit may decrease.
Highlights
For patients with multiple myeloma (MM), each additional line of therapy (LOT) is associated with lower response rates, shorter treatment duration and treatment-free intervals, and increased rates of toxicities and comorbidities
Multiple myeloma (MM) treatment options have improved in recent years, but MM remains an incurable disease with an estimated 5-year survival rate of 52% in the United States [1]
Data sources Patients with newly diagnosed MM (NDMM) were identified from 3 US databases: the OPTUMTM Commercial Claims database from January 2000–September 2018, the OPTUMTM Electronic Medical Records (EMR) database from January 2000– September 2018, and the Surveillance, Epidemiology, and End Results (SEER)-Medicare Linked database from January 2007–December 2016
Summary
For patients with multiple myeloma (MM), each additional line of therapy (LOT) is associated with lower response rates, shorter treatment duration and treatment-free intervals, and increased rates of toxicities and comorbidities. We examine frontline treatment patterns, and attrition rates by LOT among newly diagnosed MM (NDMM) patients in the United States who were eligible or ineligible for autologous stem cell transplant (ASCT). Frontline and subsequent treatment options are selected based on a patient’s age, frailty, comorbidity status, intolerance, resistance, and/or exposure to previous therapy, and disease biology [2, 3]. Patients who receive a stem cell transplant and maintenance therapy have superior outcomes compared with those who are transplant ineligible [4, 5], both groups of patients frequently experience disease relapse and require subsequent lines of therapy (LOTs). Clinical trials evaluate the efficacy and safety of a therapy at a given disease stage and can be highly selective for a patient population (ie, by restricting enrollment to patients with good performance status). Clinical trials provide valuable information for specific therapeutic regimens, there is limited information on the factors guiding treatment patterns and patient outcomes in a real-world setting
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