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4519 Characteristics of Multiple Myeloma Patients with Multiple Lines of Therapy Using Real-World US Claims Data

Health Services and Outcomes Research – Malignant Diseases
Program: Oral and Poster Abstracts
Session: 902. Health Services and Outcomes Research – Malignant Diseases: Poster III
Monday, December 7, 2015, 6:00 PM-8:00 PM
Hall A, Level 2 (Orange County Convention Center)

Eric Maiese1*, Brian Macomson, PharmD2*, Chris Kozma3*, Terra Slaton4* and Mekre Senbetta, PharmD5*

1HECOR, Janssen Scientific Affairs, LLC, Horsham, PA
2Janssen Scientific Services, LLC, Augusta, GA
3CK Consulting Associates, LLC, St. Helena Island, SC
4HECOR, CK Consulting Associates, LLC, St. Helena Island, SC
5Janssen, Horsham, PA

Background:  Multiple myeloma is an incurable disease with poor survival rate. Recently, novel treatments have focused on addressing unmet needs among heavily pre-treated patients who have failed prior therapies. The purpose of this analysis was to describe the characteristics of patients who are heavily pre-treated vs patients who were not, within 2 years of initiating MM therapy. Results of this analysis will help to understand the characteristics, including treatment patterns and burden, of MM patients who progress through lines of therapy over a relatively short time period.

Methods:  Using a US administrative claims database (Truven Health MarketScan® Database), adult patients (age ≥18) were included in the analysis if they had 1) ≥2 MM diagnoses codes (ICD-9 203.0x) on different dates between Jan 1, 2005-Mar 31, 2014 (study period); 2) MM treatment between Jan 1, 2007-Mar 31, 2012 and within 90 days of an MM diagnosis code (date of the first MM treatment set as the index date); and 3) continuous eligibility for medical insurance 24 months pre/postindex. Patients were excluded if they had 1) MM treatment during 24 months preindex; or during 24 month pre/post index had 2) moved from commercial insurance to Medicare; 3) non-MM chemotherapy; 4) pregnancy-related or stem cell transplant codes; or 5) HIV diagnosis during study period.  An algorithm using dispensing dates and days supply was developed to define line of therapy (LOT) and double refractory.  A new LOT was identified where there was a ≥60 day gap with no treatment, a ≥60 day gap followed by retreatment with the same drug, or where there was a change in therapy based on 30 day windows and the summed days supply of medication was >60 days. Refractory events were defined when a PI or IMiD had days supply for <60 days, was discontinued for ≥60 days, a different PI or IMiD was initiated and the initial drug did not appear in the next LOT.  Heavily pre-treated was defined as starting an LOT after having received ≥3 prior LOT that included a PI and IMiD or double refractory to both PI and IMiD.  Chi-square test was used to test for differences in categorical variables and Mann Whitney U test for continuous variables. 

Results:  A total of 1109 patients were included in the analysis. The percent of patients with 1, 2, 3, 4 or >4 LOT were 39.8%, 33.0%, 15.4% and 6.1% and 5.7%, respectively. A single refractory event occurred in 66 (6.0%) patients and 2 (0.2%) patients were identified as double refractory. There were 80 (7.2%) patients who were heavily pre-treated.  The heavily pre-treated group had a similar percent of males (56.3%) as the non-heavily pre-treated group (54.9%; p=0.82).  The heavily pre-treated group was slightly younger (66.1 vs 70.9 years; p=0.0008) and had a lower percent with Medicare coverage (55.0% vs 71.1%; p=0.0024). The heavily pre-treated group had a substantially higher percent of regimens that included both PI and IMiD in the 1st LOT (28.8% vs 7.4%; p<0.0001).  The most common 1st LOT drug regimens for the heavily pre-treated group were bortezomib (BOR) (21.31%), thalidomide (THAL) (21.3%), lenalidomide/bortezomib (LEN/BOR) (20.0%), and lenalidomide (LEN) (18.8%).  In the non-heavily pre-treated group the most common 1st LOT regimens were LEN (36.7%), BOR (20.4%), THAL (14.4%), and melphalan (10.1%).  Patients who were heavily pre-treated reached their 2nd LOT in fewer days than non-heavily pre-treated (152.5 vs 279.9 days; p<0.0001).  There was a much higher percent of patients using BOR/LEN in the 2nd LOT in the heavily pre-treated than non-heavily pre-treated (20.0% vs. 4.1%).

Conclusions:  In this analysis, 7.2% of non-stem cell transplant patients were heavily pre-treated at 2 years after initiating MM therapy.  Heavily pre-treated patients had a faster time to initiation of 2nd LOT. They also tended to be younger. Moreover, heavily pre-treated patients were more likely to have had both a PI and IMiD as their initial therapy.  Patients who were heavily pre-treated in this analysis may have had faster disease progression, which may have led to becoming heavily pre-treated within the follow-up time of the study. Additional research should further explore the disease and economic burden of these patients.

Disclosures: Maiese: Janssen Scientific Affairs, LLC: Employment . Macomson: Janssen Scientific Affairs, LLC: Employment . Kozma: Janssen Scientific Affairs, LLC: Consultancy . Slaton: Janssen Scientific Affairs, LLC: Consultancy . Senbetta: Janssen Scientific Affairs, LLC: Employment .

*signifies non-member of ASH