Background

While rituximab revolutionized outcomes in DLBCL, little is known regarding survival improvements at population level beyond the introduction of rituximab. The advent of novel agents, improvements in supportive care and expansion of autologous hematopoietic cell transplantation (auto-HCT) to older individuals may have improved survival of DLBCL patients. We hypothesized that outcomes for patients diagnosed with DLBCL in the U.S. has continued to improve in recent years and intended to measure improvements and identify possible disparities by comparing survival of DLBCL between two consecutive post-rituximab eras.

Methods

We used the population-based SEER-18 registry to calculate the incidence and relative survival rates (RSR) of DLBCL in the U.S. for two consecutive eras since broad availability of rituximab in upfront DLBCL treatment, 2002-2007 (era-1, early years after adoption of rituximab) and 2008-2013 (era-2, availability of novel agents, broader use of auto-HCT and improvement in supportive care). We included adult patients with microscopically confirmed DLBCL as first malignant neoplasm regardless of histologic subtype and survival follow up to the end of 2015.

Results

There were a total of 56,625 DLBCL patients diagnosed between 2002 and 2013, of which 27,306 patients were diagnosed during era-1 and 29,319 during era-2. Median follow up of survivors was 125 months in era-1 and 53 months in era-2. The median age at diagnosis was 66 years with slight male predominance in both the eras. There were no differences in age, gender, race/ethnicity and stage characteristics. There was a slight decline in incidence of DLBCL (era-1 vs. era-2), 8.11 (95% CI=8.01-8.2) vs. 7.82 (95% CI=7.73-7.91) cases per 100,000 persons (P<0.0001). Overall there was a modest improvement in DLBCL RSR, with 5-year RSR improving from 59.5% to 62.5%. Improvement was mostly evident on first year after diagnosis and affected all subsets of patients (Table), but was more pronounced in patients with advanced stage (Figure).

Conclusions

There has been limited improvement in the survival of adult patients with DLBCL beyond the introduction of rituximab, highlighting the need for experimental therapies and calling for the incorporation of novel therapies earlier in treatment, especially for high-risk cases.

Disclosures

Costa:Sanofi: Honoraria; Celgene: Honoraria, Research Funding; Karyopharm: Research Funding; Janssen: Research Funding; Amgen: Honoraria, Research Funding; BMS: Research Funding; Abbvie: Research Funding.

Author notes

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Asterisk with author names denotes non-ASH members.

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