Black/White Differences in the Treatment and Outcomes of Diffuse Large B Cell Lymphoma: A Matched Cohort Analysis.

Blood ◽  
2009 ◽  
Vol 114 (22) ◽  
pp. 1392-1392 ◽  
Author(s):  
Pareen J. Shenoy ◽  
Kevin Bumpers ◽  
Nassoma King ◽  
Taoying Huang ◽  
Neha Malik ◽  
...  

Abstract Abstract 1392 Poster Board I-414 Background: While African-Americans have a lower incidence of diffuse large B-cell lymphoma (DLBCL) than Whites (W) in the United States, there appear to be racial differences in clinical features, the use of chemoimmunotherapy(Flowers, AACR 2008), and treatment outcomes. However, previous analyses have been hampered by limited numbers of Black (B) patients (pts); lack of direct clinical information on pathology, prognostic factors, treatment, and outcomes; limited follow-up; or all three. Methods: To examine B/W differences in the use of CHOP-based chemotherapy vs. rituximab CHOP (RCHOP), we performed a retrospective, matched cohort analysis comparing the impact of race, on presenting features, treatment, and outcomes in a clinical setting with detailed data ascertainment from pathology, clinical, and pharmacy records. Patients diagnosed with DLBCL from 1981 to 2009 were identified from Emory pathology and medical records using previously published methods (Graiser, Cancer Informatics 2007). Baseline demographic data, components of the International Prognostic Index (IPI: age, performance status, lactate dehydrogenase [LDH], number of extranodal sites involved, stage), insurance status, employment status, treatment and survival data were extracted. Differences by race in baseline features and treatment category (CHOP vs. RCHOP) were analyzed using Chi-squared statistical analysis. Univariate and multivariate logistic regression analyses were performed for the entire population and cohorts matched by IPI, age, and year of diagnosis, to determine predictors of RCHOP use, 2-year and 5-year overall survival (OS). Cox regression was used to analyze the predictors of OS. Results: A total of 531 (348 W and 107 B) pts with a confirmed diagnosis of DLBCL were identified. The median age of diagnosis for B was significantly less than that for W pts (median age 46 (range: 18–87) vs. 56 (range: 18–86), respectively; p<0.001). There were no differences in stage, performance status or extranodal disease, but B pts more frequently presented with elevated LDH (50% vs. 37%, p=0.04). There were no racial differences in RCHOP use. Pts who had elevated LDH were more likely to receive RCHOP (p<0.001). W race was a predictor of improved 2yr OS. W race, early stage, IPI <2 were predictors of improved 5yr OS. However, there were no B/W differences in OS, in the CHOP cohort or the RCHOP cohort. After matching for revised IPI group, age at diagnosis, and diagnosis year B (n=104) and W (n=104) pts had similar rates of RCHOP use (41% vs. 46%), 2-yr OS, and 5-yr OS. Conclusions: These data corroborate findings that B pts present with DLBCL at a younger age. In the setting of a single institution referral center with detailed ascertainment of treatment, there do not appear to be racial differences in RCHOP use or outcomes. Since IPI, age, and year of treatment may influence treatment selection and outcomes, matching cohorts on these factors is necessary when examining B/W differences. Disclosures: Flowers: Amos Medical Faculty Development Program grant from the American Society of Hematology/Robert Wood Johnson Foundation: Research Funding.

Blood ◽  
2009 ◽  
Vol 114 (22) ◽  
pp. 898-898
Author(s):  
Neha Malik ◽  
Pareen J. Shenoy ◽  
Kevin Bumpers ◽  
Rajni Sinha ◽  
Christopher R. Flowers

Abstract Abstract 898 Background: Diffuse large B cell lymphoma (DLBCL) is the most common type of non-Hodgkin lymphoma (NHL), and can often be cured with standard chemoimmunotherapy, but there is great heterogeneity in patient outcomes. Methods: To examine the baseline characteristics and outcomes in a national cohort of patients(pts) with DLBCL we performed a retrospective cohort analysis of DLBCL cases diagnosed from 1992 to 2005 in 13 Surveillance, Epidemiology and End Results (SEER) registries. International Classification of Diseases for Oncology histology codes 9680, 9684, 9697 were used to identify cases. Cases with known race were grouped into White (W), Black (B), and others (O; Asians or Pacific Islanders, and American Indians or Alaska Natives). Subtype-specific DLBCL incidence rates were calculated for population subgroups according to age, sex, race, registry and time period, expressed as new cases per 100,000 population and age-adjusted to the 2000 US standard population. Incidence rates were compared by sex and by race by computing incidence rate ratios (IRR) and 95% Confidence Intervals (95% CI). Two- and 5-year relative survival rates (RSR) were calculated by actuarial methods. Results: Between 1992 and 2005, 34,436 cases of DLBCL were recorded in SEER. Over this period, the incidence of imunoblastic DLBCL decreased from 1.7 to 0.1 cases per 100,000 population while the incidence of DLBCL as a whole remained stable. Incidence rates were higher among W than among B or O pts with DLBCL (IRR W:B 1.52, 95% CI 1.45-1.59, W:O 1.26, 95% CI 1.21-1.31) and among those with immunoblastic DLBCL but not thymic DLBCL. 65% of B pts compared to 37% of W pts presented at age ≤60 years (p<0.001). Among pts with complete staging (n=5,285), 54% of B compared with 47% of W and 41% of O pts presented with stage III/IV disease (W vs. B p=0.05, W vs. O p=0.002). There were no differences in 2-yr RSR by gender. 2-yr RSR rates were 53% for W, 49% for O, and 46% for B pts (W vs. B p=0.02, W vs. O p=0.09), and improved from 1992 to 2001 for all racial groups. 5-yr RSR rates varied by race (46% for W, 47% for O, and 38% for B pts; (W vs. B p=0.02, W vs. O p=0.09) and gender (47% for females and 43% for males; p=0.03) and remained stable from 1992 to 1997. Conclusions: These data indicate that B pts present with DLBCL at a younger age, more advanced stage, and have inferior 2-yr and 5-yr RSR. Given the known differences in outcomes for activated B-cell (ABC) and germinal center B-cell DLBCL subtypes, to address these differences in survival it will be necessary for future studies investigating racial disparities in treatment outcomes to ascertain whether there are racial differences in the incidence of ABC DLBCL. Disclosures: Flowers: Amos Medical Faculty Development Program grant from the American Society of Hematology/Robert Wood Johnson Foundation: Research Funding.


Cancer ◽  
2010 ◽  
Vol 117 (11) ◽  
pp. 2530-2540 ◽  
Author(s):  
Pareen J. Shenoy ◽  
Neha Malik ◽  
Ajay Nooka ◽  
Rajni Sinha ◽  
Kevin C. Ward ◽  
...  

2021 ◽  
Author(s):  
Thomas Drago

Diffuse large B-cell lymphoma (DLBCL) is the most common form of Non-Hodgkin Lymphoma (NHL) in adults. Affecting nearly 7 out of every 100,000 people in the United States annually, this hematogenous neoplasm is known for its aggressiveness and rapid development. Being the most common NHL, it has been divided into several subgroups based on pathogenesis and treatment methods. In particular, subtypes such as germinal center, activated B-cell-like, and primary mediastinal diffuse large B-cell lymphomas  have been divided by their uniqueness of pathology at the cellular level. Knowing the numerous cytokines, inflammatory markers, and other microcellular processes that these lymphomas disrupt can help target an effective therapeutic at the disease.


2021 ◽  
Vol 11 (9) ◽  
pp. 844
Author(s):  
Yu-Fen Tsai ◽  
Yi-Chang Liu ◽  
Ching-I Yang ◽  
Tzer-Ming Chuang ◽  
Ya-Lun Ke ◽  
...  

Background: Hepatitis C virus (HCV) in diffuse large B-cell lymphoma (DLBCL) is associated with a higher prevalence and distinctive clinical characteristics and outcomes. Methods: A retrospective analysis of adult DLBCL patients from 2011 to 2015 was studied. Results: A total of 206 adult DLBCL were enrolled with 22 (10.7%) HCV-positive patients. Compared to HCV-negative patients, the HCV-positive group had a poor performance status (p = 0.011), lower platelet count (p = 0.029), and higher spleen and liver involvement incidences (liver involvement, p = 0.027, spleen involvement, p = 0.026), and they received fewer cycles of chemotherapy significantly due to morbidity and mortality (p = 0.048). Overall survival was shorter in HCV-positive DLBCL (25.3 months in HCV-positive vs. not reached (NR), p = 0.049). With multivariate analysis, poor performance status (p < 0.001), advanced stage (p < 0.001), less chemotherapy cycles (p < 0.001), and the presence of liver toxicity (p = 0.001) contributed to poor OS in DLBCL. Among HCV-positive DLBCL, the severity of liver fibrosis was the main risk factor related to death. Conclusion: Inferior survival of HCV-positive DLBCL was observed and associated with poor performance status, higher numbers of complications, and intolerance of treatment, leading to fewer therapy. Therefore, anti-HCV therapy, such as direct-acting antiviral agents, might benefit these patients in the future.


2019 ◽  
Vol 12 (10) ◽  
pp. e230277 ◽  
Author(s):  
Turab Jawaid Mohammed ◽  
Rohit Gosain ◽  
Rajeev Sharma ◽  
Pallawi Torka

An elderly man in the seventh decade of life was brought to the hospital with worsening mental status. Blood tests revealed anaemia and thrombocytopenia with elevated lactate dehydrogenase and serum lactate levels. CT scan showed bulky thoracic and abdominal lymphadenopathy with splenomegaly. A positron emission tomography scan confirmed the above and in addition, revealed bilateral adrenal involvement. Bone marrow biopsy revealed non-germinal centre B-cell-like (non-GCB)-diffuse large B-cell lymphoma (DLBCL). Prompt treatment with dose-adjusted etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin and rituximab with intrathecal methotrexate chemotherapy resulted in a dramatic improvement in the patient’s condition. This vignette serves as a reminder to include aggressive lymphomas like DLBCL in the differential diagnoses of patients presenting with metabolic encephalopathy and lactic acidosis. Our patient was moribund at presentation with poor sensorium and failure to thrive. The dilemma was whether to take an aggressive stand and start chemotherapy urgently or whether to stabilise the patient first and then consider the treatment of DLBCL. We make a case for initiating therapy promptly in such patients irrespective of their performance status.


2014 ◽  
Vol 89 (7) ◽  
pp. 714-720 ◽  
Author(s):  
Todd M. Gibson ◽  
Eric A. Engels ◽  
Christina A. Clarke ◽  
Charles F. Lynch ◽  
Dennis D. Weisenburger ◽  
...  

2012 ◽  
Vol 21 (9) ◽  
pp. 1520-1530 ◽  
Author(s):  
Christopher R. Flowers ◽  
Stacey A. Fedewa ◽  
Amy Y. Chen ◽  
Loretta J. Nastoupil ◽  
Joseph Lipscomb ◽  
...  

Blood ◽  
2007 ◽  
Vol 110 (11) ◽  
pp. 21-21
Author(s):  
Marek Trneny ◽  
Robert Pytlik ◽  
David Belada ◽  
Katerina Kubackova ◽  
Ingrid Vasova ◽  
...  

Abstract Background. Combined immunochemotherapy with CHOP and rituximab have improved the outcome of patients with diffuse large B-cell lymphoma (DLBCL). and related diseases. However, the cure rate of patients with IPI 3–5 or aaIPI 3 is still only about 50% with this regimen. Given the feasibility of previous CLSG regimens based on high-dose CHOP-ESHAP induction and BEAM consolidation, we have conducted a phase II trial combining this approach with rituximab immunotherapy. Patients and methods. Patients aged 18–65 years with DLBCL and age-adjusted IPI (aaIPI) 2–3 were treated with three cycles of high-dose CHOP (MegaCHOP - cyclophosphamide, 3 g/m2, vincristine 2 mg, adriamycin, 75 mg/m2, and prednisone, 300 mg/m2) with G-CSF every 3 weeks, followed by three cycles of ESHAP (etoposide, 240 mg/m2, cisplatin, 100 mg/m2, methylprednisolone, 2000 mg and Ara-C 2000 mg/m2) every 3 weeks. Four to six doses of rituximab 375 mg/m2 were administered on day 1 of each cycle of induction therapy. High-dose therapy (BEAM) followed by autologous stem cell transplant (ASCT) was used as consolidation. Radiotherapy was given to residual masses or sites of bulky disease. Primary endpoint was progression-free survival (PFS), while secondary endpoints were overall survival (OS) and feasibility of the treatment. Results. From April 2002 to October 2006, 105 consecutive patients from 10 centers were recruited. 58% were men and 42% women with median age 46 years (19–63 years). 74% of patients had stage IV disease, 92% had elevated LDH, 53% had performance status &gt;1, 55% had B symptoms and 19% had bone marrow involvement. aaIPI was 2 in 62% of patients and 3 in 38% of patients. 68% of patients received the whole treatment according to the protocol, including ASCT and radiotherapy. Stem cells mobilization according to the protocol was performed in 90% of patients and was successful in 86% of mobilized patients (77% of all patients). 73% of patients ultimately received ASCT (including 3 patients transplanted after ammended treatment) and 51% of patients received planned radiotherapy. Complete remission (CR) was achieved in 83% of all patients and partial remission (PR) in 2%. Early toxic death rate was 6% and 9% patients had primary refractory disease. Of patients who achieved CR or PR, only 6 subsequently relapsed (7%) and two suffered late toxic death (2%). With a median follow-up of 32 months for living patients, the estimated 2-year PFS is 77% and 2-year OS is 81%. Age less than median (46 years) was strongest predictor of favorable outcome (p = 0,00006 for PFS and p = 0,00013 for OS), while there was no effect of stage, LDH, performance status or aaIPI (2-year PFS 79% for aaIPI 2 and 77% for aaIPI 3, 2-year OS 81% for aaIPI 2 and 80% for aaIPI 3). Delivery of ASCT or radiotherapy did not significantly affected PFS in patients who did not suffered early progression or early toxic death, but radiotherapy modestly improved OS of these patients (p = 0,03). Conclusion. R-MEB has proved to be an effective treatment strategy for younger patients with high-risk aggressive B-cell lymphoma. Currently, CLSG is testing whether utilization of early PET scan may decrease toxicity and improve treatment tolerance while maintaining the efficacy of this regimen.


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