scholarly journals Venous-Thromboembolism Is Associated with Increased Healthcare Utilization in Elderly Patients with Diffuse Large B Cell Lymphoma

Blood ◽  
2021 ◽  
Vol 138 (Supplement 1) ◽  
pp. 753-753
Author(s):  
Radhika Gangaraju ◽  
Smita Bhatia ◽  
Kelly Kenzik

Abstract INTRODUCTION: Lymphoma is associated with a high risk of venous-thromboembolism (VTE); we have previously shown that elderly patients with diffuse large B cell lymphoma (DLBCL) have a 6.7-fold higher risk of VTE compared to control population without a history of cancer. Given this high risk, we sought to examine the impact of VTE on healthcare utilization using Surveillance, Epidemiology, and End Results Registry (SEER) data linked with Medicare. METHODS: We identified 5,537 Medicare beneficiaries diagnosed with DLBCL at age ≥66 years between 2011 and 2015, with at least 1 year of coverage prior to diagnosis, and initiation of chemotherapy within 1 year post-diagnosis. We ascertained pre-existing comorbidities for the 1 year prior to DLBCL diagnosis. Patients were followed from DLBCL diagnosis until 1 year after cancer diagnosis, or until death, loss of continuous Part A or Part B coverage, blood or marrow transplantation, or end of study (12/31/2016), whichever came first. VTE diagnosis was based on ICD 9 and ICD 10 codes for events including deep vein thrombosis (DVT) and pulmonary embolism (PE). Hospitalizations and Outpatient Visits: Total number of hospitalizations and outpatient visits were compared in DLBCL patients with and without VTE for 1 year after cancer diagnosis, using multivariable negative binomial regression, offset for person-months and adjusting for age at diagnosis, race/ethnicity, stage at diagnosis and number of pre-DLBCL comorbidities (0, 1, 2+). Predicted counts for hospitalizations and outpatient visits were estimated from the multivariable models. Healthcare Spending: Total inpatient and outpatient Medicare spending and spending per visit was estimated from multivariable quantile regression, offset for person-months contributed and adjusting for age at diagnosis, race/ethnicity, stage at diagnosis, and pre-DLBCL comorbidities (0, 1, 2+). RESULTS: Overall, 462 (8.3%) patients developed VTE within 1 year of diagnosis of DLBCL and 244 patients had a VTE history before lymphoma diagnosis. Patients with VTE after DLBCL diagnosis had increased number of hospitalizations compared to those without VTE at the 3, 6 and 12 month time points in the first year after cancer diagnosis (Table 1). The median number of hospitalizations in patients with VTE was 2 compared to 1 in those without VTE at 3 months (p<0.0001). Increased hospitalizations continued until 1 year after lymphoma diagnosis; median number of hospitalizations was 3 in those with VTE compared to 2 in those without VTE at 1 year (p<0.0001). This lead to $51,285 in Medicare spending for hospitalizations in those with VTE compared to $37,065 in those without VTE (excess Medicare spending of $14,220 in those with VTE) in the first year after DLBCL diagnosis (p<0.001). We found no difference in the cost per visit; the excess costs were due to increased number of hospitalizations. The excess hospitalizations in those with VTE compared to those without VTE were primarily related to admissions for cardiovascular problems that included PE and/or DVT (14% vs 5%, respectively; p<0.001). Patients with VTE also had increased outpatient visits in the first year (Table 2). Median number of outpatient visits was 17 in those with VTE compared to 14 in those without VTE at 1 year (p<0.001). Medicare spending for outpatient visits in patients with a VTE diagnosis after DLBCL was $13,851 in the first year compared to $5,863 in those without VTE ($7,988 excess in those with VTE, p<0.001). Similar to hospitalizations, there was no difference in the cost per outpatient visit and the excess costs were due to increased number of visits. Increased outpatient healthcare utilization was also noted in patients who had a history of VTE prior to DLBCL diagnosis compared to those without VTE (median number of outpatient visits: 18 vs 14, p<0.001). CONCLUSION: In conclusion, elderly patients with DLBCL and VTE (diagnosed both before and after DLBCL diagnosis) have substantially higher healthcare utilization compared to those without VTE, resulting from both increased hospitalizations and outpatient visits in the first year after cancer diagnosis; these translate into higher Medicare spending. These findings identify a need for thromboprophylaxis in high risk patients after DLBCL diagnosis and future studies should assess cost-benefit analysis with thromboprophylaxis. Figure 1 Figure 1. Disclosures Gangaraju: Alexion: Consultancy; Sanofi Genzyme: Consultancy.

2020 ◽  
Vol 38 (15) ◽  
pp. 1664-1675 ◽  
Author(s):  
Tanaya Shree ◽  
Qian Li ◽  
Sally L. Glaser ◽  
Ann Brunson ◽  
Holden T. Maecker ◽  
...  

PURPOSE Therapeutic advances for diffuse large B-cell lymphoma (DLBCL) have led to an increasing number of survivors. Both DLBCL and its treatments perturb the immune system, yet little is known about immune health during extended survivorship. METHODS In this retrospective cohort study, we compared 21,690 survivors of DLBCL from the California Cancer Registry (CCR) to survivors of breast, prostate, head and neck, and melanoma cancers. We linked their CCR records to a statewide database documenting hospital, emergency room, and ambulatory surgery visits and investigated the incidence of autoimmune conditions, immune deficiencies, and infections 1-10 years after cancer diagnosis. RESULTS We found elevated incidence rate ratios (IRRs) for many immune-related conditions in survivors of DLBCL compared with other cancer survivors, including significantly and consistently elevated IRRs for viral and fungal pneumonias (up to 10.8-fold), meningitis (up to 5.3-fold), as well as humoral deficiency (up to 17.6-fold) and autoimmune cytopenias (up to 12-fold). IRRs for most conditions remained high even in the late survivorship period (5-10 years after cancer diagnosis). The elevated risks could not be explained by exposure to chemotherapy, stem-cell transplantation, or rituximab, except for IRRs for humoral deficiency, which were consistently higher after the incorporation of rituximab into DLBCL treatments. CONCLUSION To our knowledge, this is the largest cohort study with extended follow-up to demonstrate impaired immune health in survivors of DLBCL. The observed persistent, elevated risks for autoimmune diseases, immune deficiencies, and infectious conditions may reflect persistent immune dysregulation caused by lymphoma or treatment and may lead to excess morbidity and mortality during survivorship. Improved understanding of these risks could meaningfully improve long-term care of patients with DLBCL.


2006 ◽  
Vol 115 (1-2) ◽  
pp. 22-27 ◽  
Author(s):  
Luigi Rigacci ◽  
Luca Nassi ◽  
Renato Alterini ◽  
Valentina Carrai ◽  
Giovanni Longo ◽  
...  

2015 ◽  
Vol 24 (11) ◽  
pp. 1521-1528 ◽  
Author(s):  
Laura Deckx ◽  
Marjan van den Akker ◽  
Mieke van Driel ◽  
Paul Bulens ◽  
Doris van Abbema ◽  
...  

eLife ◽  
2015 ◽  
Vol 4 ◽  
Author(s):  
Ruoqing Chen ◽  
Amanda Regodón Wallin ◽  
Arvid Sjölander ◽  
Unnur Valdimarsdóttir ◽  
Weimin Ye ◽  
...  

A parental cancer diagnosis is psychologically straining for the whole family. We investigated whether a parental cancer diagnosis is associated with a higher-than-expected risk of injury among children by using a Swedish nationwide register-based cohort study. Compared to children without parental cancer, children with parental cancer had a higher rate of hospital contact for injury during the first year after parental cancer diagnosis (hazard ratio [HR] = 1.27, 95% confidence interval [CI] = 1.22-1.33), especially when the parent had a comorbid psychiatric disorder after cancer diagnosis (HR = 1.41, 95% CI = 1.08-1.85). The rate increment declined during the second and third year after parental cancer diagnosis (HR = 1.10, 95% CI = 1.07-1.14) and became null afterwards (HR = 1.01, 95% CI = 0.99-1.03). Children with parental cancer also had a higher rate of repeated injuries than the other children (HR = 1.13, 95% CI = 1.12-1.15). Given the high rate of injury among children in the general population, our findings may have important public health implications.


Blood ◽  
2021 ◽  
Vol 138 (Supplement 1) ◽  
pp. 4581-4581
Author(s):  
Veronica A Guerra ◽  
Marisol Ocampo ◽  
Mike Cusnir

Abstract Introduction: DLBCL represents the most common lymphoma of the elderly, with R-CHOP remaining the standard of care. For elderly patients survival and outcomes data remains limited. Reduced dose R-mini-CHOP was demonstrated to be safe and effective treatment for elderly patients with overall survival of 58%. Defining predictor factors of response and identifying patients that benefit from R-CHOP remains essential. Methods: Retrospective analysis of elderly patients (pts) with frontline DLBCL and high-grade FL treated with R-mini-CHOP and R-CHOP between April 2014 and June 2021. Adult pts 75 years and older were included in the analysis. We performed a chart review to obtain treatment responses and analyze correlations between clinical, molecular characteristics and outcomes. A comparative study with outcomes of standard R-CHOP treatment was conducted. Primary objective was to determine safety and efficacy of R-mini-CHOP in elderly pts. Secondary objectives include overall response rates (ORR), overall survival (OS), and progression-free survival (PFS) after R-mini-CHOP compared with standard R-CHOP. Results: A total of 22 frontline elderly pts 75 years and older were included. Twenty pts (91%) were >80 years, with a median age of 83 years. Most patients had a diagnosis of DLBCL (86%), with stage III-IV in 61%. LDH was increased in 54% of pts. Fifteen pts had a high-risk IPI score (68%). Baseline characteristics are listed in Table 1. Sixteen pts (73%) completed at least 3 cycles of therapy, with a median of 4 cycles (range 1-6). Nineteen pts were evaluable for response. With a median follow-up of 16 months, the overall response rate (ORR) was 79%, including 53% complete response and 26% partial response. Figure 1. The overall survival (OS) was 36 months with a progression-free survival of 22 months and event-free survival of 16 months. With a 2-year OS and PFS of 63% and 44%, respectably, with a median duration of response of 44 months. A total of 7 pts died (32%), 3 pts from disease progression (14%), 3 pts from infection (14%), and 1 pt from bleeding (4%); and the 4-week mortality rate was 18%. Response rates were compared with a contemporary group treated with standard R-CHOP therapy. Significant differences were observed between both subgroups with an increased performance status (PS>2) (P=<0.001), LDH (P=0.015), and high-risk IPI score (P=0.002) among R-mini-CHOP pts compared to R-CHOP pts. With a significantly younger median age of 78 years for R-CHOP vs 83 years for R-mini-CHOP pts (P=<0.001). Table 1. Univariate analysis for predictors of response revealed a PS equal to 2 or higher to be significantly associated with decreased response rates. (Odds ratio 0.1, P=0.007) Among R-CHOP treated pts, the ORR was 96% with 76% complete responses, while the OS, PFS, and EFS were not reached. Figure 2. Conclusions: Dose-reduced R-mini-CHOP is an effective and safe therapy for elderly patients with a diagnosis of DLBCL and high-grade FL. Response rates compared favorably with previously reported 2-year OS 58% and PFS 47% by the GELA study. Compared with contemporary subgroup treated with R-CHOP therapy showed higher response rates with significantly improved OS and PFS. However, pts in this group were younger with a significantly lower IPI and PS. Further comparison analysis with historical R-CHOP and R-CVP therapy is undergoing Figure 1 Figure 1. Disclosures No relevant conflicts of interest to declare.


Blood ◽  
2004 ◽  
Vol 104 (11) ◽  
pp. 4577-4577
Author(s):  
Luigi Rigacci ◽  
Luca Nassi ◽  
Renato Alterini ◽  
Valentina Carrai ◽  
Franco Bernardi ◽  
...  

Abstract The results of treatment of aggressive NHL in elderly patients is relatively poor. The use of protocol specifically devised for eldery patients can reduce hematological and extrahematological toxicity but yield worst results, particularly in high-risk IPI patients. Recentely Coiffier et al. have showed that the standard therapy for patients over 60 years with aggressive lymphoma was rituximab plus CHOP. With the aim to improve dose intensity in elderly large cell lymphoma patients and intermediate-high or high-risk IPI score we planned treatment with rituximab 375 mg/sqm on day 0 and CHOP therapy on day +2 given every 2 weeks, with G-CSF starting from day + 7 to + 11 and a profilaxis with cotrimoxazole twice weekly and itraconazole 100 mg day. With an intention to treat analysis we have included in the study, from June 2002 to June 2004, 25 patients with the following characteristics: IPI score 2 in 8 patients (32%), score 3 in 10 (40%) and score 4–5 in 7 (28%). Two patients had diagnosis of follicular grade III lymphoma and the other 23 diffuse large B-cell lymphoma. Eighteen patients (72%) had abnormal value of LDH and 18 patients had one or more extranodal sites involved. The median age was 64 years (60–76), seven patients (28%) were stage II, four (16%) were stage III and fourteen (56%) were stage IV. The aims of the present study were: 1) feasibility 2) toxicity 3) response to therapy. Twenty-two patients completed the estabilished 6 cycles and were evaluable, one patient stopped the treatment after three cycles due to infections the remaining two patients are in treatment. Six patients delayed one cycle and one patient two cycles, due to trombocytopenia or neutropenia. Only eight out 135 cycles were delayed (6%). Sixteen out 23 (70%) patients obtained complete remission (CR) and after a median follow-up of 11 months (1 – 22 months) the disease-free survival was 79%, three patients (19%) relapsed. Two of these patients died rapidly after relapse and one obtained a second CR. Three out 6 patients with a partial response obtained a CR after a salvage therapy, two died and one is still in therapy. With a median follow-up of 15 months (3–25 months) the overall survival was 78%. No remarkable extrahematological toxicity was observed, in particular, as regards cardiotoxicity, we did not observe significant variation of left ventricular ejection rate in comparison with the diagnostic ones, except one patient who, after the sixth cycle, presented a significant reduction of left ventricular ejection which rapidly recovered after he was admitted at hospital. In conclusion we observed that dose intensified CHOP with rituximab was feasible and lack of severe toxicity in elderly patients with aggressive and high risk prognosis lymphoma.


Blood ◽  
2008 ◽  
Vol 112 (11) ◽  
pp. 1013-1013
Author(s):  
Akmal Safwat ◽  
Lena Specht ◽  
Flemming Hansen ◽  
Mads Hansen ◽  
Jesper Jurlander ◽  
...  

Abstract Background: To further improve the results achieved by adding Rituximab (R) and shortening chemotherapy interval in elderly patients, an effective but relatively non-toxic treatment modality is needed. We tested therefore the addition of low dose total body irradiation (LTBI) of 1,6 Gy given after chemo-immunotherapy. Methods: A multicenter, phase II trial including patients >60 yrs with stage II-IV, CD20-positive DLBCL was performed between 2003 and 2007. Patients received 6x R-CHOP-14 + 2x R alone followed by LTBI given as 2 courses of 4 daily fractions of 0,2 Gy separated by 2 weeks of rest. Radiotherapy to sites of bulky (>7.5 cm) disease was given according to the local guidelines of the participating centres. Results: Forty two patients were included. Observation time ranged from 3 to 47 months with median follow up of 24 months. The median age was 67 years; 62% had stage III or IV; 48% had B symptoms and 36% had bulky (> 7.5 cm) disease; 50% had ECOG score ≥ 1; 76% had elevated LDH and 57% had IPI of >2. Twenty four patients (57%) achieved a CR or CRu at the end of chemotherapy, while 12 (28.5%) were in PR. One of the 12 PR patients refused LTBI. Of the remaining 11 PR patients who received LTBI, 8 (82%) achieved CR in the first follow up after LTBI while the remaining 3 patients had initially stable disease but progressed shortly after. One patient (2%) progressed under chemotherapy while seven patients (17%) relapsed after achieving CR. Six of these refractory/relapsed cases presented with IPI ≥ 3. The 3-yr event-free and progression-free survival values were 64.8% (SE: 8.7%) and 73.5% (SE: 8.9%), respectively, while the 3-yr overall survival was 85.4% (SE: 5.5%). There were 3 toxic deaths (7.1%) due to sepsis occurring during chemotherapy. Ninteen of 235 cycles of CHOP (8%) were given at reduced dose levels in 3 patients (7%), while 3 cycles (1.3%) were delayed but given at 100% dose level. None of the 305 injections of Rituximab were dose reduced. Only one of 31 patients (3%) got his second LTBI cycle at 75% of the planned dose because of thrombocytopenia. CTC Gr 3–4 neutropenia occurred following 50 of 250 R-CHOP-14 cycles (20%). CTC Gr. 3–4 thrombocytopenia was seen in 8 pts (22%) following LTBI. Conclusions: Despite the high risk profile of the patient cohort enrolled in this trial, the 3-yr outcome values match the results of the best performing recent phase III clinical trials designed for elderly patients with DLBCL. Adding LTBI to 6 cycles of R-CHOP-14 was well tolerated and effective in converting the majority of PRs into CRs. Therefore, it may provide survival benefit and should be tested in a randomised setting.


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