Prognostic Impact of Extranodal Diffuse Large B-Cell Lymphoma in the Era of Immunochemotherapy and PET/CT Staging

Blood ◽  
2014 ◽  
Vol 124 (21) ◽  
pp. 1630-1630
Author(s):  
Tarec Christoffer El-Galaly ◽  
Diego Villa ◽  
Musa Alzahrani ◽  
Jakob Werner Hansen ◽  
Laurie H. Sehn ◽  
...  

Abstract Background: Extranodal disease is common in diffuse large B-cell lymphoma (DLBCL), and involvement of more than one extranodal site is associated with a worse outcome. 18F-fluorodeoxyglucose PET/CT (PET/CT) is the current state-of-the-art for staging of DLBCL, and has shown to be much more sensitive for the detection of extranodal involvement than a stand-alone CT scan. Therefore, a re-evaluation of the clinical significance of extranodal disease among PET/CT staged DLBCL patients is warranted. Patients and Methods: We retrospectively included patients from Aalborg (2007-2012), Copenhagen (2009-2012), and British Columbia (2011-2012) in the present study. The inclusion criteria were, i) newly diagnosed DLBCL, ii) R-CHOP or R-CHOP like first-line treatment, and iii) PET/CT staging. The written PET/CT files were reviewed for disease stage and extranodal sites of involvement. The relationship between number of involved sites, extranodal locations and outcome were assessed with simple Cox regression analyses. Extranodal locations with p<0.1 in univariate analysis were entered in a multivariable Cox regression analysis together with the following International Prognostic Index (IPI) factors: age > 60 years, elevated LDH, ECOG performance score >1. Results: A total of 444 patients with a median age of 65 years (range 16-90) and a male:female ratio of 1.3 were included in the study. Of these patients 28% (n=98) had Ann Arbor stage I disease, 16% (n=72) stage II disease, 16% (n=71) stage III disease, and 46% stage IV disease (n= 203). LDH was elevated in 51% (n=224), and 17% (n=74) had ECOG performance status >1. B-symptoms were present in 37% (n=164) and 26% (n=114) had a bulky mass =/> 10 cm. With a median follow-up of 2.4 years (range 0.5-6.5) in patients still alive at the time of analysis, the 3-year OS and PFS were 73% and 69%, respectively. Extranodal disease was diagnosed in 286 (64%) of the patients. The anatomic locations of extranodal disease and their relations to outcome are shown in Table I. Figure 1A and B show the PFS and OS curves when patients are grouped according to the number of involved extranodal sites. Patients with one or two extranodal sites of involvement had similar outcome (3-year PFS 68% vs. 70%), whereas all patients with involvement of more than three extranodal sites progressed. Conclusions: Extranodal involvement is diagnosed in more than half of all newly diagnosed DLBCL patients staged with PET/CT. Bone/bone marrow involvement was the most common site and associated with a worse outcome. Thus, detection of these lesions with PET/CT is clinically important. The presence of extranodal disease is generally associated with a worse outcome, but our data suggest that the optimal cut-off for prognostication in PET/CT staged patients may be more than two sites rather than more than one site, as according to the IPI. Abstract 1630 Table1: Extranodal DLBCL and their relationship with outcome in PET/CT staged patients treated with R-CHOP. Empty boxes represent variables not included in multivariate models. Site Frequency, n (%) HR, univariate HR, multivariate PFS OS PFS OS Lung 33 (7%) 1.56, p=0.002 1.46, p=0.26 Not significant Liver 34 (8%) 2.39, p=0.001 2.43, p=0.002 Not significant Not significant Bone/bone marrow (PET/CT) 127 (29%) 2.49, p<0.001 2.53, p<0.001 1.77, p=0.007 1.66, p=0.03 Bone marrow indolent NHL (biopsy) 28 (6%) 0.86, p=0.70 0.94, p=0.87 Bone marrow DLBCL (biopsy) 43 (10%) 2.55, p<0.001 2.66, p<0.001 Not significant Not significant Gastrointestinal 35 (8%) 1.27, p=0.43 1.02, p=0.96 Kidney 13 (3%) 2.10, p=0.06 1.63, p=0.29 Not significant Soft tissue and muscle 46 (10%) 1.18, p=0.58 1.17, p=0.64 Paranasal sinus 15 (3%) 1.57, p=0.28 1.69, p=0.25 Pleural fluid 16 (4%) 2.82, p=0.005 3.23, p=0.003 2.43, p=0.02 2.53, p=0.02 Testicular 13/252 (5%) 2.42, p=0.22 1.81, p=0.41 Female genitals 10/192 (5%) 3.38, p=0.006 3.76, p=0.003 Figure 1A and B: PFS (Figure 1A) and OS (Figure 1B) in patients grouped according to the number of extranodal sites involved: zero (blue), 1 (green), 2 (grey), 3 (purple), >4 (red). Figure 1A and B:. PFS (Figure 1A) and OS (Figure 1B) in patients grouped according to the number of extranodal sites involved: zero (blue), 1 (green), 2 (grey), 3 (purple), >4 (red). Disclosures No relevant conflicts of interest to declare.

Oncotarget ◽  
2016 ◽  
Vol 7 (14) ◽  
pp. 19072-19080 ◽  
Author(s):  
Jin-Hua Liang ◽  
Jin Sun ◽  
Li Wang ◽  
Lei Fan ◽  
Yao-Yu Chen ◽  
...  

2011 ◽  
Vol 91 (5) ◽  
pp. 687-695 ◽  
Author(s):  
Junshik Hong ◽  
Yukyung Lee ◽  
Yeonjeong Park ◽  
Seog Gyun Kim ◽  
Kyung Hoon Hwang ◽  
...  

Blood ◽  
2011 ◽  
Vol 118 (21) ◽  
pp. 5204-5204
Author(s):  
Junshik Hong ◽  
Yukyung Lee ◽  
Seog Gyun Kim ◽  
Kyung Hoon Hwang ◽  
Soon Ho Park ◽  
...  

Abstract Abstract 5204 Backgrounds: As a bone marrow bopsy (BMB) is a painful and invasive procedure with a restrictive reliability as only a limited area of the bone marrow (BM) can be evaluated, role of FDG-PET/CT to demonstrate lymphomatous BM involvement as an alternative or at least a complementary to BMB is an area of interest. Several previous studies exist but most of them included heterogeneous types of lymphomas with various treatments. Patients and methods: To evaluate the role of FDG-PET/CT in detecting BM involvement, pre-treatment bilateral BMBs and FDG-PET/CT scans of 89 patients with diffuse large B-cell lymphoma (DLBCL) treated with standard immunochemotherapy, rituximab-CHOP were reviewed and analyzed. Uptake more than liver parenchyma intensity on FDG-PET/CT was interpreted as 'with a possibility' of involvement. The final interpretation on the possibility of BM involvement in each patient was reported after discussion among three nuclear medicine physicians and results of BMB were blinded at the time of FDG-PET/CT review. Fourteen patients (15.7%) had lymphomatous involvement based on BMB (BMB+) and 17 patients (19.1%) had the possibility of BM involvement on FDG-PET/CT (FDG-PET/CT+). Seventy-two patients (80.8%) had concordant results between BMB and FDG-PET/CT (7 patients were positive for both and 65 patients were negative for both), but 17 patients (19.2%) had a discordant interpretation (7 patients were BMB+ and FDG-PET/CT-, and 10 for BMB- and FDG-PET/CT+; table 1). Although BMB+ patients had an inferior 2-year EFS (37.0% vs. 79.8%, p < 0.001) and OS (36.3% vs. 81.0%, p < 0.001) compared to BMB- patients, no differences in EFS (62.6% vs. 72.7%, p = 0.185) and OS (59.4% vs. 78.0%, p = 0.146) were shown between FDG-PET/CT+ and FDG-PET/CT- patients. Six of 7 patients with BMB+ and FDG-PET/CT+ had a diffuse involvement on FDG-PET/CT whereas 9 of 10 patients with BMB- and FDG-PET/CT+ had a focal BM involvement on FDG-PET/CT (table 2). Six of 7 patients with diffuse involvement on FDG-PET/CT were BMB+ whereas only 1 of 10 patients with focal BM involvement on FDG-PET/CT were BMB+ (table 2). It is likely therefore that patients with diffuse BM involvement on FDG-PET/CT had higher probability for BMB+ and they might have poorer survival than those with focal BM involvement. Conclusion: The results suggest that FDG-PET/CT had a limited value to detect BM involvement in patients with DLBCL. It may not be justified to upgrade patient's Ann Arbor stage to IV according to focal hypermetabolic BM lesion on FDG-PET/CT. Until additional results on the role of FDG-PET/CT in detecting BM involvement available, FDG-PET/CT should be used as an adjuvant rather than an alternative in detecting BM involvement in patients with newly diagnosed DLBCL. Disclosures: No relevant conflicts of interest to declare.


Blood ◽  
2009 ◽  
Vol 114 (22) ◽  
pp. 5006-5006
Author(s):  
Ru Feng ◽  
Meng Xu ◽  
Yongqiang Wei ◽  
Fen Huang ◽  
Tong Zhao

Abstract Abstract 5006 Diffuse large B-cell lymphoma (DLBCL) has an obvious heterogeneity for a set of morphological, immunological phenotype, genetics and clinical manifestations. We found some patients suffered in bone invovlement at early stage. However some patients are not even if many of primary lesions or at the advanced stage. Is this is a universal or accident phenomenon? Is there any regularity for the occurrence of bone invovlement? As we all know, CD44 is a important antigent in normal development of B cells, which express in post-germinal center. It has a negative contro with the expression of Bcl-6, and has a a positive control with Stat-3. CD44 is also a cell surface glycoprotein and the principle receptor for hyaluronan and have multiple splice forms, such as CD44H and CD44v6. In the immune system, CD44 is called a homing receptor. The goal of our study is to evaluate if using a panel of markers such as CD20, CD44H, CD44v6,Bcl-6, Mum-l and Stat3 by immunohistochemistry defines prognosis in patients with DLBCL. We expect to find out some effective indexes for prognosis and bone marrow involvement. Materials and Methods Results 1. Case imformation: There are male 67 cases (55.8%) and 53 cases (44.2%) of female in the 120 cases. The median age is 55 years. 77 cases of primary lymph nodes (60%) and 48 cases of primary lymph node outside (40%). The Median follow-up of 120 patient was17 months, range to 6-148 month 2. The percentage of expression for CD20, CD44H, CD44v6, Bcl-6, Stat3 and Mum-1 in the 120 cases studied were as follows: 95.0%, 66.0%, 55.8%,54.2%,41.7%,46.7%. 3. Survival for single factor and multi-factor analysis: The single factor survival analysis showed that Hans group, Bcl-6/Stat-3 group, chemotherapy ± Rituximab, age, systemic symptoms, LDH level, bone marrow involvement, IPI score, number of extranodal involvement, Bcl-6, CD44H, CD44v6 on the survival of patients with DLBCL influential. In the Cox multivariate analysis, only chemotherapy ± Rituximab, age, extranodal involvement and CD44v6 have a significant statistical significance on the survival of patients with DLBCL (P = 0.000, 0.001, 0.000 and 0.009 respectively). 4. The associativity with antigen expression and clinical factors. It showed that the expression of CD44H had a positive correlation with bone marrow involvement (P 0.022), and implied a poor effect (P 0.003). The expression of CD44v6 also had a negative correlation with effect (P 0.000) and had a positive correlation with bone marrow involvement (P 0.052). The expression of Bcl-6 had a negative correlation with age and extranodal involvement (P 0.025 A0.005);the expression of Stat-3 had a negative correlation with pathology stage (P 0.030); the expression of Mum-1 had a positive correlation with age and extranodal involvement (P 0.014 A0.023), but had a negative correlation with bone marrow involvement (P 0.028). The rest had no statistics, P>0.05. 5. The associativity with antigens expression. It showed that the expressions of CD44H and CD44v6 had a positive correlation (P 0.000); the expression of CD44v6 and Stat-3 also had a positive correlation (P 0.045); the expression of Bcl-6 with Stat-3, Mum-1 had a negative correlation (P 0.013 A0.000);the expression of Stat-3 and Mum-1 also had a positive correlation (P 0.007). 6. Bcl-6 (-) ACD44v6 (+) and Stat-3 (+) provide actively singal to choose rituximab for DLBCL patients. Conclusions ACKNOWLEDGMENTS. We thank Hilda Ye for helpes and discussions. Disclosures No relevant conflicts of interest to declare.


2017 ◽  
Vol 6 (11) ◽  
pp. 2507-2514 ◽  
Author(s):  
Tzu-Hua Chen-Liang ◽  
Taida Martín-Santos ◽  
Andrés Jerez ◽  
Guillermo Rodríguez-García ◽  
Leonor Senent ◽  
...  

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