Clinical Outcomes in Patients with Diffuse Large B Cell Lymphoma with Partial Responses to First-Line R-CHOP Chemotherapy: Prognostic Value of Secondary IPI Scores and FDG-PET

Blood ◽  
2016 ◽  
Vol 128 (22) ◽  
pp. 4205-4205
Author(s):  
Hyewon Lee ◽  
Yu Ri Kim ◽  
Soo-Jeong Kim ◽  
Yong Park ◽  
Hyeon-Seok Eom ◽  
...  

Abstract Background: Rituximab-containing chemoimmunotherapy (R-CHOP) is a standard treatment for patients with diffuse large B cell lymphoma (DLBCL), with a high response rate. Achievement of only a partial response (PR) was regarded as treatment failure, but data on their prognosis are limited to date. Distinguishing PR from CR is not always clear because of controversies in interpreting 18-fluorodeoxyglucose positron emission tomography (FDG-PET) in rituximab-era. Recent advances have prompted a revision in the response criteria, as recently suggested at the 12th International Conference of Malignant Lymphomas (ICML), emphasizing the prognostic significance of FDG-PET results interpreted using the five-point Deauville score. Based on such changes, the prognosis of PR patients should be re-evaluated. Patients and Methods: We conducted a retrospective multicenter study on behalf of the Consortium for Improving Survival of Lymphoma (CISL), to investigate survival outcomes and to define prognostic factors for PR patients after first-line treatment. A total of 758 patients with histologically proven DLBCL, who received the R-CHOP regimen between January 2005 and December 2013, were assessed. Among them, patients who achieved a PR defined by both computed tomography (CT) and FDG-PET at the end of R-CHOP were included in further analysis. Clinical information at diagnosis and after treatment was collected to determine the prognostic factors affecting the clinical outcome of PR patients. FDG-PET scans were reviewed by physicians and nuclear medicine experts in each institution and interpreted using the Deauville five-point scale. The prognostic role of secondary International Prognostic Index after R-CHOP (IPI2), assessed by restaging, age, performance status, residual multiple extranodal involvements and lactate dehydrogenase (LDH) levels, was evaluated. Progression-free survival (PFS2) and overall survival (OS2), measured from the date of the response assessment after R-CHOP to further progression or death, were determined by Kaplan-Meier methods with log-rank test. We also performed t-tests, χ2 tests, and Cox proportional hazard analysis. Statistical significance was accepted when two-sided p values were <0.05. Results: In total, 88 (11.6%) patients partially responded to R-CHOP with a median age of 53.5 years were searched. Over a median follow-up of 47.8 months, 3-year PFS2 and OS2 rates were 58.8% and 69.4%, respectively. The IPI2 scores were 0-1 (low) in 68.2% and ≥2 (high) in 31.8% of patients. The Deauville scores after R-CHOP were 2-3 (low) in 57.9% and 4 (high) in 42.0% of patients. High (≥2) and low (0-1) IPI2 groups represented 28% and 72% of 3-year PFS2 rates (p <0.001). Patients with Deauville score 4 were also associated with worse 3-year PFS2 rates than those with a lower score (2-3) (40.4% vs. 71.1%, p=0.009). For OS2, IPI2 (47.6% vs. 77.7%, p=0.013) and Deauville score (57.5% vs. 75.3%, p=0.067) were prognostic, although the effect of the Deauville score was not statistically significant. A high-risk group, defined by the IPI2-Deauville index (Table 1), showed significantly lower 3-year rates of PFS2 (17.1% vs. 69.3%, p<0.001) and OS2 (43.4% vs. 75.1%, p=0.006) compared with other groups (Figure 1). In a multivariate analysis, the IPI2-Deauville index was an independent prognostic factor for disease progression (HR 1.76, 95% CI 1.15-2.69, p=0.009), adjusted with initial IPI score and bone marrow involvement at diagnosis. For OS2, the index did not remain significant in a multivariate analysis. Conclusion: Our data shows that patients with DLBCL who achieved a PR to R-CHOP is still a heterogeneous group, and IPI2 and Deauville scores can be useful prognostic factors in addition to initial IPI at diagnosis. Validation through future prospective study would be valuable. Disclosures No relevant conflicts of interest to declare.

2010 ◽  
Vol 84 (6) ◽  
pp. 493-498 ◽  
Author(s):  
Dai Chihara ◽  
Yasuhiro Oki ◽  
Shouji Ine ◽  
Harumi Kato ◽  
Hiroshi Onoda ◽  
...  

Blood ◽  
2012 ◽  
Vol 120 (21) ◽  
pp. 748-748
Author(s):  
Stephen Paul Robinson ◽  
Ariane Boumendil ◽  
Herve Finel ◽  
Harry C Schouten ◽  
Peter Dreger

Abstract Abstract 748 Introduction. The current standard of care for patients who fail first line therapy for diffuse large B cell lymphoma (DLBCL) comprises salvage chemotherapy and an autologous stem cell transplant (SCT). With the development of effective first line immunochemotherapy studies have suggested that the results of salvage autologous SCT have deteriorated and that alternative strategies are required. Myeloablative (MA) allogeneic SCT for DLBCL has been rarely used due largely to the toxicity of the procedure. Consequently reduced intensity conditioning (RIC) regimens prior to allogeneic SCT have been developed. Given these developments we have studied the outcome of both autologous and allogeneic SCT for DLBCL over the last decade. Methods. The EBMT database was searched for patients satisfying the following criteria;- diagnosis DLBCL, diagnosis between 2002 and 2010, age 18–65, first SCT procedure, chemosensitive relapse or primary refractory disease/refractory relapse. Cumulative incidence analysis of non-relapse mortality (NRM) and relapse rate (RR) and Kaplan-Meier estimates of disease free survival (DFS) and overall survival (OS) were calculated. Results. Outcomes for patients with chemosensitive relapse. The 1 and 4 year NRM rates were:- 3.2% and 6.4% for autoSCT, 11.7% and 20% for RIC alloSCT and 20% and 23.9% for MA alloSCT respectively (hazard ratio (HR) RIC allo 4.0, HR MA allo 4.5 both p<0.0001). Time from diagnosis to transplant >1 year was the only other factor associated with a higher NRM. The 4 year RR was 49% for autoSCT, 44.5% for RICalloSCT and 39.4% for MA alloSCT (ns). Only female sex was associated with a lower RR (HR 0.81 p=0.004). The 4 year DFS was 45.5%, 37% and 37% for autoSCT, RICalloSCT and MA alloSCT respectively. The DFS was worse for those patients undergoing a MA alloSCT (HR 1.6 p= 0.007). Female patients (HR 0.88 p=0.05) and those transplanted more than 1 year after diagnosis (HR 0.83 p=0.016) experienced a superior DFS. The 4 year OS was 55%, 57% and 42% for autologous SCT, RIC alloSCT and MA alloSCT respectively. The OS was worse for patients undergoing a MA alloSCT (HR 2.2, p=0.0002) and those over the age of 50 at transplant (HR 1.2, p=0.02). Outcomes for patients with chemosensitive relapse transplanted within 1 year of diagnosis. In this subgroup of patients 585, 20 and 17 received an autologous SCT, RICalloSCT and MA alloSCT respectively. The 4 year DFS was 44.6%, 51.7% and 50.4% and the 4 year OS was 54%, 75.8%, and 59.8% for autoSCT, RIC alloSCT and MA alloSCT respectively. The cohorts were too small to permit a multivariate analysis. Outcomes for patients with primary refractory and refractory relapse. The 1 and 4 year NRM rates were:- 6.6% and 7.3% for autoSCT, 15.4% and 15.4% for RIC alloSCT and 19.2% and 19.2% for MA alloSCT respectively. MA alloSCT (HR 2.9, p=0.004) and female sex (HR 1.7, p=0.04) were the only factors associated with a higher NRM. The 4 year RR was 73% for autoSCT, 81.5% for RICalloSCT and 61.3% for MA alloSCT (ns). Only female sex was associated with a lower RR (HR 0.77 p=0.08). The 4 year DFS was 20.7%, 3.9% and 20.7% for autoSCT, RICalloSCT and MA alloSCT respectively. The DFS was significantly better for female patients (HR 0.82 p= 0.04). The 4 year OS was 28%, 8.6% and 17.9% for autologous SCT, RIC alloSCT and MA alloSCT respectively. In multivariate analysis OS was significantly worse for patients undergoing a MA alloSCT (HR 1.5, p=0.02). The year of transplant and the use of immunochemotherapy as first line therapy had no impact on transplant outcomes. Conclusions. Over the last decade patients with chemosensitive relapse can achieve prolonged DFS following an autoSCT at a rate similar to that observed in the pre-Rituximab era. The NRM following an allogeneic SCT continues to be significant without being associated with lower relapse rates although the outcomes following a RICalloSCT are comparable to those following an autoSCT. Disclosures: No relevant conflicts of interest to declare.


2015 ◽  
Vol 39 (5) ◽  
pp. 810-815 ◽  
Author(s):  
Hugo J.A. Adams ◽  
John M.H. de Klerk ◽  
Rob Fijnheer ◽  
Ben G.F. Heggelman ◽  
Stefan V. Dubois ◽  
...  

2021 ◽  
pp. 1-9
Author(s):  
François Allioux ◽  
Damaj Gandhi ◽  
Jean-Pierre Vilque ◽  
Cathy Nganoa ◽  
Anne-Claire Gac ◽  
...  

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Pierre Decazes ◽  
Vincent Camus ◽  
Elodie Bohers ◽  
Pierre-Julien Viailly ◽  
Hervé Tilly ◽  
...  

Abstract Background 18F-FDG PET/CT is a standard for many B cell malignancies, while blood DNA measurements are emerging tools. Our objective was to evaluate the correlations between baseline PET parameters and circulating DNA in diffuse large B cell lymphoma (DLBCL) and classical Hodgkin lymphoma (cHL). Methods Twenty-seven DLBCL and forty-eight cHL were prospectively included. Twelve PET parameters were analysed. Spearman’s correlations were used to compare PET parameters each other and to circulating cell-free DNA ([cfDNA]) and circulating tumour DNA ([ctDNA]). p values were controlled by Benjamini–Hochberg correction. Results Among the PET parameters, three different clusters for tumour burden, fragmentation/massiveness and dispersion parameters were observed. Some PET parameters were significantly correlated with blood DNA parameters, including the total metabolic tumour surface (TMTS) describing the tumour–host interface (e.g. ρ = 0.81 p < 0.001 for [ctDNA] of DLBLC), the tumour median distance between the periphery and the centroid (medPCD) describing the tumour’s massiveness (e.g. ρ = 0.81 p < 0.001 for [ctDNA] of DLBLC) and the volume of the bounding box including tumours (TumBB) describing the disease’s dispersion (e.g. ρ = 0.83 p < 0.001 for [ctDNA] of DLBLC). Conclusions Some PET parameters describing tumour burden, fragmentation/massiveness and dispersion are significantly correlated with circulating DNA parameters of DLBCL and cHL patients. These results could help to understand the pathophysiology of B cell malignancies.


2021 ◽  
Vol 39 (S2) ◽  
Author(s):  
L. Pezzullo ◽  
G. Cassiordor0 ◽  
R. Rosamilio ◽  
I. Ferrara ◽  
S. Luponio ◽  
...  

2019 ◽  
Vol 61 (1) ◽  
pp. 40-45 ◽  
Author(s):  
Anne-Ségolène Cottereau ◽  
Christophe Nioche ◽  
Anne-Sophie Dirand ◽  
Jérôme Clerc ◽  
Franck Morschhauser ◽  
...  

2013 ◽  
Vol 104 (9) ◽  
pp. 1245-1251 ◽  
Author(s):  
Young Wha Koh ◽  
Hee Sang Hwang ◽  
Se Jin Jung ◽  
Chansik Park ◽  
Dok Hyun Yoon ◽  
...  

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