scholarly journals Prognostic significance of bone marrow infiltration detected by PET-CT in newly diagnosed diffuse large B cell lymphoma

Oncotarget ◽  
2016 ◽  
Vol 7 (14) ◽  
pp. 19072-19080 ◽  
Author(s):  
Jin-Hua Liang ◽  
Jin Sun ◽  
Li Wang ◽  
Lei Fan ◽  
Yao-Yu Chen ◽  
...  
2013 ◽  
Vol 197 (3) ◽  
pp. 776-781 ◽  
Author(s):  
Laura Marconato ◽  
Valeria Martini ◽  
Luca Aresu ◽  
Michele Sampaolo ◽  
Fabio Valentini ◽  
...  

2018 ◽  
Vol 9 (7) ◽  
pp. 1231-1238 ◽  
Author(s):  
Yumei Chen ◽  
Mingge Zhou ◽  
Jianjun Liu ◽  
Gang Huang

Blood ◽  
2011 ◽  
Vol 118 (21) ◽  
pp. 1626-1626
Author(s):  
Luigi Rigacci ◽  
Alberto Fabbri ◽  
Benedetta Puccini ◽  
Enrico Orciuolo ◽  
Alice Pietrini ◽  
...  

Abstract Abstract 1626 Diffuse large B cell lymphoma (DLBCL) is one of the most common types of non-Hodgkin's lymphoma. R-CHOP21 (C21) is considered the standard therapy but a large number of studies tested R-CHOP14 (C14). The aim of our study was to evaluate retrospectively a cohort of patients (pts) treated with C21 or C14. All pts with diagnosis of DLBCL or follicular grade IIIb lymphoma, treated with curative intent were accrued. From January 2002 to December 2010, 123 pts were treated with C21 and 142 were treated with C14. The median age was 63 (range 19–89). The two cohorts of pts were balanced for all clinical characteristics a part for age (<65 or >64 years) with more aged pts in C21 arm (p 0.000), PS with more advanced PS (2–3) in C21 arm (0.000) and LDH value which was more frequently elevated in C14 arm (p: 0.002). After induction therapy 190 pts (71%) obtained a complete remission: 82/123 (67%) after C21 and 108/142 (75%) after C14. After a median period of observation of 31 months 81 pts relapsed, 42 (51%) in the C21 arm and 39 (36%) in the C14 arm. Considering the two therapies, C21 vs C14, no differences were reported in OS, PFS and DFS: 61% vs 68%, 59% vs 58% and 74% vs 61% respectively. In univariate analysis OS was lower in older pts (p: 0.02), advanced stage (p: 0.02), symptomatic disease (p: 0.05), elevated LDH (p: 0.001), bone marrow infiltration (p: 0.02) and intermediate or high risk IPI (p: 0.000); PFS was lower in advanced stage (p: 0.002), symptomatic disease (p: 0.009), elevated LDH (p: 0.001), bone marrow infiltration (p: 0.001) and intermediate high risk IPI (p: 0.000). In multivariate analysis OS was significantly better in low-intermediate IPI risk pts (p: 0.000) and in pts treated with C14 (p: 0.02); the PFS was better in low-intermediate IPI risk pts (p: 0.000). Considering only pts with low or low-intermediate IPI we observed that OS was significantly superior in the group treated with C14 (90% vs 64% p: 0.03), moreover in young pts (< 65 years) OS was better in pts treated with C14 (81% vs 58% p: 0.05). As expected hematological grade III/IV toxicity was more frequent in pts treated with C14, all pts but three (2%) completed the therapy without delay or dose reduction. No differences in extra-hematological toxicity were observed. Conclusions: In conclusion our results confirm that C14 do not improve the results of the standard C21 in the whole lymphoma population but in a subset of pts, young and low/intermediate risk pts, the C14 scheme seems to improve the OS. We will enlarge the cohort of studied patients but further prospective randomized studies are needed to verify this preliminary observations. 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 ◽  
...  

Blood ◽  
2010 ◽  
Vol 116 (21) ◽  
pp. 3127-3127
Author(s):  
Nina Wagner-Johnston ◽  
Nancy L. Bartlett ◽  
Jacqueline E. Payton ◽  
Kathryn Trinkaus ◽  
Akash Sharma ◽  
...  

Abstract Abstract 3127 Background: Circulating nucleic acids have been explored as tumor markers in several malignancies. Lymphoma offers a special opportunity to develop tumor DNA markers. Normal B cells undergo Ig rearrangements to generate antibody diversity. In B cell malignancies, the Ig gene rearrangements are monoclonal. Molecular diagnostic tests are widely employed in tumor specimens to detect these clone-specific Ig rearrangements when histology and immunohistochemistry are ambiguous. While long-lived plasma cells can secrete Ig over years, a B cell can only release its unique clone once. In order to sustain the presence of Ig DNA, ongoing cellular proliferation and death is required, suggesting that detection in the plasma may be a specific marker for presence of lymphoma. We previously reported our experience in screening plasma from patients (pts) with AIDS-related lymphomas (Blood 110(11):1579, 2007). The feasibility of this approach and promising results led to a pilot study evaluating clonal Ig DNA in pts with newly diagnosed diffuse large B cell lymphoma (DLBCL) without HIV. Methods: Plasma is screened for clonal Ig DNA using standardized fluorescently-labeled multiplex primers (InVivoScribe) targeting IgH rearrangements. Rearranged Ig DNA is amplified by polymerase chain reaction (PCR), and the amplified products are separated by size using capillary electrophoresis. International prognostic index (IPI) scores and results of baseline PET/CT scans, including standardized uptake value (SUV)max scores are collected from pts to determine the impact of these findings on the ability to detect clonal Ig DNA. Results: Of 36 plasma specimens evaluated to date, 28 (78%) had clonal IgH rearrangements. Clonal and polyclonal controls yielded appropriate results. Tumor specimens are available from 22 patients, including 19 formalin-fixed paraffin-embedded (FFPE) and 5 fresh frozen tissue (FFT) specimens (2 pts have both FFPE and FFT). Eight FFPE tumor specimens have been evaluated; monoclonal IgH rearrangements were present in 5 (63%), 2 had polyclonal rearrangements, and 1 had no detectable IgH rearrangements. The median IPI scores were 1.5 (75% of pts had scores of 0–2) for the group without detectable plasma clonal Ig DNA and 2 (67% of pts had scores of 0–2) for the group with detectable plasma clonal Ig DNA. Wilcoxon 2-sample test demonstrated no difference between the 2 groups with respect to IPI scores (p= 0.50). Pre-treatment PET/CT scans were interpreted as positive in 30 of 33 pts. Two pts with negative PET/CT and corresponding IPI scores of 0 and 1 respectively, did not have detectable plasma clonal Ig DNA. One pt with a negative PET/CT had an IPI score of 0 and had detectable clonal Ig DNA in the plasma. In a T-test comparison, there was no evidence for a difference in SUVmax among pts with and without detectable clonal Ig DNA (p = 0.31). Conclusions: Circulating clonal Ig DNA is detectable in pts with newly diagnosed DLBCL even with low IPI scores and negative PET/CT scans. Relatively small pt numbers limit the interpretation of the IPI/FDG-PET findings with respect to the detection of clonal Ig DNA in the plasma, and larger studies are needed to better appreciate if there is any correlation. Studies are ongoing to determine whether clonal Ig plasma DNA persists after the initiation of therapy, and whether the presence of clonal Ig DNA in plasma might complement information obtained from early interim FDG-PET in identifying patients likely to fail conventional therapy. Continued analysis of paired tumor/plasma specimens will clarify if plasma clonal Ig DNA is tumor derived. Disclosures: No relevant conflicts of interest to declare.


Leukemia ◽  
2015 ◽  
Vol 30 (1) ◽  
pp. 238-242 ◽  
Author(s):  
T P Vassilakopoulos ◽  
G A Pangalis ◽  
S Chatziioannou ◽  
S Papageorgiou ◽  
M K Angelopoulou ◽  
...  

2019 ◽  
Vol 60 (10) ◽  
pp. 2477-2482 ◽  
Author(s):  
Uri Greenbaum ◽  
Itai Levi ◽  
Odelia Madmoni ◽  
Yotam Lior ◽  
Kayed Al-Athamen ◽  
...  

2011 ◽  
Vol 86 (3) ◽  
pp. 246-255 ◽  
Author(s):  
Olivera Markovic ◽  
Dragomir Marisavljevic ◽  
Vesna Cemerikic ◽  
Maja Perunicic ◽  
Sasa Savic ◽  
...  

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