Lymphoid Neoplasia

2017 ◽  
Vol 47 (1) ◽  
pp. 53-70 ◽  
Author(s):  
Emily D. Rout ◽  
Paul R. Avery
Keyword(s):  
2021 ◽  
Vol 11 (4) ◽  
pp. 249
Author(s):  
Irene Dogliotti ◽  
Simone Ragaini ◽  
Francesco Vassallo ◽  
Elia Boccellato ◽  
Gabriele De Luca ◽  
...  

Background. Bendamustine is a cytotoxic alkylating drug with a broad range of indications as a single agent or in combination therapy in lymphoid neoplasia patients. However, its tolerability in elderly patients is still debated. Methods: An observational, retrospective study was carried out; patients with chronic lymphocytic leukemia (CLL) or lymphoma, aged ≥ 65 years old, treated with bendamustine-based regimens in first or subsequent lines between 2010 and 2020 were considered eligible. Results: Overall, 179 patients aged ≥ 65 years were enrolled, 53% between 71 and 79 years old. Cumulative Illness Rating Scale (CIRS) comorbidity score was ≥6 in 54% patients. Overall survival (OS) at 12 months was 95% (95% confidence interval [CI]: 90–97%); after a median follow up of 50 months, median OS was 84 months. The overall response rate was 87%, with 56% complete responses; the median time to progression (TTP) was 61 months. The baseline factors affecting OS by multivariable analysis were sex, histological diagnosis, renal function, and planned bendamustine dose, while only type of lymphoma and bendamustine dose impacted on TTP. Main adverse events were neutropenia (grade ≥ 3: 43%) and infections (any grade: 36%), with 17% of patients requiring hospital admission. Conclusions: The responses to bendamustine, as well as survival, are relevant even in advanced age patients, with a manageable incidence of acute toxicity.


Animals ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 1477
Author(s):  
Tamsyn Stephenson ◽  
Natasha Speight ◽  
Wai Yee Low ◽  
Lucy Woolford ◽  
Rick Tearle ◽  
...  

Koala retrovirus, a recent discovery in Australian koalas, is endogenised in 100% of northern koalas but has lower prevalence in southern populations, with lower proviral and viral loads, and an undetermined level of endogenisation. KoRV has been associated with lymphoid neoplasia, e.g., lymphoma. Recent studies have revealed high complexity in southern koala retroviral infections, with a need to clarify what constitutes positive and negative cases. This study aimed to define KoRV infection status in Mount Lofty Ranges koalas in South Australia using RNA-seq and proviral analysis (n = 216). The basis for positivity of KoRV was deemed the presence of central regions of the KoRV genome (gag 2, pol, env 1, and env 2) and based on this, 41% (89/216) koalas were positive, 57% (124/216) negative, and 2% inconclusive. These genes showed higher expression in lymph node tissue from KoRV positive koalas with lymphoma compared with other KoRV positive koalas, which showed lower, fragmented expression. Terminal regions (LTRs, partial gag, and partial env) were present in SA koalas regardless of KoRV status, with almost all (99.5%, 215/216) koalas positive for gag 1 by proviral PCR. Further investigation is needed to understand the differences in KoRV infection in southern koala populations.


2014 ◽  
Vol 03 (10) ◽  
pp. 560-565 ◽  
Author(s):  
Photis Beris ◽  
Monika Nagy ◽  
Daniel Robert ◽  
Kaveh Samii ◽  
Tom McKee ◽  
...  

Blood ◽  
1966 ◽  
Vol 27 (4) ◽  
pp. 435-448 ◽  
Author(s):  
ROBERT C. MELLORS ◽  
Dolores A. Landy ◽  
David Bardell

Abstract Malignant lymphoma was found in 4 of 20 NZB/Bl mice (of the 61st generation) selected for laboratory examinations and autopsy at 9 to 11 months of age. The malignant lymphomas were of two histologic types, reticulum cell sarcoma and pleomorphic malignant lymphoma, the latter term being used to designate malignant neoplasms arising in lymphatic tissue, composed of mesenchymal cells of diverse appearance—mainly plasma cells of blast, immature, mature and Russell-body types but also large primitive (stem) cells, reticulum cells, and lymphocytes of large and small size—and frequently associated with gammopathies. One of the reticulum cell sarcomas was transplantable to, and produced lethal disseminated growth in, other NZB/Bl mice. In each example of malignant lymphoma, warm hemagglutinins (to papain-treated mouse red cells) were demonstrable in serum. Autoimmune hemolytic disease and chronic membranous glomerulonephritis, both of common occurrence in NZB/Bl mice of comparable age, were also present. In one instance of pleomorphic malignant lymphoma, hypergammaglobulinemia of unusual quantity and quality drew attention to the possibility of lymphomatous disease. Some evidence was brought forth indicating that in the majority of instances the autoimmune diseases preceded the malignant lymphomas. While the coexistence of autoimmunity and lymphoid neoplasia conceivably reflects nothing more than chance occurrence, other interpretations were considered: the proliferative advantage engendered in immunologically competent cells in autoimmune disease may be a step in the direction of lymphoid neoplasia; or, in some instances autoantibodies may be produced by, or in response to, the neoplastic lymphoid cells.


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