Abstract:Background: B-cell chronic lymphocytic leukemia (BCLL) in dogs generally is considered an indolent disease, but previous studies indicate a wide range in survival times.Objectives: We hypothesized that BCLL has a heterogeneous clinical course, similar to chronic lymphocytic leukemia in humans. We aimed to assess presentation and outcome in dogs with BCLL and evaluate the prognostic relevance of clinical and flow cytometric factors. Animals: One hundred and twenty-one dogs with BCLL diagnosed by flow cytometry.… Show more
“…12,25 However, dogs with lymphocytosis in this study appeared to have a much more aggressive clinical course with an OS of 133 days, as compared to a MST of 300 to 480 days 12,24 for dogs with BCLL, despite a majority of dogs having a lymphocytosis of <60 000/μL which was associated with an improved prognosis for dogs with BCLL. 12 MCL, another subtype comprised of small to intermediate-sized B-cells, primarily affects the spleen in dogs and nodal MCL appears quite uncommon. 3,20,21 We hypothesized that Ki67 expression, which is a marker of cellular proliferation, would be a useful prognostic factor for small cell B-cell lymphoma.…”
Section: Clinical Outcome and Survival Analysiscontrasting
confidence: 53%
“…12,24 It is possible dogs with BCLL were included in this study as a subset of BCLL cases can have nodal involvement. 12,25 However, dogs with lymphocytosis in this study appeared to have a much more aggressive clinical course with an OS of 133 days, as compared to a MST of 300 to 480 days 12,24 for dogs with BCLL, despite a majority of dogs having a lymphocytosis of <60 000/μL which was associated with an improved prognosis for dogs with BCLL. 12 MCL, another subtype comprised of small to intermediate-sized B-cells, primarily affects the spleen in dogs and nodal MCL appears quite uncommon.…”
Section: Clinical Outcome and Survival Analysismentioning
confidence: 99%
“…We previously measured Ki67 expression on control B-cells from healthy dog blood and lymph node samples (n = 12). 12…”
Background
Nodal small cell B‐cell lymphoma subtypes in dogs cannot be distinguished by flow cytometry and information regarding treatment, prognosis, and outcome are limited.
Hypothesis/Objectives
Objectives were to describe outcome in dogs with nodal small cell B‐cell lymphoma diagnosed by flow cytometry and correlate clinical and laboratory data with survival. We hypothesized that B‐cell Ki67 expression measured by flow cytometry is associated with shorter progression free survival (PFS) and overall survival (OS).
Animals
Forty‐nine dogs with nodal small cell B‐cell lymphoma, defined by >80% CD21+ B‐cells by flow cytometry and small‐sized B‐cells by forward scatter.
Methods
Retrospective study reviewing treatment and outcome data extracted from medical records. Percentage of Ki67‐expressing B‐cells was measured by flow cytometry. Clinical, laboratory, and flow cytometry data were assessed for association with outcome.
Results
Median percentage of B‐cell Ki67 was 41% (range, 3%‐97%). Median PFS was 119 days and median OS was 222 days (n = 49). Among cases treated with CHOP‐based chemotherapy (n = 32), median PFS was 70 days, median OS was 267 days, and 50% of cases achieved complete response. Low percentage of B‐cell Ki67 (≤11%) was associated with prolonged OS by univariable analysis. Greater age, substage B, high B‐cell CD25 expression and low B‐cell CD21 and class II major histocompatibility complex expression by flow cytometry were independently associated with shorter OS.
Conclusions and Clinical Importance
Most nodal small cell B‐cell lymphoma cases had aggressive disease. Low Ki67 expression can help identify cases with better prognosis. Age, substage, and flow cytometry variables are useful prognostic factors.
“…12,25 However, dogs with lymphocytosis in this study appeared to have a much more aggressive clinical course with an OS of 133 days, as compared to a MST of 300 to 480 days 12,24 for dogs with BCLL, despite a majority of dogs having a lymphocytosis of <60 000/μL which was associated with an improved prognosis for dogs with BCLL. 12 MCL, another subtype comprised of small to intermediate-sized B-cells, primarily affects the spleen in dogs and nodal MCL appears quite uncommon. 3,20,21 We hypothesized that Ki67 expression, which is a marker of cellular proliferation, would be a useful prognostic factor for small cell B-cell lymphoma.…”
Section: Clinical Outcome and Survival Analysiscontrasting
confidence: 53%
“…12,24 It is possible dogs with BCLL were included in this study as a subset of BCLL cases can have nodal involvement. 12,25 However, dogs with lymphocytosis in this study appeared to have a much more aggressive clinical course with an OS of 133 days, as compared to a MST of 300 to 480 days 12,24 for dogs with BCLL, despite a majority of dogs having a lymphocytosis of <60 000/μL which was associated with an improved prognosis for dogs with BCLL. 12 MCL, another subtype comprised of small to intermediate-sized B-cells, primarily affects the spleen in dogs and nodal MCL appears quite uncommon.…”
Section: Clinical Outcome and Survival Analysismentioning
confidence: 99%
“…We previously measured Ki67 expression on control B-cells from healthy dog blood and lymph node samples (n = 12). 12…”
Background
Nodal small cell B‐cell lymphoma subtypes in dogs cannot be distinguished by flow cytometry and information regarding treatment, prognosis, and outcome are limited.
Hypothesis/Objectives
Objectives were to describe outcome in dogs with nodal small cell B‐cell lymphoma diagnosed by flow cytometry and correlate clinical and laboratory data with survival. We hypothesized that B‐cell Ki67 expression measured by flow cytometry is associated with shorter progression free survival (PFS) and overall survival (OS).
Animals
Forty‐nine dogs with nodal small cell B‐cell lymphoma, defined by >80% CD21+ B‐cells by flow cytometry and small‐sized B‐cells by forward scatter.
Methods
Retrospective study reviewing treatment and outcome data extracted from medical records. Percentage of Ki67‐expressing B‐cells was measured by flow cytometry. Clinical, laboratory, and flow cytometry data were assessed for association with outcome.
Results
Median percentage of B‐cell Ki67 was 41% (range, 3%‐97%). Median PFS was 119 days and median OS was 222 days (n = 49). Among cases treated with CHOP‐based chemotherapy (n = 32), median PFS was 70 days, median OS was 267 days, and 50% of cases achieved complete response. Low percentage of B‐cell Ki67 (≤11%) was associated with prolonged OS by univariable analysis. Greater age, substage B, high B‐cell CD25 expression and low B‐cell CD21 and class II major histocompatibility complex expression by flow cytometry were independently associated with shorter OS.
Conclusions and Clinical Importance
Most nodal small cell B‐cell lymphoma cases had aggressive disease. Low Ki67 expression can help identify cases with better prognosis. Age, substage, and flow cytometry variables are useful prognostic factors.
“…The estimated median RFP and lymphoma related survival time for all dogs were 414 days (95% confidence interval (CI), range 228–600 days) and 442 days (95% CI, range 236–648 days), respectively, in a study published by Pioggi et al [ 49 ]. Another study reported 121 cases treated by chemotherapy, with a median survival time (MST) of 300 days (range 1–1644 days) [ 50 ]. In yet another study, median RFP was 196 days (range 22–1656 days) and OST was 292 days (range 40–2246 days) of dogs receiving CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisolone) based protocols [ 51 ].…”
Various mechanisms are known to be involved in the development of multidrug resistance during cancer treatment. P-glycoprotein (P-gp) decreases the intracellular concentrations of cytotoxic drugs by an energy-dependent efflux mechanism. The aim of this study was to investigate the predictive value of P-gp function based on the evaluation of P-gp activity in tumor cells obtained from canine B-cell lymphoma patients at diagnosis. P-gp function of 79 immunophenotyped canine lymphoma samples was determined by flow cytometry using the Calcein assay. Dogs were treated with either the CHOP or the L-CHOP protocol, a subset of relapsed patients received L-asparaginase and lomustine rescue treatments. Among the 79 dogs, the median overall survival time was 417 days, and the median relapse-free period was 301 days. 47 percent of the samples showed high P-gp activity, which was significantly higher in Stage IV cancer patients compared to Stage II + III and V. Whereas staging was associated with major differences in survival times, we found that the intrinsic P-gp activity of tumor cells measured at diagnosis is not predictive for therapy outcome. Further studies are needed to identify the intrinsic and acquired resistant mechanisms that shape therapy response and survival in B-cell canine lymphoma patients.
“…In fact, many bulldogs were started on prednisone and chlorambucil with a presumptive diagnosis of chronic lymphocytic leukaemia based on blood film review. In humans and dogs, B‐cell chronic lymphocytic leukaemia (B‐CLL) is considered an indolent disease, in which many patients with early‐stage disease can be monitored without therapy 1,16–19 . Polyclonal B‐cell lymphocytosis of English bulldogs (PBLEB), a recently described non‐neoplastic disease of predominantly young, male English bulldogs is also indolent and characterized by an expansion of small mature B lymphocytes without peripheral lymph node involvement 13 .…”
T-cell leukemia/lymphoma accounts for roughly 30% of all types of lymphoproliferative neoplasia in dogs. Two forms of T-cell lymphoma (T-zone and peripheral T-cell lymphoma) exhibit breed-specific predilections. During the course of routine immunophenotyping, we observed a breed-specific presentation of a unique form of T-cell leukaemia in young English bulldogs. To describe the clinical presentation and
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.