Dramatic and Sustained Hematologic Complete Remission with Denileukin Diftitox (ONTAK®) in a Patient with Refractory Adult T-Cell Leukemia (ATL).

Blood ◽  
2005 ◽  
Vol 106 (11) ◽  
pp. 4638-4638
Author(s):  
Sheryl L. Ziegler ◽  
Connie Augustyniak ◽  
Leo I. Gordon ◽  
Andrew M. Evens

Abstract Background: Acute ATL is an aggressive hematologic malignacy with a median survival of 9 months. It is a malignant disease of mature activated T-cells caused by human T-cell lymphotropic virus (HTLV-I). Chemotherapy is disappointing for ATL, particulary for acute ATL. Antiretroviral therapy with combination interferon/zivodudine increases responses and improves survival. However, the disease is characterized by repeated relapses with few novel therapeutic options available for patients. Allogeneic stem cell transplant is the only known cure for ATL. We present a case report of refractory acute ATL and relapsed leukemic meningitis with marked clinical response and hematologic remission to single-agent denileukin diftitox. Method: The patient (pt) is a 55 year-old black man (from Mississippi) who presented Janurary 2004 with mild fatigue, lymphocytosis and was found to be in chronic-phase ATL. Peripheral blood (PB) flow cytometry showed a 72% clonal T-cell population: CD3+, CD7−, CD5+, CD2+, CD4+, and CD25+. Serology was + for HTLV-1 and T-cell genes were rearranged. Results: The pt was initially observed without therapy. Within 6 months, he developed profound fagtigue, weight loss, severe headaches, eye pain, tinnitus and myalgias. White blood count (WBC) increased and acute ATL and leukemic meningitis was diagnosed. The pt began daily zidovudine/α interferon (1 gram and 9 million units, respectively) and intrathecal (IT) methotrexate. Cerebral spinal fluid (CSF) cleared with slight decrease in WBC, and improvement in symptoms. He relapsed 5 months later with reccurrence of constitutional and CNS symptoms. Repeated ommaya catheter CSF analysis at that time was negative, however, a lumbar puncture was floridly positive. The pt subsequently began daily aresenic trioxide and weekly pegylated interferon therapy. There was a transient decline in symtoms and WBC with clearing of the CSF, although the patient quickly relapsed with massive PB and CSF infiltration of ATL cells (PB absolute lymphocyte count 89.3 cc3/mm3) and severe constitutional symtpoms including 20 pound weight loss. Acute T-cell Leukemia Treatment Time Line Acute T-cell Leukemia Treatment Time Line At this relapse, the pts CSF T-cells were 87% CD25-positive. Denileukin diftitox was started at 18 μg/kg/day IV(days 1–5) every 21 days with concurrent IT cytarabine. The only other concomitant medications were diflucan and gabapentin (no steroids given at any time). The pt had rapid resolution of all symptoms and normalization of the WBC following his 1st cycle. The pt has tolerated 8 denileukin diftitox cycles well. PB flow cytometry now shows 1% CD25 T-cell positivity. The pt is currently asymptomatic and proceeding to 6/6 matched sibling allogeneic transplant. Conclusion: This case demonstrates a marked and sustained response to single-agent denilekin difitox. There is 1 published case of ATL treated with denileukin diftitox. However, that pt was also treated with hyper-CVAD chemotherapy. Despite the anecdotal nature of this case, we believe it is important to report this information, especially in a disease with often few therapeutic options.

2007 ◽  
Vol 7 (7) ◽  
pp. 472-474 ◽  
Author(s):  
Andrew M. Evens ◽  
Sheryl L. Ziegler ◽  
Rohit Gupta ◽  
Connie Augustyniak ◽  
Leo I. Gordon ◽  
...  

2016 ◽  
Vol 59 (4) ◽  
pp. 569 ◽  
Author(s):  
RekhaA Nair ◽  
Renu Sukumaran ◽  
JayasudhaA Vasudevan

Blood ◽  
2005 ◽  
Vol 106 (11) ◽  
pp. 881-881 ◽  
Author(s):  
Richard R. Furman ◽  
Genadi Iosava ◽  
Luis Isola ◽  
Farhad Ravandi ◽  
Mamia Zodelava ◽  
...  

Abstract Inherited deficiency of purine nucleoside phosphorylase (PNP) is associated with a profound loss of T-cells. This rare clinical condition provides a model for developing specific inhibitors of PNP as therapy for T-cell malignancies. Forodesine is a specific PNP inhibitor that raises plasma 2′-deoxyguanosine (dGuo) and intracellular dGTP levels, leading to T-cell apoptosis. The objective of this study was to determine the efficacy and safety of forodesine in patients with relapsed or refractory T-cell leukemia. Patients received IV forodesine 40 mg/m2 5 days each week (1 cycle) for a total of 6 cycles (8 cycles if dose escalation needed after cycle 2). To date, 21 patients have been treated, 19 of which are T-ALL. Results are based on available data from 13 T-ALL patients. Median number of prior regimens was 4 (range: 1–6). Overall response rate was 38%, including 3 patients with complete response (CR) (23%) and 2 patients with partial response (PR) (15%). Three patients had stable disease and 5 patients had disease progression. Time to progression (TTP) for the 3 CR patients was 80, 119, and 160+ days. One CR patient continues to receive treatment. TTP for the 2 PR patients was 89 and 40 days. Plasma dGuo was elevated in all patients (range: 3.4 to 88.5 μM; predose levels ≤0.004 μM). Treatment was well tolerated. One serious adverse event possibly drug related was CMV pneumonitis in 1 patient. The most common adverse events possibly drug related were nausea (33%), headache (26%), anemia (20%), thrombocytopenia (20%), and weakness (20%). In 1 patient, after 2 doses of forodesine, WBC count dropped dramatically, requiring interruption of treatment for 2 weeks because of tumor lysis syndrome (Figure). After 2 cycles of treatment, the patient achieved a CR. By week 3, platelets and neutrophils recovered, indicating a specificity of forodesine for leukemic cell populations. These study results show that forodesine is active, with minimal toxicity, as a single agent in relapsed or refractory T-cell leukemia. Additional clinical efficacy and safety data will be presented. Effect of Forodesine on Blood Components in One T-All Patient Effect of Forodesine on Blood Components in One T-All Patient


PeerJ ◽  
2021 ◽  
Vol 9 ◽  
pp. e10692
Author(s):  
Jie Meng ◽  
Rui Su ◽  
Luping Wang ◽  
Bo Yuan ◽  
Ling Li

Background The bark of Uncaria rhynchophylla has been traditionally used to treat convulsion, bleeding, hypertension, auto-immune conditions, cancer, and other diseases. The main focus of this research is done for the purpose of exploring the antitumor activity and mechanism of action (MOA) for hirsutine isolated from U. rhynchophylla. Methods Jurkat clone E6-1 cells were treated using 10, 25 and 50 μM for 48 h. Inhibition of cell proliferation due to hirsutine treatment was evaluated by CCK8 assay. Flow cytometry was applied to ascertain Jurkat cell cycle progression and apoptosis after treatment with 10, 25 and 50 μM hirsutine for 48 h. The expression and level of the apoptosis-related genes and proteins was analyzed by Real-time Quantitative polymerase chain reaction (qPCR) and Western blotting method, respectively. Results CCK8 analyses revealed that hirsutine could significantly inhibit the proliferation of Jurkat clone E6-1 cells, in a concentration and time-dependent fashion. Flow cytometry assays revealed that hirsutine could drive apoptotic death and G0/G1 phase arrest in Jurkat cells. Apoptotic cells frequencies were 4.99 ± 0.51%, 13.69 ± 2.00% and 40.21 ± 15.19%, and respective cell cycle arrest in G0/G1 accounted for 34.85 ± 1.81%, 42.83 ± 0.70% and 49.12 ± 4.07%. Simultaneously, compared with the control group, Western blot assays indicated that the up-regulation of pro-apoptotic Bax, cleaved-caspase3, cleaved-caspase9 and Cyto c proteins, as well as the down-regulation of Bcl-2 protein which guards against cell death, might be correlated with cell death induction and inhibition of cell proliferation. QPCR analyses indicated that hirsutine could diminish BCL2 expression and, at the same time, improve Bax, caspase-3 and caspase-9 mRNA levels, thus reiterating a putative correlation of hirsutine treatment in vitro with apoptosis induction and inhibition of cell proliferation (p-value < 0.05). Excessive hirsutine damages the ultrastructure in mitochondria, leading to the release of Cyt c from the mitochondria to cytoplasm in Jurkat clone E6-1 cells, thereby inducing the activated caspase cascade apoptosis process through a mitochondria-mediated pathway. Conclusion An important bioactive constituent—hirsutine—appears to have antitumor effects in human T-cell leukemia, thus enlightening the use of phytomedicines as a novel source for tumor therapy. It is speculated that hirsutine may induce apoptosis of Jurkat Clone E6-1 cells through the mitochondrial apoptotic pathway.


Blood ◽  
2010 ◽  
Vol 116 (21) ◽  
pp. 4144-4144
Author(s):  
Yamin Tian ◽  
Seiichiro Kobayashi ◽  
Nobuhiro Ohno ◽  
Masamichi Isobe ◽  
Mayuko Tsuda ◽  
...  

Abstract Abstract 4144 [Background] Adult T-cell leukemia (ATL) is a malignant disorder caused by human T-cell leukemia virus type I (HTLV-I). Morphological discrimination of leukemic cells from non-leukemic T cells is often difficult in ATL since ATL cells reveal morphological diversity except for typical “flower cells”. Although a study using CD3 gating in flow cytometry reported that ATL cells were distinguishable as a CD3low population from normal lymphocytes, these cells were not well characterised as ATL cells. Considering that defective expression of CD7 as well as CD3 is common in ATL cells, we applied multi-color flow cytometry to detect a putative leukemia-specific cell population in the peripheral blood from ATL patients. [Methods and Results] (1) In flow cytometry, after dead-cell and monocyte removal, CD4+ T lymphocytes were gated on the CD3 versus CD4 plot. Based on cell density and fluorescence intensity of CD3 and CD7 in this population, we designated three subpopulations on this plot: CD3highCD7high, CD3dimCD7dim and CD3dimCD7low(Results of a representative ATL and a control sample are shown in Figure). The proportion of the CD3dim/CD7low subpopulation was significantly higher in acute-type ATL CD4+ lymphocytes than in normal controls(Figure). (2) To extensively characterise this subpopulation, we next estimated the HTLV-I proviral load by quantitative real-time PCR after FACS sorting based on this CD3 versus CD7 plot. In all patient samples, HTLV-I proviral integration was detected in all subpopulations. However, the proviral load was significantly higher in the CD3dim/CD7low subpopulation compared to the CD3high/CD7high subpopulation. Almost all of the cells in the CD3dim/CD7low subpopulation were HTLV-I infected. (3) We next examined CCR4 and CD25 expression in each subpopulation. Both CCR4 and CD25 expression levels were maintained at very low and similar levels throughout all subpopulations in normal control cells and in the CD3high/CD7high subpopulation of patients with ATL as well. In contrast, CCR4 expression was significantly up-regulated in CD3dim/CD7low subpopulation of patients with ATL compared to the CD3high/CD7high subpopulation (MFI: 36.5±17.2 vs. 3.8±1.1). The expression of CD25 was also up-regulated in the subpopulation (MFI: 7.8±8.0 vs. 2.7±1.6). (4) Monoclonal expansion of HTLV-I-infected cells in the CD3dim/CD7low subpopulation was indicated by the genomic integration site analysis using a long inverse polymerase chain reaction (PCR) method. (5) We reviewed the glass-slide specimens of FACS-sorted samples to evaluate the morphology of each subpopulation on the CD3 versus CD7 plot. Atypical lymphocytes with morphology such as a notch in the nucleus were observed in all subpopulations. The majority of sorted cells from CD3dim/CD7low subpopulation showed “flower cell”-like morphology. (6) We also detected a small CD3dim/CD7dim subpopulation other than the CD3dim/CD7low and CD3high/CD7high subpopulations in all patients with acute-type ATL who were analysed(Figure). This subpopulation contained the same clone as the CD3dim/CD7low subpopulation, although a phenotypical difference existed between these subpopulations. [Conclusion] (1) Above findings indicate that leukemic T cells are specifically enriched in a unique CD3dim/CD7low subpopulation of CD4+ T cells in acute-type ATL. This multi-color FACS system may be useful for precisely monitoring disease during chemotherapy, detecting minimal residual disease and analysing ATL cells. (2) Previous reports have revealed that HTLV-I-infected cells transform through multi-step oncogenesis. Detailed analysis of these three subpopulations (CD3high/CD7high, CD3dim/CD7dim and CD3dim/CD7low) may give some insight into oncogenesis of HTLV-I-infected cells. Disclosures: No relevant conflicts of interest to declare.


Blood ◽  
2020 ◽  
Vol 136 (Supplement 1) ◽  
pp. 33-33
Author(s):  
Hugo Henrique de Freitas Ferreira ◽  
Alessandra Suelen Jardim Silva ◽  
Lenilton Silva DA Silva Júnior ◽  
Gustavo Henrique de Medeiros Oliveira ◽  
Maria das Graças Pereira Araujo ◽  
...  

Introduction:Adult T-cell leukemia / lymphoma (ATLL) is a rare type of malignant haemopathy with the Human T-Cell Lymphotropic Virus type I (HTLV-1) as its etiologic agent. The clinical picture includes skin lesions, hypercalcemia, elevated lactate dehydrogenase (LDH), adenomegaly, myelopathy and leukocytosis with atypical TCD4 lymphocytes.Objective:To report a case of a patient from the city of Macau-RN, with ATLL, presenting skin lesions, weight loss (&gt; 13%), leukocytosis and supraclavicular lymph node enlargement. Case Description: Male patient, bricklayer, 67-year-old, hypertensive, was admitted to a hospital in Natal-RN, with severe itching, diffuse exanthematic skin lesions for 13 days, adynamia, associated with progressive, weight loss (P: 73Kg, 63Kg -13.6%), hyporexia, feverish (37.8 ° C), insidious and progressive drowsiness. Physical examination showed palpable lymphadenomegaly in the right supraclavicular chain, 1 cm, mobile and painless. Painful abdomen on deep palpation in the right hypochondrium and left iliac fossa, moderate hepatosplenomegaly. The blood count showed leukocytosis with the presence of atypical lymphocytes with convoluted nucleus (Flow-Cell), Creatinine (6.81), urea 349, hyperuricemia (14.9 mg / dL), hypercalcemia (12.8), LDH (723), Alkaline phosphatase (1388) GGT (183). Abdominal, kidney and urinary tract ultrasound revealed acute pancreatitis with signs of saponification (steatonecrosis of peripancreatic fat) and bilateral acute parenchymal nephropathy, respectively. The transthoracic echocardiogram identified aortic and mitral valve sclerosis. Immunophenotyping by flow cytometry found lymphoproliferative disease of mature TCD4 + cells, and the diagnosis of ATLL was confirmed by the serological reagent for HTLV-1. From then on, adequate treatment for ATLL was started with reversion of the clinical period, currently being followed up on an outpatient basis.Conclusions:The multiprofessional performance with accurate clinical investigation associated and specific laboratory exams such as immunophenotyping by flow cytometry and serological tests are essential for the early diagnosis and treatment of ATLL, a rare entity in the state of Rio Grande do Norte., Brazil and that high mortality when not diagnosed and treated early. Disclosures No relevant conflicts of interest to declare.


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