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Published in: Medical Oncology 1/2015

01-01-2015 | Original Paper

Topotecan combined with Ifosfamide, Etoposide, and l-asparaginase (TIEL) regimen improves outcomes in aggressive T-cell lymphoma

Authors: YaJuan Shao, Mei Guan, ShuChang Chen, Ning Jia, YuZhou Wang

Published in: Medical Oncology | Issue 1/2015

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Abstract

This study evaluated the efficacy and safety of a new regimen consisting of Topotecan, Ifosfamide, Etoposide, and l-asparaginase (TIEL) in treating aggressive T-cell lymphoma. Twenty-four patients were included in the research, eighteen males and six females. Half of the patients were in stages III and IV, and nearly half of them experienced failure of at least one regimen. Eleven were diagnosed as peripheral T-cell lymphoma (PTCL), five extranodal NK/T-cell lymphoma, non-specific, four angioimmunoblastic, and four anaplastic large-cell lymphoma (2 ALK positive). Patients were given 98 cycles of TIEL altogether. The responsive rate to TIEL was 76.9 % among 13 cases who received the regimen as the first-line treatment. Among 11 cases, TIEL was the second- or more-line treatment, the responsive rate was 63.6 %. The median PFS was 32.0 ± 21.0 (95 % CI 0–73.29) months. Median overall survival (OS) was not reached yet. Approximately 41.3 % of patients showed the third- to fourth-degree hematological side effects. Non-hematological toxicity included nausea, vomiting, diarrhea, and abnormal liver function. Among those patients received l-asparaginase, nine experienced mild abnormal coagulation function after 7 days of initiating chemotherapy, and no pancreatic injury was found. TIEL regimen is effective for aggressive T-cell lymphoma with controllable side effect and can be used for more patients.
Literature
1.
go back to reference The Non-Hodgkin’s Lymphoma Classification Project. A clinical evaluation of the international lymphoma study group classification of non-Hodgkin’s lymphoma. Blood. 1997;89(11):3909–18. The Non-Hodgkin’s Lymphoma Classification Project. A clinical evaluation of the international lymphoma study group classification of non-Hodgkin’s lymphoma. Blood. 1997;89(11):3909–18.
2.
go back to reference Sun J, Yang Q, Lu Z, et al. Distribution of lymphoid neoplasms in China: analysis of 4,638 cases according to the World Health Organization classification. Am J Clin Pathol. 2012;138(3):429–34.PubMedCrossRef Sun J, Yang Q, Lu Z, et al. Distribution of lymphoid neoplasms in China: analysis of 4,638 cases according to the World Health Organization classification. Am J Clin Pathol. 2012;138(3):429–34.PubMedCrossRef
3.
go back to reference Kwong YL, Kim WS, Lim ST, et al. SMILE for natural killer/T-cell lymphoma: analysis of safety and efficacy from the Asia Lymphoma Study Group. Blood. 2012;120(15):2973–80.PubMedCrossRef Kwong YL, Kim WS, Lim ST, et al. SMILE for natural killer/T-cell lymphoma: analysis of safety and efficacy from the Asia Lymphoma Study Group. Blood. 2012;120(15):2973–80.PubMedCrossRef
4.
go back to reference Yang L, Liu H, Xu XH, et al. Retrospective study of modified SMILE chemotherapy for advanced-stage, relapsed, or refractory extranodal natural killer (NK)/T cell lymphoma, nasal type. Med Oncol. 2013;30(4):720–6.PubMedCrossRef Yang L, Liu H, Xu XH, et al. Retrospective study of modified SMILE chemotherapy for advanced-stage, relapsed, or refractory extranodal natural killer (NK)/T cell lymphoma, nasal type. Med Oncol. 2013;30(4):720–6.PubMedCrossRef
5.
go back to reference Ping LY, Zheng W, Wang XP. Safety and adverse event profiling of pegylated L-asparaginase combined chemotherapy in the treatment of lymphoma. Zhong Hua Yi Xue Za Zhi. 2012;92(46):3257–60. Ping LY, Zheng W, Wang XP. Safety and adverse event profiling of pegylated L-asparaginase combined chemotherapy in the treatment of lymphoma. Zhong Hua Yi Xue Za Zhi. 2012;92(46):3257–60.
6.
go back to reference Ramya LN, Doble M, Rekha VP. L-asparaginase as potent anti-leukemic agent and its significance of having reduced glutaminase side activity for better treatment of acute lymphoblastic leukaemia. Appl Biochem Biotechnol. 2012;167(8):2144–59.PubMedCrossRef Ramya LN, Doble M, Rekha VP. L-asparaginase as potent anti-leukemic agent and its significance of having reduced glutaminase side activity for better treatment of acute lymphoblastic leukaemia. Appl Biochem Biotechnol. 2012;167(8):2144–59.PubMedCrossRef
7.
go back to reference Yong W, Zheng W, Zhang Y, et al. L-asparaginase-based regimen in the treatment of refractory midline nasal/nasal-type T/NK-cell lymphoma. Int J Hematol. 2003;78(2):163–7.PubMedCrossRef Yong W, Zheng W, Zhang Y, et al. L-asparaginase-based regimen in the treatment of refractory midline nasal/nasal-type T/NK-cell lymphoma. Int J Hematol. 2003;78(2):163–7.PubMedCrossRef
8.
go back to reference Kraut EH, Balcerzak SP, Young D, et al. A phase II study of topotecan in non-Hodgkin’s lymphoma: an Ohio State University phase II research consortium study. Cancer Invest. 2002;20(2):174–9.PubMedCrossRef Kraut EH, Balcerzak SP, Young D, et al. A phase II study of topotecan in non-Hodgkin’s lymphoma: an Ohio State University phase II research consortium study. Cancer Invest. 2002;20(2):174–9.PubMedCrossRef
9.
go back to reference Wiernik PH, Li H, Weller E, et al. Activity of topotecan 21-day infusion in patients with previously treated large cell lymphoma: long-term follow-up of an Eastern Cooperative Oncology Group study (E5493). Leuk Lymphoma. 2012;53(6):1137–42.PubMedCentralPubMedCrossRef Wiernik PH, Li H, Weller E, et al. Activity of topotecan 21-day infusion in patients with previously treated large cell lymphoma: long-term follow-up of an Eastern Cooperative Oncology Group study (E5493). Leuk Lymphoma. 2012;53(6):1137–42.PubMedCentralPubMedCrossRef
10.
go back to reference Crump M, Couban S, Meyer R, et al. Phase II study of sequential topotecan and etoposide in patients with intermediate grade non-Hodgkin’s lymphoma: a National Cancer Institute of Canada Clinical Trials Group study. Leuk Lymphoma. 2002;43(8):1581–7.PubMedCrossRef Crump M, Couban S, Meyer R, et al. Phase II study of sequential topotecan and etoposide in patients with intermediate grade non-Hodgkin’s lymphoma: a National Cancer Institute of Canada Clinical Trials Group study. Leuk Lymphoma. 2002;43(8):1581–7.PubMedCrossRef
11.
go back to reference Schmitz N, Trümper L, Ziepert M, et al. Treatment and prognosis of mature T-cell and NK-cell lymphoma: an analysis of patients with T-cell lymphoma treated in studies of the German High-Grade Non-Hodgkin Lymphoma Study Group. Blood. 2010;116(18):3418–25.PubMedCrossRef Schmitz N, Trümper L, Ziepert M, et al. Treatment and prognosis of mature T-cell and NK-cell lymphoma: an analysis of patients with T-cell lymphoma treated in studies of the German High-Grade Non-Hodgkin Lymphoma Study Group. Blood. 2010;116(18):3418–25.PubMedCrossRef
12.
go back to reference Vose J, Armitage J, Weisenburger D, et al. International peripheral T-cell and natural killer/T-cell lymphoma study: pathology findings and clinical outcomes. J Clin Oncol. 2008;26(25):4124–30.PubMedCrossRef Vose J, Armitage J, Weisenburger D, et al. International peripheral T-cell and natural killer/T-cell lymphoma study: pathology findings and clinical outcomes. J Clin Oncol. 2008;26(25):4124–30.PubMedCrossRef
13.
go back to reference Escalon MP, Liu NS, Yang Y, et al. Prognostic factors and treatment of patients with T-cell non-Hodgkin lymphoma: the M.D. Anderson Cancer Center experience. Cancer. 2005;103(10):2091–8.PubMedCrossRef Escalon MP, Liu NS, Yang Y, et al. Prognostic factors and treatment of patients with T-cell non-Hodgkin lymphoma: the M.D. Anderson Cancer Center experience. Cancer. 2005;103(10):2091–8.PubMedCrossRef
14.
go back to reference Iriyama N, Takahashi H, Hatta Y, et al. Efficacy of a dose-intensified CHOP (Double-CHOP) regimen for peripheral T-cell lymphomas. Oncol Rep. 2012;29(2):805–11.PubMed Iriyama N, Takahashi H, Hatta Y, et al. Efficacy of a dose-intensified CHOP (Double-CHOP) regimen for peripheral T-cell lymphomas. Oncol Rep. 2012;29(2):805–11.PubMed
15.
go back to reference Cheng MF, Chatterjee S, Berger NA. Schedule-dependent cytotoxicity of topotecan alone and in combination chemotherapy regimens. Oncol Res. 1994;6:269–79.PubMed Cheng MF, Chatterjee S, Berger NA. Schedule-dependent cytotoxicity of topotecan alone and in combination chemotherapy regimens. Oncol Res. 1994;6:269–79.PubMed
16.
go back to reference Kaufmann SH, Peereboom D, Buckwalter CA, et al. Cytotoxic effects of topotecan combined with various anticancer agents in human cancer cell lines. J Natl Cancer Inst. 1996;88(11):734–41.PubMedCrossRef Kaufmann SH, Peereboom D, Buckwalter CA, et al. Cytotoxic effects of topotecan combined with various anticancer agents in human cancer cell lines. J Natl Cancer Inst. 1996;88(11):734–41.PubMedCrossRef
17.
go back to reference Smith SM, Johnson JL, Niedzwiecki D, et al. Sequential doxorubicin and topotecan in relapsed/refractory aggressive non-Hodgkin’s lymphoma: results of CALGB 59906. Leuk Lymphoma. 2006;47(8):1511–7.PubMedCrossRef Smith SM, Johnson JL, Niedzwiecki D, et al. Sequential doxorubicin and topotecan in relapsed/refractory aggressive non-Hodgkin’s lymphoma: results of CALGB 59906. Leuk Lymphoma. 2006;47(8):1511–7.PubMedCrossRef
18.
go back to reference Perkins JB, Goldstein SC, Dawson JL, et al. Phase I Study of Topotecan, Ifosfamide, and Etoposide (TIME) with autologous stem cell transplant in refractory cancer: pharmacokinetic and pharmacodynamics correlates. Clin Cancer Res. 2011;17(24):7743–53.PubMedCrossRef Perkins JB, Goldstein SC, Dawson JL, et al. Phase I Study of Topotecan, Ifosfamide, and Etoposide (TIME) with autologous stem cell transplant in refractory cancer: pharmacokinetic and pharmacodynamics correlates. Clin Cancer Res. 2011;17(24):7743–53.PubMedCrossRef
19.
go back to reference Voloschin AD, Betensky R, Wen PY, et al. Topotecan as salvage therapy for relapsed or refractory primary central nervous system lymphoma. J Neuro Oncol. 2008;86(2):211–5.CrossRef Voloschin AD, Betensky R, Wen PY, et al. Topotecan as salvage therapy for relapsed or refractory primary central nervous system lymphoma. J Neuro Oncol. 2008;86(2):211–5.CrossRef
20.
go back to reference Verma N, Kumar K, Kaur G, et al. L-asparaginase: a promising chemotherapeutic agent. Crit Rev Biotechnol. 2007;27(1):45–62.PubMedCrossRef Verma N, Kumar K, Kaur G, et al. L-asparaginase: a promising chemotherapeutic agent. Crit Rev Biotechnol. 2007;27(1):45–62.PubMedCrossRef
21.
go back to reference Foss FM, Sjak-Shie N, Goy A, et al. A multicenter phase II trial to determine the safety and efficacy of combination therapy with denileukin diftitox and cyclophosphamide, doxorubicin, vincristine and prednisone in untreated peripheral T-cell lymphoma: the CONCEPT study. Leuk Lymphoma. 2013;54(7):1373–9.PubMedCrossRef Foss FM, Sjak-Shie N, Goy A, et al. A multicenter phase II trial to determine the safety and efficacy of combination therapy with denileukin diftitox and cyclophosphamide, doxorubicin, vincristine and prednisone in untreated peripheral T-cell lymphoma: the CONCEPT study. Leuk Lymphoma. 2013;54(7):1373–9.PubMedCrossRef
22.
go back to reference Damaj G, Gressin R, Bouabdallah K, et al. Results from a prospective, open-label, phase II trial of bendamustine in refractory or relapsed T-cell lymphomas: the BENTLY trial. J Clin Oncol. 2013;31(1):104–10.PubMedCrossRef Damaj G, Gressin R, Bouabdallah K, et al. Results from a prospective, open-label, phase II trial of bendamustine in refractory or relapsed T-cell lymphomas: the BENTLY trial. J Clin Oncol. 2013;31(1):104–10.PubMedCrossRef
Metadata
Title
Topotecan combined with Ifosfamide, Etoposide, and l-asparaginase (TIEL) regimen improves outcomes in aggressive T-cell lymphoma
Authors
YaJuan Shao
Mei Guan
ShuChang Chen
Ning Jia
YuZhou Wang
Publication date
01-01-2015
Publisher
Springer US
Published in
Medical Oncology / Issue 1/2015
Print ISSN: 1357-0560
Electronic ISSN: 1559-131X
DOI
https://doi.org/10.1007/s12032-014-0402-0

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