2015, Number 4
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Rev Hematol Mex 2015; 16 (4)
Efficacy and safety of two schemes of rescue chemotherapy administered to patients with relapse of acute lymphoblastic leukemia
Alvarado-Ibarra M, Tapia-Enríquez AL, López-Hernández M, Álvarez-Vera JL, Ortiz-Zepeda M, Ramos-León E
Language: Spanish
References: 25
Page: 271-280
PDF size: 457.58 Kb.
ABSTRACT
Background: The course and prognosis of patients with acute lymphoblastic leukemia (ALL) in adults persist still bad despite the new treatment with which account, a significant percentage of patients experience relapse and rescue schemes offer low frequencies of complete remission (CR) with major toxicity and treatment related mortality (TRM); with overall survival and disease free survival shortened.
Objective: To compare the efficacy and safety of chemotherapy rescue schemes administered to patients with relapsed acute lymphoblastic leukemia treated at the Hematology Service of CMN 20 de Noviembre, in Mexico City.
Patients and method: A retrospective, longitudinal and comparative cohort, from January 2000 to January 2015, were included patients over 15 years of age with relapsed ALL who received chemotherapy rescue schemes of own protocols called LAL or LAMMP-A; we reviewed their clinical, electronic and tracking sheets designed for hematologists of the Service. The complete remission was evaluated at day 28 postchemotherapy and haematological and non-haematological toxicity was evaluated according to WHO classification.
Results: A total of 48 patients were evaluable, 12 treated with LAL and 36 treated with LAMMP-A; they were no differences in sex, age, risk, leukocyte count, bone marrow blasts, lactic dehydrogenase and time to relapse (p≥0.4). The overall complete remission was 28%, in the LAMMP-A group, the complete remission was attained in 23% and was 63% in those treated with LAL (p=0.021). Sex showed influence on the complete remission in patients treated with LAMMP A with remission of 21% of men and 77% of women (p =0.001), blasts count less than 50% and the risk of leukemia also showed prognostic influence on complete remission in the patientes receiving the LAL protocol (p≤0.024). The only predictor of survival was the RC. The treatment related mortality was 22%, with no differences in terms of hematologic and non hematologic toxicity and hospitalization days.
Conclusions: Chemotherapy rescue schedules used in CMN 20 de Noviembre, ISSSTE, in Mexico City, offer complete remission similar to those reported in the literature, with TRM ant toxicity also similar, LAL scheme has a higher frequency of complete remission when compared with LAMMP-A scheme, finding no difference in relation to safety and treatment related mortality.
REFERENCES
Pui CH, Robison LL, Look At. Acute lymphoblastic leukemia. Lancet 2008;371:1030-1043.
Vardiman JW, Thiele J, Arber DA, Brunning RD, et al. The 2008 revision of the World Health Organization (WHO) classification of myeloid neoplasms and acute leukemia: rationale and important changes. Blood 2009;114:937-951.
Jabbour EJ, Faderl S, Kantarjian HM. Adult acute lymphoblastic leukemia. Mayo Clin Proc 2005;80:1517-1527.
Siegel R, MA J, Zou Z, Jemal A. Cancer Statistics, 2014. CA Cancer J Clin 2014;64:9-29.
Rowe M. Prognostic factors in adult acute lymphoblastic leukaemia. Br J Haematol 2010:150:389-405.
Moorman AV, Chilton L, Wilkinson J, Ensor HM, et al. A population-based cytogenetic study of adults with acute lymphoblastic leukemia. Blood 2010:115:206-214.
Rowe JM, Buck G, Burnett AK, Chopra R, et al. Induction therapy for adults with acute lymphoblastic leukaemia: results of more than 1500 patients from the international ALL trial: MRC UKALL XII/ECOG E2993. Blood 2005;106:3760-3767.
Moorman AV, Harrison CJ, Buck GA, et al. Karyotype is an independent prognostic factor in adult acute lymphoblastic leukemia (ALL): analysis of cytogenetic data from patients treated on the Medical Research Council (MRC) UKALLXII/Eastern Cooperative Oncology Group (ECOG) 2993 trial. Blood 2007:109:3189-3197.
Schultz KR, Pullen DJ, Sather HN, Shuster JJ, et al. Risk- and response-based classification of childhood B-precursor acute lymphoblastic leukemia: a combined analysis of prognostic markers from the Pediatric Oncology Group (POG) and Children’s Cancer Group (CCG). Blood 2007:109:926-935.
Fielding AK, Richards SM, Chopra R, Lazarus HM, et al. Outcome of 609 adults after relapse of acute lymphoblastic leukaemia (ALL); an MRC UKALL12/ECOG 2993 study. Blood 2007;109:944-950.
Oriol A, Vives S, Hernández-Rivas JM. Outcome after relapse of acute lymphoblastic leukemia in adult patients included in four consecutive risk-adapted trials by the PETHEMA Study Group. Hematologica 2010;95:589-596.
Zwaan CM, Rizzari C, Mechinaud F,Lancaster DL, et al. Dasatinib in children and adolescents with relapsed or refractory leukemia: results of the CA180-018 phase I doseescalation study of the Innovative Therapies for Children with Cancer Consortium. J Clin Oncol 2013;31:2460-2468.
Benjamini O, Dumlao TL, Kantarjian H, O’Brien S, et al. Phase II trial of hyper CVAD and dasatinib in patients with relapsed Philadelphia chromosome positive acutelymphoblastic leukemia or blast phase chronic myeloid leukemia. Am J Hematol 2014;89:282-287.
Faderl S, Thomas DA, O’Brien S, Ravandi F, et al. Augmented hyper-CVAD based on dose-intensified vincristine, dexamethasone, and asparaginase in adult acutelymphoblastic leukemia salvage therapy. Clin Lymphoma Myeloma Leuk 2011;11:54-59.
Françoise Huguet, Thibaut Leguay, Emmanuel Raffoux, Philippe Rousselot, et al . Clofarabine for the treatment of Adult Acute Lymphoid Leukemia A review article by the GRAALL intergroup. Leukemia Lymphoma 2014;4:1-39.
Ahn JS, Yang DH, Jung SH, Lee JJ, et al. Clinical efficacy of mitoxantrone and Ara-C with or without etoposide salvage chemotherapy in adult patients with relapsed or refractory acute lymphoblastic leukemia: retrospective multicenter study of the Korean Adult ALL Working Party. Acta Haematol 2015;133:91-97.
Liedtke M, Dunn T, Dinner S, Coutré SE, et al. Salvage therapy with mitoxantrone, etoposide and cytarabine in relapsed or refractory acute lymphoblastic leukemia. Leuk Res 2014;38:1441-1445.
Gökbuget N, Stanze D, Beck J, Diedrich H, et al. Outcome of relapsed adult lymphoblastic leukemia depends on response to salvage chemotherapy, prognostic factors, and performance of stem cell transplantation. Blood 2012;120:2032-2041.
López-Hernández MA, Alvarado-Ibarra M, Jiménez-Alvarado RM, De Diego-Flores JE, González-Avante C. Adolescentes con leucemia aguda linfoblástica de novo: eficacia y seguridad de un protocolo pediátrico versus uno de adultos. Gac Méd Méx 2008;144:485-489.
DeAngelo DJ, Yu D, Johnson JL, et al. Nelarabine induces complete remissions in adults with relapsed or refractory T lineage acute lymphoblastic leukemia or lymphoblastic lymphoma: Cancer and Leukemia Group B study 19801. Blood 2007;109:5136-5142.
Topp MS, Gökbuget N, Zugmaier G, Klappers P, et al. Phase II trial of the anti-CD19 bispecific T cell-engager blinatumomab shows hematologic and molecular remissions in patients with relapsed or refractory B-precursor acute lymphoblastic leukemia. JCO 2014:32:4134-4140.
Faderl S, Thomas Da, O’brien S, Ravandi F, et al. Augmented hyper-CVAD based on dose-intensified vincristine, dexamethasone, and asparaginase in adult acute lymphoblastic leukemia salvage therapy. Clin Lymphoma Myeloma Leuk 2011;11:54-59.
Wolach O, Stone RM. Blinatumomab for the Treatment of Philadelphia chromosome-negative, precursor B-cell acute lymphoblastic leukemia. Clin Cancer Res 2015;21:4262-4269.
Weiss MA, Aliff TB, Frankel SR, Kalayco ME, et al. A single, high dose of idarubicin combined with cytarabine as induction therapy for adult patients with recurrent or refractory acute lymphoblastic leukemia. Cancer 2002;95:581-587.
Domínguez SJ, Rodríguez Garrido JN, Sanchez M, Martín E. Efectividad y seguridad del régimen FLAG-IDA en leucemias agudas resistentes o recidivantes. Farm Hosp 2012;36:261-267.