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Erschienen in: Indian Journal of Hematology and Blood Transfusion 3/2021

18.01.2021 | Short Communication

Study of Three Cases of Primary Refractory T Cell ALL

verfasst von: Reema Singh, Narender Tejwani, Narendra Agrawal, Jyotsna Kapoor, Vishvdeep Khushoo, Pallavi Mehta, Rayaz Ahmed, Dinesh Bhurani

Erschienen in: Indian Journal of Hematology and Blood Transfusion | Ausgabe 3/2021

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Abstract

A significant proportion of T cell acute lymphoblastic leukemia (T-ALL) patients do not achieve complete remission after 4 weeks of induction chemotherapy or relapse early. Salvage chemotherapy for such patients usually results in poor outcome which can be up to 20–30% survival with allogeneic BMT. Nelarabine combined with chemotherapy, in COG AALL0434 study, showed 4-year disease-free survival of 54.8% in patients with primary refractory T ALL. An allogeneic BMT in such patients may further improve outcome. In this report, three patients with primary refractory T cell ALL including a case of ETP-ALL and near ETP-ALL were treated with Nelarabine combined with COG based regime and thereafter an allogeneic stem cell transplantation. All three patients achieved a complete remission with negative minimal residual disease status with one course of therapy, received allo SCT (MSD = 2, Haplo = 1) and are surviving in complete remission at 12 months, 14 months and 25 months of follow up. This report highlights that primary refractory T ALL patient can be successfully treated with Nelarabine in combination with chemotherapy and consolidation with allogeneic SCT to provide maximum chances of long-term survival and cure.
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Metadaten
Titel
Study of Three Cases of Primary Refractory T Cell ALL
verfasst von
Reema Singh
Narender Tejwani
Narendra Agrawal
Jyotsna Kapoor
Vishvdeep Khushoo
Pallavi Mehta
Rayaz Ahmed
Dinesh Bhurani
Publikationsdatum
18.01.2021
Verlag
Springer India
Erschienen in
Indian Journal of Hematology and Blood Transfusion / Ausgabe 3/2021
Print ISSN: 0971-4502
Elektronische ISSN: 0974-0449
DOI
https://doi.org/10.1007/s12288-020-01392-8

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