Cytarabine, Ki‐67, and SOX11 in patients with mantle cell lymphoma receiving rituximab‐containing autologous stem cell transplantation during first remission. Issue 18 (17th June 2013)

• Record Type: Journal Article
• Authors: Chakhachiro, Zaher I.; Saliba, Rima M.; Okoroji, Grace‐Julia; Korbling, Martin; Alousi, Amin M.; Betul, Oran; Anderlini, Paolo; Ciurea, Stefan O.; Popat, Uday; Champlin, Richard; Samuels, Barry I.; Medeiros, L. Jeffrey; Bueso‐Ramos, Carlos; Khouri, Issa F.
• Is Part Of: Cancer. Volume 119:Issue 18(2013)
• Page Start: 3318
• Page End: 3325
• Publication Date: 2013-06-17
• Subjects: Cancer -- Periodicals; Cancer -- Cytopathology -- Periodicals; 616.99405
• DOI: 10.1002/cncr.28219
• Languages: English
• ISSNs: 0008-543X

Abstract

<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="cncr28219-sec-0001" sec-type="section"> <title>BACKGROUND</title> <p>In the current study, the authors report the results of 39 patients with mantle cell lymphoma (MCL) who were treated with chemotherapy and high‐dose rituximab‐containing autologous stem cell transplantation (ASCT) during their first disease remission.</p> </sec> <sec id="cncr28219-sec-0002" sec-type="section"> <title>METHODS</title> <p>The median age of the patients was 54 years. At the time of diagnosis, 87% of patients had Ann Arbor stage IV disease, and 77% had bone marrow involvement. A Ki‐67 level of > 30% was found in 11 of 27 patients (40%), and SOX11 (SRY [sex determining region Y)‐box 11] expression was found to be positive in 17 of 18 patients (94%). Twenty‐seven patients (69%) underwent induction therapy with high‐dose cytarabine‐containing chemotherapy. Rituximab was administered during stem cell collection at a dose of 1000 mg/m<sup>2</sup> on days +1 and +8 after ASCT.</p> </sec> <sec id="cncr28219-sec-0003" sec-type="section"> <title>RESULTS</title> <p>The estimated 4‐year overall survival and progression‐free survival rates were 82% and 59%, respectively. Twelve patients experienced disease recurrence. Fifteen of 16 patients who were alive and in complete remission at 36 months remained so at a median follow‐up of 69 months (range, 38 months‐145 months). The only determinant of recurrence risk found was a Ki‐67 level of > 30%. Seven of 11 patients with a Ki‐67 level > 30% experienced disease recurrence within the first 3 years versus only 3 of 16 patients with a Ki‐67 level ≤ 30% (<italic>P</italic> = .02). Patients who received high‐dose cytarabine did not have a significantly different risk of developing disease recurrence compared with other patients (<italic>P</italic> = .7).</p> </sec> <sec id="cncr28219-sec-0004" sec-type="section"> <title>CONCLUSIONS</title> <p>Administering ASCT with rituximab during stem cell collection and immediately after transplantation may induce a continuous long‐term disease remission in patients with MCL with a Ki‐67 level of ≤ 30%. <bold><italic>Cancer</italic> 2013;119:3318–25</bold>. © <italic>2013 American Cancer Society</italic>.</p> </sec> </abstract>