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仅MYC基因重排而非扩增与弥漫性大B细胞淋巴瘤和无法分类的B细胞淋巴瘤患者的不良预后相关。

Sole rearrangement but not amplification of MYC is associated with a poor prognosis in patients with diffuse large B cell lymphoma and B cell lymphoma unclassifiable.

作者信息

Landsburg Daniel J, Falkiewicz Marissa K, Petrich Adam M, Chu Benjamin A, Behdad Amir, Li Shaoying, Medeiros L Jeffrey, Cassaday Ryan D, Reddy Nishitha M, Bast Martin A, Vose Julie M, Kruczek Kimberly R, Smith Scott E, Patel Priyank, Hernandez-Ilizaliturri Francisco, Karmali Reem, Rajguru Saurabh, Yang David T, Maly Joseph J, Blum Kristie A, Zhao Weiqiang, Vanslambrouck Charles, Nabhan Chadi

机构信息

Division of Hematology/Oncology, University of Pennsylvania, Philadelphia, PA, USA.

Robert Wood Johnson Medical School, Rutgers University, New Brunswick, NJ, USA.

出版信息

Br J Haematol. 2016 Nov;175(4):631-640. doi: 10.1111/bjh.14282. Epub 2016 Jul 29.

Abstract

Rearrangement of MYC is associated with a poor prognosis in patients with diffuse large B cell lymphoma (DLBCL) and B cell lymphoma unclassifiable (BCLU), particularly in the setting of double hit lymphoma (DHL). However, little is known about outcomes of patients who demonstrate MYC rearrangement without evidence of BCL2 or BCL6 rearrangement (single hit) or amplification (>4 copies) of MYC. We identified 87 patients with single hit lymphoma (SHL), 22 patients with MYC-amplified lymphoma (MYC amp) as well as 127 DLBCL patients without MYC rearrangement or amplification (MYC normal) and 45 patients with DHL, all treated with either R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone) or intensive induction therapy. For SHL and MYC amp patients, the 2-year progression-free survival rate (PFS) was 49% and 48% and 2-year overall survival rate (OS) was 59% and 71%, respectively. SHL patients receiving intensive induction experienced higher 2-year PFS (59% vs. 23%, P = 0·006) but similar 2-year OS as compared with SHL patients receiving R-CHOP. SHL DLBCL patients treated with R-CHOP, but not intensive induction, experienced significantly lower 2-year PFS and OS (P < 0·001 for both) when compared with MYC normal patients. SHL patients appear to have a poor prognosis, which may be improved with receipt of intensive induction.

摘要

MYC重排与弥漫性大B细胞淋巴瘤(DLBCL)和无法分类的B细胞淋巴瘤(BCLU)患者的不良预后相关,尤其是在双打击淋巴瘤(DHL)的情况下。然而,对于那些显示MYC重排但无BCL2或BCL6重排证据(单打击)或MYC扩增(>4拷贝)的患者的预后知之甚少。我们确定了87名单打击淋巴瘤(SHL)患者、22名MYC扩增淋巴瘤(MYC amp)患者、127名无MYC重排或扩增的DLBCL患者(MYC正常)以及45名DHL患者,所有患者均接受了R-CHOP(利妥昔单抗、环磷酰胺、阿霉素、长春新碱、泼尼松)或强化诱导治疗。对于SHL和MYC amp患者,2年无进展生存率(PFS)分别为49%和48%,2年总生存率(OS)分别为59%和71%。接受强化诱导的SHL患者2年PFS更高(59%对23%,P = 0·006),但与接受R-CHOP的SHL患者相比,2年OS相似。与MYC正常的患者相比,接受R-CHOP而非强化诱导治疗的SHL DLBCL患者2年PFS和OS显著更低(两者P均<0·001)。SHL患者似乎预后不良,接受强化诱导可能会改善预后。

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