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The prognostic value of bone marrow involvement at the molecular level in aggressive lymphoma
被引:2
|作者:
Goldschmidt, Neta
[1
]
Darawshy, Fares
[1
]
Kleinstern, Geffen
[2
]
Slyusarevsky, Elena
[1
]
Pogrebijski, Galina
[1
]
Krichevsky, Svetlana
[1
]
Ben-Yehuda, Dina
[1
]
Gatt, Moshe E.
[1
]
机构:
[1] Hadassah Hebrew Univ, Med Ctr, Dept Hematol, Jerusalem, Israel
[2] Hadassah Hebrew Univ, Med Ctr, Sch Publ Hlth, Jerusalem, Israel
关键词:
Gene rearrangement;
bone marrow;
diffuse large B-cell lymphoma;
peripheral T-cell lymphoma;
B-CELL LYMPHOMA;
MINIMAL RESIDUAL DISEASE;
RECEPTOR GENE REARRANGEMENTS;
R-IPI;
IMMUNOGLOBULIN;
PCR;
BIOPSY;
PET/CT;
D O I:
10.1080/10428194.2016.1201569
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
We retrospectively studied the prognostic role of molecular (gene rearrangement, GRR) bone marrow (BM) involvement in diffuse large B-cell lymphoma (DLBCL, 424 patients) and in peripheral T-cell lymphoma (PTCL, 67 patients). When correlating BM GRR to histological findings at diagnosis, the GRR test was more sensitive (p = 0.036) but less specific (p<0.0001) in PTCL than in DLBCL. For DLBCL (but not PTCL), a positive BM GRR correlated with advanced stage (p = 0.0001) and high IPI (p = 0.002), and worsened the progression free survival (PFS) (p = 0.05) and overall survival (OS) (p = 0.01), irrespective of rituximab treatment. Histologic negative/GRR positive cases had worse PFS/OS (p<0.0001) than histologic/GRR double negative cases, however BM GRR was not an independent prognostic survival factor. End-of-treatment BM GRR did not predict survival. We conclude that BM GRR is unjustified as a prognostic tool for PTCL and should be reserved for a subset of DLBCL patients with negative histology of the BM.
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页码:45 / 52
页数:8
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