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Evaluation of the CLL-IPI in relapsed and refractory chronic lymphocytic leukemia in idelalisib phase-3 trials
被引:15
作者:
Soumerai, Jacob D.
[1
,2
]
Ni, Ai
[2
]
Xing, Guan
[3
]
Huang, Julie
[3
]
Furman, Richard R.
[4
]
Jones, Jeffrey
[5
]
Sharman, Jeffrey P.
[6
]
Hallek, Michael
[7
]
Adewoye, Adeboye H.
[3
]
Dubowy, Ronald
[3
]
Dreiling, Lyndah
[3
]
Zelenetz, Andrew D.
[2
]
机构:
[1] Massachusetts Gen Hosp, Boston, MA 02114 USA
[2] Mem Sloan Kettering Canc Ctr, 1275 York Ave, New York, NY 10021 USA
[3] Gilead Sci Inc, 353 Lakeside Dr, Foster City, CA 94404 USA
[4] New York Presbyterian Hosp, Weill Cornell Med Coll, New York, NY USA
[5] Ohio State Univ, Comprehens Canc Ctr, Columbus, OH 43210 USA
[6] Willamette Valley Canc Inst & Res Ctr, Springfield, OR USA
[7] Univ Cologne, Cologne, Germany
关键词:
Chronic lymphocytic leukemia;
CLL-IPI;
idelalisib;
lymphoma;
leukemia;
prognostication;
GENE MUTATION STATUS;
GENOMIC ABERRATIONS;
ZAP-70;
EXPRESSION;
CD38;
SURVIVAL;
COMBINATION;
OFATUMUMAB;
PREDICTOR;
RITUXIMAB;
IBRUTINIB;
D O I:
10.1080/10428194.2018.1540782
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
The CLL-IPI is a risk-weighted prognostic model for previously untreated patients with chronic lymphocytic leukemia (CLL), but has not been evaluated in patients with relapsed CLL or on novel therapies. We evaluated the CLL-IPI in 897 patients with relapsed/refractory CLL in 3 randomized trials testing idelalisib (PI3K inhibitor). The CLL-IPI identified patients as low (2.2%), intermediate (12.8%), high (48.7%), and very high (36.2%) risk and was prognostic for survival (log-rank p<.0001; C-statistic 0.706). Of CLL-IPI factors, age >65, 2-microglobulin >3.5mg/L, unmutated immunoglobulin heavy chain variable region gene, and deletion 17p/TP53 mutation were independently prognostic, but Rai I-IV or Binet B/C was not. The CLL-IPI is prognostic for survival in relapsed CLL and with idelalisib therapy. However, low/intermediate risk is uncommon, and regression parameters of individual factors in this risk-weighted model appear different in relapsed CLL. Reassessment of the weighting of the individual variables might optimize the model in this setting.
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页码:1438 / 1446
页数:9
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