Response criteria for NHL:: Importance of 'normal' lymph node size and correlations with response rates

被引:58
作者
Grillo-López, AJ
Cheson, BD
Horning, SJ
Peterson, BA
Carter, WD
Varns, CL
Klippenstein, DL
Shen, CD
机构
[1] Idec Pharmaceut Corp, San Diego, CA 92121 USA
[2] NCI, CTEP, Rockville, MD USA
[3] Stanford Univ, Palo Alto, CA 94304 USA
[4] Univ Minnesota, Minneapolis, MN USA
[5] San Diego Diagnost Radiol, San Diego, CA USA
[6] Roswell Pk Canc Inst, Buffalo, NY 14263 USA
关键词
clinical trials; non-Hodgkin's lymphoma; response criteria;
D O I
10.1023/A:1008332713631
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Oncologic literature cites many different definitions of critical response measurements. Patients and methods: Response criteria (RC) for non-Hodgkin's lymphoma (NHL) were developed by lymphoma experts, endorsed by international lymphoma clinicians, and applied to a 166-patient rituximab (Rituxan(R), MabThera(R)) trial by a third-party, blinded panel of NHL experts (LEXCOR). Retrospectively, we analyzed this data using variations of the original RC and comparing with recently published RC. Results: The definition of a 'normal' lymph node affected the complete response (CR) rate (less than or equal to 1.0 x 1.0 cm, 6%; less than or equal to 1.5 x 1.5 cm, 18%; less than or equal to 2.0 x 2.0 cm, 28%); overall response rate (ORR) was not affected. CR rates increased progressively without greater than or equal to 28 days response confirmation: 12% vs. 6% (less than or equal to 1.0 x 1.0 cm), 26% vs. 18% (less than or equal to 1.5 x 1.5 cm), and 36% vs. 28% (less than or equal to 2.0 x 2.0 cm). CR rate and duration of response (DR) were unaffected when only the six largest, rather than all lesions, were measured. When the new RC were applied, CR rate (32%) was higher and DR (13.9 months) and time to progression (15.6 months) were shorter in complete responders. Conclusions: Standard RC must be consistently and rigorously applied for accurate comparisons between studies.
引用
收藏
页码:399 / 408
页数:10
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