The efficacy and tolerability of adriamycin, bleomycin, vinblastine, dacarbazine and Stanford V in older Hodgkin lymphoma patients: a comprehensive analysis from the North American intergroup trial E2496

被引:117
作者
Evens, Andrew M. [1 ]
Hong, Fangxin [2 ,3 ]
Gordon, Leo I. [4 ]
Fisher, Richard I. [5 ]
Bartlett, Nancy L. [6 ]
Connors, Joseph M. [7 ]
Gascoyne, Randy D. [7 ]
Wagner, Henry [8 ]
Gospodarowicz, Mary [9 ]
Cheson, Bruce D. [10 ]
Stiff, Patrick J. [11 ]
Advani, Ranjana [12 ]
Miller, Thomas P. [13 ]
Hoppe, Richard T. [12 ]
Kahl, Brad S. [14 ]
Horning, Sandra J. [15 ]
机构
[1] Univ Massachusetts, Sch Med, Worcester, MA 01655 USA
[2] Dana Farber Canc Inst, Boston, MA 02115 USA
[3] Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USA
[4] Northwestern Univ, Feinberg Sch Med, Chicago, IL 60611 USA
[5] Univ Rochester, Rochester, NY USA
[6] Washington Univ, St Louis, MO USA
[7] BC Canc Agcy Ctr Lymphoid Canc, Vancouver, BC, Canada
[8] Penn State Canc Inst, Hershey, PA USA
[9] Princess Margaret Hosp, Toronto, ON M4X 1K9, Canada
[10] Georgetown Univ Hosp, Washington, DC 20007 USA
[11] Loyola Univ, Chicago, IL 60611 USA
[12] Univ Arizona, Tucson, AZ USA
[13] Stanford Univ, Palo Alto, CA 94304 USA
[14] Univ Wisconsin, Madison, WI USA
[15] Genentech Inc, San Francisco, CA 94080 USA
基金
美国国家卫生研究院;
关键词
Hodgkin lymphoma; elderly; treatment-related toxicity; bleomycin lung toxicity; EPSTEIN-BARR-VIRUS; LONG-TERM SURVIVAL; ELDERLY-PATIENTS; DISEASE PATIENTS; POPULATION; CHEMOTHERAPY; TOXICITY; INTENSITY; PROGNOSIS; OUTCOMES;
D O I
10.1111/bjh.12222
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
There is a lack of contemporary prospective data examining the adriamycin, bleomycin, vinblastine, dacarbazine (ABVD) and Stanford V (SV; doxorubicin, vinblastine, mechlorethamine, vincristine, bleomycin, etoposide, prednisone) regimens in older Hodgkin lymphoma (HL) patients. Forty-four advanced-stage, older HL patients (aged60years) were treated on the randomized study, E2496. Toxicities were mostly similar between chemotherapy regimens, although 24% of older patients developed bleomycin lung toxicity (BLT), which occurred mainly with ABVD (91%). Further, the BLT-related mortality rate was 18%. The overall treatment-related mortality for older HL patients was 9% vs. 0 center dot 3% for patients aged <60years (P<0 center dot 001). Among older patients, there were no survival differences between ABVD and SV. According to age, outcomes were significantly inferior for older versus younger patients (5-year failure-free survival: 48% vs. 74%, respectively, P=0 center dot 002; 5-year overall survival: 58% and 90%, respectively, P<0 center dot 0001), although time-to-progression (TTP) was not significantly different (5-year TTP: 68% vs. 78%, respectively, P=0 center dot 37). Furthermore, considering progression and death without progression as competing risks, the risk of progression was not different between older and younger HL patients (5years: 30% and 23%, respectively, P=0 center dot 30); however, the incidence of death without progression was significantly increased for older HL patients (22% vs. 9%, respectively, P<0 center dot 0001). Altogether, the marked HL age-dependent survival differences appeared attributable primarily to non-HL events.
引用
收藏
页码:76 / 86
页数:11
相关论文
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