PROSPECTIVE MULTICENTER TRIAL FOR THE RESPONSE-ADAPTED TREATMENT OF HIGH-GRADE MALIGNANT NON-HODGKINS-LYMPHOMAS - UPDATED RESULTS OF THE COP-BLAM/IMVP-16 PROTOCOL WITH RANDOMIZED ADJUVANT RADIOTHERAPY

被引:39
作者
ENGELHARD, M
MEUSERS, P
BRITTINGER, G
BRACK, N
DORNOFF, W
ENNE, W
GASSMANN, W
GERHARTZ, H
HALLEK, M
HEISE, J
HETTCHEN, W
HUHN, D
KABELITZ, K
KUSE, R
LENGFELDER, E
LUDWIG, F
MEUTHEN, I
RADTKE, H
SCHADECK, C
SCHOBER, C
SCHUMACHER, E
SIEGERT, W
STAIGER, HJ
TERHARDT, E
THIEL, E
THOMAS, M
WAGNER, T
WILLEMS, MG
WILMANNS, W
ZWINGERS, T
STEIN, H
TIEMANN, M
LENNERT, K
机构
关键词
NON-HODGKIN LYMPHOMA; RANDOMIZED TRIAL; RESPONSE-ADAPTED STRATEGY;
D O I
10.1093/annonc/2.suppl_2.177
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In a prospective multicenter trial the efficiency of the response-adapted COP-BLAM/IMVP-16 protocol to induce complete remissions (CR) in high-grade malignant non-Hodgkin's lymphomas as well as the prognostic relevance of adjuvant radiotherapy were investigated. From 1986-1989, 548 patients (median age 56 years) with stage II-IV (Ann Arbor) disease were treated with five cycles of COP-BLAM followed by two cycles of IMVP-16. If only a partial remission was obtained at the time of first restaging (RS) after three cycles (delayed response), treatment was switched to IMVP-16 (two to five courses) immediately. Patients achieving CR by the second RS after chemotherapy were randomized to adjuvant radiotherapy or observation. Responses to chemotherapy were 63% CR in patients completing the second RS (N = 350) or 72% if patients achieving late CR by consolidating radiotherapy are added; responses were 58% or 65% if all deaths prior to the second RS are included (N = 50). Overall and relapse-free survival were 71% and 68% at one year and 63% at two years. Multivariate risk factor analysis proved the early (by first RS) CR response to possess predominant prognostic relevance for survival. A significant advantage of adjuvant radiotherapy over no further treatment for duration of CR is not yet discernible. These results emphasize the importance of a rapidly achieved CR, thus contributing to the design of future trials.
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收藏
页码:177 / 180
页数:4
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