The Stanford V regimen is effective in patients with good risk Hodgkin lymphoma but radiotherapy is a necessary component

被引:5
作者
Abuzetun, Jamil Y. [2 ]
Loberiza, Fausto
Vose, Julie
Bierman, Philip
Greg Bociek, R.
Enke, Charles
Bast, Martin
Weisenburger, Dennis
Armitage, James O. [1 ]
机构
[1] Univ Nebraska, Med Ctr, Hematol Oncol Sect, Omaha, NE 68198 USA
[2] Creighton Univ, Med Ctr, Omaha, NE USA
关键词
Hodgkin lymphoma; radiotherapy; Stanford V regimen; COMBINATION CHEMOTHERAPY; DISEASE; ABVD; TRIAL; STAGE; BULKY; MOPP;
D O I
10.1111/j.1365-2141.2008.07500.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
One-hundred and thirteen patients between the ages of 15 and 88 years with biopsy proven, untreated Hodgkin lymphoma were treated by physicians in the Nebraska Lymphoma Study Group using the Stanford V regimen (bleomycin, doxorubicin, etoposide, mechlorethamine, prednisone, vinblastine and vincristine) between January 1997 and January 2006. With a median follow-up of all surviving patients of 63 months, the 5-year overall survival (OS) was 84% and the 5-year progression-free survival (PFS) was 74%. Age > 60 years, other than nodular sclerosing histological subtype, Ann Arbor Stage III/IV, and the presence of B-symptoms significantly predicted treatment outcome. Patients with 0-2 of these factors had a 5-year PFS and OS of 80% and 89% vs. 20% and 40% for patients with 3 or 4 factors. Patients who received radiotherapy had a superior 5-year PFS (86% vs. 42%) and OS (96% vs. 53%). Patients with 0-2 adverse risk factors who received radiotherapy had an excellent treatment outcome with 5-year PFS of 88% and a 5-year OS of 97%. The Stanford V chemotherapy regimen has an excellent treatment outcome for good prognosis patients with Hodgkin lymphoma. The results are compromised when radiotherapy is not utilized.
引用
收藏
页码:531 / 537
页数:7
相关论文
共 17 条
[1]  
*AJCC, 2002, AJCC CANC STAG MAN
[2]   BRIEF CHEMOTHERAPY, STANFORD-V, AND ADJUVANT RADIOTHERAPY FOR BULKY OR ADVANCED-STAGE HODGKINS-DISEASE - A PRELIMINARY-REPORT [J].
BARTLETT, NL ;
ROSENBERG, SA ;
HOPPE, RT ;
HANCOCK, SL ;
HORNING, SJ .
JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (05) :1080-1088
[3]  
BONADONNA G, 1975, CANCER, V36, P252, DOI 10.1002/1097-0142(197507)36:1<252::AID-CNCR2820360128>3.0.CO
[4]  
2-7
[5]   CHEMOTHERAPY OF ADVANCED HODGKINS-DISEASE WITH MOPP, ABVD, OR MOPP ALTERNATING WITH ABVD [J].
CANELLOS, GP ;
ANDERSON, JR ;
PROPERT, KJ ;
NISSEN, N ;
COOPER, MR ;
HENDERSON, ES ;
GREEN, MR ;
GOTTLIEB, A ;
PETERSON, BA .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 327 (21) :1478-1484
[6]  
COX DR, 1972, J R STAT SOC B, V34, P187
[7]   COMBINATION CHEMOTHERAPY IN TREATMENT OF ADVANCED HODGKINS DISEASE [J].
DEVITA, VT ;
SERPICK, AA ;
CARBONE, PP .
ANNALS OF INTERNAL MEDICINE, 1970, 73 (06) :881-+
[8]   Standard and increased-dose BEACOPP chemotherapy compared with COPP-ABVD for advanced Hodgkin's disease [J].
Diehl, V ;
Franklin, J ;
Pfreundschuh, M ;
Lathan, B ;
Paulus, U ;
Hasenclever, D ;
Tesch, H ;
Herrmann, R ;
Dörken, B ;
Müller-Hermelink, H ;
Dühmke, E ;
Loeffler, M .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (24) :2386-2395
[9]   ABVD versus modified Stanford V versus MOPPEBVCAD with optional and limited radiotherapy in intermediate- and advanced-stage Hodgkin's lymphoma: Final results of a multicenter randomized trial by the Intergruppo Italiano Linfomi [J].
Gobbi, PG ;
Levis, A ;
Chisesi, T ;
Broglia, C ;
Vitolo, U ;
Stelitano, C ;
Pavone, V ;
Cavanna, L ;
Santini, G ;
Merli, F ;
Liberati, M ;
Baldini, L ;
Deliliers, GL ;
Angelucci, E ;
Bordonaro, R ;
Federico, M .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (36) :9198-9207
[10]   A prognostic score for advanced Hodgkin's disease [J].
Hasenclever, D ;
Diehl, V .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (21) :1506-1514