Long-term events in adult patients with clinical stage IA-IIa nonbulky Hodgkin's lymphoma treated with four cycles of doxorubicin, bleomycin,vinblastine, and dacarbazine and adjuvant radiotherapy: A single-institution 15-year follow-up

被引:68
作者
Brusamolino, Ercole
Baio, Ambrogia
Orlandi, Ester
Arcaini, Luca
Passamonti, Francesco
Griva, Vassiliki
Casagrande, William
Pascutto, Cristiana
Franchini, Pietro
Lazzarino, Mario
机构
[1] Univ Pavia, Policlin San Matteo, Ist Ricovero & Cura Carattere Sci, Clin Ematol, I-27100 Pavia, Italy
[2] Univ Pavia, Policlin San Matteo, Ist Ricovero & Cura Carattere Sci, Serv Radioterapia Oncol, I-27100 Pavia, Italy
关键词
D O I
10.1158/1078-0432.CCR-06-1420
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Purpose: To report on long-term events after short doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD) chemotherapy and adjuvant radiotherapy in favorable early-stage Hodgkin's lymphoma. Experimental Design: We monitored late events and causes of death over 15 years (median follow-up, 120 months) in 120 patients with nonbulky stage IA-IIA Hodgkin's lymphoma, treated with four cycles of ABVD and limited radiotherapy. Pulmonary and cardiac function tests were done throughout the follow-up. Outcome measures included cause-specific mortality, standardized mortality ratio, and standardized incidence ratio for secondary neoplasia. Results: Projected 15-year event-free and overall survival were 78% and 86%, and tumor mortality was 3%. Standardized mortality ratio was significantly higher than 1 for both males (2.8; P = 0.029) and females (9.4; P = 0.003). The risk of cardiovascular events at 5 and 12 years was 5.5% and 14%, with a median latent time of 67 months (range: 23-179 months) from the end of radiotherapy. Pulmonary toxicity developed in 8% of patients; all had received mediastinal irradiation and the median time from radiotherapy to pulmonary sequelae was 76 weeks (range: 50-123 weeks). The risk of secondary neoplasia at 5 and 12 years was 4% and 8%, respectively, with no cases of leukemia. Fertility was preserved. Conclusions: Long-term events were mostly related to radiotherapy; the role of short ABVD chemotherapy was very limited, as documented by fertility preservation and lack of secondary myelodysplasia/leukemia. A proportion of patients died from causes unrelated to disease progression and the excess mortality risk was mostly due to the occurrence of secondary neoplasms and cardiovascular diseases. A moderate dose reduction of radiotherapy from 40-44 Gy to 30-36 Gy did not decrease the risk of late complications; abolishing radiotherapy in nonbulky early-stage Hodgkin's lymphoma is being evaluated.
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页码:6487 / 6493
页数:7
相关论文
共 34 条
[1]
Cardiovascular status in long-term survivors of Hodgkin's disease treated with chest radiotherapy [J].
Adams, MJ ;
Lipsitz, SR ;
Colan, SD ;
Tarbell, NJ ;
Treves, ST ;
Diller, L ;
Greenbaum, N ;
Mauch, P ;
Lipshultz, SE .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (15) :3139-3148
[2]
Long-term cause-specific mortality of patients treated for Hodgkin's disease [J].
Aleman, BMP ;
van den Belt-Dusebout, AW ;
Klokman, WJ ;
van't Veer, MB ;
Bartelink, H ;
van Leeuwen, FE .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (18) :3431-3439
[3]
[Anonymous], ANN ONCOL S3
[4]
Secondary amenorrhea after Hodgkin's lymphoma is influenced by age at treatment, stage of disease, chemotherapy regimen, and the use of oral contraceptives during therapy: A report from the German Hodgkin's lymphoma study group [J].
Behringer, K ;
Breuer, K ;
Reineke, T ;
May, M ;
Nogova, L ;
Klimm, B ;
Schmitz, T ;
Wildt, L ;
Diehl, V ;
Engert, A .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (30) :7555-7564
[5]
ABVD plus subtotal nodal versus involved-field radiotherapy in early-stage Hodgkin's disease: Long-term results [J].
Bonadonna, G ;
Bonfante, V ;
Viviani, S ;
Di Russo, A ;
Villani, F ;
Valagussa, P .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (14) :2835-2841
[6]
EARLY-STAGE HODGKINS-DISEASE - LONG-TERM RESULTS WITH RADIOTHERAPY ALONE OR COMBINED RADIOTHERAPY AND CHEMOTHERAPY [J].
BRUSAMOLINO, E ;
LAZZARINO, M ;
ORLANDI, E ;
CANEVARI, A ;
MORRA, E ;
CASTELLI, G ;
ALESSANDRINO, EP ;
PAGNUCCO, G ;
ASTORI, C ;
LIVRAGHI, A ;
CORBELLA, F ;
FRANCHINI, P ;
BERNASCONI, C .
ANNALS OF ONCOLOGY, 1994, 5 :S101-S106
[7]
Brusamolino E, 1998, HAEMATOLOGICA, V83, P812
[8]
Brusamolino E, 2000, HAEMATOLOGICA, V85, P1032
[10]
State-of-the-art therapeutics: Hodgkin's lymphoma [J].
Connors, JM .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (26) :6400-6408