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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Phase 2 study of PVAG (prednisone, vinblastine, doxorubicin, gemcitabine) in elderly patients with early unfavorable or advanced stage Hodgkin lymphoma.
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Phase 2 study of PVAG (prednisone, vinblastine, doxorubicin, gemcitabine) in elderly patients with early unfavorable or advanced stage Hodgkin lymphoma.

机译:PVAG(泼尼松,长春碱,阿霉素,吉西他滨)在老年早期或晚期霍奇金淋巴瘤患者中的2期研究。

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摘要

Approximately 20% of all Hodgkin lymphoma (HL) patients are older than 60 years and have a poor prognosis, mainly because of increased treatment-related toxicity resulting in reduced overall dose intensity and more treatment-related mortality. To possibly improve the treatment of elderly HL patients, the German Hodgkin Study Group developed a new regimen, PVAG (prednisone, vinblastine, doxorubicin, and gemcitabine). In this multicenter phase 2 study, elderly HL patients in early unfavorable and advanced stages received 6 to 8 cycles of PVAG and additional radiotherapy if they were not in complete remission (CR) after chemotherapy. Endpoints included feasibility, acute toxicity, and response rate. Fifty-nine patients 60 to 75 years of age (median, 68 years) were eligible for analysis; 93% had advanced stage disease. WHO grade 3/4 toxicities were documented in 43 patients; 46 patients responded with CR/CR uncertain (78%). Within 37 months median observation time, 15 progressions or relapses and 17 deaths were observed, of which 8 were related to HL and 1 was the result of treatment-related toxicity. The 3-year estimates for overall survival and progression-free survival were 66% (95% CI, 50%-78%) and 58% (95% CI, 43%-71%), respectively. We conclude that PVAG is safe and feasible in elderly HL patients. This trial was registered at www.clinicaltrials.gov as #NCT00147875.
机译:所有霍奇金淋巴瘤(HL)患者中约20%年龄超过60岁且预后较差,这主要是由于与治疗相关的毒性增加,导致总体剂量强度降低和与治疗相关的死亡率增加。为了改善老年HL患者的治疗效果,德国霍奇金研究小组开发了一种新的方案PVAG(强的松,长春碱,阿霉素和吉西他滨)。在这项多中心2期研究中,处于早期不利阶段和晚期阶段的老年HL患者如果接受化疗后仍未完全缓解(CR),则应接受6至8周期的PVAG和额外的放疗。终点包括可行性,急性毒性和反应率。年龄为60至75岁(中位数为68岁)的59例患者符合分析条件。 93%患有晚期疾病。记录到43例患者的WHO 3/4毒性。 46例患者的CR / CR不确定(78%)。在中位观察时间的37个月内,观察到15例进展或复发,观察到17例死亡,其中8例与HL相关,1例与治疗相关的毒性反应。 3年总生存期和无进展生存期估计分别为66%(95%CI,50%-78%)和58%(95%CI,43%-71%)。我们得出结论,PVAG在老年HL患者中是安全可行的。该试验已在www.clinicaltrials.gov上注册为#NCT00147875。

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