Rossini Fausto, Terruzzi Elisabetta, Perego Daniele, Miccolis Isabella, Rivolta Franca, Manca Elena, Pogliani Enrico M
Hematology Unit, Ospedale S. Gerardo, Via Donizetti 106, 20052 Monza (MI), Italy.
Cancer. 2004 Jan 15;100(2):350-5. doi: 10.1002/cncr.11907.
Doxorubicin cardiotoxicity is one of the most serious side effects of the cyclophosphamide, doxorubicin, vincristine, and prednisone chemotherapy, regimen, especially among elderly patients. In the CEOP regimen, epirubicin was substituted for doxorubicin to reduce cardiotoxicity.
Between March 1984 and September 1998, 186 previously untreated patients with a histologically confirmed diagnosis of intermediate- or high-grade non-Hodgkin lymphoma according to the Working Formulation were treated with CEOP (cyclophosphamide, 750 mg/m(2), epirubicin, 75 mg/m(2), vincristine, 1.4 mg/m(2); and prednisone, 60 mg per day orally on Days 1-5). Of 186 patients, 85 (45.7%) had Stage IV disease, and 60 (32.3%) had an International Prognostic Index score > 2. Comorbidity was present in 36 patients (19.3%).
Complete remission (CR) was achieved in 119 patients (64.3%), and partial remission was achieved in 30 patients (16.2%). Among the patients who achieved a CR, 95 (79.8%) were still disease free at a median follow-up time of 86.9 months (range, 14-200 months). The remaining 24 patients experienced disease recurrence, at a median follow-up time of 19 months (range, 3-101 months). The relative dose intensities were 0.69, 0.89, and 0.80 for vincristine, epirubicin, and cyclophosphamide, respectively. Two patients died of toxicity due to infection. Two patients, 59 and 73 years old, respectively, experienced arrhythmia. Another patient, age 64 years, who had a myocardial infarction 10 years earlier, had angina. One patient with hypertension experienced cardiac failure. No patients died of cardiac toxicity.
Long-term follow-up confirmed that CEOP is an effective and well-tolerated chemotherapy regimen for intermediate- and high-grade lymphoma. The results were promising, especially among elderly patients.
阿霉素心脏毒性是环磷酰胺、阿霉素、长春新碱和泼尼松化疗方案最严重的副作用之一,在老年患者中尤为如此。在CEOP方案中,表柔比星替代了阿霉素以降低心脏毒性。
1984年3月至1998年9月期间,186例既往未经治疗、根据工作分类法组织学确诊为中或高度非霍奇金淋巴瘤的患者接受了CEOP方案治疗(环磷酰胺750mg/m²、表柔比星75mg/m²、长春新碱1.4mg/m²;泼尼松在第1 - 5天每天口服60mg)。186例患者中,85例(45.7%)为IV期疾病,60例(32.3%)国际预后指数评分>2。36例患者(19.3%)存在合并症。
119例患者(64.3%)达到完全缓解(CR),30例患者(16.2%)达到部分缓解。在达到CR的患者中,95例(79.8%)在中位随访时间86.9个月(范围14 - 200个月)时仍无疾病。其余24例患者疾病复发,中位随访时间19个月(范围3 - 101个月)。长春新碱、表柔比星和环磷酰胺的相对剂量强度分别为0.69、0.89和0.80。2例患者死于感染毒性。2例患者分别为59岁和73岁,出现心律失常。另1例64岁患者10年前曾发生心肌梗死,出现心绞痛。1例高血压患者发生心力衰竭。无患者死于心脏毒性。
长期随访证实CEOP是治疗中高度淋巴瘤的一种有效且耐受性良好的化疗方案。结果令人鼓舞,尤其是在老年患者中。