Comella P, Abate G, Comella G, Bruni G S, Zarrilli D, Pergola M
Tumori. 1980 Dec 31;66(6):749-56. doi: 10.1177/030089168006600610.
From January 1978 to June 1979, 29 selected, previously untreated patients with unfavorable histology of non-Hodgkin's lymphomas (12 DPDL, 7 DM, 9 DH and 1 DU) were submitted to the combination chemotherapy CHOP (cyclophosphamide, 750 mg/m2 i.v. on day 1; adriamycin, 50 mg/m2 i.v. on day 1; vincristine, 1.4 mg/m2 i.v. on day 1, and prednisone, 100 mg p.o. on day 1 through 5) every 21 days. Eighteen patients were in early stage (I or II) and 11 of them were also submitted to involved field radiotherapy (60Co), immediately before (stage I) or during (stage II) the chemotherapy, with a mean dosage of 4,500 rad. The remaining 11 patients were in advanced stage (III or IV) of disease and were treated with chemotherapy alone. We obtained 20 complete remissions (68%), 8 partial remissions (28%) and 1 no response (4%) to therapy. Sixteen of 18 patients (89%) in early stages and 4 of 11 patients (36%) in advanced stages achieved a complete remission. The bone marrow toxicity of the chemotherapy was moderate. Nausea, vomiting and diarrhea were frequent but well controlled by the support therapy. The actuarial survival rate of patients, after 18 months of follow-up, is 41% (40% in complete remission). The patients who achieved a complete remission are alive and 65% of them still relapse free. We believe that the combination chemotherapy CHOP improves the complete remission rate as well as the survival of patients with unfavorable histology of non-Hodgkin's lymphomas.
1978年1月至1979年6月,选取29例先前未经治疗、组织学类型不良的非霍奇金淋巴瘤患者(12例弥漫性组织细胞性淋巴瘤、7例弥漫性混合细胞性淋巴瘤、9例弥漫性小裂细胞性淋巴瘤和1例弥漫性大细胞性淋巴瘤),每21天接受CHOP联合化疗(环磷酰胺,第1天静脉注射750mg/m²;阿霉素,第1天静脉注射50mg/m²;长春新碱,第1天静脉注射1.4mg/m²;泼尼松,第1天至第5天口服100mg)。18例患者处于早期(I期或II期),其中11例在化疗前(I期)或化疗期间(II期)还接受了累及野放射治疗(60钴),平均剂量为4500拉德。其余11例患者处于疾病晚期(III期或IV期),仅接受化疗。治疗后获得20例完全缓解(68%)、8例部分缓解(28%)和1例无反应(4%)。18例早期患者中有16例(89%)、11例晚期患者中有4例(36%)实现完全缓解。化疗的骨髓毒性为中度。恶心、呕吐和腹泻常见,但通过支持治疗可得到良好控制。随访18个月后患者的精算生存率为41%(完全缓解患者为40%)。实现完全缓解的患者仍存活,其中65%仍无复发。我们认为CHOP联合化疗可提高组织学类型不良的非霍奇金淋巴瘤患者的完全缓解率及生存率。