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[阿霉素、ACNU和长春地辛联合化疗治疗原发性肺腺癌]

[Combination chemotherapy of primary adenocarcinoma of the lung using adriamycin, ACNU, and vindesine].

作者信息

Yoneda S, Min K Y, Honma T, Yoshida S, Nakagawa H

出版信息

Gan To Kagaku Ryoho. 1983 Apr;10(4 Pt 1):961-6.

PMID:6575723
Abstract

Since July 1980, thirty patients with inoperable adenocarcinoma of the lung have been treated with ANV. Induction chemotherapy (Adriamycin 35 mg/m2 i.v. days 1 and 22, ACNU 2 mg/kg i.v. day 1, vindesine 2 mg/m2 i.v. days 1, and 22) was given for 2 courses (or 1 course) at 3-week intervals. Maintenance chemotherapy was performed with reduced doses and elongated intervals. Characteristics of 30 patients were as follows: 13 males and 17 females; mean age 55 (range 32-77); mean PS 1.6, prior chemotherapy 3 cases; tumor involving bone (53%), brain (20%) and cervical node (23%). Of 27 patients who received no prior chemotherapy, 2 patients were unmeasurable because of pleural effusion. After one course of induction chemotherapy, 7 out of 25 patients achieved PR (response rate: 28%), 5 MRS (20%), 10 NCS, and 3 PDS. When patients were divided into the youngers (32-59 years old, mean 47) and the older (60-77 years old, mean 67), the youngers showed apparently higher response rate (6/17, 35%) than the olders (1/8, 13%). When patients were divided into three groups by the grade of cell differentiation, response rates were 0/5 (0%) in the well differentiated group, 2/6 (33%) in the moderately differentiated group, and 5/11 (45%) in the poorly differentiated group. The median survival time for all patients was 9 months; the younger 8 months, the older 9 months, well differentiated 11 months, moderately differentiated 9 months, and poorly differentiated 7 months. Survival time of responders was not significantly (P greater than 0.05) longer than that of non-responders. Toxicities were mild: leucopenia (less than 4,000) found in 85%, thrombocytopenia (less than 100,000) in 8%, anorexia in 54%, nausea and vomiting in 39%, and alopecia in 82%.

摘要

自1980年7月以来,30例无法手术的肺癌腺癌患者接受了ANV治疗。诱导化疗(阿霉素35mg/m²静脉注射,第1天和第22天;ACNU 2mg/kg静脉注射,第1天;长春地辛2mg/m²静脉注射,第1天和第22天)每3周进行2个疗程(或1个疗程)。维持化疗采用减量和延长间隔时间的方式。30例患者的特征如下:男性13例,女性17例;平均年龄55岁(范围32 - 77岁);平均PS为1.6,3例曾接受过化疗;肿瘤累及骨(53%)、脑(20%)和颈部淋巴结(23%)。在27例未曾接受过化疗的患者中,2例因胸腔积液无法测量。经过1个疗程的诱导化疗后,25例患者中有7例达到PR(缓解率:28%),5例MRS(20%),10例NCS,3例PDS。将患者分为较年轻组(32 - 59岁,平均47岁)和较年长组(60 - 77岁,平均67岁),较年轻组的缓解率(6/17,35%)明显高于较年长组(1/8,13%)。按细胞分化程度将患者分为三组,高分化组的缓解率为0/5(0%),中分化组为2/6(33%),低分化组为5/11(45%)。所有患者的中位生存时间为9个月;较年轻组为8个月,较年长组为9个月,高分化组为11个月,中分化组为9个月,低分化组为7个月。缓解者的生存时间与未缓解者相比无显著差异(P大于0.05)。毒性反应较轻:85%的患者出现白细胞减少(低于4000),8%的患者出现血小板减少(低于100000),54%的患者出现厌食,39%的患者出现恶心和呕吐,82%的患者出现脱发。

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