Meguro S, Kobayashi T, Chinen T, Usui N, Yamazaki H, Kobayashi A, Nagata T, Yokoyama K, Kuraishi Y, Ichiba K, Abe M
Gan To Kagaku Ryoho. 1982 Jul;9(6):1012-8.
Recent advances in the chemotherapy of malignant diseases, particularly, in hematopoietic malignancies, has opened oncologists' eyes in wonder, whereas the chemotherapy of solid malignant diseases including the carcinoma of the lung is not satisfactory compared with the results of other modalities such as radiotherapy and surgery. The chemotherapy, however, gradually becomes a great importance because the majority of the cases of lung cancer is that of advanced one. Between June, 1974 and December 1980 we experienced 54 inoperable cases of lung cancers among which there were 11 cases diagnosed as an anaplastic carcinoma. The combination chemotherapy of vincristine (1 mg/body, iv, day 1), methotrexate (30 mg/body, iv, day 1 and 5), ACNU (100mg/body, iv, day 2) and adriamycin (40mg/m2, iv, day 2) was employed. Vincristine and methotrexate were given every 3 weeks and ACNU and adriamycin were repeated every 9 weeks. If the moderate degree of neuropathy due to vincristine occurred it was suspended and methotrexate was stopped if WBC was less than 2000/mm or if patients were suffered from stomatitis which disturbed their swallowing. According to the response criteria of Koyama-Saito 4, cases were responded and one of them survived 17 months after the initiation of above 4-drug combination chemotherapy, although she received another combination chemotherapy because of the relapse of disease. The combination chemotherapy of ACNU and adriamycin was tried to utilize the advantage of their time different effects on the bone marrow suppression and to cover heterogenous histopathological diagnosis of anaplastic carcinoma. The heterogeneity of anaplastic carcinoma included undifferentiated squamous cell carcinoma, adenocarcinoma, large cell carcinoma and even small cell carcinoma. In taking consideration of these points, the drug-combination was designed. Clinically, however, the long resting period made the tumor regrow in some cases due to severe delayed myelosuppression by the combination of ACNU and adriamycin. Thus, more cautiously-designed combination should be considered.
恶性疾病化疗方面的最新进展,尤其是造血系统恶性肿瘤的化疗进展,令肿瘤学家惊叹不已。然而,与放疗和手术等其他治疗方式的效果相比,包括肺癌在内的实体恶性疾病的化疗效果并不理想。不过,由于大多数肺癌病例处于晚期,化疗的重要性日益凸显。1974年6月至1980年12月期间,我们收治了54例无法手术的肺癌患者,其中11例被诊断为间变性癌。采用了长春新碱(1mg/体,静脉注射,第1天)、甲氨蝶呤(30mg/体,静脉注射,第1天和第5天)、阿糖胞苷(100mg/体,静脉注射,第2天)和阿霉素(40mg/m²,静脉注射,第2天)的联合化疗方案。长春新碱和甲氨蝶呤每3周给药一次,阿糖胞苷和阿霉素每9周重复给药一次。如果出现因长春新碱导致的中度神经病变,则暂停用药;如果白细胞低于2000/mm³,或者患者出现影响吞咽的口腔炎,则停止使用甲氨蝶呤。根据小山 - 斋藤4的疗效标准,部分病例有反应,其中1例在开始上述四联化疗后存活了17个月,不过她因疾病复发接受了另一种联合化疗。尝试使用阿糖胞苷和阿霉素的联合化疗,以利用它们对骨髓抑制的不同时间效应优势,并涵盖间变性癌的异质性组织病理学诊断。间变性癌的异质性包括未分化鳞状细胞癌、腺癌、大细胞癌甚至小细胞癌。考虑到这些因素,设计了药物组合。然而在临床实践中,由于阿糖胞苷和阿霉素联合使用导致严重的延迟性骨髓抑制,较长的休息期使得部分病例中的肿瘤复发。因此,应考虑设计更为谨慎的联合化疗方案。