Karrer K, Shields T W, Denck H, Hrabar B, Vogt-Moykopf I, Salzer G M
Northwestern University Medical School, Department of Surgery, Chicago, IL 60611.
J Thorac Cardiovasc Surg. 1989 Feb;97(2):168-76.
In a cooperative international lung cancer multimodality treatment trial, 112 patients with small cell lung cancer underwent initial surgical resection and were then randomized to receive one of two intensive postoperative chemotherapeutic regimens, followed by prophylactic cranial irradiation in the disease-free patients. Regimen A consisted of eight courses of cyclophosphamide, doxorubicin, and vincristine and regimen B of two courses of three sequential drug combinations: (1) cyclophosphamide, lomustine, and methotrexate; (2) cyclophosphamide, doxorubicin, and vincristine; and (3) ifosfamid and etoposide. In 47 patients the diagnosis was known preoperatively and in 65 it was not confirmed until the resected specimen was examined (all diagnoses were reviewed by a referee pathologist). Each patient was classified by the pathologic TNM characteristics. There were 38 patients with stage I disease, 39 patients with stage II, and 35 patients with stage IIIa disease. In stage IIIa there were nine patients with T3 N0-1 disease and 26 with T1-3 N2 disease (most N2 disease was clinically undetected until thoracotomy or was discovered only by routine histologic examination of the resected mediastinal nodes). Early survival rates at 24 months calculated by the life table method are as follows: stage I, 76%; stage II, 56%; and stage IIIa, 49% (T3 N0-1, 89%; T1-3 N2, 35%). Survival rates at 36 months are 62%, 50%, and 41% (74% and 29%), respectively. The projected 36-month survival rate for 43 patients with N0 disease is 65%; for 43 with N1 disease, 52%; and for 26 with N2 disease, 29%. No difference in survival has been noted in either chemotherapy treatment group. It is concluded that initial surgical resection for limited small cell cancer (stage I, II, and T3 N0-1) followed by intensive chemotherapy is an appropriate therapeutic approach. For T1-3 N2 disease the results are inconclusive.
在一项国际合作的肺癌多模式治疗试验中,112例小细胞肺癌患者接受了初始手术切除,然后被随机分配接受两种强化术后化疗方案之一,无病患者随后接受预防性颅脑照射。方案A由八个疗程的环磷酰胺、阿霉素和长春新碱组成,方案B由两个疗程的三种连续药物组合组成:(1)环磷酰胺、洛莫司汀和甲氨蝶呤;(2)环磷酰胺、阿霉素和长春新碱;(3)异环磷酰胺和依托泊苷。47例患者术前已明确诊断,65例患者直到切除标本检查后才得以确诊(所有诊断均由一名裁判病理学家复查)。每位患者根据病理TNM特征进行分类。有38例I期疾病患者,39例II期患者,35例IIIA期患者。在IIIA期,有9例T3 N0 - 1疾病患者和26例T1 - 3 N2疾病患者(大多数N2疾病在开胸手术前临床未被发现,或仅通过切除纵隔淋巴结的常规组织学检查才被发现)。采用寿命表法计算的24个月早期生存率如下:I期,76%;II期,56%;IIIA期,49%(T3 N0 - 1,89%;T1 - 3 N2,35%)。36个月生存率分别为62%、50%和41%(74%和29%)。43例N0疾病患者预计36个月生存率为65%;43例N1疾病患者为52%;26例N2疾病患者为29%。两个化疗治疗组在生存率方面均未发现差异。得出的结论是,对于局限性小细胞癌(I期、II期和T3 N0 - 1),初始手术切除后进行强化化疗是一种合适的治疗方法。对于T1 - 3 N2疾病,结果尚无定论。