Takita H, Blumenson L E, Raghavan D
Department of Thoracic Surgery and Oncology, Division of Surgical Oncology, Buffalo 14263, USA.
J Surg Oncol. 1995 Jul;59(3):147-50. doi: 10.1002/jso.2930590303.
Previously, we reported an effective chemotherapeutic combination regimen for non-small cell lung carcinoma (NSCLC): cisplatinum, doxorubicin, cyclophosphamide, CCNU, and vincristine (PACCO). Forty-one patients with a diagnosis of NSCLC Stages III-A and III-B were entered into the protocol of neoadjuvant PACCO chemotherapy. Following two courses of chemotherapy, the patients were evaluated for surgical therapy. The overall response rate to the chemotherapy was 60%. Subsequently, 65% of the patients underwent surgical resection. The overall estimated median survival was 18 months. The survival of patients in III-A was 36 months and that of III-B was 18 months (95% confidence lower bounds for III-A: 8 months and for III-B: 13 months). There was one chemotherapy-related mortality but no surgical mortality. Neoadjuvant chemotherapy with PACCO regiment offers an alternative to chemoradiation therapy, without increasing the surgical mortality, and should be validated in a randomized clinical trial. For successful neoadjuvant chemotherapy of Stage III NSCLC, chemotherapy combination which would give a high response rate without significant side effects must be chosen.
此前,我们报道了一种针对非小细胞肺癌(NSCLC)的有效化疗联合方案:顺铂、阿霉素、环磷酰胺、洛莫司汀和长春新碱(PACCO)。41例诊断为NSCLCⅢA期和ⅢB期的患者进入新辅助PACCO化疗方案。经过两个疗程的化疗后,对患者进行手术治疗评估。化疗的总体缓解率为60%。随后,65%的患者接受了手术切除。总体估计中位生存期为18个月。ⅢA期患者的生存期为36个月,ⅢB期患者的生存期为18个月(ⅢA期的95%置信区间下限:8个月;ⅢB期:13个月)。有1例与化疗相关的死亡,但无手术死亡。PACCO方案的新辅助化疗为放化疗提供了一种替代方案,且不增加手术死亡率,应在随机临床试验中进行验证。对于Ⅲ期NSCLC的新辅助化疗成功而言,必须选择一种能产生高缓解率且无明显副作用的化疗联合方案。