Shepherd F A, Ginsberg R J, Haddad R, Feld R, Sagman U, Evans W K, DeBoer G, Maki E
Department of Medicine, Toronto Hospital, Ontario, Canada.
J Clin Oncol. 1993 Aug;11(8):1592-7. doi: 10.1200/JCO.1993.11.8.1592.
In an attempt to assess the response to treatment and survival of a group of patients treated with standard chemotherapy and radiotherapy, we undertook a retrospective review of small-cell lung cancer (SCLC) patients treated by the University of Toronto Lung Oncology Group.
We reviewed the records of 264 patients with limited SCLC who were treated from 1976 to 1985. Based on radiologic review and physical examination, patients were assigned to three prognostic groups: group 1 (very limited SCLC), negative mediastinoscopy and/or no evidence of mediastinal nodes on radiologic review; group 2, x-ray evidence of mediastinal node involvement or a positive mediastinoscopy; group 3, supraclavicular adenopathy or x-ray evidence of pneumonic consolidation, pleural effusion, or atelectasis. All patients received combination chemotherapy, radiotherapy to the primary site, and prophylactic cranial irradiation.
Complete response was seen in 52% of patients and partial response in 29%. Response rates did not differ among the three prognostic subgroups. The median survival time for patients in group 1 was 15.7 months, compared with 12 months for group 2 and 11 months for group 3 (P = .0175). Projected 5-year survival for group 1 was 18%, compared with only 6% and 2% for groups 2 and 3, respectively. There was no difference among the prognostic subgroups with respect to either local or distant recurrence rates.
Using simple clinical staging techniques, we were able to identify a subgroup of patients with very limited SCLC who had a significantly better prognosis. We recommend that randomized clinical trials stratify patients according to the presence or absence of clinically detectable mediastinal lymphadenopathy.
为了评估一组接受标准化化疗和放疗的患者的治疗反应及生存率,我们对多伦多大学肺部肿瘤学组治疗的小细胞肺癌(SCLC)患者进行了一项回顾性研究。
我们回顾了1976年至1985年期间接受治疗的264例局限性SCLC患者的记录。根据影像学检查和体格检查,将患者分为三个预后组:第1组(极局限性SCLC),纵隔镜检查阴性和/或影像学检查无纵隔淋巴结证据;第2组,有纵隔淋巴结受累的X线证据或纵隔镜检查阳性;第3组,锁骨上淋巴结肿大或有肺炎实变、胸腔积液或肺不张的X线证据。所有患者均接受联合化疗、原发部位放疗和预防性颅脑照射。
52%的患者出现完全缓解,29%的患者出现部分缓解。三个预后亚组的缓解率无差异。第1组患者的中位生存时间为15.7个月,第2组为12个月,第3组为11个月(P = 0.0175)。第1组预计五年生存率为18%,相比之下,第2组和第3组分别仅为6%和2%。预后亚组在局部或远处复发率方面无差异。
通过简单的临床分期技术,我们能够识别出一组极局限性SCLC患者,他们的预后明显更好。我们建议随机临床试验根据临床上是否可检测到纵隔淋巴结肿大对患者进行分层。