Newman S B, DeMeester T R, Golomb H M, Hoffman P C, Little A G, Raghavan V
J Thorac Cardiovasc Surg. 1983 Aug;86(2):180-5.
Twenty patients with postsurgical, modified Stage II (T2 N1 M0, T1 N1 M0) non-small cell bronchogenic carcinoma were seen between 1974 and 1981 and were evaluated in a retrospective manner. Fifteen patients had T2 N1 M0 lesions, while 5 patients had T1 N1 M0 disease. Eight patients were treated with surgical resection alone, of whom seven had died, with a median survival of 12.0 months. Four patients received surgical resection and postoperative radiation therapy, of whom two have died, with a median survival not reached at 37 months. Eight patients were treated with surgical resection, radiation therapy, and adjuvant chemotherapy including cyclophosphamide (C), doxorubicin (A), methotrexate (M), and procarbazine (P). Six patients are alive and free of disease, with a median survival not yet reached at 72 months. There is a significant survival advantage for the 12 patients treated with combined modality therapy (surgical resection + radiation therapy; surgical resection + radiation therapy + chemotherapy) compared to the eight patients treated with SR alone (p less than 0.01), and for the eight patients receiving chemotherapy versus the 12 patients who did not (p less than 0.01). In spite of thorough clinical and surgical staging, patients with T1 and T2 primary tumors with N1 disease have a high relapse rate, predominantly in metastatic sites. Adjuvant radiation therapy and chemotherapy appear to benefit these patients with modified Stage II non-small cell bronchogenic carcinoma.
1974年至1981年间,共观察了20例手术后改良II期(T2 N1 M0、T1 N1 M0)非小细胞支气管源性癌患者,并进行了回顾性评估。15例患者为T2 N1 M0病变,5例患者为T1 N1 M0疾病。8例患者仅接受手术切除治疗,其中7例死亡,中位生存期为12.0个月。4例患者接受了手术切除及术后放疗,其中2例死亡,37个月时中位生存期未达到。8例患者接受了手术切除、放疗及包括环磷酰胺(C)、阿霉素(A)、甲氨蝶呤(M)和丙卡巴肼(P)在内的辅助化疗。6例患者存活且无疾病,72个月时中位生存期尚未达到。与仅接受手术切除的8例患者相比,接受综合治疗(手术切除+放疗;手术切除+放疗+化疗)的12例患者有显著的生存优势(p<0.01),接受化疗的8例患者与未接受化疗的12例患者相比也有显著优势(p<0.01)。尽管进行了全面的临床和手术分期,但T1和T2原发性肿瘤伴N1疾病的患者复发率较高,主要发生在转移部位。辅助放疗和化疗似乎对这些改良II期非小细胞支气管源性癌患者有益。