Chen L M, Ignacio L, Jacobs R, Kozloff M, Telfer M, Elahi R, Evans R, Vijayakumar S
Department of Radiation and Cellular Oncology, University of Chicago, Illinois 60637, USA.
Radiat Oncol Investig. 1999;7(1):49-53. doi: 10.1002/(sici)1520-6823(1999)7:1<49::aid-roi7>3.0.co;2-8.
This phase II study was designed to utilize conformal radiation therapy with cisplatin and oral etoposide in patients with stage III or locally recurrent non-small-cell lung cancer to determine tolerance and toxicity of therapy. From April 1992-February 1996, 18 patients with pathologically confirmed stage IIIA, IIIB, or locally recurrent non-small-cell lung cancer (NSCLC) were entered on study. Metastatic workup included a CT scan of the thorax and upper abdomen as well as a bone scan. Chemotherapy consisted of IV cisplatin (100 mg/m2) with IV etoposide (25 mg/m2) on day 1; oral etoposide was given (50 mg/m2) days 2-14. Using three-dimensional planning, 40-45 Gy were delivered to the clinical target volume, followed by a boost to the gross tumor volume for a total of 70 Gy. Patients with recurrent disease received 40-50 Gy in total. Eighteen patients were enrolled: 16 patients were treated with curative intent and were evaluable for outcome. Two patients were treated for locally recurrent NSCLC and were not included in the outcome analysis. Stages included IIIA (44%) and stage IIIB (54%). Forty-four percent had T3/4 tumors, and 69% had N2/3 disease. Overall survival at 1 year was 64%, while 2-year overall survival was 50%. Distant metastasis-free survival at 1 year was 67%, and at 2 years 60%. The 1-year chest progression-free survival was 57%, and at 2 years 50%. Sixty-three percent required hospitalization for dehydration or neutropenia. Fifty-six percent developed leukopenia (<1,000 cells/microl) sometime during the therapy. We conclude that concurrent cisplatin and oral etoposide with conformal radiation therapy provide encouraging results in stage III lung cancer. The major toxicities of this therapy included leukopenia, thrombocytopenia, and mucosal esophagitis. Local progression of disease continues to be a problem with the current doses given. Future studies should evaluate dose escalation of radiation therapy with limited volumes, utilizing conformal radiation and chemotherapy to improve local control and potentially impact upon distant metastases.
本II期研究旨在对III期或局部复发的非小细胞肺癌患者采用顺铂和口服依托泊苷同步放疗法,以确定该疗法的耐受性和毒性。1992年4月至1996年2月,18例经病理确诊为IIIA期、IIIB期或局部复发的非小细胞肺癌(NSCLC)患者进入研究。转移灶检查包括胸部和上腹部CT扫描以及骨扫描。化疗方案为第1天静脉注射顺铂(100mg/m²)和静脉注射依托泊苷(25mg/m²);第2 - 14天口服依托泊苷(50mg/m²)。采用三维计划,向临床靶体积给予40 - 45Gy照射,随后对大体肿瘤体积进行追加照射,总量达70Gy。复发患者共接受40 - 50Gy照射。共纳入18例患者:16例接受根治性治疗,可对结局进行评估。2例因局部复发的NSCLC接受治疗,未纳入结局分析。分期包括IIIA期(44%)和IIIB期(54%)。44%的患者有T3/4肿瘤,69%的患者有N2/3疾病。1年总生存率为64%,2年总生存率为50%。1年无远处转移生存率为67%,2年为60%。1年胸部无进展生存率为57%,2年为50%。63%的患者因脱水或中性粒细胞减少需要住院治疗。56%的患者在治疗期间出现白细胞减少(<1000个细胞/微升)。我们得出结论,顺铂和口服依托泊苷同步放疗法在III期肺癌治疗中取得了令人鼓舞的结果。该疗法的主要毒性包括白细胞减少、血小板减少和食管黏膜炎症。按照目前的剂量给药,疾病局部进展仍是一个问题。未来的研究应评估在有限体积内提高放疗剂量,采用适形放疗和化疗以改善局部控制,并可能对远处转移产生影响。