顺铂和口服依托泊苷三维适形放疗治疗III期非小细胞肺癌的II期同步放化疗研究结果

L M Chen, L Ignacio, R Jacobs, M Kozloff, M Telfer, R Elahi, R Evans, S Vijayakumar
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引用次数: 16

摘要

这项II期研究旨在利用顺铂和口服依托泊苷对III期或局部复发的非小细胞肺癌患者进行适形放射治疗,以确定治疗的耐受性和毒性。从1992年4月至1996年2月,18例病理证实为IIIA期、IIIB期或局部复发的非小细胞肺癌(NSCLC)患者进入研究。转移性检查包括胸部和上腹部的CT扫描以及骨扫描。化疗方案为:第1天IV顺铂(100mg /m2) + IV依托泊苷(25mg /m2);口服依托泊苷(50 mg/m2),第2-14天。采用三维规划,将40-45 Gy送入临床靶体积,然后将总肿瘤体积增加70 Gy。复发患者总剂量为40 ~ 50 Gy。18名患者入组:16名患者接受治疗并可评估结果。2例患者接受局部复发性NSCLC治疗,未纳入结果分析。分期包括IIIA期(44%)和IIIB期(54%)。44%的人患有T3/4肿瘤,69%的人患有N2/3肿瘤。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年生存率为60%。1年胸部无进展生存率为57%,2年为50%。63%的人因脱水或中性粒细胞减少而住院。56%的人患上白细胞减少症(
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Results of a phase II concurrent chemoradiotherapy study using three-dimensional conformal radiotherapy with cisplatin and oral etoposide in stage III nonsmall-cell lung cancer.

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.

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