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首页> 外文期刊>Neoplasma: Journal of Experimental and Clinical Oncology >The addition of induction chemotherapy with etoposide, ifosfamide, and cisplatin failed to improve therapeutic outcome of concurrent chemoradiotherapy in patients with locally advanced non-small cell lung cancer - single institution retrospective ana
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The addition of induction chemotherapy with etoposide, ifosfamide, and cisplatin failed to improve therapeutic outcome of concurrent chemoradiotherapy in patients with locally advanced non-small cell lung cancer - single institution retrospective ana

机译:依托泊苷,异环磷酰胺和顺铂的诱导化疗不能改善局部晚期非小细胞肺癌患者同时放化疗的治疗效果-单机构回顾性分析

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Although chemoradiotherapy (CRT) is a standard treatment for unresectable locally advanced non-small cell lung cancer (NSCLC), the optimal sequencing remains to be determined. We retrospectively compared the treatment results of induction chemotherapy followed by concurrent CRT (induction group, 32 patients) with those of concurrent CRT alone (concurrent group, 41 patients) in unresectable stage IIIA/IIIB NSCLC patients. In induction group, 2 cycles of induction chemotherapy (etoposide/ifosfamide/cisplatin: 24 patients, others: 8 patients) were followed by concurrent CRT (60 Gy/30 fractions, 6 mg/m2 of cisplatin daily), while the same concurrent CRT was administered in concurrent group. Clinicopathologic characteristics including age, weight loss, histologic types, and clinical stage did not show significant differences between two groups except for a higher proportion of patients with ECOG performance status 2 in concurrent group (3% vs. 27%, p=0.015). Overall toxicity was generally acceptable with 1 treatment-related death from tracheoesophageal fistula in induction group. The response rates after concurrent CRT were 41% for induction group and 54% for concurrent group, which showed no significant difference (p=0.560). With median follow-up of 13 (1-92) months, there was a trend toward an advantage for concurrent group in median progression-free survival (6 months vs 8.3 months, p=0.067) and overall survival (12 months vs. 14.5 months, p=0.059). In multivariate analysis, only more than 10% weight loss within 6 months was significantly associated with poor survival (p=0.001). In conclusion, the addition of induction chemotherapy to concurrent CRT did not show any advantage over concurrent CRT alone in locally advanced NSCLC.
机译:尽管放化疗(CRT)是不可切除的局部晚期非小细胞肺癌(NSCLC)的标准治疗方法,但最佳测序尚待确定。我们回顾性地比较了不可切除的IIIA / IIIB期NSCLC患者中,同步化疗后同时进行CRT(诱导组,32例)与单纯同期CRT(同时组,41例)的治疗结果。在诱导组中,进行2轮诱导化疗(依托泊苷/异环磷酰胺/顺铂:24例,其他:8例),然后进行同期CRT(60 Gy / 30份,每天6 mg / m2顺铂),同时进行同期CRT被并发组管理。两组患者的临床病理特征(包括年龄,体重减轻,组织学类型和临床分期)没有显示出显着差异,但同时组中具有较高ECOG功能状态2的患者比例较高(3%vs. 27%,p = 0.015)。诱导组中因气管食管瘘造成的1例与治疗相关的死亡,总体毒性一般是可以接受的。并发CRT后,诱导组的反应率为41%,并发组为54%,差异无统计学意义(p = 0.560)。中位随访时间为13(1-92)个月,并发组在中位无进展生存期(6个月vs 8.3个月,p = 0.067)和总生存期(12个月vs 14.5)方面有优势个月,p = 0.059)。在多变量分析中,在6个月内体重减轻仅超过10%与存活率低显着相关(p = 0.001)。总之,在局部晚期NSCLC中,并发CRT加诱导化疗与单独并发CRT相比没有任何优势。

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