Le Quynh-Thu X, Moon James, Redman Mary, Williamson Stephen K, Lara Primo N, Goldberg Zelanna, Gaspar Laurie E, Crowley John J, Moore Dennis F, Gandara David R
Stanford University, Stanford, CA, USA.
J Clin Oncol. 2009 Jun 20;27(18):3014-9. doi: 10.1200/JCO.2008.21.3868. Epub 2009 Apr 13.
A SWOG pilot study (S0004) showed that tirapazamine (TPZ) when combined with concurrent chemoradiotherapy yielded a promising median survival of 22 months in limited-stage small-cell lung cancer (LSCLC). We report results of the phase II study designed to confirm this result.
The concurrent phase consisted of two cycles of cisplatin, etoposide, and once-daily radiation to 61 Gy. TPZ was given at 260 mg/m(2) on days 1, 29, and at 160 mg/m(2) on days 8, 10, 12, 36, 38, and 40. Consolidation consisted of two cycles of cisplatin and etoposide. Complete responders received prophylactic cranial irradiation. Results were considered promising if the median survival time was at least 21 months and of no further interest if < or = 14 months.
S0222 was closed early due to a report of excess toxicity for TPZ in a head and neck cancer trial elsewhere. Of planned 85 patients, 69 were accrued. In 68 assessable patients, 17 (25%) had grade 3 to 4 esophagitis and eight (12%) had grade 3 febrile neutropenia during the concurrent phase. There were three possible treatment-related deaths, two in concurrent phase (one progressive disease not otherwise specified within 30 days, one pericardial effusion) and one in consolidation phase (esophageal hemorrhage). At a median follow-up of 35 months, median progression-free survival was 11 months (95% CI, 10 to 13 months) and median overall survival was 21 months (95% CI, 17 to 33 months).
S0222 showed acceptable levels of toxicity and similar promising median survival as S0004. Further study of hypoxia-targeted therapy is warranted in LSCLC.
一项西南肿瘤协作组(SWOG)的试点研究(S0004)表明,替拉扎明(TPZ)与同步放化疗联合应用时,在局限期小细胞肺癌(LSCLC)中产生了有前景的22个月中位生存期。我们报告旨在证实这一结果的II期研究结果。
同步治疗阶段包括两个周期的顺铂、依托泊苷以及每日一次放疗至61 Gy。TPZ在第1天、第29天给予260 mg/m²,在第8天、第10天、第12天、第36天、第38天和第40天给予160 mg/m²。巩固治疗包括两个周期的顺铂和依托泊苷。完全缓解者接受预防性脑照射。如果中位生存时间至少为21个月,则结果被认为有前景;如果小于或等于14个月,则不再进一步关注。
由于其他地方一项头颈部癌试验中报告了TPZ的毒性过高,S0222提前结束。在计划的85例患者中,有69例入组。在68例可评估患者中,17例(25%)在同步治疗阶段出现3至4级食管炎,8例(12%)出现3级发热性中性粒细胞减少。有3例可能与治疗相关的死亡,2例在同步治疗阶段(1例在30天内未明确的疾病进展,1例心包积液),1例在巩固治疗阶段(食管出血)。中位随访35个月时,中位无进展生存期为11个月(95%可信区间,10至13个月),中位总生存期为21个月(95%可信区间,17至33个月)。
S0222显示出可接受的毒性水平,且中位生存期与S0004相似,有前景。对LSCLC进行缺氧靶向治疗的进一步研究是必要的。