Suppr超能文献

炎性或局部复发性乳腺癌患者中同时应用维利帕尼联合胸部和区域淋巴结放疗:TBCRC 024 期 I 多中心研究。

Concurrent Veliparib With Chest Wall and Nodal Radiotherapy in Patients With Inflammatory or Locoregionally Recurrent Breast Cancer: The TBCRC 024 Phase I Multicenter Study.

机构信息

Reshma Jagsi, Felix Y. Feng, Corey Speers, Michael Sabel, Anne F. Schott, and Lori Pierce, University of Michigan; Kent A. Griffith, University of Michigan School of Public Health, Ann Arbor, MI; Jennifer R. Bellon and Beth Overmoyer, Dana-Farber Cancer Institute, Boston, MA; Wendy A. Woodward, The University of Texas MD Anderson Cancer Center, Houston, TX; Janet K. Horton, Duke University School of Medicine, Durham, NC; and Alice Ho, Cedars-Sinai Medical Center, Los Angeles, CA.

出版信息

J Clin Oncol. 2018 May 1;36(13):1317-1322. doi: 10.1200/JCO.2017.77.2665. Epub 2018 Mar 20.

Abstract

Purpose Locoregional control for inflammatory breast cancers and chest wall recurrences is suboptimal, which has motivated interest in radiosensitization to intensify therapy. Preclinical studies have suggested a favorable therapeutic index when poly (ADP-ribose) polymerase inhibitors are used as radiosensitizers; clinical investigation is necessary to establish appropriate dosing and confirm safety. Patients and Methods We conducted a multi-institutional phase I study of veliparib and concurrent radiotherapy (RT) to the chest wall and regional lymph nodes in 30 patients with inflammatory or locally recurrent breast cancer after complete surgical resection. RT consisted of 50 Gy to the chest wall and regional lymph nodes plus a 10-Gy boost. A Bayesian time-to-event continual reassessment method escalated dose through four levels, with a 30% targeted rate of dose-limiting toxicity (DLT) measured during the 6 weeks of treatment plus 4 weeks of follow-up. DLTs were defined as confluent moist desquamation > 100 cm, nonhematologic toxicity grade ≥ 3, toxicity that requires an RT dose delay > 1 week, absolute neutrophil count < 1,000/mm, platelet count < 50,000/mm, or hemoglobin < 8.0 g/dL if possibly, probably, or definitely related to study treatment. Results Five DLTs occurred: Four were moist desquamation (two each at 100 and 150 mg twice a day), and one was neutropenia (at 200 mg twice a day). The crude rate of any grade 3 toxicity (regardless of attribution) was 10% at year 1, 16.7% at year 2, and 46.7% at year 3. At year 3, six of 15 surviving patients had severe fibrosis in the treatment field. Conclusion Although severe acute toxicity did not exceed 30% even at the highest tested dose, nearly half of surviving patients demonstrated grade 3 adverse events at 3 years, which underscores the importance of long-term monitoring of toxicity in trials of radiosensitizing agents.

摘要

目的

炎性乳腺癌和胸壁复发的局部区域控制效果不佳,这促使人们关注放射增敏作用以加强治疗。临床前研究表明,聚(ADP-核糖)聚合酶抑制剂作为放射增敏剂具有良好的治疗指数;需要进行临床研究以确定适当的剂量并确认其安全性。

患者和方法

我们对 30 例完全手术后的炎性或局部复发性乳腺癌患者进行了一项多中心 I 期研究,评估 veliparib 联合胸部和区域淋巴结放射治疗(RT)。RT 采用 50 Gy 照射胸壁和区域淋巴结,外加 10 Gy 的增量。贝叶斯时间事件连续评估方法通过四个剂量水平进行剂量递增,目标剂量限制性毒性(DLT)发生率为 30%,在 6 周的治疗和 4 周的随访期间进行评估。DLT 定义为弥漫性湿性脱皮> 100 cm²,非血液学毒性≥3 级,需要 RT 剂量延迟> 1 周,中性粒细胞绝对计数< 1000/mm³,血小板计数< 50000/mm³,或血红蛋白< 8.0 g/dL,如果可能、可能或肯定与研究治疗相关。

结果

发生了 5 例 DLT:4 例为湿性脱皮(2 例分别为 100 和 150 mg 每日 2 次),1 例为中性粒细胞减少(200 mg 每日 2 次)。第 1 年任何 3 级毒性(无论归因如何)的粗发生率为 10%,第 2 年为 16.7%,第 3 年为 46.7%。第 3 年,15 例存活患者中有 6 例在治疗区域出现严重纤维化。

结论

尽管即使在最高测试剂量下,严重的急性毒性也未超过 30%,但近一半的存活患者在 3 年内出现 3 级不良事件,这突出表明在放射增敏剂试验中需要长期监测毒性。

相似文献

引用本文的文献

3
PARP inhibitors combined with radiotherapy: are we ready?聚(ADP-核糖)聚合酶抑制剂联合放疗:我们准备好了吗?
Front Pharmacol. 2023 Oct 26;14:1234973. doi: 10.3389/fphar.2023.1234973. eCollection 2023.
5
Tailoring Treatment for Patients with Inflammatory Breast Cancer.为炎性乳腺癌患者制定治疗方案。
Curr Treat Options Oncol. 2023 Jun;24(6):580-593. doi: 10.1007/s11864-023-01077-0. Epub 2023 Apr 12.

本文引用的文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验