Department of Radiation Oncology, The University of TexasMDAnderson Cancer Center, Houston, Texas 77030, USA.
Oncologist. 2013;18(3):265-70. doi: 10.1634/theoncologist.2012-0348. Epub 2013 Feb 12.
Radiation recall is an acute inflammatory reaction within a previously irradiated field triggered by chemotherapy administration. We observed a series of patients with unexpectedly severe reactions that included radiation recall and delayed healing when patients received the microtubule stabilizer ixabepilone (Ixempra; Bristol-Myers Squibb, Princeton, NJ) after radiation. We therefore decided to evaluate our experience in patients receiving ixabepilone following radiotherapy.
We performed a retrospective chart review of all patients treated with curative intent in the Department of Radiation Oncology at the MD Anderson Cancer Center from 2008-2011 who received any ixabepilone after completion of external-beam radiation therapy. These patients received adjuvant ixabepilone on one of two protocols, either for locally advanced breast cancer or for metastatic breast cancer. In total, 19 patients were identified and their charts were subsequently reviewed for evidence of ixabepilone-related toxicity.
Of the 19 patients identified who received ixabepilone following radiation therapy, three (15.8%) had unexpectedly serious reactions in the months following radiation therapy. Complications included delayed wound closure and drain placement into the seroma, intense erythema, and delayed wound closure and grade 4 chest wall necrosis requiring latissimus flap and skin grafting. The average number of days between the end of radiation therapy and documentation of reaction was 99.
Ixabepilone chemotherapy may induce radiation recall and delayed wound healing when used shortly after the completion of external-beam radiotherapy. Significant clinical interactions have not been previously reported and merit further evaluation.
辐射召回是一种在先前接受过放射治疗的区域内发生的急性炎症反应,由化疗药物引发。我们观察到一系列患者出现了出乎意料的严重反应,包括辐射召回和延迟愈合,这些患者在接受放射治疗后接受微管稳定剂伊沙匹隆(Ixempra;百时美施贵宝,新泽西州普林斯顿)。因此,我们决定评估我们在接受放射治疗后接受伊沙匹隆治疗的患者的经验。
我们对 2008 年至 2011 年期间在 MD 安德森癌症中心放射肿瘤科接受根治性治疗且在完成外照射放疗后接受任何伊沙匹隆治疗的所有患者进行了回顾性图表审查。这些患者根据两种方案之一接受辅助伊沙匹隆治疗,一种用于局部晚期乳腺癌,另一种用于转移性乳腺癌。共确定了 19 例患者,随后对其病历进行了审查,以确定是否存在与伊沙匹隆相关的毒性证据。
在接受放射治疗后接受伊沙匹隆治疗的 19 例患者中,有 3 例(15.8%)在放射治疗后数月出现意外严重反应。并发症包括伤口延迟闭合和引流管置入到血清肿中、剧烈红斑以及伤口延迟闭合和 4 级胸壁坏死,需要Latissimus 皮瓣和植皮。放射治疗结束与反应记录之间的平均天数为 99 天。
伊沙匹隆化疗在完成外照射放疗后不久使用时可能会引发辐射召回和延迟伤口愈合。以前没有报道过明显的临床相互作用,值得进一步评估。