Sirachainan Nongnuch, Boongird Atthaporn, Swangsilpa Thiti, Klaisuban Wipawi, Lusawat Apasri, Hongeng Suradej
Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, 10400, Thailand.
Department of Surgery, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, 10400, Thailand.
Childs Nerv Syst. 2017 Jun;33(6):893-897. doi: 10.1007/s00381-017-3409-y. Epub 2017 Apr 24.
The outcome of children with high-grade gliomas (HGGs) treated with radiation and adjuvant chemotherapy remains poor. The expression of epidermal growth factor receptor (EGFR) has been established in children with HGGs. This report demonstrated the outcomes of adjuvant nimotuzumab, an EGFR inhibitor, with irinotecan in pediatric HGGs.
Children with newly diagnosed HGGs were enrolled. Two weeks after surgery, nimotuzumab with a dose of 150 mg/m was given every week during radiation. After completion of radiation, a 4-week cycle of nimotuzumab (150 mg/m) at week 1 and 3 and irinotecan (125 mg/m) at week 1, 2, and 3 was given.
Sixteen patients (5 females, 11 males), with a mean ± SD age of 8.2 ± 3.5 years were included. Tumors were located at the supratentorial region (50.0%), infratentorial region (43.8%), and both locations (6.2%). The 5-year PFS and OS were 19.9 ± 11.6 and 31.5 ± 13.0%, respectively. Median times of PFS and OS were 1.8 and 1.9 years, respectively. Prognostic factors related to good outcome were the location of tumor at the supratentorial region or outside brainstem and the extension of surgery. Side effects were minimal, with grade 1 anemia in three patients and diarrhea in one patient. Although, the adjuvant regimen of nimotuzumab and irinotecan slightly increases the overall outcome when compared to the historical study, the advantages of this protocol were minimal side effect, short period of hospitalization, and improved OS in patients who received extensive surgery.
接受放疗和辅助化疗的高级别胶质瘤(HGG)患儿的预后仍然很差。表皮生长因子受体(EGFR)的表达已在HGG患儿中得到证实。本报告展示了辅助使用EGFR抑制剂尼妥珠单抗联合伊立替康治疗儿童HGG的疗效。
纳入新诊断的HGG患儿。术后两周开始,放疗期间每周给予剂量为150mg/m²的尼妥珠单抗。放疗结束后,在第1周和第3周给予4周周期的尼妥珠单抗(150mg/m²),在第1、2和3周给予伊立替康(125mg/m²)。
纳入16例患者(5例女性,11例男性),平均年龄为8.2±3.5岁。肿瘤位于幕上区域(50.0%)、幕下区域(43.8%)和两个区域均有(6.2%)。5年无进展生存期(PFS)和总生存期(OS)分别为19.9±11.6%和31.5±13.0%。PFS和OS的中位时间分别为1.8年和1.9年。与良好预后相关的预后因素是肿瘤位于幕上区域或脑干外以及手术切除范围。副作用轻微,3例患者出现1级贫血,1例患者出现腹泻。尽管与历史研究相比,尼妥珠单抗和伊立替康的辅助治疗方案略微提高了总体疗效,但该方案的优势在于副作用小、住院时间短以及接受广泛手术的患者OS有所改善。