1. Tandem High-Dose Chemotherapy and Autologous Stem Cell Transplantation for Atypical Teratoid/Rhabdoid Tumor
- Author
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Keon Hee Yoo, Yoo Sook Joung, Ji Hye Kim, Yeon-Lim Suh, Do Hoon Lim, Hyung Jin Shin, Ji Won Lee, Eun Sang Yi, Hong Hoe Koo, Young Bae Choi, and Ki Woong Sung
- Subjects
Oncology ,Male ,Cancer Research ,medicine.medical_specialty ,medicine.medical_treatment ,Hematopoietic stem cell transplantation ,Pilot Projects ,Transplantation, Autologous ,Disease-Free Survival ,Carboplatin ,03 medical and health sciences ,chemistry.chemical_compound ,0302 clinical medicine ,Autologous stem-cell transplantation ,Internal medicine ,medicine ,Chemotherapy ,Humans ,Adverse effect ,Child ,Rhabdoid Tumor ,Radiotherapy ,business.industry ,Induction chemotherapy ,Infant ,Induction Chemotherapy ,medicine.disease ,Combined Modality Therapy ,Radiation therapy ,Brain neoplasms ,chemistry ,030220 oncology & carcinogenesis ,Child, Preschool ,Atypical teratoid rhabdoid tumor ,Original Article ,Female ,Neoplasm Recurrence, Local ,business ,030217 neurology & neurosurgery ,Stem Cell Transplantation - Abstract
Purpose We prospectively evaluated the effectiveness of tandem high-dose chemotherapy and autologous stem cell transplantation (HDCT/auto-SCT) in improving the survival of patients with atypical teratoid/rhabdoid tumors while reducing the risks of late adverse effects from radiotherapy (RT). Materials and Methods For young children (< 3 years old), tandem HDCT/auto-SCT was administered after six cycles of induction chemotherapy. RT was deferred until after 3 years of age unless the tumor showed relapse or progression. For older patients (> 3 years old), RT including reduced-dose craniospinal RT (23.4 or 30.6 Gy) was administered either after two cycles of induction chemotherapy or after surgery, and tandem HDCT/auto-SCT was administered after six cycles of induction chemotherapy. Results A total of 13 patients (five young and eight older) were enrolled from November 2004 to June 2012. Eight patients, including all five young patients, had metastatic disease at diagnosis. Six patients (four young and two older) experienced progression before initiation of RT, and seven were able to proceed to HDCT/auto-SCT without progression during induction treatment. Three of six patients who experienced progression during induction treatment underwent HDCT/auto-SCT as salvage treatment. All five young patients died from disease progression. However, four of the eight older patients remain progression-freewith a median follow-up period of 64 months (range, 39 to 108 months). Treatment-related late toxicities were acceptable. Conclusion The required dose of craniospinal RT might be reduced in older patients if the intensity of chemotherapy is increased. However, early administration of RT should be considered to prevent early progression in young patients.
- Published
- 2016