Donaldson S S
Department of Radiation Oncology, Stanford University School of Medicine, CA 94305.
Arch Surg. 1989 Sep;124(9):1015-20. doi: 10.1001/archsurg.1989.01410090021003.
Approximately two thirds of children with rhabdomyosarcoma will be cured of their tumor and become long-term survivors. Multidisciplinary care has brought about improvements in survival. Yet our therapies of today are suboptimal in many situations and demand intense effort toward improving cure rates and quality of life. Rhabdomyosarcoma is a complex childhood malignancy with differing anatomic sites of presentation and varying histologic subtypes, each presenting with unique patterns of growth, making it inappropriate to consider the disease a single entity. Avenues of future research involve cytogenetic and molecular genetic investigations that will aid in diagnosis and screening and, it is hoped, guide clinicians to more specific therapy.
大约三分之二的横纹肌肉瘤患儿将治愈肿瘤并成为长期幸存者。多学科护理已使生存率得到提高。然而,我们目前的治疗方法在许多情况下并不理想,需要付出巨大努力来提高治愈率和生活质量。横纹肌肉瘤是一种复杂的儿童恶性肿瘤,其发病的解剖部位不同,组织学亚型各异,每种亚型都有独特的生长模式,因此不宜将该疾病视为单一实体。未来的研究方向包括细胞遗传学和分子遗传学研究,这将有助于诊断和筛查,并有望指导临床医生采用更具针对性的治疗方法。