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Delayed Primary Excision with Subsequent Modification of Radiotherapy Dose for Intermediate Risk Rhabdomyosarcoma (RMS): A Report from the Childrens Oncology Group (COG) Soft Tissue Sarcoma Committee

机译:中度危险性横纹肌肉瘤(RMS)的放射治疗剂量的延迟初次切除及随后的修改:儿童肿瘤学组(COG)软组织肉瘤委员会的报告

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摘要

The majority of intermediate risk Rhabdomyosarcoma (RMS) patients have gross residual disease (Group III) after their first operative procedure. It is currently not known if local control rates can be maintained when, following induction chemotherapy, the radiation therapy (RT) dose is decreased after a delayed primary excision (DPE). To answer this question we evaluated patients enrolled on COG D9803 (1999-2005) who had Group III tumors of the bladder dome, extremity, or trunk (thorax, abdomen, pelvis) were candidates for DPE at week 12 if the primary tumor appeared resectable. RT dose was then adjusted by the completeness of DPE: no evidence of disease (NED) 36 Gy, microscopic residual (MR) 41.4 Gy, and gross residual disease (GRD) 50.4 Gy. A total of 161 Group III patients were evaluated (24 bladder dome, 63 extremity, and 74 trunk). Seventy-three patients (45%) underwent DPE which achieved removal of all gross disease in 61 (84%) who were then eligible for reduced RT dose [43/73 received 36 Gy, 19/73 received 41.4 Gy]. The local 5-year failure rate (0% for bladder dome, 7% for extremity and 20% for trunk) was similar to IRS-IV, which did not encourage DPE and did not allow for DPE adapted RT dose reduction. In conclusion, DPE was performed in 45% of Group III RMS patients with tumors at select anatomic sites (bladder dome, extremity and trunk), and 84% of those who had DPE were eligible for RT dose reduction. Local control outcomes were similar to historic results with RT alone.
机译:大多数中等风险的横纹肌肉瘤(RMS)患者在首次手术后均患有严重残留疾病(III组)。目前尚不清楚,在诱导化疗后,延迟初次切除(DPE)后降低放射治疗(RT)剂量时,能否维持局部控制率。为了回答这个问题,我们评估了在COG D9803(1999-2005)入组的患者中,如果原发性肿瘤可以切除,则其膀胱穹,、四肢或躯干(胸部,腹部,骨盆)的III组肿瘤在第12周时应作为DPE的候选人。然后通过DPE的完整性来调整RT剂量:无疾病证据(NED)36 Gy,无微观残留(MR)41.4 Gy,有总残留疾病(GRD)50.4 Gy。总共对161名III组患者进行了评估(24个膀胱穹,、 63个四肢和74个躯干)。 73例患者(45%)接受了DPE治疗,这些患者中有61例(84%)的全部疾病得以清除,然后有资格降低RT剂量[43/73接受36 Gy,19/73接受41.4 Gy]。局部5年失败率(膀胱穹顶为0%,四肢为7%,躯干为20%)与IRS-IV相似,IRS-IV不鼓励DPE,也不允许DPE适应性降低RT剂量。结论是,DPE是在45%的III类RMS肿瘤患者中进行的,这些患者在特定的解剖部位(膀胱穹,、四肢和躯干)有肿瘤,而84%的DPE患者符合降低RT剂量的条件。局部控制的结果与仅使用放疗的历史结果相似。

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