Dantonello Tobias M, Int-Veen Christoph, Winkler Peter, Leuschner Ivo, Schuck Andreas, Schmidt Bernhard F, Lochbuehler Helmut, Kirsch Sylvia, Hallmen Erika, Veit-Friedrich Iris, Bielack Stefan S, Niggli Felix, Kazanowska Bernarda, Ladenstein Ruth, Wiebe Thomas, Klingebiel Thomas, Treuner Joern, Koscielniak Ewa
Olgahospital, Pediatrics 5 (Oncology, Hematology, Immunology), Klinikum Stuttgart, Bismarckstrasse 8, D-70176 Stuttgart, Germany.
J Clin Oncol. 2008 Jan 20;26(3):406-13. doi: 10.1200/JCO.2007.12.2382.
Evaluation of primary tumor-, treatment-, and patient-related factors predicting relapse pattern, risk, and survival after relapse with the aim to design a risk-adapted, tumor-directed surveillance program for patients with localized rhabdomyosarcoma (RMS).
One thousand one hundred sixty-four patients with nonmetastatic RMS achieved complete remission at the end of multimodal therapy in the consecutive trials of the Cooperative Weichteilsarkom Studiengruppe (CWS)-81, CWS-86, CWS-91, and CWS-96 between 1980 and 2002 (median follow-up, 5 years). Three hundred thirty-seven of these individuals developed either locoregional, metastatic, or combined relapses. Predictive factors for relapse, its pattern, and postrelapse survival were analyzed.
Age, histology, tumor size, tumor site, postsurgical stage, and omission of radiotherapy were identified as factors associated with an increased relapse risk in multivariate analyses. Relapse rates did not differ among the CWS trials. Median time to relapse was 1.43 years from first diagnosis (range, 0.13 to 13.5 years). There were 217 locoregional, 72 metastatic, and 48 combined recurrences. Only two patients developed metastases more than 4 years after diagnosis, and both had combined recurrences. Five-year postrelapse survival was 24%. Patient subsets with consistent relapse pattern, risk, and postrelapse survival rates were identified on the basis of histologic subtype and tumor size.
Initial patient and tumor characteristics predict pattern and risk of relapse and also correlate with postrelapse survival probabilities. In localized RMS, tumor-directed follow-up should focus on the primary site. Screening for metastatic relapse may not be necessary more than 4 years after diagnosis. The identification of subgroups with distinctive pattern and risk of relapse may be used to develop risk-adapted, tumor-directed guidance for detection of recurrent disease in localized RMS.
评估原发性肿瘤、治疗及患者相关因素对横纹肌肉瘤(RMS)复发模式、风险及复发后生存的预测作用,旨在为局限性横纹肌肉瘤患者设计一个风险适应性、针对肿瘤的监测方案。
1980年至2002年期间,在合作横纹肌肉瘤研究组(CWS)-81、CWS-86、CWS-91和CWS-96的连续试验中,1164例非转移性横纹肌肉瘤患者在多模式治疗结束时达到完全缓解(中位随访时间为5年)。其中337例患者出现局部区域复发、远处转移或混合性复发。分析复发的预测因素、复发模式及复发后生存情况。
在多因素分析中,年龄、组织学类型、肿瘤大小、肿瘤部位、术后分期及未进行放疗被确定为与复发风险增加相关的因素。CWS各项试验的复发率无差异。从首次诊断到复发的中位时间为1.43年(范围为0.13至13.5年)。有217例局部区域复发、72例远处转移和48例混合性复发。仅2例患者在诊断后4年以上出现转移,且均为混合性复发。复发后5年生存率为24%。根据组织学亚型和肿瘤大小确定了复发模式、风险及复发后生存率一致的患者亚组。
患者和肿瘤的初始特征可预测复发模式和风险,也与复发后生存概率相关。在局限性横纹肌肉瘤中,针对肿瘤的随访应聚焦于原发部位。诊断后4年以上可能无需筛查远处转移复发。识别具有独特复发模式和风险的亚组可用于为局限性横纹肌肉瘤复发病变的检测制定风险适应性、针对肿瘤的指导方案。