Andreou Dimosthenis, Werner Mathias, Pink Daniel, Traub Frank, Schuler Markus K, Gosheger Georg, Jobke Björn, Reichardt Peter, Tunn Per-Ulf
a Department of General Orthopaedics and Tumour Orthopaedics , Münster University Hospital , Münster , Germany .
b Department of Orthopaedic Oncology , Sarcoma Centre Berlin-Brandenburg, HELIOS Klinikum Berlin-Buch , Berlin , Germany .
Int J Hyperthermia. 2016;32(2):159-64. doi: 10.3109/02656736.2015.1109146. Epub 2015 Dec 15.
Histological response assessment following neoadjuvant treatment can help identify patients at a higher risk for systemic disease progression. Our goal was to evaluate whether mitotic count and the amount of viable tumour following neoadjuvant isolated limb perfusion (ILP) for primary, locally advanced, non-metastatic, high-grade extremity soft tissue sarcoma correlate with prognosis.
This study is a retrospective analysis of 61 patients who underwent neoadjuvant ILP followed by surgical resection with curative intent between 2001 and 2011. Non-parametric analyses were carried out with the Mann-Whitney U and the Wilcoxon signed-rank test. Survival curves were calculated with the Kaplan-Meier method and compared with the log-rank test.
The median follow-up was 44 months for all patients and 55 months for survivors. The amount of viable tumour after ILP had no correlation with overall (OS) (P = 0.227) or event-free (EFS) (P = 0.238) survival probability. Patients with a low mitotic count after ILP had a significantly higher OS (P < 0.001), EFS (P = 0.002) and post-relapse survival probability (P = 0.030) compared to patients with an intermediate or high mitotic count.
The mitotic count following ILP for primary, high-grade, locally advanced, non-metastatic soft tissue sarcoma appears to significantly correlate with prognosis. If these results are validated in a prospective setting, they could provide a rationale for the design of adjuvant systemic chemotherapy trials with the goal of improving the prognosis of patients with an intermediate or high mitotic count after ILP.
新辅助治疗后的组织学反应评估有助于识别系统性疾病进展风险较高的患者。我们的目标是评估原发性、局部晚期、非转移性、高级别肢体软组织肉瘤新辅助隔离肢体灌注(ILP)后的有丝分裂计数和存活肿瘤量是否与预后相关。
本研究是对2001年至2011年间接受新辅助ILP并随后进行根治性手术切除的61例患者的回顾性分析。采用Mann-Whitney U检验和Wilcoxon符号秩检验进行非参数分析。用Kaplan-Meier方法计算生存曲线,并与对数秩检验进行比较。
所有患者的中位随访时间为44个月,幸存者为55个月。ILP后存活肿瘤量与总生存期(OS)(P = 0.227)或无事件生存期(EFS)(P = 0.238)的生存概率均无相关性。与有丝分裂计数中等或较高的患者相比,ILP后有丝分裂计数低的患者的OS(P < 0.001)、EFS(P = 0.002)和复发后生存概率(P = 0.030)显著更高。
原发性、高级别、局部晚期、非转移性软组织肉瘤ILP后的有丝分裂计数似乎与预后显著相关。如果这些结果在前瞻性研究中得到验证,它们可为辅助性全身化疗试验的设计提供理论依据,以改善ILP后有丝分裂计数中等或较高患者的预后。