Szumera-Ciećkiewicz Anna, Bobak Klaudia, Spałek Mateusz J, Sokół Kamil, Wągrodzki Michał, Owczarek Daria, Kawecka Monika, Puton Beata, Koseła-Paterczyk Hanna, Rutkowski Piotr, Czarnecka Anna M
Department of Pathology, Maria Sklodowska-Curie National Research Institute of Oncology, 02781 Warsaw, Poland.
Diagnostic Hematology Department, Institute of Hematology and Transfusion Medicine, 00791 Warsaw, Poland.
Cancers (Basel). 2023 May 29;15(11):2960. doi: 10.3390/cancers15112960.
Marginally resectable and unresectable soft tissue sarcomas (STS) remain a therapy challenge due to the lack of highly active treatment. The aim of the study was to identify a biomarker to predict the pathological response (PR) to preplanned treatment of these STSs.
In the phase II clinical trial (NCT03651375), locally advanced STS patients received preoperative treatment with a combination of doxorubicin-ifosfamide chemotherapy and 5 × 5 Gy radiotherapy. PR to the treatment was classified using the European Organization for Research and Treatment of Cancer-Soft Tissue and Bone Sarcoma Group recommendations. We have chosen HIF-1α, CD163, CD68, CD34, CD105, and γH2AFX proteins, rendering different biological phenomena, for biomarker study.
Nineteen patients were enrolled and in four cases a good PR was reported. The high expression of HIF-1α before surgery showed a negative correlation with PR, which means a poor response to therapy. Furthermore, the samples after surgery had decreased expression of HIF-1α, which confirmed the correlation with PR. However, high expression of γH2AFX positively correlated with PR, which provides better PR. The high number of positive-staining TAMs and the high IMVD did not correlate with PR.
HIF1α and γH2AFX could be potential biomarkers for PR prediction after neoadjuvant treatment in STS.
由于缺乏高效的治疗方法,边缘可切除和不可切除的软组织肉瘤(STS)仍然是治疗上的挑战。本研究的目的是确定一种生物标志物,以预测这些STS对预先计划治疗的病理反应(PR)。
在II期临床试验(NCT03651375)中,局部晚期STS患者接受了阿霉素-异环磷酰胺化疗和5×5 Gy放疗联合的术前治疗。根据欧洲癌症研究与治疗组织-软组织和骨肉瘤组的建议对治疗的PR进行分类。我们选择了呈现不同生物学现象的HIF-1α、CD163、CD68、CD34、CD105和γH2AFX蛋白进行生物标志物研究。
纳入19例患者,其中4例报告有良好的PR。术前HIF-1α的高表达与PR呈负相关,这意味着对治疗反应不佳。此外,术后样本中HIF-1α的表达降低,这证实了与PR的相关性。然而,γH2AFX的高表达与PR呈正相关,这意味着更好的PR。高数量的阳性染色肿瘤相关巨噬细胞(TAM)和高微血管密度(IMVD)与PR无关。
HIF1α和γH2AFX可能是STS新辅助治疗后PR预测的潜在生物标志物。