Markovic Svetomir N, Galli Filippo, Suman Vera J, Nevala Wendy K, Paulsen Andrew M, Hung Joseph C, Gansen Denise N, Erickson Lori A, Marchetti Paolo, Wiseman Gregory A, Signore Alberto
Department of Oncology, Mayo Clinic, Rochester, MN, USA.
Department of Immunology, Mayo Clinic, Rochester, MN, USA.
Oncotarget. 2018 Jul 13;9(54):30268-30278. doi: 10.18632/oncotarget.25666.
Early in the course of immunotherapy there is frequently a transient enlargement of tumor masses (pseudo-progression) due to tumor infiltration by TILs. Current clinical imaging modalities are not able to distinguished pseudo-progression from true tumor progression. Thus, patients often remain on treatment 4-8 weeks longer to confirm disease progression. Nuclear medicine offers the possibility to image immune cells and potentially discriminate pseudo-progression and progression. We conducted a pilot study in patients with metastatic melanoma receiving ipilimumab (IPI) or pembrolizumab (PEMBRO) to assess safety and feasibility of SPECT/CT imaging with Tc- interleukin-2 (Tc-HYNIC-IL2) to detect TILs and distinguish between true progression from pseudo- progression. Scans were performed prior to and after 12w treatment. After labelling,Tc-HYNIC-IL2 was purified and diluted in 10 mL of 5% glucose with 0.1% human serum albumin. Of the 5 patients (2 treated with IPI and 3 with PEMBRO) enrolled, two failed to complete the second scan as they discontinued IPI due grade 3 colitis (1 patient) or patient refusal after developing multiple toxicities attributed to IPI (1 patient). Following the first scan, one patient reported to have a grade 1 pruritus with grade 1 pain. No other toxicities attributed to the radiopharmaceutical infusion were reported. Metastatic lesions could be visualized by Tc-IL2 imaging and there was positive correlation between size and Tc-HYNIC-IL2 uptake, both before and after 12 weeks of therapy. The results of this pilot study demonstrate the safety and feasibility of Tc-IL2 imaging and has led to a number of hypotheses to be tested in future studies.
在免疫治疗过程早期,由于肿瘤浸润淋巴细胞(TILs)浸润肿瘤,肿瘤肿块常出现短暂增大(假进展)。目前的临床成像方式无法区分假进展和真正的肿瘤进展。因此,患者通常会继续治疗4 - 8周以确认疾病进展。核医学提供了对免疫细胞成像并潜在区分假进展和进展的可能性。我们对接受伊匹单抗(IPI)或派姆单抗(PEMBRO)治疗的转移性黑色素瘤患者进行了一项初步研究,以评估用锝 - 白细胞介素 - 2(Tc - HYNIC - IL2)进行SPECT/CT成像检测TILs并区分真正进展与假进展的安全性和可行性。在治疗12周前后进行扫描。标记后,将Tc - HYNIC - IL2纯化并在含有0.1%人血清白蛋白的10 mL 5%葡萄糖中稀释。在纳入的5名患者(2名接受IPI治疗,3名接受PEMBRO治疗)中,两名患者未能完成第二次扫描,因为其中1名患者因3级结肠炎停用IPI,另1名患者在出现多种归因于IPI的毒性反应后拒绝继续治疗。第一次扫描后,一名患者报告有1级瘙痒和1级疼痛。未报告其他归因于放射性药物输注的毒性反应。转移性病变可通过Tc - IL2成像显示,并且在治疗12周前后,病变大小与Tc - HYNIC - IL2摄取之间均存在正相关。这项初步研究的结果证明了Tc - IL2成像的安全性和可行性,并提出了一些有待未来研究检验的假设。