Fleten Karianne Giller, Lund-Andersen Christin, Waagene Stein, Abrahamsen Torveig Weum, Mørch Yrr, Boye Kjetil, Torgunrud Annette, Flatmark Kjersti
Department of Tumor Biology, Institute for Cancer Research, Oslo University Hospital, The Norwegian Radium Hospital, Oslo, Norway; Faculty of Medicine, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Department of Tumor Biology, Institute for Cancer Research, Oslo University Hospital, The Norwegian Radium Hospital, Oslo, Norway.
Transl Oncol. 2020 Aug;13(8):100793. doi: 10.1016/j.tranon.2020.100793. Epub 2020 May 21.
Mucinous peritoneal metastases (PM) generally respond poorly to systemic treatment, and there is a clear unmet need for new treatment strategies to improve survival and quality of life for patients with PM. In this work, the growth inhibitory effect of five drugs (oxaliplatin (OXA; 5 mg/kg), irinotecan (IRI; 60 mg/kg), cabazitaxel (CBZ; 15 or 30 mg/kg), regorafenib (REG; 10, 30 or 60 mg/kg), and capecitabine (CAP; 359 or 755 mg/kg) was investigated in three orthotopic patient-derived xenograft models that mimic mucinous PM. Drugs were administered intraperitoneally (i.p.) as monotherapy weekly for 4 weeks (OXA, IRI), as one single i.p. injection (CBZ), or orally (REG, CAP) daily 5 of 7 days per week for four weeks, and i.p. tumor growth and survival were monitored and compared between treatment groups. The i.p. administered drugs (OXA, IRI, CBZ) had the strongest growth inhibitory effect, with OXA being most efficacious, completely inhibiting tumor growth in the majority of the animals. CBZ and IRI also strongly inhibited tumor growth, but with more variation in efficacy between the models. A moderate reduction in tumor growth was observed in all models treated with REG, while CAP had little to no growth inhibitory effect. Targeted next-generation-sequencing has identified mutational profiles typically associated with PM (mutations in KRAS, GNAS, and BRAF oncogenes), supporting the representativeness of the models. The results presented in this work support the continued exploration of i.p. treatment protocols for PM, with OXA remaining and CBZ emerging as particularly interesting candidates for further studies.
黏液性腹膜转移瘤(PM)对全身治疗的反应通常较差,显然迫切需要新的治疗策略来提高PM患者的生存率和生活质量。在这项研究中,在三种模拟黏液性PM的原位患者来源异种移植模型中,研究了五种药物(奥沙利铂(OXA;5mg/kg)、伊立替康(IRI;60mg/kg)、卡巴他赛(CBZ;15或30mg/kg)、瑞戈非尼(REG;10、30或60mg/kg)和卡培他滨(CAP;359或755mg/kg)的生长抑制作用。药物作为单一疗法通过腹腔内(i.p.)给药,每周一次,共4周(OXA、IRI),或作为单次腹腔内注射(CBZ),或口服(REG、CAP),每周7天中的5天,持续4周,监测并比较各治疗组的腹腔内肿瘤生长和生存率。腹腔内给药的药物(OXA、IRI、CBZ)具有最强的生长抑制作用,其中OXA最为有效,在大多数动物中完全抑制了肿瘤生长。CBZ和IRI也强烈抑制肿瘤生长,但各模型之间的疗效差异更大。在所有接受REG治疗的模型中,肿瘤生长均有中度降低,而CAP几乎没有生长抑制作用。靶向新一代测序已确定了通常与PM相关的突变谱(KRAS、GNAS和BRAF癌基因中的突变),支持了模型的代表性。这项研究的结果支持继续探索PM的腹腔内治疗方案,OXA仍然是,而CBZ则成为进一步研究特别有吸引力的候选药物。