[Sensitivity of colorectal cancer organoids to hyperthermic intraperitoneal chemotherapy with lobaplatin]

Zhonghua Wei Chang Wai Ke Za Zhi. 2024 May 25;27(5):486-494. doi: 10.3760/cma.j.cn441530-20230613-00201.
[Article in Chinese]

Abstract

Objective: To investigate the sensitivity of tumor organoids derived from samples of colorectal cancer to lobaplatin and oxaliplatin hyperthermic perfusion in vitro and to assist clinical development of hyperthermic intraperitoneal chemotherapy. Method: Tumor samples and relevant clinical data were collected from patients with pathologically confirmed colorectal cancer in the Sixth Affiliated Hospital of Sun Yat-sen University from July 2021 to December 2022. Organoids were cultured and tumor tissue were passaged. In vitro hyperthermic perfusion experiments were performed on organoids with good viability. Firstly, 10 organoids were treated with oxaliplatin and lobaplatin at the following six concentrations: 1 000, 250, 62.5, 15.6, 3.9, and 0.98 μmol/L. The organoids were exposed to oxaliplatin at 42℃ for 30 minutes and to lobaplatin at 42℃ for 60 minutes. Dose-response curves of responses to in vitro hyperthermic perfusion with these two drugs were constructed and evaluated. Clinical doses of oxaliplatin and lobaplatin were further tested on 30 organoids. This testing revealed oxaliplatin was effective at 579 µmol/L at a hyperthermic perfusion temperature of 42℃ for 30 min and lobaplatin was effective at 240 µmol/L at a hyperthermic perfusion temperature of 42℃ for 60 minutes. Result: Thirty-two tumor organoids were cultured from samples of colorectal cancer. The median concentration required for oxaliplatin to eliminate 50% of tumor cells (IC50) was 577.45 µmol/L (IQR: 1846.09 µmol/L). The median IC50 for lobaplatin was 85.04 µmol/L (IQR: 305.01 µmol/L).The difference between the two groups was not statistically significant (Z=1.784, P=0.084). In seven of 10 organoids, lobaplatin showed a greater IC50 after in vitro hyperthermic perfusion than did oxaliplatin. Testing of 30 organoids with clinical doses of oxaliplatin and lobaplatin revealed that oxaliplatin achieved an average inhibition rate of 39.6% (95%CI: 32.1%‒47.0%), whereas the average rate of inhibition for lobaplatin was 89.7% (95%CI: 87.0%‒92.3%): this difference is statistically significant (t=‒15.282, P<0.001). Conclusion: The rate of inhibition achieved by hyperthermic perfusion of lobaplatin in vitro is better than that achieved by hyperthermic perfusion with oxaliplatin. Lobaplatin is more effective than oxaliplatin when administered by hyperthermic intraperitoneal perfusion and therefore has the potential to replace oxaliplatin in this setting.

目的: 利用结直肠癌患者来源的肿瘤类器官作为临床前模型,对比洛铂与奥沙利铂体外热灌注的药物敏感性,以辅助临床制定腹腔热灌注化疗方案。 方法: 收集2021年7月至2022年12月期间中山大学附属第六医院经病理确诊为结直肠癌的患者手术后切下的部分肿瘤组织及获取的相关临床资料,对肿瘤组织进行类器官培养及传代,对活性良好的类器官进行体外热灌注实验。首先使用10例类器官分别进行6种浓度梯度(1 000、250、62.5、15.6、3.9和0.98 μmol/L)的奥沙利铂和洛铂体外热灌注实验,奥沙利铂于42℃环境下与类器官接触30 min,洛铂于42℃环境下与类器官接触60 min,根据绘制的剂量反应曲线,评估两种药物体外热灌注剂量反应能力。进一步使用30例类器官进行奥沙利铂和洛铂临床剂量的测试,奥沙利铂浓度为579 μmol/L,热灌注温度为42℃,时间为30 min;洛铂浓度为240 μmol/L,热灌注温度为42℃,时间为60 min。评估奥沙利铂和洛铂两种药物的体外热灌注敏感性。 结果: 成功培养了32例结直肠癌患者的肿瘤类器官。奥沙利铂消除50%肿瘤细胞所需的浓度(IC50)中位数为577.45 μmol/L(IQR:1 846.09 μmol/L);洛铂的IC50中位数为85.04 μmol/L(IQR:305.01 μmol/L),两者比较差异无统计学意义(Z=1.784,P=0.084);10个类器官中有7个结果显示洛铂体外热灌注IC50大于奥沙利铂。30例类器官在奥沙利铂和洛铂临床剂量下的测试结果显示:奥沙利铂的平均抑制率为39.6%(95%CI:32.1%~47.0%),洛铂的平均抑制率为89.7%(95%CI:87.0%~92.3%),两者比较差异有统计学意义(t=-15.282,P<0.001)。 结论: 洛铂体外热灌注的抑制率优于奥沙利铂,有希望代替奥沙利铂成为更好的腹腔热灌注化疗药物。.

Publication types

  • English Abstract

MeSH terms

  • Antineoplastic Agents / administration & dosage
  • Colorectal Neoplasms* / drug therapy
  • Colorectal Neoplasms* / pathology
  • Colorectal Neoplasms* / therapy
  • Cyclobutanes* / administration & dosage
  • Female
  • Humans
  • Hyperthermia, Induced / methods
  • Hyperthermic Intraperitoneal Chemotherapy*
  • Male
  • Organoids*
  • Organoplatinum Compounds* / administration & dosage
  • Organoplatinum Compounds* / therapeutic use
  • Oxaliplatin* / administration & dosage
  • Oxaliplatin* / pharmacology
  • Oxaliplatin* / therapeutic use

Substances

  • Cyclobutanes
  • lobaplatin
  • Organoplatinum Compounds
  • Oxaliplatin
  • Antineoplastic Agents