School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Int J Cancer. 2024 May 15;154(10):1794-1801. doi: 10.1002/ijc.34845. Epub 2024 Feb 5.
DNA methyltransferase inhibitors (DNMTi) have demonstrated benefit in reversing resistance to systemic therapies for several cancer types. In a phase II trial of guadecitabine and irinotecan compared to regorafenib or TAS-102 in pts with advanced mCRC refractory to irinotecan. Patients with mCRC refractory to irinotecan were randomized 2:1 to guadecitabine and irinotecan (Arm A) vs standard of care regorafenib or TAS-102 (Arm B) on a 28-day cycle. Between January 15, 2016 and October 24, 2018, 104 pts were randomized at four international sites, with 96 pts undergoing treatment, 62 in Arm A and 34 in Arm B. Median overall survival was 7.15 months for Arm A and 7.66 months for Arm B (HR 0.93, 95% CI: 0.58-1.47, P = .75). The Kaplan-Meier rates of progression free survival at 4 months were 32% in Arm A and 26% in Arm B. Common ≥Grade 3 treatment related adverse events in Arm A were neutropenia (42%), anemia (18%), diarrhea (11%), compared to Arm B pts with neutropenia (12%), anemia (12%). Guadecitabine and irinotecan had similar OS compared to standard of care TAS-102 or regorafenib, with evidence of target modulation. Clinical trial information: NCT01896856.
DNA 甲基转移酶抑制剂 (DNMTi) 在逆转几种癌症类型对系统治疗的耐药性方面显示出益处。在一项比较 guadecitabine 和伊立替康与regorafenib 或 TAS-102 在对伊立替康耐药的晚期 mCRC 患者中的 II 期试验中。对伊立替康耐药的 mCRC 患者按 2:1 随机分配至 guadecitabine 和伊立替康(A 组)与标准治疗 regorafenib 或 TAS-102(B 组),每 28 天为一个周期。在 2016 年 1 月 15 日至 2018 年 10 月 24 日期间,在四个国际中心随机分配了 104 名患者,96 名患者接受了治疗,其中 62 名在 A 组,34 名在 B 组。A 组的中位总生存期为 7.15 个月,B 组为 7.66 个月(HR 0.93,95%CI:0.58-1.47,P=0.75)。A 组的 4 个月无进展生存期的 Kaplan-Meier 率为 32%,B 组为 26%。A 组常见的≥3 级治疗相关不良事件为中性粒细胞减少(42%)、贫血(18%)、腹泻(11%),而 B 组为中性粒细胞减少(12%)、贫血(12%)。Guadecitabine 和伊立替康的 OS 与标准治疗 TAS-102 或 regorafenib 相似,具有靶标调节的证据。临床试验信息:NCT01896856。