Irinotecan plus raltitrexed as second-line treatment in locally advanced or metastatic colorectal cancer patients: a prospective open-label, single-arm, multi-center, phase II study

被引:2
作者
Cheng, Yu [1 ,2 ,3 ,4 ]
Teng, Zan [1 ,2 ,3 ,4 ]
Zhang, Yanqiao [5 ]
Jin, Bo [1 ,2 ,3 ,4 ]
Zheng, Zhendong [6 ]
Man, Li [7 ]
Wang, Zhenghua [8 ]
Teng, Yuee [1 ,2 ,3 ,4 ]
Yu, Ping [1 ,2 ,3 ,4 ]
Shi, Jing [1 ,2 ,3 ,4 ]
Luo, Ying [1 ,2 ,3 ,4 ]
Wang, Ying [9 ]
Zhang, Jingdong [10 ]
Zhang, Huijuan [11 ]
Liu, Jiwei [12 ]
Chen, Hao [13 ]
Xiao, Jiawen [14 ]
Zhao, Lei [1 ,2 ,3 ,4 ]
Zhang, Lingyun [1 ,2 ,3 ,4 ]
Jiang, Yu [15 ]
Chen, Ying [1 ,2 ,3 ,4 ]
Zhang, Jian [16 ]
Wang, Chang [17 ]
Liu, Sa [18 ]
Qu, Jinglei [1 ,2 ,3 ,4 ]
Qu, Xiujuan [1 ,2 ,3 ,4 ]
Liu, Yunpeng [1 ,2 ,3 ,4 ]
机构
[1] China Med Univ, Hosp 1, Dept Oncol, Shenyang, Liaoning, Peoples R China
[2] China Med Univ, Hosp 1, Key Lab Anticanc Drugs & Biotherapy Liaoning Prov, Shenyang, Liaoning, Peoples R China
[3] Liaoning Prov Clin Res Ctr Canc, Shenyang, Liaoning, Peoples R China
[4] Minist Educ, Key Lab Precis Diag & Treatment Gastrointestinal, Shenyang, Liaoning, Peoples R China
[5] Harbin Med Univ, Canc Hosp, Dept Oncol, Harbin, Heilongjiang, Peoples R China
[6] Gen Hosp Northern Theater Command, Dept Oncol, Shenyang, Liaoning, Peoples R China
[7] Anshan Canc Hosp, Dept Oncol, Anshan, Liaoning, Peoples R China
[8] Jinzhou Med Univ, Affiliated Hosp 1, Dept Oncol, Jinzhou, Liaoning, Peoples R China
[9] China Med Univ, Dept Oncol, Shengjing Hosp, Shenyang, Liaoning, Peoples R China
[10] Liaoning Canc Hosp, Dept Oncol, Shenyang, Liaoning, Peoples R China
[11] Tieling Cent Hosp, Dept Oncol, Tieling, Liaoning, Peoples R China
[12] Dalian Med Univ, Affiliated Hosp 1, Dept Oncol, Dalian, Liaoning, Peoples R China
[13] Liaoyang Liaohua Hosp, Dept Oncol, Liaoyang, Liaoning, Peoples R China
[14] Shenyang Fifth People Hosp, Dept Oncol, Shenyang, Peoples R China
[15] Panjin Cent Hosp, Dept Obstet & Gynecol, Panjin, Liaoning, Peoples R China
[16] Liaoyang City Cent Hosp, Dept Neurosurg, Liaoyang, Liaoning, Peoples R China
[17] First Hosp Jilin Univ, Dept Oncol Neurosurg, Changchun, Jilin, Peoples R China
[18] China Med Univ, Affiliated Hosp 4, Dept Oncol, Shenyang, Liaoning, Peoples R China
关键词
Raltitrexed; Colorectal cancer; Second-line chemotherapy; 1ST-LINE CHEMOTHERAPY; OXALIPLATIN; DEFICIENCY; TOXICITY; TRIAL;
D O I
10.1186/s12885-024-12831-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundColorectal cancer is the third most common cancer and the second leading cause of cancer death. There are limited therapeutic options for the treatment of locally advanced or metastatic colorectal cancers which fail first-line chemotherapy. Phase I/II studies showed that the combined application of the raltitrexed and irinotecan has significant synergistic effect and acceptable toxicity. However, most of these previous studies have relatively small sample size.MethodsThis is a prospective open-label, single-arm, multi-center, Phase II trial. Brief inclusion criteria: patients were aged 18 to 75 years with locally advanced or metastatic colorectal cancer after failure of 5-FU and oxaliplatin therapy. Enrolled patients received raltitrexed (3 mg/m2, d1) and irinotecan (180 mg/m2, d1) each 21-day cycle until disease progression or unacceptable toxicity. The primary endpoint was progression-free survival, and the secondary endpoints were disease control rate, objective response rate, overall survival and safety.ResultsA total of 108 patients were enrolled between September 2016 and May 2020. The median age was 61 years, ECOG 1 score accounts for 67.6%, the rest were ECOG 0. A total of 502 cycles were completed, with an average of 4.6 cycles and a median of 4 cycles. 108 patients were evaluated, with an objective response rate of 17.6%, and disease control rate of 76.9%. The median follow-up time was 27 months (range:3.1-61.0 m) at data cut-off on March 2023. Median progression-free survival was 4.9 months (95% CI 4.1-5.7) and median overall survival was 13.1 months (95% CI 12.2-15.5). The most common adverse events that were elevated are alanine aminotransferase increased, aspartate aminotransferase increased, fatigue, diarrhoea, neutrocytopenia, thrombocytopenia, hypohemoglobin, and leukocytopenia. Most of the adverse events were Grade I/II, which were relieved after symptomatic treatment, and there were no treatment-related cardiotoxicities and deaths.ConclusionsThe combination of raltitrexed and irinotecan as second-line treatment for mCRC could be a reliable option after failure of standard 5-Fu-first-line chemotherapy in locally advanced or metastatic colorectal cancers, especially for patients with 5-FU intolerance (cardiac events or DPD deficiency patients).Trial registrationClinicalTrials.gov identifier: NCT03053167, registration date was 14/2/2017.
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