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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.
Cheng, Yu; Teng, Zan; Zhang, Yanqiao; Jin, Bo; Zheng, Zhendong; Man, Li; Wang, Zhenghua; Teng, Yuee; Yu, Ping; Shi, Jing; Luo, Ying; Wang, Ying; Zhang, Jingdong; Zhang, Huijuan; Liu, Jiwei; Chen, Hao; Xiao, Jiawen; Zhao, Lei; Zhang, Lingyun; Jiang, Yu; Chen, Ying; Zhang, Jian; Wang, Chang; Liu, Sa; Qu, Jinglei; Qu, Xiujuan; Liu, Yunpeng.
Affiliation
  • Cheng Y; Department of Oncology, The First Hospital of China Medical University, Shenyang, Liaoning Province, China.
  • Teng Z; Key Laboratory of Anticancer Drugs and Biotherapy of Liaoning Province, the First Hospital of China Medical University, Shenyang, Liaoning Province, China.
  • Zhang Y; Liaoning Province Clinical Research Center for Cancer, Shenyang, Liaoning Province, China.
  • Jin B; Key Laboratory of Precision Diagnosis and Treatment of Gastrointestinal Tumors, Ministry of Education, Shenyang, Liaoning Province, China.
  • Zheng Z; Department of Oncology, The First Hospital of China Medical University, Shenyang, Liaoning Province, China.
  • Man L; Key Laboratory of Anticancer Drugs and Biotherapy of Liaoning Province, the First Hospital of China Medical University, Shenyang, Liaoning Province, China.
  • Wang Z; Liaoning Province Clinical Research Center for Cancer, Shenyang, Liaoning Province, China.
  • Teng Y; Key Laboratory of Precision Diagnosis and Treatment of Gastrointestinal Tumors, Ministry of Education, Shenyang, Liaoning Province, China.
  • Yu P; Department of Oncology, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang Province, China.
  • Shi J; Department of Oncology, The First Hospital of China Medical University, Shenyang, Liaoning Province, China.
  • Luo Y; Key Laboratory of Anticancer Drugs and Biotherapy of Liaoning Province, the First Hospital of China Medical University, Shenyang, Liaoning Province, China.
  • Wang Y; Liaoning Province Clinical Research Center for Cancer, Shenyang, Liaoning Province, China.
  • Zhang J; Key Laboratory of Precision Diagnosis and Treatment of Gastrointestinal Tumors, Ministry of Education, Shenyang, Liaoning Province, China.
  • Zhang H; Department of Oncology, Northern Theater Command General Hospital, Shenyang, Liaoning Province, China.
  • Liu J; Department of Oncology, Anshan Cancer Hospital, Anshan, Liaoning Province, China.
  • Chen H; Department of Oncology, The First Affiliated Hospital Of Jinzhou Medical University, Jinzhou, Liaoning Province, China.
  • Xiao J; Department of Oncology, The First Hospital of China Medical University, Shenyang, Liaoning Province, China.
  • Zhao L; Key Laboratory of Anticancer Drugs and Biotherapy of Liaoning Province, the First Hospital of China Medical University, Shenyang, Liaoning Province, China.
  • Zhang L; Liaoning Province Clinical Research Center for Cancer, Shenyang, Liaoning Province, China.
  • Jiang Y; Key Laboratory of Precision Diagnosis and Treatment of Gastrointestinal Tumors, Ministry of Education, Shenyang, Liaoning Province, China.
  • Chen Y; Department of Oncology, The First Hospital of China Medical University, Shenyang, Liaoning Province, China.
  • Zhang J; Key Laboratory of Anticancer Drugs and Biotherapy of Liaoning Province, the First Hospital of China Medical University, Shenyang, Liaoning Province, China.
  • Wang C; Liaoning Province Clinical Research Center for Cancer, Shenyang, Liaoning Province, China.
  • Liu S; Key Laboratory of Precision Diagnosis and Treatment of Gastrointestinal Tumors, Ministry of Education, Shenyang, Liaoning Province, China.
  • Qu J; Department of Oncology, The First Hospital of China Medical University, Shenyang, Liaoning Province, China.
  • Qu X; Key Laboratory of Anticancer Drugs and Biotherapy of Liaoning Province, the First Hospital of China Medical University, Shenyang, Liaoning Province, China.
  • Liu Y; Liaoning Province Clinical Research Center for Cancer, Shenyang, Liaoning Province, China.
BMC Cancer ; 24(1): 1082, 2024 Sep 02.
Article in En | MEDLINE | ID: mdl-39223545
ABSTRACT

BACKGROUND:

Colorectal 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.

METHODS:

This 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.

RESULTS:

A 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 (range3.1-61.0 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.

CONCLUSIONS:

The 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 REGISTRATION ClinicalTrials.gov identifier NCT03053167, registration date was 14/2/2017.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Quinazolines / Thiophenes / Colorectal Neoplasms / Antineoplastic Combined Chemotherapy Protocols / Irinotecan Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: BMC Cancer Journal subject: NEOPLASIAS Year: 2024 Document type: Article Affiliation country: China Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Quinazolines / Thiophenes / Colorectal Neoplasms / Antineoplastic Combined Chemotherapy Protocols / Irinotecan Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: BMC Cancer Journal subject: NEOPLASIAS Year: 2024 Document type: Article Affiliation country: China Country of publication: United kingdom