Literature DB >> 27446580

Different schedules of irinotecan administration: A meta-analysis.

Yi Shao1, Hui Lv1, Dian-Sheng Zhong1.   

Abstract

The concept of the UDP glucuronosyltransferase family 1 member A1 genotype-directed schedule of irinotecan administration is still far from being introduced into clinical practice, and the efficacy and toxicity of irinotecan are in part schedule-dependent. The objective of the present meta-analysis was to determine the efficacy and adverse effects of 3-weekly vs. weekly irinotecan for the treatment of solid tumors. The PubMed, EMBASE and Cochrane Library databases and the search engines Google Scholar and Medical Martix were searched for randomized controlled trials to compare the two regimens of irinotecan administration. The results of the meta-analysis indicated that the 3-weekly regimen yielded a longer time to progression, while other measures of efficacy, such as the objective response rate and overall survival of patients with solid tumors were similar between the two regimens of irinotecan administration. Furthermore, the group receiving the 3-weekly regimen had a lower incidence of grade 3/4 diarrhea and a higher rate of grade 3/4 neutropenia compared with the group receiving the weekly regimen. However, these results require confirmation by large-sample, multicenter, randomized, controlled trials.

Entities:  

Keywords:  colorectal carcinoma; irinotecan; meta-analysis; schedule; solid tumor

Year:  2016        PMID: 27446580      PMCID: PMC4950879          DOI: 10.3892/mco.2016.920

Source DB:  PubMed          Journal:  Mol Clin Oncol        ISSN: 2049-9450


  23 in total

1.  Dose-finding and pharmacokinetic study to optimize the dosing of irinotecan according to the UGT1A1 genotype of patients with cancer.

Authors:  Federico Innocenti; Richard L Schilsky; Jacqueline Ramírez; Linda Janisch; Samir Undevia; Larry K House; Soma Das; Kehua Wu; Michelle Turcich; Robert Marsh; Theodore Karrison; Michael L Maitland; Ravi Salgia; Mark J Ratain
Journal:  J Clin Oncol       Date:  2014-06-23       Impact factor: 44.544

Review 2.  Irinotecan in the treatment of colorectal cancer: clinical overview.

Authors:  U Vanhoefer; A Harstrick; W Achterrath; S Cao; S Seeber; Y M Rustum
Journal:  J Clin Oncol       Date:  2001-03-01       Impact factor: 44.544

3.  UGT1A1 genotype-guided phase I study of irinotecan, oxaliplatin, and capecitabine.

Authors:  Matthew P Goetz; Heidi A McKean; Joel M Reid; Sumithra J Mandrekar; Angelina D Tan; Mary A Kuffel; Stephanie L Safgren; Renee M McGovern; Richard M Goldberg; Axel A Grothey; Robert McWilliams; Charles Erlichman; Matthew M Ames
Journal:  Invest New Drugs       Date:  2013-10-10       Impact factor: 3.850

4.  Irinotecan pharmacogenetics: a finished puzzle?

Authors:  Mitch A Phelps; Alex Sparreboom
Journal:  J Clin Oncol       Date:  2014-06-23       Impact factor: 44.544

5.  Rationale for the dosage and schedule of CPT-11 (irinotecan) selected for phase II studies, as determined by European phase I studies.

Authors:  J P Armand; Y M Extra; G Catimel; D Abigerges; M Marty; M Clavel
Journal:  Ann Oncol       Date:  1996-10       Impact factor: 32.976

6.  Randomized phase II window trial of two schedules of irinotecan with vincristine in patients with first relapse or progression of rhabdomyosarcoma: a report from the Children's Oncology Group.

Authors:  Leo Mascarenhas; Elizabeth R Lyden; Philip P Breitfeld; David O Walterhouse; Sarah S Donaldson; Charles N Paidas; David M Parham; James R Anderson; William H Meyer; Douglas S Hawkins
Journal:  J Clin Oncol       Date:  2010-09-13       Impact factor: 44.544

Review 7.  Irinotecan (CPT-11): pharmacology and clinical applications.

Authors:  N Masuda; S Kudoh; M Fukuoka
Journal:  Crit Rev Oncol Hematol       Date:  1996-09       Impact factor: 6.312

8.  Randomized phase II study of two irinotecan schedules for patients with metastatic breast cancer refractory to an anthracycline, a taxane, or both.

Authors:  Edith A Perez; David W Hillman; James A Mailliard; James N Ingle; J Michael Ryan; Tom R Fitch; Kendrith M Rowland; Carl G Kardinal; James E Krook; John W Kugler; Shaker R Dakhil
Journal:  J Clin Oncol       Date:  2004-07-15       Impact factor: 44.544

9.  Two different schedules of irinotecan (CPT-11) in patients with advanced colorectal carcinoma relapsing after a 5-fluorouracil and leucovorin combination. A randomized study.

Authors:  N Tsavaris; N Ziras; C Kosmas; T Giannakakis; P Gouveris; M Vadiaka; A Dimitrakopoulos; D Karadima; S Rokana; E Papalambros; G Papastratis; H Margaris; H Tsipras; A Polyzos
Journal:  Cancer Chemother Pharmacol       Date:  2003-09-23       Impact factor: 3.333

10.  Randomised trial of irinotecan versus fluorouracil by continuous infusion after fluorouracil failure in patients with metastatic colorectal cancer.

Authors:  P Rougier; E Van Cutsem; E Bajetta; N Niederle; K Possinger; R Labianca; M Navarro; R Morant; H Bleiberg; J Wils; L Awad; P Herait; C Jacques
Journal:  Lancet       Date:  1998-10-31       Impact factor: 79.321

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  1 in total

1.  Phase 1 study of alisertib (MLN8237) and weekly irinotecan in adults with advanced solid tumors.

Authors:  Thomas J Semrad; Edward J Kim; I-Yeh Gong; Tianhong Li; Scott Christensen; Mili Arora; Jonathan W Riess; David R Gandara; Karen Kelly
Journal:  Cancer Chemother Pharmacol       Date:  2021-05-15       Impact factor: 3.288

  1 in total

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