Literature DB >> 8633249

CPT-11: an original spectrum of clinical activity.

M L Rothenberg1.   

Abstract

Due to its novel mechanism of action, CPT-11 (irinotecan) has significant in vitro activity against a variety of solid tumors, including those particularly resistant to other cytotoxic agents. This activity has been confirmed in clinical trials of single-agent CPT-11 conducted in Japan, Europe, and the United States. In chemotherapy-naive patients with advanced non-small cell lung cancer, a response rate of 32% to 34% has been shown in Japan with CPT-11 monotherapy, although this has been improved to within the range of 43% to 54% using CPT-11 in combination with cisplatin. Prior chemotherapy appears to reduce the response rate substantially in this setting, although the mechanisms of cross-resistance are unknown. CPT-11 is also active in small cell lung cancer, with a single agent response rate of 47% in patients previously treated with cisplatin. As might be expected, CPT-11 is more active when combined with cisplatin as first-line chemotherapy for small cell lung cancer, with Japanese investigators reporting an average response rate of 85%. Consistent results from studies of colorectal cancer in Japan, the United States, and Europe, indicate that CPT-11 is active as a single agent in patients who have developed progressive disease following 5-fluorouracil (5-FU)-based treatment. In patients with metastatic colorectal cancer, approximately 18% to 27% of patients with 5-FU refractory disease and 15% to 32% of patients who are chemotherapy-naive respond to single agent therapy. Efforts to combine CPT-11 with 5-FU with or without folinic acid are ongoing. There is less clinical experience with CPT-11 in the treatment of other solid tumors, but activity has been reported in phase II trials of patients with squamous cell carcinoma of the uterine cervix or skin, and in those with cancer of the ovary, stomach, or pancreas and in patients with lymphoma. While notable objective response rates have been reported for single agent CPT-11, the precise role of this drug in the treatment of patients with solid tumors has yet to be defined, especially as part of first-line therapy. CPT-11 appears to be one of the most exciting new drugs to reach clinical development in the past decade, and its seemingly wide spectrum of clinical activity suggests that it may have a substantial impact on the treatment of many of the most common epithelial malignancies.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8633249

Source DB:  PubMed          Journal:  Semin Oncol        ISSN: 0093-7754            Impact factor:   4.929


  8 in total

Review 1.  Clinical pharmacokinetics of irinotecan.

Authors:  G G Chabot
Journal:  Clin Pharmacokinet       Date:  1997-10       Impact factor: 6.447

2.  Irinotecan plus carboplatin in patients with extensive-disease small-cell lung cancer.

Authors:  Young Saing Kim; Se Hoon Park; Sun Young Kyung; Sun Jin Sym; Sang Pyo Lee; Jeong Woong Park; Sung Hwan Jung; Jinny Park; Eun Kyung Cho; Jae Hoon Lee; Dong Bok Shin
Journal:  Med Oncol       Date:  2010-03-03       Impact factor: 3.064

3.  Irinotecan monotherapy as third-line or later treatment in advanced gastric cancer.

Authors:  Akitaka Makiyama; Kohei Arimizu; Gen Hirano; Chinatsu Makiyama; Yuzo Matsushita; Tsuyoshi Shirakawa; Hirofumi Ohmura; Masato Komoda; Keita Uchino; Kyoko Inadomi; Shuji Arita; Hiroshi Ariyama; Hitoshi Kusaba; Yudai Shinohara; Miyuki Kuwayama; Tatsuhiro Kajitani; Hisanobu Oda; Taito Esaki; Koichi Akashi; Eishi Baba
Journal:  Gastric Cancer       Date:  2017-08-10       Impact factor: 7.370

Review 4.  A review of the pharmacology and clinical activity of new chemotherapy agents for the treatment of colorectal cancer.

Authors:  A A Adjei
Journal:  Br J Clin Pharmacol       Date:  1999-09       Impact factor: 4.335

5.  Phase I dose escalation study of gemcitabine plus irinotecan in advanced solid tumors.

Authors:  Elizabeth Dugan; Roxanne Truax; Kellen L Meadows; Gerald C Blobe; Michael A Morse; Nishan H Fernando; Jon P Gockerman; William P Petros; Herbert I Hurwitz
Journal:  Anticancer Res       Date:  2009-12       Impact factor: 2.480

6.  A multicenter, phase I, dose-escalation study to assess the safety, tolerability, and pharmacokinetics of etirinotecan pegol in patients with refractory solid tumors.

Authors:  Gayle S Jameson; John T Hamm; Glen J Weiss; Carlos Alemany; Stephen Anthony; Michele Basche; Ramesh K Ramanathan; Mitesh J Borad; Raoul Tibes; Allen Cohn; Ioana Hinshaw; Robert Jotte; Lee S Rosen; Ute Hoch; Michael A Eldon; Robert Medve; Katrina Schroeder; Erica White; Daniel D Von Hoff
Journal:  Clin Cancer Res       Date:  2012-11-07       Impact factor: 12.531

7.  Phase I study of the combination of irinotecan hydrochloride, carboplatin, and dexamethasone for the treatment of relapsed or refractory malignant lymphoma.

Authors:  Junji Suzumiya; Hitoshi Suzushima; Kouichi Maeda; Seiichi Okamura; Atae Utsunomiya; Tunefumi Shibuya; Kazuo Tamura
Journal:  Int J Hematol       Date:  2004-04       Impact factor: 2.490

8.  Phase I study of cisplatin and irinotecan combined with concurrent hyperfractionated accelerated thoracic radiotherapy for locally advanced non-small cell lung carcinoma.

Authors:  Yuichi Takiguchi; Reiko Uruma; Yoshiko Asaka-Amano; Katsushi Kurosu; Yasunori Kasahara; Nobuhiro Tanabe; Koichiro Tatsumi; Takashi Uno; Hisao Itoh; Takayuki Kuriyama
Journal:  Int J Clin Oncol       Date:  2005-12       Impact factor: 3.850

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.