Literature DB >> 12023787

Phase I trials of pemetrexed.

Frank V Fossella1, Ulrich Gatzemeier.   

Abstract

The maximum tolerated dose of the multitargeted antifolate drug pemetrexed is 600 mg/m(2) every 3 weeks in heavily pretreated patients without folic acid supplementation. However, with folic acid supplementation, higher doses have been given without limiting side effects. The dose-limiting toxicities of pemetrexed are neutropenia, asthenia, and thrombocytopenia. Other adverse effects include anemia, anorexia, rash, nausea, vomiting, peripheral edema, diarrhea, mucositis, and reversible elevations of transaminase and creatinine levels. Multiple pemetrexed combination phase I trials have been completed or are underway. Without folic acid supplementation, pemetrexed doses of 400 to 600 mg/m(2)could be safely administered with full therapeutic doses of irinotecan, gemcitabine, cisplatin, carboplatin, oxaliplatin, and 5-fluorouracil. Preliminary data from other ongoing trials (with folic acid and vitamin B(12) supplementation) have similarly shown that pemetrexed doses of at least 400 to 500 mg/m(2) can be safely administered with therapeutic doses of vinorelbine, docetaxel, and paclitaxel. Combination studies of pemetrexed with agents active in breast cancer (doxorubicin, epirubicin, and cyclophosphamide) and chest radiotherapy are also now underway. Adverse effects of these combinations have included neutropenia, anemia, thrombocytopenia, asthenia, vomiting, diarrhea, rash, nausea, anorexia, mucositis, and reversible transaminase elevation. The phase I trials of pemetrexed have consistently shown activity against a broad range of tumor types, including colorectal cancer, pancreatic cancer, breast cancer, non-small cell lung cancer, and mesothelioma. This activity has been noted not only in the combination trials, but when pemetrexed is given as a single agent as well. Pemetrexed is a promising drug. It is active against a broad range of cancers, and it has manageable side effects that seem to be lessened with folic acid and vitamin B(12) supplementation. Copyright 2002, Elsevier Science (USA). All rights reserved.

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Year:  2002        PMID: 12023787     DOI: 10.1053/sonc.2002.30764

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


  5 in total

1.  Phase I study of pemetrexed and pegylated liposomal doxorubicin in patients with refractory breast, ovarian, primary peritoneal, or fallopian tube cancer.

Authors:  Donald A Richards; David Loesch; Svetislava J Vukelja; Hillary Wu; William J Hyman; Jeffery Nieves; Yunfei Wang; Simin Hu; Oluwatoyin O Shonukan; Datchen F Tai
Journal:  Invest New Drugs       Date:  2010-03-30       Impact factor: 3.850

Review 2.  Novel antifolate drugs.

Authors:  W Thomas Purcell; David S Ettinger
Journal:  Curr Oncol Rep       Date:  2003-03       Impact factor: 5.075

3.  An eQTL-based method identifies CTTN and ZMAT3 as pemetrexed susceptibility markers.

Authors:  Yujia Wen; Eric R Gamazon; Wasim K Bleibel; Claudia Wing; Shuangli Mi; Bridget E McIlwee; Shannon M Delaney; Shiwei Duan; Hae Kyung Im; M Eileen Dolan
Journal:  Hum Mol Genet       Date:  2011-12-13       Impact factor: 6.150

4.  Phase 2 trial of pemetrexed in children and adolescents with refractory solid tumors: a Children's Oncology Group study.

Authors:  Anne B Warwick; Suman Malempati; Mark Krailo; Allen Melemed; Richard Gorlick; Matthew M Ames; Stephanie L Safgren; Peter C Adamson; Susan M Blaney
Journal:  Pediatr Blood Cancer       Date:  2012-06-28       Impact factor: 3.167

Review 5.  Potential role of pemetrexed in metastatic breast cancer patients pre-treated with anthracycline or taxane.

Authors:  Li-Yan Zhou; Ye-Hui Shi; Yong-Sheng Jia; Zhong-Sheng Tong
Journal:  Chronic Dis Transl Med       Date:  2015-03-23
  5 in total

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