Literature DB >> 10577855

Phase II study of oral platinum drug JM216 as first-line treatment in patients with small-cell lung cancer.

E Fokkema1, H J Groen, J Bauer, D R Uges, C Weil, I E Smith.   

Abstract

PURPOSE: This multicenter phase II trial was performed to determine tumor efficacy and tolerance of the oral platinum drug JM216 in patients with small-cell lung cancer (SCLC). PATIENTS AND METHODS: Patients with SCLC limited disease unfit for intensive chemotherapy or those with extensive disease received JM216 120 mg/m(2)/d for 5 consecutive days every 3 weeks. Individual dose escalation to 140 mg/m(2)/d was allowed if toxicity was </= grade 2 according to the National Cancer Institute Common Toxicity Criteria. Tumor response was evaluated according to World Health Organization criteria.
RESULTS: Twenty-seven patients were assessable for toxicity and 26 for tumor response. Eighty-eight cycles were administered. Common Toxicity Criteria grade 3 and 4 hematologic toxicities were neutropenia in 15.9% and 3.7%, lymphocytopenia in 47.6% and 17.1%, and thrombocytopenia in 19.5% and 10.3% of cycles, respectively. One patient suffered from neutropenic fever. Nausea, vomiting, and diarrhea were the most common nonhematologic toxicities. Except for grade 4 diarrhea in one patient, no grade 4 nonhematologic toxicity was observed. No severe neurotoxicity or nephrotoxicity was observed. Tumor response rate was 10 of 26 (38%; 95% confidence interval, 19% to 58%), excluding five unconfirmed partial responses. No complete responses were observed. Median overall time to progression was 110 days (range, 5 to 624 days). Median overall survival time was 210 days (range, 5 to 624 days).
CONCLUSION: Oral JM216 is active in previously untreated patients with SCLC and shows mild toxicities.

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Year:  1999        PMID: 10577855     DOI: 10.1200/JCO.1999.17.12.3822

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  13 in total

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2.  Phase I study of JM-216 (an oral platinum analogue) in combination with paclitaxel in patients with advanced malignancies.

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3.  Platinum-(IV)-derivative satraplatin induced G2/M cell cycle perturbation via p53-p21(waf1/cip1)-independent pathway in human colorectal cancer cells.

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4.  High seroprevalence of human herpesvirus type 8 infection in males with advanced lung carcinoma.

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Journal:  Med Microbiol Immunol       Date:  2014-08-15       Impact factor: 3.402

5.  A phase I trial of the oral platinum analogue JM216 with concomitant radiotherapy in advanced malignancies of the chest.

Authors:  C M George; D J Haraf; A M Mauer; S A Krauss; P C Hoffman; C M Rudin; L Szeto; E E Vokes
Journal:  Invest New Drugs       Date:  2001       Impact factor: 3.850

6.  Phase 1 trial and pharmacokinetic study of the oral platinum analog satraplatin in children and young adults with refractory solid tumors including brain tumors.

Authors:  Srivandana Akshintala; Leigh Marcus; Katherine E Warren; Robert F Murphy; Tristan M Sissung; Anjali Srivastava; Wendy J Goodspeed; Anne Goodwin; Carmen C Brewer; Christopher Zalewski; Kelly A King; AeRang Kim; William D Figg; Brigitte C Widemann
Journal:  Pediatr Blood Cancer       Date:  2015-01-03       Impact factor: 3.167

7.  Phase II study of oral bis (aceto) ammine dichloro (cyclohexamine) platinum (IV) (JM-216, BMS-182751) given daily x 5 in hormone refractory prostate cancer (HRPC).

Authors:  Tahir Latif; Laura Wood; Cindy Connell; David C Smith; David Vaughn; David Lebwohl; David Peereboom
Journal:  Invest New Drugs       Date:  2005-01       Impact factor: 3.850

8.  The new platinum(IV) derivative LA-12 shows stronger inhibitory effect on Hsp90 function compared to cisplatin.

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Review 9.  Satraplatin: leading the new generation of oral platinum agents.

Authors:  Ashish Bhargava; Ulka N Vaishampayan
Journal:  Expert Opin Investig Drugs       Date:  2009-11       Impact factor: 6.206

Review 10.  Satraplatin in hormone-refractory prostate cancer and other tumour types: pharmacological properties and clinical evaluation.

Authors:  Mark J McKeage
Journal:  Drugs       Date:  2007       Impact factor: 9.546

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