Literature DB >> 23841031

Phase 1 study of intravenous rigosertib (ON 01910.Na), a novel benzyl styryl sulfone structure producing G2/M arrest and apoptosis, in adult patients with advanced cancer.

Takao Ohnuma1, Deborah Lehrer, Chen Ren, Sool Yeon Cho, Manoj Maniar, Lewis Silverman, Max Sung, Herbert F Gretz, Vladimir Benisovich, Shyamala Navada, Eugene Akahoho, Eric Wilck, David R Taft, John Roboz, Francois Wilhelm, James F Holland.   

Abstract

Rigosertib (ON 01910.Na), a synthetic novel benzyl styryl sulfone, was administered to 28 patients with advanced cancer in a Phase I trial in order to characterize its pharmacokinetic profile, determine the dose-limiting toxicities (DLT), define the recommended phase II dose (RPTD) and to document any antitumor activity. Patients with advanced malignant neoplasms refractory to standard therapy were given escalating doses of rigosertib (50, 100, 150, 250, 325, 400, 650, 850, 1,050, 1,375, 1,700 mg/m(2)/24h) as a 3-day continuous infusion (CI) every 2 weeks. An accelerated Fibonacci titration schedule with specified decreases for toxicities was used for escalation until grade ≥2 toxicity occurred. Intrapatient dose escalation was allowed if toxicity was grade ≤2 and the disease remained stable. Plasma pharmacokinetics (PK) and urinary PK assessments were studied in the 1st and 4th cycles. Twenty-nine patients (12 men and 17 women; age 36-87 y with a median of 63 y) were registered, but one died before study drug was given. Twenty-eight patients received a median of 3 cycles of therapy. Most common grade ≥2 toxicities attributable to rigosertib included fatigue, anorexia, vomiting and constipation. DLTs included muscular weakness, hyponatremia, neutropenia, delirium and confusional state. Risk factors for severe toxicities include pre-existing neurological dysfunction or advanced gynecologic cancer after pelvic surgery. Rigosertib pharmacokinetics showed rapid plasma distribution phases and urinary excretion. Elevations in plasma Cmax and AUC due to decreases in plasma clearance were associated with acute grade ≥3 toxicities. Of 22 evaluable patients, 9 (41%) achieved a best overall response of stable disease; all other patients (n=13; 59%) progressed. The median progression-free survival time was 50 days (95% confidence interval [CI]: 37-80 days). Nine (41%) patients survived for over 1 y. In summary, prolonged IV infusions of rigosertib were generally well tolerated. Nine (41%) patients achieved stable disease and 9 (41%) patients survived for over 1 year. The RPTD appears to be 850 mg/m(2)/24hr CI x 3 days. (ClinicalTrials.gov identifier: NCT01538537).

Entities:  

Keywords:  ON01910.Na; Rigosertib; phase 1 study; phosphatidylinositol-3-kinase; polo-like kinase

Year:  2013        PMID: 23841031      PMCID: PMC3696538     

Source DB:  PubMed          Journal:  Am J Cancer Res        ISSN: 2156-6976            Impact factor:   6.166


  10 in total

1.  Effect of ON 01910.Na, an anticancer mitotic inhibitor, on cell-cycle progression correlates with RanGAP1 hyperphosphorylation.

Authors:  Irina A Oussenko; James F Holland; E Premkumar Reddy; Takao Ohnuma
Journal:  Cancer Res       Date:  2011-06-06       Impact factor: 12.701

2.  Treatment of higher risk myelodysplastic syndrome patients unresponsive to hypomethylating agents with ON 01910.Na.

Authors:  Mahesh Seetharam; Alice C Fan; Mai Tran; Liwen Xu; John P Renschler; Dean W Felsher; Kunju Sridhar; Francois Wilhelm; Peter L Greenberg
Journal:  Leuk Res       Date:  2011-09-14       Impact factor: 3.156

3.  ON01910, a non-ATP-competitive small molecule inhibitor of Plk1, is a potent anticancer agent.

Authors:  Kiranmai Gumireddy; M V Ramana Reddy; Stephen C Cosenza; R Boominathan; R Boomi Nathan; Stacey J Baker; Nabisa Papathi; Jiandong Jiang; James Holland; E Premkumar Reddy
Journal:  Cancer Cell       Date:  2005-03       Impact factor: 31.743

4.  Clinical application and proposal for modification of the International Working Group (IWG) response criteria in myelodysplasia.

Authors:  Bruce D Cheson; Peter L Greenberg; John M Bennett; Bob Lowenberg; Pierre W Wijermans; Stephen D Nimer; Antonio Pinto; Miloslav Beran; Theo M de Witte; Richard M Stone; Moshe Mittelman; Guillermo F Sanz; Steven D Gore; Charles A Schiffer; Hagop Kantarjian
Journal:  Blood       Date:  2006-04-11       Impact factor: 22.113

5.  Directed therapy for patients with myelodysplastic syndromes (MDS) by suppression of cyclin D1 with ON 01910.Na.

Authors:  Matthew J Olnes; Aarthie Shenoy; Barbara Weinstein; Loretta Pfannes; Kelsey Loeliger; Zachary Tucker; Xin Tian; Minjung Kwak; Francois Wilhelm; Agnes S M Yong; Irina Maric; Manoj Maniar; Phillip Scheinberg; Jerome Groopman; Neal S Young; Elaine M Sloand
Journal:  Leuk Res       Date:  2012-04-21       Impact factor: 3.156

6.  BI 2536, a potent and selective inhibitor of polo-like kinase 1, inhibits tumor growth in vivo.

Authors:  Martin Steegmaier; Matthias Hoffmann; Anke Baum; Péter Lénárt; Mark Petronczki; Martin Krssák; Ulrich Gürtler; Pilar Garin-Chesa; Simone Lieb; Jens Quant; Matthias Grauert; Günther R Adolf; Norbert Kraut; Jan-Michael Peters; Wolfgang J Rettig
Journal:  Curr Biol       Date:  2007-02-08       Impact factor: 10.834

7.  Accelerated titration designs for phase I clinical trials in oncology.

Authors:  R Simon; B Freidlin; L Rubinstein; S G Arbuck; J Collins; M C Christian
Journal:  J Natl Cancer Inst       Date:  1997-08-06       Impact factor: 13.506

8.  Phase I study of ON 01910.Na, a novel modulator of the Polo-like kinase 1 pathway, in adult patients with solid tumors.

Authors:  Antonio Jimeno; Jing Li; Wells A Messersmith; Daniel Laheru; Michelle A Rudek; Manoj Maniar; Manuel Hidalgo; Sharyn D Baker; Ross C Donehower
Journal:  J Clin Oncol       Date:  2008-10-27       Impact factor: 44.544

9.  Validation and implementation of a liquid chromatography/tandem mass spectrometry assay to quantitate ON 01910.Na, a mitotic progression modulator, in human plasma.

Authors:  Jing Li; Ming Zhao; Antonio Jimeno; Ping He; M V Ramana Reddy; Manuel Hidalgo; Ross C Donehower; Michelle A Rudek
Journal:  J Chromatogr B Analyt Technol Biomed Life Sci       Date:  2007-06-07       Impact factor: 3.205

10.  Styryl sulfonyl compounds inhibit translation of cyclin D1 in mantle cell lymphoma cells.

Authors:  A Prasad; I-W Park; H Allen; X Zhang; M V R Reddy; R Boominathan; E P Reddy; J E Groopman
Journal:  Oncogene       Date:  2009-02-09       Impact factor: 9.867

  10 in total
  4 in total

Review 1.  Real-time nanoscale proteomic analysis of the novel multi-kinase pathway inhibitor rigosertib to measure the response to treatment of cancer.

Authors:  Alice C Fan; Jennifer J O'Rourke; Dave R Praharaj; Dean W Felsher
Journal:  Expert Opin Investig Drugs       Date:  2013-08-12       Impact factor: 6.206

Review 2.  Genome maintenance in retinoblastoma: Implications for therapeutic vulnerabilities.

Authors:  Chunsik Lee; Jong Kyong Kim
Journal:  Oncol Lett       Date:  2022-04-29       Impact factor: 3.111

Review 3.  Present and Future Perspective on PLK1 Inhibition in Cancer Treatment.

Authors:  Michela Chiappa; Serena Petrella; Giovanna Damia; Massimo Broggini; Federica Guffanti; Francesca Ricci
Journal:  Front Oncol       Date:  2022-06-02       Impact factor: 5.738

4.  Novel induction of CD40 expression by tumor cells with RAS/RAF/PI3K pathway inhibition augments response to checkpoint blockade.

Authors:  Chi Yan; Nabil Saleh; Jinming Yang; Caroline A Nebhan; Anna E Vilgelm; E Premkumar Reddy; Joseph T Roland; Douglas B Johnson; Sheau-Chiann Chen; Rebecca L Shattuck-Brandt; Gregory D Ayers; Ann Richmond
Journal:  Mol Cancer       Date:  2021-06-06       Impact factor: 41.444

  4 in total

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