Literature DB >> 28436582

Phase I study of bortezomib in combination with irinotecan in patients with relapsed/refractory high-risk neuroblastoma.

Rajen Mody1, Lili Zhao2, Gregory Anthony Yanik1, Valerie Opipari1,3.   

Abstract

PURPOSE: Prognosis for relapsed/refractory high-risk neuroblastoma (HR-NBL) remains poor. Bortezomib, a proteasome inhibitor, has shown preclinical activity against NBL as a single agent and in combination with cytotoxic chemotherapy including irinotecan. PATIENTS AND METHODS: Eighteen HR-NBL patients with primary refractory (n = 8) or relapsed (n = 10) disease were enrolled in a Phase I study using modified Time To Event Continual Reassessment Method. Bortezomib (1.2 mg/m2 /day) was administered on days 1, 4, 8, and 11 intravenously (IV) and irinotecan was given IV on days 1-5 (35, 40, or 45 mg/m2 /day, on dose levels [DL] 1-3, respectively). The maximum tolerated dose (MTD), dose-limiting toxicity (DLT), and response rate were examined.
RESULTS: Eighteen NBL patients were evaluable for toxicity; 17 were evaluable for response assessment. A total of 142 courses were delivered (mean 8.2, median 2, range 1-48), with two patients receiving more than 40 courses of therapy. Two DLTs were reported, including a grade 4 thrombocytopenia (DL2) and a grade 3 irritability (DL3). MTD was estimated as DL3. Two of 17 (12%) evaluable patients showed objective responses (ORs) lasting more than 40 courses, including 1 partial remission and 1 complete remission. Four patients (23%) had prolonged stable disease (SD) lasting six or more courses, with a total of 35% study patients demonstrating clinical benefit in the form of prolonged OR or SD.
CONCLUSION: The combination of bortezomib and irinotecan was well tolerated by patients with relapsed/refractory NBL with favorable toxicity profile. It also showed modest but promising clinical activity and merits further testing in Phase II studies.
© 2017 Wiley Periodicals, Inc.

Entities:  

Keywords:  irinotecan; proteasome inhibitor; relapsed/refractory high-risk neuroblastoma

Mesh:

Substances:

Year:  2017        PMID: 28436582     DOI: 10.1002/pbc.26563

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  5 in total

1.  Heme Oxygenase Inhibition Sensitizes Neuroblastoma Cells to Carfilzomib.

Authors:  Ignazio Barbagallo; Cesarina Giallongo; Giovanni Li Volti; Alfio Distefano; Giuseppina Camiolo; Marco Raffaele; Loredana Salerno; Valeria Pittalà; Valeria Sorrenti; Roberto Avola; Michelino Di Rosa; Luca Vanella; Francesco Di Raimondo; Daniele Tibullo
Journal:  Mol Neurobiol       Date:  2018-06-10       Impact factor: 5.590

2.  Role of GOLPH3 and TPX2 in Neuroblastoma DNA Damage Response and Cell Resistance to Chemotherapy.

Authors:  Marzia Ognibene; Marina Podestà; Alberto Garaventa; Annalisa Pezzolo
Journal:  Int J Mol Sci       Date:  2019-09-25       Impact factor: 5.923

Review 3.  Heme Oxygenase-1 in Central Nervous System Malignancies.

Authors:  Giuseppe Sferrazzo; Michelino Di Rosa; Eugenio Barone; Giovanni Li Volti; Nicolò Musso; Daniele Tibullo; Ignazio Barbagallo
Journal:  J Clin Med       Date:  2020-05-21       Impact factor: 4.241

4.  Italian Precision Medicine in Pediatric Oncology: Moving beyond Actionable Alterations.

Authors:  Fabio Pastorino; Mario Capasso; Chiara Brignole; Serena Giglio; Veronica Bensa; Sueva Cantalupo; Vito Alessandro Lasorsa; Annalisa Tondo; Rossella Mura; Angela Rita Sementa; Alberto Garaventa; Mirco Ponzoni; Loredana Amoroso
Journal:  Int J Mol Sci       Date:  2022-09-23       Impact factor: 6.208

Review 5.  Novel Therapies for Relapsed and Refractory Neuroblastoma.

Authors:  Peter E Zage
Journal:  Children (Basel)       Date:  2018-10-31
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.