Literature DB >> 28420721

Phase I Study of Fenretinide Delivered Intravenously in Patients with Relapsed or Refractory Hematologic Malignancies: A California Cancer Consortium Trial.

Ann M Mohrbacher1, Allen S Yang1, Susan Groshen2, Shivaani Kummar3, Martin E Gutierrez4, Min H Kang5, Denice Tsao-Wei2, C Patrick Reynolds6, Edward M Newman7, Barry J Maurer8.   

Abstract

Purpose: A phase I study was conducted to determine the MTD, dose-limiting toxicities (DLT), and pharmacokinetics of fenretinide delivered as an intravenous emulsion in relapsed/refractory hematologic malignancies.Experimental Design: Fenretinide (80-1,810 mg/m2/day) was administered by continuous infusion on days 1 to 5, in 21-day cycles, using an accelerated titration design.
Results: Twenty-nine patients, treated with a median of three prior regimens (range, 1-7), were enrolled and received the test drug. Ninety-seven courses were completed. An MTD was reached at 1,280 mg/m2/day for 5 days. Course 1 DLTs included 6 patients with hypertriglyceridemia, 4 of whom were asymptomatic; 2 patients experienced DLT thrombocytopenia (asymptomatic). Of 11 patients with response-evaluable peripheral T-cell lymphomas, two had complete responses [CR, progression-free survival (PFS) 68+ months; unconfirmed CR, PFS 14+ months], two had unconfirmed partial responses (unconfirmed PR, PFS 5 months; unconfirmed PR, PFS 6 months), and five had stable disease (2-12 cycles). One patient with mature B-cell lymphoma had an unconfirmed PR sustained for two cycles. Steady-state plasma levels were approximately 10 mcg/mL (mid-20s μmol/L) at 640 mg/m2/day, approximately 14 mcg/mL (mid-30s μmol/L) at 905 mg/m2/day, and approximately 22 mcg/mL (mid-50s μmol/L) at 1,280 mg/m2/day.Conclusions: Intravenous fenretinide obtained significantly higher plasma levels than a previous capsule formulation, had acceptable toxicities, and evidenced antitumor activity in peripheral T-cell lymphomas. A recommended phase II dosing is 600 mg/m2 on day 1, followed by 1,200 mg/m2 on days 2 to 5, every 21 days. A registration-enabling phase II study in relapsed/refractory PTCL (ClinicalTrials.gov identifier: NCT02495415) is ongoing. Clin Cancer Res; 23(16); 4550-5. ©2017 AACR. ©2017 American Association for Cancer Research.

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Year:  2017        PMID: 28420721      PMCID: PMC5559312          DOI: 10.1158/1078-0432.CCR-17-0234

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  17 in total

1.  Involvement of reactive oxygen species in N-(4-hydroxyphenyl)retinamide-induced apoptosis in cervical carcinoma cells.

Authors:  N Oridate; S Suzuki; M Higuchi; M F Mitchell; W K Hong; R Lotan
Journal:  J Natl Cancer Inst       Date:  1997-08-20       Impact factor: 13.506

2.  N-(4-hydroxyphenyl)retinamide elevates ceramide in neuroblastoma cell lines by coordinate activation of serine palmitoyltransferase and ceramide synthase.

Authors:  H Wang; B J Maurer; C P Reynolds; M C Cabot
Journal:  Cancer Res       Date:  2001-07-01       Impact factor: 12.701

3.  Increase of ceramide and induction of mixed apoptosis/necrosis by N-(4-hydroxyphenyl)- retinamide in neuroblastoma cell lines.

Authors:  B J Maurer; L S Metelitsa; R C Seeger; M C Cabot; C P Reynolds
Journal:  J Natl Cancer Inst       Date:  1999-07-07       Impact factor: 13.506

4.  N-(4-hydroxyphenyl)retinamide increases ceramide and is cytotoxic to acute lymphoblastic leukemia cell lines, but not to non-malignant lymphocytes.

Authors:  P H O'Donnell; W-X Guo; C P Reynolds; B J Maurer
Journal:  Leukemia       Date:  2002-05       Impact factor: 11.528

5.  Treatment of advanced stages of Philadelphia chromosome-positive chronic myelogenous leukemia with interferon-alpha and low-dose cytarabine.

Authors:  H M Kantarjian; M J Keating; E H Estey; S O'Brien; S Pierce; M Beran; C Koller; E Feldman; M Talpaz
Journal:  J Clin Oncol       Date:  1992-05       Impact factor: 44.544

6.  Phase II study of oral capsular 4-hydroxyphenylretinamide (4-HPR/fenretinide) in pediatric patients with refractory or recurrent neuroblastoma: a report from the Children's Oncology Group.

Authors:  Judith G Villablanca; Wendy B London; Arlene Naranjo; Patrick McGrady; Matthew M Ames; Joel M Reid; Renee M McGovern; Sarah A Buhrow; Hollie Jackson; Enno Stranzinger; Brenda J Kitchen; Paul M Sondel; Marguerite T Parisi; Barry Shulkin; Gregory A Yanik; Susan L Cohn; C Patrick Reynolds
Journal:  Clin Cancer Res       Date:  2011-09-09       Impact factor: 12.531

7.  Identification of dihydroceramide desaturase as a direct in vitro target for fenretinide.

Authors:  Mehrdad Rahmaniyan; Robert W Curley; Lina M Obeid; Yusuf A Hannun; Jacqueline M Kraveka
Journal:  J Biol Chem       Date:  2011-05-04       Impact factor: 5.157

8.  Differential effects of N-(4-hydroxyphenyl)retinamide and retinoic acid on neuroblastoma cells: apoptosis versus differentiation.

Authors:  M Ponzoni; P Bocca; V Chiesa; A Decensi; V Pistoia; L Raffaghello; C Rozzo; P G Montaldo
Journal:  Cancer Res       Date:  1995-02-15       Impact factor: 12.701

9.  Phase I trial of fenretinide delivered orally in a novel organized lipid complex in patients with relapsed/refractory neuroblastoma: a report from the New Approaches to Neuroblastoma Therapy (NANT) consortium.

Authors:  Barry J Maurer; Min H Kang; Judith G Villablanca; Jitka Janeba; Susan Groshen; Katherine K Matthay; Paul M Sondel; John M Maris; Hollie A Jackson; Fariba Goodarzian; Hiroyuki Shimada; Scarlett Czarnecki; Beth Hasenauer; C Patrick Reynolds; Araz Marachelian
Journal:  Pediatr Blood Cancer       Date:  2013-06-29       Impact factor: 3.167

10.  Tolerability of the synthetic retinoid Fenretinide (HPR).

Authors:  A Costa; W Malone; M Perloff; F Buranelli; T Campa; G Dossena; A Magni; M Pizzichetta; C Andreoli; M Del Vecchio
Journal:  Eur J Cancer Clin Oncol       Date:  1989-05
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  11 in total

Review 1.  Clinical development of fenretinide as an antineoplastic drug: Pharmacology perspectives.

Authors:  Jason P Cooper; C Patrick Reynolds; Hwangeui Cho; Min H Kang
Journal:  Exp Biol Med (Maywood)       Date:  2017-04-21

2.  Efficacy of Optimized Treatment Protocol Using LAU-7b Formulation against Ovalbumin (OVA) and House Dust Mite (HDM) -Induced Allergic Asthma in Atopic Hyperresponsive A/J Mice.

Authors:  Mina Youssef; Juan B De Sanctis; Cynthia Kanagaratham; Shao Tao; Eisha Ahmed; Danuta Radzioch
Journal:  Pharm Res       Date:  2020-01-08       Impact factor: 4.200

Review 3.  Sphingolipids and Lymphomas: A Double-Edged Sword.

Authors:  Alfredo Pherez-Farah; Rosa Del Carmen López-Sánchez; Luis Mario Villela-Martínez; Rocío Ortiz-López; Brady E Beltrán; José Ascención Hernández-Hernández
Journal:  Cancers (Basel)       Date:  2022-04-19       Impact factor: 6.575

Review 4.  Harnessing the power of sphingolipids: Prospects for acute myeloid leukemia.

Authors:  Johnson Ung; Su-Fern Tan; Todd E Fox; Jeremy J P Shaw; Luke R Vass; Pedro Costa-Pinheiro; Francine E Garrett-Bakelman; Michael K Keng; Arati Sharma; David F Claxton; Ross L Levine; Martin S Tallman; Myles C Cabot; Mark Kester; David J Feith; Thomas P Loughran
Journal:  Blood Rev       Date:  2022-04-09       Impact factor: 10.626

5.  Fenretinide induces a new form of dynamin-dependent cell death in pediatric sarcoma.

Authors:  Eva Brack; Marco Wachtel; Anja Wolf; Andres Kaech; Urs Ziegler; Beat W Schäfer
Journal:  Cell Death Differ       Date:  2020-03-06       Impact factor: 15.828

6.  A phase I study of intravenous fenretinide (4-HPR) for patients with malignant solid tumors.

Authors:  Jacob S Thomas; Anthony B El-Khoueiry; Barry J Maurer; Susan Groshen; Jacek K Pinski; Everardo Cobos; David R Gandara; Heinz J Lenz; Min H Kang; C Patrick Reynolds; Edward M Newman
Journal:  Cancer Chemother Pharmacol       Date:  2021-01-10       Impact factor: 3.333

Review 7.  Pulmonary Delivery of Fenretinide: A Possible Adjuvant Treatment In COVID-19.

Authors:  Isabella Orienti; Giovanna Angela Gentilomi; Giovanna Farruggia
Journal:  Int J Mol Sci       Date:  2020-05-27       Impact factor: 5.923

Review 8.  The SUMO Pathway in Hematomalignancies and Their Response to Therapies.

Authors:  Mathias Boulanger; Rosa Paolillo; Marc Piechaczyk; Guillaume Bossis
Journal:  Int J Mol Sci       Date:  2019-08-09       Impact factor: 5.923

9.  A new bioavailable fenretinide formulation with antiproliferative, antimetabolic, and cytotoxic effects on solid tumors.

Authors:  Isabella Orienti; Federica Francescangeli; Maria Laura De Angelis; Katia Fecchi; Lucilla Bongiorno-Borbone; Michele Signore; Angelo Peschiaroli; Alessandra Boe; Alessandro Bruselles; Angelita Costantino; Adriana Eramo; Valentina Salvati; Giovanni Sette; Paola Contavalli; Lello Zolla; Toshihiko Oki; Toshio Kitamura; Massimo Spada; Alessandro Giuliani; Marta Baiocchi; Filippo La Torre; Gerry Melino; Marco Tartaglia; Ruggero De Maria; Ann Zeuner
Journal:  Cell Death Dis       Date:  2019-07-23       Impact factor: 8.469

10.  A novel oral micellar fenretinide formulation with enhanced bioavailability and antitumour activity against multiple tumours from cancer stem cells.

Authors:  Isabella Orienti; Valentina Salvati; Giovanni Sette; Massimo Zucchetti; Lucilla Bongiorno-Borbone; Angelo Peschiaroli; Lello Zolla; Federica Francescangeli; Mariella Ferrari; Cristina Matteo; Ezia Bello; Antonio Di Virgilio; Mario Falchi; Maria Laura De Angelis; Marta Baiocchi; Gerry Melino; Ruggero De Maria; Ann Zeuner; Adriana Eramo
Journal:  J Exp Clin Cancer Res       Date:  2019-08-22
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