Literature DB >> 19877111

A phase 2 clinical trial of nab-paclitaxel in previously treated and chemotherapy-naive patients with metastatic melanoma.

Evan M Hersh1, Steven J O'Day, Antoni Ribas, Wolfram E Samlowski, Michael S Gordon, Deganit E Shechter, Alicia A Clawson, Rene Gonzalez.   

Abstract

BACKGROUND: nab-Paclitaxel (ABI-007, Abraxane), a 130-nM, albumin-bound (nab) particle form of Cremophor-free paclitaxel, is approved for metastatic breast cancer. In the current study, the efficacy and safety of nab-paclitaxel were evaluated in previously treated and chemotherapy-naive patients with metastatic melanoma (MM).
METHODS: Patients with histologically or cytologically confirmed, measurable MM were enrolled. nab-Paclitaxel was administered intravenously weekly for 3 of 4 weeks at a dose of 100 mg/m(2) (in previously treated patients) or 150 mg/m(2) (in chemotherapy-naive patients).
RESULTS: Thirty-seven patients were treated in each cohort. The response rate was 2.7% in the previously treated cohort and 21.6% in the chemotherapy-naive cohort; the response plus stable disease rate was 37.8% and 48.6% in the previously treated and chemotherapy-naive cohorts, respectively. The median progression-free survival (PFS) was 3.5 months and 4.5 months, and the median survival was 12.1 months and 9.6 months, respectively. The probability of being alive and free of disease progression at 6 months was 27% for the previously treated cohort and 34% for the chemotherapy-naive cohort; the probability of surviving 1 year was 49% and 41%, respectively, for the previously treated and chemotherapy-naive cohorts. Approximately 78% of the previously treated patients and 49% of the chemotherapy-naive patients were treated without dose reduction. Eight (22%) chemotherapy-naive patients discontinued therapy because of toxicities. Drug-related toxicities included grade 3 to 4 (graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events [version 3.0]) neuropathy, alopecia, neutropenia, and fatigue.
CONCLUSIONS: nab-Paclitaxel was found to be well tolerated and demonstrated activity in both previously treated and chemotherapy-naive patients with MM. The response rate, PFS, and survival compared favorably with current standard dacarbazine therapy and combination therapies for melanoma. nab-Paclitaxel therapy of MM should be investigated further in controlled clinical trials. Cancer 2010. (c) 2010 American Cancer Society. Copyright 2010 American Cancer Society.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 19877111     DOI: 10.1002/cncr.24720

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  37 in total

Review 1.  Overcoming the challenges in the effective delivery of chemotherapies to CNS solid tumors.

Authors:  Hemant Sarin
Journal:  Ther Deliv       Date:  2010-08

Review 2.  Latest advances in chemotherapeutic, targeted, and immune approaches in the treatment of metastatic melanoma.

Authors:  Darshil J Shah; Roxana S Dronca
Journal:  Mayo Clin Proc       Date:  2014-04       Impact factor: 7.616

Review 3.  Advances in cutaneous melanoma.

Authors:  Enrique Espinosa; Alfonso Berrocal; José Antonio López Martín; María González Cao; Pablo Cerezuela; José Ignacio Mayordomo; Salvador Martín Algarra
Journal:  Clin Transl Oncol       Date:  2012-05       Impact factor: 3.405

4.  A phase II trial of nab-paclitaxel (ABI-007) and carboplatin in patients with unresectable stage IV melanoma : a North Central Cancer Treatment Group Study, N057E(1).

Authors:  Lisa A Kottschade; Vera J Suman; Thomas Amatruda; Robert R McWilliams; Bassam I Mattar; Daniel A Nikcevich; Robert Behrens; Tom R Fitch; Anthony J Jaslowski; Svetomir N Markovic
Journal:  Cancer       Date:  2010-11-08       Impact factor: 6.860

Review 5.  The role of chemotherapy in the modern management of melanoma.

Authors:  Rebecca Jane Lee; Noor Ul-Ain-Tariq; Alberto Fusi; Samantha Bowyer; Paul Lorigan
Journal:  Melanoma Manag       Date:  2014-12-04

Review 6.  What is the role of chemotherapy in the treatment of melanoma?

Authors:  Ahmed I Megahed; Henry B Koon
Journal:  Curr Treat Options Oncol       Date:  2014-06

7.  Systemic delivery of nanoparticle formulation of novel tubulin inhibitor for treating metastatic melanoma.

Authors:  Vaibhav Mundra; Yang Peng; Virender Kumar; Wei Li; Duane D Miller; Ram I Mahato
Journal:  Drug Deliv Transl Res       Date:  2015-06       Impact factor: 4.617

Review 8.  Optimal management of metastatic melanoma: current strategies and future directions.

Authors:  Marta Batus; Salman Waheed; Carl Ruby; Lindsay Petersen; Steven D Bines; Howard L Kaufman
Journal:  Am J Clin Dermatol       Date:  2013-06       Impact factor: 7.403

9.  A phase I study of hepatic arterial infusion of nab-paclitaxel in combination with intravenous gemcitabine and bevacizumab for patients with advanced cancers and predominant liver metastases.

Authors:  Apostolia M Tsimberidou; Yang Ye; Jennifer Wheler; Aung Naing; David Hong; Uchechi Nwosu; Kenneth R Hess; Robert A Wolff
Journal:  Cancer Chemother Pharmacol       Date:  2013-02-03       Impact factor: 3.333

10.  Phase I trial of biochemotherapy with cisplatin, temozolomide, and dose escalation of nab-paclitaxel combined with interleukin-2 and interferon-α in patients with metastatic melanoma.

Authors:  Anas Alrwas; Nicholas E Papadopoulos; Suzanne Cain; Sapna P Patel; Kevin B Kim; Tawania L Deburr; Roland Bassett; Wen-Jen Hwu; Agop Y Bedikian; Michael A Davies; Scott E Woodman; Patrick Hwu
Journal:  Melanoma Res       Date:  2014-08       Impact factor: 3.599

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.