Literature DB >> 12057119

Metastatic melanoma.

W Sun1, L M Schuchter.   

Abstract

The overall survival for patients with metastatic melanoma ranges from 4.7 to 11 months, with a median survival of 8.5 months. Standard treatment for patients with metastatic melanoma has not been defined. The range of treatment options includes close observation, surgical resection of isolated metastases, therapy with dacarbazine, combination chemotherapy, and participation in clinical trials. Numerous chemotherapeutic agents have shown activity in the treatment of malignant melanoma. Dacarbazine (DTIC-Dome; Bayer Corporation, West Haven, CT) has a response rate of 15% to 20% and remains the reference agent for the treatment of metastatic disease. Additional agents with single-agent activity include cisplatin, (Platinol-AQ; Bristol-Myers Oncology, Princeton, NJ); carmustine (BiCNU; Bristol-Myers Oncology, Princeton, NJ); paclitaxel (Taxol; Bristol-Myers Squibb, Princeton, NJ); and docetaxel (Taxotere; Rhone-Poulenc Rorer Pharmaceuticals, Collegeville, PA). Temozolomide (Temodar; Schering-Plough, Kenilworth, NJ), which is essentially an oral form of dacarbazine but with greater central nervous system penetrance, is associated with a response rate of 20%. Combination chemotherapy with or without tamoxifen has been extensively evaluated in patients with metastatic melanoma. Although the initial results with the Dartmouth regimen (dacarbazine, cisplatin, carmustine, and tamoxifen) were associated with overall response rates of 50% to 55% in single-institution studies, results from larger multicenter studies reveal responses rates ranging from 10% to 20%. Based on the results of several clinical trials, there is no evidence that the addition of tamoxifen improves the response rate. Another combination regimen is cisplatin, vinblastine, and dacarbazine (CVD), which is associated with a 20% to 25% response rate. There has been widespread interest in developing immunotherapies against metastatic melanoma. Interferon (IFN)-alfa and interleukin (IL)-2 as single agents have produced response rates in the 15% to 20% range. Biochemotherapy, which is a combination of immunotherapy and cytotoxic chemotherapy, has been studied in patients with metastatic melanoma. Multiple phase II studies have demonstrated high response rates but unclear impact on overall survival. Therapy is associated with significant toxicity. Ongoing randomized clinical trials will clarify the role of biochemotherapy in patients with metastatic melanoma. Ongoing new approaches to treatment include the therapeutic use of vaccines alone or in combination with cytokines.

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Year:  2001        PMID: 12057119     DOI: 10.1007/s11864-001-0033-5

Source DB:  PubMed          Journal:  Curr Treat Options Oncol        ISSN: 1534-6277


  25 in total

1.  Complete responses and long-term survivals after systemic chemotherapy for patients with advanced malignant melanoma.

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Journal:  Cancer       Date:  1989-01-15       Impact factor: 6.860

2.  Combination chemotherapy with cisplatin, carmustine, dacarbazine, and tamoxifen in metastatic melanoma.

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Review 3.  The treatment of metastatic melanoma with chemotherapy and biologics.

Authors:  M B Atkins
Journal:  Curr Opin Oncol       Date:  1997-03       Impact factor: 3.645

4.  Sequential chemoimmunotherapy in the treatment of metastatic melanoma.

Authors:  J M Richards; N Mehta; K Ramming; P Skosey
Journal:  J Clin Oncol       Date:  1992-08       Impact factor: 44.544

Review 5.  High-dose recombinant interleukin 2 therapy for patients with metastatic melanoma: analysis of 270 patients treated between 1985 and 1993.

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Journal:  J Clin Oncol       Date:  1999-07       Impact factor: 44.544

6.  Dimethyl triazeno imidazole carboxamide and combination therapy for melanoma. IV. Late results after complete response to chemotherapy (Central Oncology Group protocols 7130, 7131, and 7131A).

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Journal:  Cancer       Date:  1984-03-15       Impact factor: 6.860

7.  Metastasectomy in malignant melanoma.

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Journal:  Surgery       Date:  1994-03       Impact factor: 3.982

8.  Interferon alfa-2b adjuvant therapy of high-risk resected cutaneous melanoma: the Eastern Cooperative Oncology Group Trial EST 1684.

Authors:  J M Kirkwood; M H Strawderman; M S Ernstoff; T J Smith; E C Borden; R H Blum
Journal:  J Clin Oncol       Date:  1996-01       Impact factor: 44.544

9.  Randomized phase III trial of treatment with high-dose interleukin-2 either alone or in combination with interferon alfa-2a in patients with advanced melanoma.

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Journal:  J Clin Oncol       Date:  1993-10       Impact factor: 44.544

10.  Prognostic factors in 1,521 melanoma patients with distant metastases.

Authors:  A Barth; L A Wanek; D L Morton
Journal:  J Am Coll Surg       Date:  1995-09       Impact factor: 6.113

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  23 in total

Review 1.  Genetic alterations of PTEN in human melanoma.

Authors:  Almass-Houd Aguissa-Touré; Gang Li
Journal:  Cell Mol Life Sci       Date:  2011-11-11       Impact factor: 9.261

2.  Antimetastatic activity and low systemic toxicity of tetradecyl gallate in a preclinical melanoma mouse model.

Authors:  Claudriana Locatelli; Deborah Regina Carvalho; Alessandra Mascarello; Clarissa Amorin Silva de Cordova; Rosendo Augusto Yunes; Ricardo Jose Nunes; Celso Pilati; Tânia Beatriz Creczynski-Pasa
Journal:  Invest New Drugs       Date:  2011-01-08       Impact factor: 3.850

3.  Tanapoxvirus lacking a neuregulin-like gene regresses human melanoma tumors in nude mice.

Authors:  Tiantian Zhang; Yogesh R Suryawanshi; Dennis H Kordish; Helene M Woyczesczyk; David Jeng; Karim Essani
Journal:  Virus Genes       Date:  2016-10-13       Impact factor: 2.332

Review 4.  Targeting BRAF in advanced melanoma: a first step toward manageable disease.

Authors:  Adina Vultur; Jessie Villanueva; Meenhard Herlyn
Journal:  Clin Cancer Res       Date:  2011-03-29       Impact factor: 12.531

5.  Prospective multicenter phase II trial of systemic ADH-1 in combination with melphalan via isolated limb infusion in patients with advanced extremity melanoma.

Authors:  Georgia M Beasley; Jonathan C Riboh; Christina K Augustine; Jonathan S Zager; Steven N Hochwald; Stephen R Grobmyer; Bercedis Peterson; Richard Royal; Merrick I Ross; Douglas S Tyler
Journal:  J Clin Oncol       Date:  2011-02-22       Impact factor: 44.544

6.  Serine palmitoyltransferase inhibitor myriocin induces growth inhibition of B16F10 melanoma cells through G(2) /M phase arrest.

Authors:  Y-S Lee; K-M Choi; M-H Choi; S-Y Ji; S Lee; D-M Sin; K-W Oh; Y-M Lee; J-T Hong; Y-P Yun; H-S Yoo
Journal:  Cell Prolif       Date:  2011-06-06       Impact factor: 6.831

Review 7.  Resistance to BRAF inhibitors: unraveling mechanisms and future treatment options.

Authors:  Jessie Villanueva; Adina Vultur; Meenhard Herlyn
Journal:  Cancer Res       Date:  2011-12-01       Impact factor: 12.701

8.  Bisphosphonamidate clodronate prodrug exhibits selective cytotoxic activity against melanoma cell lines.

Authors:  Marie R Webster; Chandrashekhar Kamat; Nick Connis; Ming Zhao; Ashani T Weeraratna; Michelle A Rudek; Christine L Hann; Caren L Freel Meyers
Journal:  Mol Cancer Ther       Date:  2013-12-05       Impact factor: 6.261

9.  Molecular determinants of melanoma malignancy: selecting targets for improved efficacy of chemotherapy.

Authors:  Jinming Yang; Snjezana Zaja-Milatovic; Yee-Mon Thu; Francis Lee; Richard Smykla; Ann Richmond
Journal:  Mol Cancer Ther       Date:  2009-03-10       Impact factor: 6.261

10.  Dead cells in melanoma tumors provide abundant antigen for targeted delivery of ionizing radiation by a mAb to melanin.

Authors:  Ekaterina Dadachova; Joshua D Nosanchuk; Li Shi; Andrew D Schweitzer; Annie Frenkel; Jerome S Nosanchuk; Arturo Casadevall
Journal:  Proc Natl Acad Sci U S A       Date:  2004-10-05       Impact factor: 11.205

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