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The effect of tamoxifen and cisplatin on the disease-free and overall survival of patients with high risk malignant melanoma
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  • Published: 06 June 2000

The effect of tamoxifen and cisplatin on the disease-free and overall survival of patients with high risk malignant melanoma

  • E F McClay1,
  • M E T McClay1,
  • L Monroe2,
  • P L Baron2,
  • D J Cole2,
  • P H O'Brien2,
  • J S Metcalf2 &
  • …
  • J C Maize2 

British Journal of Cancer volume 83, pages 16–21 (2000)Cite this article

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Abstract

The adjuvant treatment of high-risk malignant melanoma remains problematic. Previously we reported moderate success in the treatment of metastatic disease using tamoxifen, cisplatin, dacarbazine and carmustine. Based upon data that suggested tamoxifen and cisplatin were the active agents in this regimen, we initiated a phase II trial of this combination in the adjuvant setting. We treated 153 patients with 4 cycles of tamoxifen (160 mg day–1, days 1–7) and cisplatin (100 mg m–2, day 2) for 28-day intervals. Patients received an anti-nausea regimen of dexamethasone with ondansetron or granisetron. During the first 2 years of follow-up, patients were evaluated every 2 months with a history, physical exam, laboratory work and computed tomography scans of the chest, abdomen and pelvis every 4 months. Thereafter, patients were evaluated every 3 months and radiographic studies were performed if necessary. Currently, with a median follow-up of 36 months, the disease-free survival (DFS) is 68.4% and overall survival (OS) is 84.5%. Kaplan–Meier analysis predicts a 5-year DFS of 62% with an OS of 79%. Relapses after 20 months have been rare. No effect of gender or number of positive lymph nodes was noted, however, stage of disease prior treatment was a factor. The major toxicity proved to be gastrointestinal in nature with nausea the most prevalent symptom. Minimal renal, haematologic and neurologic toxicity occurred. These preliminary results suggest that there is a positive impact of tamoxifen and cisplatin on both the DFS and OS of high-risk malignant melanoma patients. The 5-year projected DFS and OS compare favourably with those reported for the ECOG 1684 trial and warrant confirmation in a prospective randomized trial. © 2000 Cancer Research Campaign

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  • 16 November 2011

    This paper was modified 12 months after initial publication to switch to Creative Commons licence terms, as noted at publication

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Authors and Affiliations

  1. Department of Medicine, Division of Hematology/Oncology, and the Cancer Center, , University of California, 9500 Gilman Drive, San Diego, La Jolla, 92093-0063, CA, USA

    E F McClay & M E T McClay

  2. Departments of Medicine, Surgery and Dermatology and the Hollings Cancer Center, Medical University of South Carolina, 86 Jonathan Lucas Street, Charleston, 29403-5851, SC, USA

    L Monroe, P L Baron, D J Cole, P H O'Brien, J S Metcalf & J C Maize

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  3. L Monroe
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From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/

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McClay, E., McClay, M., Monroe, L. et al. The effect of tamoxifen and cisplatin on the disease-free and overall survival of patients with high risk malignant melanoma. Br J Cancer 83, 16–21 (2000). https://doi.org/10.1054/bjoc.1999.1220

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  • Received: 30 June 1999

  • Revised: 16 November 1999

  • Accepted: 08 December 1999

  • Published: 06 June 2000

  • Issue date: 01 July 2000

  • DOI: https://doi.org/10.1054/bjoc.1999.1220

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Keywords

  • tamoxifen
  • cisplatin
  • adjuvant therapy
  • melanoma

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