Dacarbazine combined targeted therapy versus dacarbazine alone in patients with malignant melanoma: a meta-analysis

Guan Jiang1, Rong-Hua Li2, Chao Sun2

  • 1Department of Dermatology, Affiliated Hospital of Xuzhou Medical College, Xuzhou, 221002, China; Jiangsu Key Laboratory of Biological Cancer Therapy, Xuzhou Medical College, Xuzhou, 221002, China; Center for Disease Control and Prevention of Xuzhou City, Xuzhou, 221002, China.

Plos One
|December 16, 2014
PubMed
Abstract

Insights

Dacarbazine (DTIC)-based combination therapies show improved response and survival for metastatic melanoma patients compared to DTIC alone. However, these combinations also lead to a higher incidence of adverse events like nausea, vomiting, and neutropenia.

Area of Science:

  • Oncology
  • Dermatology

Background:

  • Malignant melanoma is an aggressive skin cancer with limited treatment options.
  • Dacarbazine (DTIC) is a standard first-line treatment for metastatic melanoma, but its efficacy is often limited.
  • Low response rates with single-agent DTIC necessitate exploration of alternative therapeutic strategies.

Purpose of the Study:

  • To compare the efficacy and safety of DTIC monotherapy versus DTIC-based combination therapies in advanced metastatic melanoma.
  • To evaluate overall response and 1-year survival rates in patients receiving different DTIC treatment regimens.
  • To assess the incidence of adverse events associated with DTIC-based combination treatments.

Main Methods:

  • A meta-analysis of nine randomized controlled trials (RCTs) involving 2,481 patients was conducted.
  • Literature search was performed across major electronic databases from 2003 to 2013.
  • Primary outcomes included overall response and 1-year survival; secondary outcomes focused on adverse events.

Main Results:

  • DTIC-based combination therapies demonstrated superior overall response rates (RR = 1.60, 95% CI: 1.27-2.01) compared to DTIC alone.
  • A significant improvement in 1-year survival was observed with combination therapies (RR = 1.26, 95% CI: 1.14-1.39).
  • Combination therapies were associated with increased adverse events, including nausea (RR = 1.23), vomiting (RR = 1.73), and neutropenia (RR = 1.75).

Conclusions:

  • DTIC-based combination therapies offer a moderate improvement in overall response and 1-year survival for metastatic melanoma.
  • The enhanced efficacy of combination therapies comes at the cost of an increased incidence of adverse events.
  • Further large-scale, high-quality, placebo-controlled, double-blind trials are warranted to validate these findings.

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