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Encapsulation of Cancer Therapeutic Agent Dacarbazine Using Nanostructured Lipid Carrier
Published on: April 26, 2016
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.
Background:
Malignant melanoma is the most aggressive and deadly form of skin cancer. Dacarbazine (DTIC) has been the approved first-line treatment for metastatic melanoma in routine clinical practice. However, response rates with single-agent DTIC are low. The objective of this study was to compare the efficacy and safety of DTIC with or without placebo and DTIC-based combination therapies in patients with advanced metastatic melanoma.
Methods:
We searched from electronic databases such as The Cochrane Library, MEDLINE, EBSCO, EMBASE, Ovid, CNKI, and CBMDisc from 2003 to 2013. The primary outcome measures were overall response and 1-year survival, and the secondary outcome measurements were adverse events.
Results:
Nine randomized controlled trials (RCTs) involving 2,481 patients were included in the meta-analysis. DTIC-based combination therapies was superior to DTIC alone in overall response (combined risk ratio [RR] = 1.60, 95% confidence interval [CI]: 1.27-2.01) and 1-year survival (combined RR = 1.26, 95% CI: 1.14-1.39). Patients with DTIC-based combination therapies had higher incidence of adverse events including nausea (combined RR = 1.23, 95% CI: 1.10-1.36), vomiting (combined RR = 1.73, 95% CI: 1.41-2.12) and neutropenia (combined RR = 1.75, 95% CI: 1.42-2.16) compared to the group for DTIC alone.
Conclusion:
These data suggested that DTIC-based combination therapies could moderately improve the overall response and the 1-year survival but increased the incidence of adverse events. Further large-scale, high-quality, placebo-controlled, double-blind trials are needed to confirm this conclusion.
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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