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Synergistic effects of intratumor administration of cis-diamminedichloroplatinum(II) combined with local hyperthermia
K Kitamura1, H Kuwano, H Matsuda
1Department of Surgery II, Kyushu University, Fukuoka, Japan.
Journal of Surgical Oncology
|November 1, 1992
Summary
Local hyperthermia combined with intratumor injection of cisplatin (DDP) significantly enhanced anticancer effects in a rodent melanoma model. This combination therapy improved prognosis without causing severe side effects.
Area of Science:
- Oncology
- Cancer Research
- Pharmacology
Background:
- Cis-diamminedichloroplatinum (II) (DDP) is a platinum-based chemotherapy agent.
- Local hyperthermia (LHT) can enhance the efficacy of certain cancer treatments.
- B16 melanoma is a common model for studying melanoma progression and treatment.
Purpose of the Study:
- To investigate the synergistic effect of LHT and intratumor injection (i.t.) of DDP on B16 melanoma.
- To evaluate the impact of combined therapy on tumor growth and survival in a rodent model.
- To assess potential side effects such as renal injury and metastasis.
Main Methods:
- Rodent model with implanted B16 melanoma tumors.
- Administration of DDP via intratumor injection (i.t.) or intraperitoneal (i.p.) injection.
- Application of local hyperthermia (LHT) at 42.5°C for 30 minutes post-DDP administration.
- Monitoring tumor growth ratio (TGR) and mean survival time.
Main Results:
- DDP (3 mg/kg i.t.) with LHT resulted in a tumor growth ratio (TGR) of 1.1 in experiment I and 0.5 in experiment II.
- Statistically significant differences in TGR were observed compared to control groups (P < 0.01).
- Mean survival time was significantly improved with combined therapy (42.1 days in exp I, 50.2 days in exp II; P < 0.001 in exp II).
Conclusions:
- Concomitant intratumor chemotherapy with DDP and local hyperthermia significantly enhances anticancer effects.
- This combined approach improves prognosis in B16 melanoma-bearing rodents.
- The treatment did not induce severe renal injury or promote hematogenic metastasis.