Purpose Identifying and predicting the effectiveness of carboplatin and evaluating its combination with paclitaxel to avoid chemo-resistance may exhibit in some advanced malignancies. Methods Models involving in vivo i.p. growth of human ovarian cancer cells (OCC1, CAOV3), mammary (4T1), and non-small cell lung cancer (NSCLC) tumors in athymic nude mice were used. Doses of (180, 60, 100, and 225 mg/kg) carboplatin in those xenograft growths were, respectively, applied. MTT proliferation assay was performed on samples of human ovarian cancer cell line 2774 incubated with different concentrations of carboplatin (20, 40, 60, 80, and 100 lg/mL). Predicting the response of NSCLC tumor model to carboplatin and evaluation to four cycles of carboplatin combined with paclitaxel at 50 and 15 mg/kg, respectively, in ovarian tumorgraft were performed. Results The energy yield by the carboplatin doses in OCC1, CAOV3, and 4T1 xenograft growths was perfectly correlated (r = 1) with the carboplatin dose logarithm. An efficient dose-energy model with perfect fit (R 2 = 1) has been established estimated energy yield by carboplatin doses. The response of NSCLC tumor model and growth inhibition in samples of cell line 2774 were predicted 100 % identical to those actually induced. Effectiveness of the paclitaxel/carboplatin combination in the ovarian tumorgraft model was *7 times that induced by carboplatin alone.
ConclusionsThe therapeutic response to carboplatin should be predicted prior to therapy using dose-energy model to avoid non-optimal treatments. Paclitaxel/carboplatin combination is an effective way to control tumor growth in epithelial ovarian cancer patients using lower doses of carboplatin with acceptable toxicity.