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In vitro investigation of a combination of two drugs, cisplatin and carboplatin, as a function of the area under thec/t curve

  • Original Paper
  • Experimental Oncology
  • Published:
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Abstract

The log/log relationship between the IC50 of cisplatin or carboplatin and the exposure time, determined by human tumor clonogenic assay (HTCA) and MTTAI (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay with additional incubation) using PC-14 cells, exhibited a straight line with a slope of −1, indicating that both drugs have AUC-dependent cytotoxicity (AUC, area under thec/t curve). The combined effect of cisplatin and carboplatin was estimated by the median-effect analysis using HTCA, and it was additive when the AUC ratio (AUC of free platinum from carboplatin/that from cisplatin) was low (3.2, 6.5 or 13.1 in each of PC-7, PC-9, PC-14, H-69, and K562). However, it was significantly worse at a higher AUC ratio (19.5 in PC-7, PC-9, and PC-14). The log/log relationship of each drug, determined by MTTAI using human bone marrow cells, showed that each drug exerts an AUC-dependent cytotoxicity on marrow granulocytes. When cisplatin and carboplatin were combined at an AUC ratio of 14, the therapeutic index was significantly better than that of carboplatin alone and less than that of cisplatin alone using K562, PC-9 and PC-14, indicating the usefulness of this combined therapy for tumor cells with high sensitivity to platinum compounds at this AUC ratio.

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Abbreviations

HTCA :

human tumor clonogenic assay

AUC :

area under the concentration/time curve

FCS :

fetal calf serum

TI :

therapeutic index

CI :

combination index

MTT :

3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide

MTTAI :

MTT assay with additional incubation

References

  • Chou TC, Talalay P (1985) Dose-effect analysis with microcomputers. Elsevier, UK, p1

    Google Scholar 

  • Evans BD, Raju KS, Calvert AH, Harland SJ, Wiltshaw E (1983) Phase study of JM-8, a new platinum analog, in advanced ovarian carcinoma. Cancer Treat Rep 67:997–1000

    PubMed  Google Scholar 

  • Gandara DR, Wold H, Peres EA, Deisseroth AB, Meyers DF, Hanningan KM, Gregorio WD (1989) Cisplatin dose intensity in non-small cell lung cancer: phase II results of a day 1 and day 8 high-dosc regimen. J Natl Cancer Inst 81:790–794

    PubMed  Google Scholar 

  • Ginsberg RJ, Kris MG, Armstrong JG (1993) Cancer of the lung. In: DeVita VT Jr, Hellman S, Rosenberg SA (eds) Cancer: principle and practice of oncology, 4th edn. Lippincott, Philadelphia, pp 673–723

    Google Scholar 

  • Gralla RJ, Casperc ES, Kelsen DP, Braun DW, Dukeman ME, Martini N, Young CW, Golbey RB (1981) Cisplatin and vindesine combination chemotherapy for advanced carcinoma of the lung: a randomized trial investigating two dosage schedules. Ann Intern Med 95:412–420

    Google Scholar 

  • Hamburger AM, Salmon SE (1977) Primary bioassay of human tumor stem cells. Science 197:461

    PubMed  Google Scholar 

  • Hayata Y, Tsuji K (1975) Lung cancer (in Japanese). In: Ohboshi S, Sugano H (eds) Culture of human cancer cells. Asakurashoten, Tokyo, p 131

    Google Scholar 

  • Knox RJ, Friedros F, Lydall DA, Roberts JJ (1986) Mechanism of cytotoxicity of anticancer platinum drugs: evidence thatcis-diammine-dichloroplatinum(II) andcis-diammine(1,1-cyclobutanedicarboxylato)platinum (II) differ only in the kinetics of their interaction with DNA. Cancer Res 46:1972–1979

    PubMed  Google Scholar 

  • Kobayashi K, Takemoto T, Hino M, Hayashihara K, Nakahiro K, Wasai S, Niitani H (1992) Estimating doses of anti-cancer agents in sensitivity tests in vitro (in Japanese). Jpn J Cancer Chemother 19:399–403

    Google Scholar 

  • Koeller JM, Trump DL, Tutsch KD, Earhart RH, Davis TE, Tormey DC (1986) Phase I clinical trial and pharmacokinetics of Carboplatin (NSC241240) by single monthly 30-minute infusion, Cancer 57:222–225

    PubMed  Google Scholar 

  • Kreisman H, Goutsou M, Mondea SC, Graziano SL, Costanza ME, Green MR (1990) Cisplatin-carboplatin therapy in extensive non-small cell lung cancer: a Cancer and Leukemia Group B study. Eur J Cancer 26:1057–1060

    PubMed  Google Scholar 

  • Kris MG, Gralla RJ, Wertheim MS, Kelsen DP, O'Connell JP, Burke MT, Fiore JJ, Cibas IR, Heelan RT (1986) Trial of the combination of mitomycin, vindesine and cisplatin in patients with advanced non-small cell lung cancer. Cancer Treat Rep 70:1091–1096.

    PubMed  Google Scholar 

  • Ozawa S, Sugiyama Y, Mitsuhashi Y, Kobayashi T, Inaba M (1988) Cell killing action of cycle phase-non-specific antitumor agents is dependent on concentration-time product. Cancer Chemother Pharmacol 21:185–190

    PubMed  Google Scholar 

  • Piccart MJ, Nogaret JM, Marcelis L, Ries HL, Kains JP, Gobert P, Domange AM, Sculier JP, Gompel C (1990) Cisplatin combined with carboplatin: a new way of intensification of platinum dose in the treatment of advanced ovarian cancer. J Natl Cancer Inst 82:703–707

    PubMed  Google Scholar 

  • Ruckdeschel JC, Finkelstein DM, Ettinger DS, Creech RH, Mason BA, Joss RA, Vogl S (1986) A randomized trial of the four most active regimens for metastatic non-small cell lung cancer. J Clin Oncol 4:14–22

    PubMed  Google Scholar 

  • Sasaki Y, Tamura T, Eguchi K, Shinkai T, Fujiwara Y, Fukuda M, Ohe Y, Bungo M, Horiuchi N, Niimi S, Minato K, Nakagawa K, Saijo N (1989) Pharmacokinetics of (glycolato-O,O′)-diammine platinum II, a new platinum derivative, in comparison with cisplatin and carboplatin. Cancer Chemother Pharmacol 23:243

    PubMed  Google Scholar 

  • Takahashi H, Sakai Y, Saijo N, Sakurai M, Nakano H, Nagasawa K, Hoshi A, Jett RJ, Hong WA (1987) In vitro colony inhibition of carboplatin against stomach and lung cancer cell lines in comparison with cisplatin. Cancer Chemother Pharmacol 19:197–200

    PubMed  Google Scholar 

  • Takemoto T (1993) A comparative study of chemosensitivity tests in vitro for AUC-dependent drugs focusing on the usefulness of MTT assay with drug washout and additional incubation (M-MTT) (in Japanese). J Nippon Med Sch 60:140–155

    Google Scholar 

  • Yoshimura A, Gemma A, Yoshimori K, Shibuya M, Niitani H, Yamada K, Ando M, Takenaka K, Hasegawa H, Tsuboi E (1992) A phase I trial of combination of cisplatin and carboplatin in advanced non-small cell lung cancer. An intensification of two platinum compounds (in Japanese). J Jpn Lung Cancer Soc 32:827–835

    Google Scholar 

  • Yoshimura A, Yamano Y, Gemma A, Yoshimori K, Hayashihara K, Taniguchi Y, Uematsu K, Shibuya M, Kudoh S, Niitani H, Hasegawa K, Tsuboi E (1993) An early phase II trial combining cisplatin and carboplatin in advanced non-small cell lung cancer (in Japanese). Jpn J Cancer Chemother 20:503–508

    Google Scholar 

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This work was supported by grants from the Ministry of Health and Welfare of Japan

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Kobayashi, K., Kudoh, S., Takemoto, T. et al. In vitro investigation of a combination of two drugs, cisplatin and carboplatin, as a function of the area under thec/t curve. J Cancer Res Clin Oncol 121, 715–720 (1995). https://doi.org/10.1007/BF01213317

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  • DOI: https://doi.org/10.1007/BF01213317

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