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Hematological Toxicity: Biological Basis

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Complications of Cancer Chemotherapy

Part of the book series: Recent Results in Cancer Research ((RECENTCANCER,volume 49))

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Abstract

A shortage of leukocytes and platelets may be treated by transfusions, as will be discussed by others. A search for a more efficient treatment or prevention of haemopoietic failure after chemotherapy has not yielded a better treatment. Autologous bone marrow transplantation after single high dose cytostatic therapy was not a successful method to combat toxicity. The biological basis of bone marrow toxicity should be studied in more detail to find better means to combat it. A retrospective look for the reason why bone marrow transplantation failed, indicates that stem cell loss was not the cause of death after single dose chemotherapy. Animal studies confirm, that X-ray lethality but not the mortality after chemotherapy may be prevented by stem cell replacement.

Parts of the work were carried out in programs of the EORTC Stem Cell Club and the EORTC Screening Pharmacology Group.

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Abbreviations

VCR:

Vincristine

VLB:

Vinblastine

BCNU1 :

Bis-Chloro-aethyl Nitroso Urea

Myl2 :

Myleran (Busulfan)

Iso3 :

Isophosphamide

MUST:

Mechlorethamine

Trilo3 :

Trilophosphamide

CCNU1 :

Cyclohexyl-Chloroethyl-Nitroso Urea

Nor-M:

Bis-chloro-ethylamine

TEM5 :

Triethylene Melamine

ACA6 :

Aminochlorambucil

MCCNU1 :

Methyl-Cyclohexyl-Chloroethyl Nitroso Urea

Cyclo3 :

Cyclophosphamide

DAHM:

Di-AnHydro-MannitoI7

DMM:

DiMethyl-Myleran7

5FU4 :

5 Fluoro-Uracil

15 MeVN:

15 MeV neutron irradiation

Melph:

Melphalan

X:

300 keV X-rays.

CFU:

haemopoietic spleen colony forming stem cell

3HTdR:

tritiated thymidine (9 Ci/mMol.)

VM26:

4-demethyl-epipodophyllotoxin-thenylidene glucoside, supplied by Sandoz

References

  • BekkumD. W. van: Foreign bone marrow transplantation following fractionated wholebody irradiation in mice. In: Radiation effects in physics, chemistry and biology, p. 362 (Ed.: M. Ebert and A. Howard), Amsterdam: North Holland Publishing Co. 1963.

    Google Scholar 

  • Bruce, D. L., Lin, H. S., Bruce,W. R.: Reduction of colony-forming cell sensitivity to arabinyl cytosine by halothane anaesthesia. Cancer Res. 30, 1803 (1970).

    PubMed  CAS  Google Scholar 

  • Byron, J. W.: Evidence for adrenergic receptor initiating DNA synthesis in haemopoietic stem cells. Exp. Cell Res. 71, 228 (1972).

    Article  PubMed  CAS  Google Scholar 

  • Byron, J. W.: Drug receptors and the haemopoietic stem cell. Nature New Biol. 241, 152 (1973).

    PubMed  CAS  Google Scholar 

  • Putten L. M. van, Lelieveld, P., Kram-idsengaL. K. J.: Cell-cycle specificity and therapeutic effectiveness of cytostatic agents. Cancer Chemother. Reports Part 1, 56, 6 (1972).

    Google Scholar 

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© 1974 Springer-Verlag Berlin · Heidelberg

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van Putten, L.M. (1974). Hematological Toxicity: Biological Basis. In: Mathé, G., Oldham, R.K. (eds) Complications of Cancer Chemotherapy. Recent Results in Cancer Research, vol 49. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-80848-7_3

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  • DOI: https://doi.org/10.1007/978-3-642-80848-7_3

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-80850-0

  • Online ISBN: 978-3-642-80848-7

  • eBook Packages: Springer Book Archive

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