TY - JOUR
T1 - Effect of oxygen level on the enhancement of tumor response to radiation by perfluorochemical emulsions or a bovine hemoglobin preparation
AU - Teicher, Beverly A.
AU - Herman, Terence S.
AU - Hopkins, Robert E.
AU - Menon, Krishna
N1 - Funding Information:
Supported by NIH grant No. POl-19589 and a grant from E.I. Du Pont de Nemours & Co., Chemicals and Pigments Department, Deepwater, NJ and a gift from Biopure, Inc., Boston, MA. Accepted for publication 29 March 1991.
PY - 1991/9
Y1 - 1991/9
N2 - Attempts to correct tumor hypoxia with oxygen-carrying solutions have used high concentrations of inspired oxygen (Fi02 100% or 95%). In the clinic, however, obtaining such high levels of FiO2 using mask ventilation in older patients or in children may be difficult. Since lower levels of F102 had not been previously tested, we examined the antitumor efficacy of FiO. levels of 65, 85, and 95% breathed for 1 hr prior to and during irradiation used with the concentrated perfluorochemical emulsion F44E, the less concentrated emulsion, FluosolDA, or a new preparation consisting of purified bovine hemoglobin solution, PBHS. When tested in mice bearing the Lewis lung carcinoma with 2, 3, or 4 Gy daily for 5 days, daily Fluosol-DA produced only a small increase in the slope of the tumor growth delay versus irradiation alone, when used with 85% FiO2 (dose modifying factor [DMF] 1.3), but produced a DMF of 2.1 with 95% FiO2 Various concentrations of F44E (2, 4, or 8 g PFC/kg) each required a 95% FiO2 for full effect but the 8 g/kg dose had a discernable effect with an FiO2 of 65% and 85% (DMF 1.25 and 1.30, respectively). For PBHS, in contrast, a DMF of 1.6 was observed at 20% FiO2 but surprisingly this increased further to 2.1 with 95% FiO2 Further investigations of PBHS with irradiation demonstrated that daily administration of PBHS (12 ml/kg) 1 hr before single Xray fractions of 5, 10, 15, or 20 Gy with 20% FiO, resulted in a DMF of 1.6-1.7 in the FSaIIC fibrosarcoma compared with irradiation alone when ascertained by tumor cell excision assay. These results indicate that to achieve maximum antitumor benefit with these oxygen-carrying solutions with radiation therapy, care must be taken to insure that FiO2 levels near 100% are achieved.
AB - Attempts to correct tumor hypoxia with oxygen-carrying solutions have used high concentrations of inspired oxygen (Fi02 100% or 95%). In the clinic, however, obtaining such high levels of FiO2 using mask ventilation in older patients or in children may be difficult. Since lower levels of F102 had not been previously tested, we examined the antitumor efficacy of FiO. levels of 65, 85, and 95% breathed for 1 hr prior to and during irradiation used with the concentrated perfluorochemical emulsion F44E, the less concentrated emulsion, FluosolDA, or a new preparation consisting of purified bovine hemoglobin solution, PBHS. When tested in mice bearing the Lewis lung carcinoma with 2, 3, or 4 Gy daily for 5 days, daily Fluosol-DA produced only a small increase in the slope of the tumor growth delay versus irradiation alone, when used with 85% FiO2 (dose modifying factor [DMF] 1.3), but produced a DMF of 2.1 with 95% FiO2 Various concentrations of F44E (2, 4, or 8 g PFC/kg) each required a 95% FiO2 for full effect but the 8 g/kg dose had a discernable effect with an FiO2 of 65% and 85% (DMF 1.25 and 1.30, respectively). For PBHS, in contrast, a DMF of 1.6 was observed at 20% FiO2 but surprisingly this increased further to 2.1 with 95% FiO2 Further investigations of PBHS with irradiation demonstrated that daily administration of PBHS (12 ml/kg) 1 hr before single Xray fractions of 5, 10, 15, or 20 Gy with 20% FiO, resulted in a DMF of 1.6-1.7 in the FSaIIC fibrosarcoma compared with irradiation alone when ascertained by tumor cell excision assay. These results indicate that to achieve maximum antitumor benefit with these oxygen-carrying solutions with radiation therapy, care must be taken to insure that FiO2 levels near 100% are achieved.
KW - Fluosol-DA
KW - Hemoglobin
KW - Radiation sensitization
KW - Radiation sensitizers
KW - Tumor hypoxia
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U2 - 10.1016/0360-3016(91)90737-O
DO - 10.1016/0360-3016(91)90737-O
M3 - Article
C2 - 1917627
AN - SCOPUS:0026091775
VL - 21
SP - 969
EP - 974
JO - International Journal of Radiation Oncology Biology Physics
JF - International Journal of Radiation Oncology Biology Physics
SN - 0360-3016
IS - 4
ER -