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. 2020 May 23;19:1534735420922579. doi: 10.1177/1534735420922579

Table 2.

In Vivo Experiments of Combination Sodium Bicarbonate With Other Anticancer Therapies.

Anticancer Therapy Tumor Type Animal Models Administration of NaHCO3 Outcomes (Anticancer Therapy+ NaHCO3 Versus Anticancer Therapy) Reference
Chemotherapy
 Doxorubicin (2.0 mg/kg ip) Breast cancer MCF-7 xenograft 200 mM NaHCO3 po ad libitum pHe of MCF-7 xenografts raised the therapeutic effectiveness improved 29
 Mitoxantrone (12 mg/kg iv) Breast cancer C3H allograft 0.7 mL 1M NaHCO3 by gavage 3.3-fold increase of therapeutic index 30
0.7 mL 1M NaHCO3 ip injection
Molecular targeting therapy
 VEGFR2 inhibitor: sunitinib (40 mg/kg po) Colorectal cancer HT29 xenograft 200 mM NaHCO3 po ad libitum Tumor growth delayed; the number of blood vessels decreased; tumor necrosis increased; VEGFR2 expression in the vessels increased tumor growth delayed 34
MC-38 allograft
 mTORC1 inhibitor: rapamycin (3 mg/kg ip) Colorectal cancer HT29 xenograft 200 mM NaHCO3 po ad libitum Tumor growth delayed; tumor necrosis increased; necrotic tumor surface increased 33
MC-38 allograft
Immunotherapy
 Anti-PD1 therapy Melanoma B16 allograft 200mM NaHCO3 po ad libitum Modest effect on tumor growth (P < .05) 25
Pancreatic cancer Panc02 allograft Tumor growth delayed (P < .005)
 Anti-CTLA4 therapy Melanoma B16 allograft No effect on tumor growth (P = .54)
 Anti PD1/CTLA4 Melanoma B16 allograft No effect on tumor growth
 Adoptive T-cell therapy Melanoma B16 allograft No effect on tumor growth
Long-term (120 day) survival rate (40% vs 10%)
T-cell persistence increased

Abbreviations: ip, intraperitoneal; po, per os (orally); iv, intravenous; VEGFR2, vascular endothelial growth factor rectptor-2; mTORC1, mechanistic target of rapamycin complex-1; CTLA-4, cytolytic T lymphocyte-associated antigen-4; PD-1, programmed death-1.