Table 2. In Vivo Studiesa

Reference Animal Model Outcome
[2] Four transplantable rodent tumors (L1210 lymphoid leukemia, P388 lymphocytic leukemia, B16 melanoma, and Walker 256 carcinosarcoma)No antitumor activity of amygdalin alone (25–3,200 mg/kg); potentiation of toxicity of amygdalin when combined with beta glucosidase
[3] Three transplantable rodent tumors (osteogenic sarcoma, Lewis lung carcinoma, and P388 leukemia)No antitumor activity at 20% of lethal dose (LD20)
[4] DMBA-induced rat mammary carcinoma and the following transplanted experimental tumors: sarcoma 180, plasma cell tumor LPC-1, leukemia L1210, Mecca lymphosarcoma, Ridgway osteogenic sarcoma, sarcoma T241, mammary carcinoma E0771, Taper liver tumor, Ehrlich carcinoma (solid and ascites), and Walker carcinosarcoma 256Not effective at treating, preventing, or delaying development of tumors
[6] B16 melanoma and BW5147 AKR leukemiaIneffective
[9] Murine mammary adenocarcinomaNo effect of amygdalin alone. Enhanced antitumor activity of combination of oral vitamin A, amygdalin given intramuscularly, and enzymes injected into and around the tumor
[10] Human breast and colon xenograftsInactive
[19] HeLa human cervical cancer cell xenograftsModest tumor growth inhibition in mice receiving 300 mg/kg intraperitoneally daily for 14 days

DMBA = dimethylbenz-alpha-anthracene; kg = kilogram(s); mg = milligram(s).

aFor additional information and definition of terms, see text and the NCI Dictionary of Cancer Terms.

From: Laetrile/Amygdalin (PDQ®)

Cover of PDQ Cancer Information Summaries
PDQ Cancer Information Summaries [Internet].
Bethesda (MD): National Cancer Institute (US); 2002-.

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