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Toxicology studies on antineoplaston AS2-5 injections in cancer patients

Drugs Under Experimental and Clinical Research
|January 1, 1986
PubMed

Insights

Antineoplaston AS2-5, a phenylacetylglutamine derivative, showed mild side effects in cancer patients. Two complete remissions were observed, with one lung cancer patient remaining disease-free for over 5 years.

Area of Science:

  • Oncology
  • Pharmacology

Background:

  • Antineoplaston AS2-5 is a phenylacetylglutamine derivative and a degradation product of Antineoplaston A10.
  • This study investigates the toxicological profile and efficacy of Antineoplaston AS2-5 in patients with various neoplastic diseases.

Purpose of the Study:

  • To evaluate the safety and efficacy of Antineoplaston AS2-5 in patients with advanced cancers.
  • To assess treatment outcomes, including remission rates, stabilization, and disease progression.

Main Methods:

  • Intravenous daily administration of Antineoplaston AS2-5 via subclavian vein catheter.
  • Treatment duration ranged from 41 to 436 days, with a maximum dosage of 167.6 mg/kg/24 h.
  • Involved 13 patients with 15 types of neoplastic diseases, including lung, breast, and colon cancers.

Main Results:

  • The treatment was generally well-tolerated, with mild side effects such as febrile reactions and joint swelling.
  • Beneficial effects included increased platelet count and plasma globulin concentration.
  • Achieved two complete remissions (laryngeal and lung cancer), one mixed response, four stabilizations, and six cases of disease progression.

Conclusions:

  • Antineoplaston AS2-5 demonstrated a favorable safety profile with potential anti-neoplastic activity.
  • Complete remission in advanced lung cancer, sustained for over 5 years, suggests significant therapeutic potential.
  • Further research is warranted to explore its efficacy in broader cancer populations.

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