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This information is for educational purposes only. Off-label drug use carries risks. Always consult a qualified physician before using any drug outside its approved indication.

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Hydroxychloroquine

Hydroxychloroquine Sulphate

Brand names: Plaquenil

Quinoline Antimalarial / DMARDImmune Modulatormoderate evidenceActive Clinical Trials

ORIGINALLY APPROVED FOR

Malaria, Rheumatoid Arthritis, Lupus

Hydroxychloroquine (HCQ) inhibits autophagy — the process cancer cells use to recycle damaged components and survive under stress (including chemotherapy stress). By raising lysosomal pH, HCQ prevents the final step of autophagy (autolysosome degradation), trapping cancer cells in a pro-death state. It is being extensively tested as a chemotherapy sensitiser — multiple Phase I/II trials show it enhances the efficacy of various cytotoxic agents.

Molecular Pathways Targeted

Autophagy InhibitionLysosomal pHToll-Like ReceptorsmTORChloroquine Pathway

Mechanism of Action in Cancer

Accumulates in lysosomes → raises lysosomal pH → blocks acid-dependent hydrolytic enzymes → prevents autolysosome degradation → autophagy blockade → cancer cell stress and death. Synergises with many chemotherapies by preventing cancer cell 'escape' via autophagy recycling.

Cancers Studied

PancreaticGlioblastomaMultiple MyelomaColorectalBreastLungMelanoma

Typical Off-Label Dosing

200–400 mg daily (same as standard autoimmune dosing). Must not exceed 5 mg/kg body weight/day to avoid retinal toxicity. Requires baseline and annual ophthalmology monitoring. Typically used as combination adjunct with chemotherapy.

* Dosing information from research literature only. Not a prescription. Requires physician supervision.

Cautions & Drug Interactions

  • Retinal toxicity with long-term use — mandatory baseline and annual eye exams
  • QT prolongation — ECG monitoring recommended, avoid with other QT-prolonging drugs
  • Hypoglycaemia — monitor blood sugar
  • Muscle weakness and neuropathy with long-term use
  • Contraindicated in G6PD deficiency
  • Evidence as monotherapy is weak — best studied as combination with conventional treatment
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