ChemotherapyFDA-approvedSecond-line

Irinotecan

How it works

Irinotecan is a topoisomerase I inhibitor that interferes with DNA replication, preventing cancer cells from growing and dividing.

Cancer types

Pancreatic CancerAll patients

Efficacy

Irinotecan has been shown to improve overall survival and quality of life in patients with pancreatic cancer, although the response rates are generally modest.

Side effects

Moderate

Side effects can be significant and may require dose adjustments or supportive medication, but the treatment is usually continued.

Evidence from research

StudyCancer typeStageEfficacy
Testing Chemo-Immunotherapy for Pancreatic CancerPancreatic Cancerphase-2Source →
New Treatment Combination Shows Promise for Metastatic Colorectal CancerColorectal Cancerphase-2The objective response rate was 18.3%, and the disease control rate was 83.3%.Source →
Testing M6620 and Irinotecan in Patients with Advanced Solid TumorsLung Cancerphase-1Source →
Cancer Cells' Fat Metabolism Linked to Chemotherapy ResistanceColorectal Cancerlab-studySource →
Liposomal irinotecan shows promise in treating breast cancer with brain metastasesBreast Cancerphase-2The intracranial objective response rate was 22.0% among patients with progressive brain metastases.Source →
Combining Nanoparticles and Medication to Boost Pancreatic Cancer TreatmentPancreatic Canceranimal-studySource →
Combining Cancer Drugs Improves Immune Response in Lab ExperimentsColorectal Cancerlab-studyThis neutrophil-based formulation resulted in a >4-fold increase in the ratios of the amount of both IRI and GAL accumulated in tumors to the dosage administration.Source →
Engineered Nanocarriers Improve Irinotecan Delivery for Colon CancerColorectal Cancerlab-studyThe P-DSPE-PEG-Ir LP exhibited significant tumor growth delay as compared to untreated and blank formulation-treated groups.Source →
New Treatment Shows Promise for Advanced Pancreatic CancerPancreatic Cancermeta-analysisThe use of nal-IRI resulted in significantly improved progression-free survival (pooled mean difference=1.01 months, 95% confidence interval [CI]=0.97-1.05, p<0.01) and overall survival (pooled mean difference=0.29 months, 95%CI=0.18-0.39, p<0.01), as well as significantly better overall response rate (pooled odds ratio=2.06, 95%CI=1.30-3.27, p=0.002) compared to other second-line regimens.Source →
New Study Helps Optimize Chemotherapy for Colorectal Cancer PatientsColorectal Cancerphase-1Source →
Comparing Two Cancer Treatments in Metastatic Colorectal CancerColorectal Cancerphase-3There was no significant difference in median overall survival between treatment groups (9.1 months vs 10.1 months).Source →
Liposomal Irinotecan in Biliary Tract Cancer: A Meta-AnalysisPancreatic Cancermeta-analysisThe combination therapy exhibited a statistically significant decrease in the risk of progression (hazard ratio 0.70; 95% confidence interval 0.50-0.97)Source →
Older patients with pancreatic cancer may benefit from liposomal irinotecan treatmentPancreatic CancerobservationalThe median overall survival and progression-free survival of the entire cohort were 8.5 and 3.6 months, respectively.Source →

This information is provided for general education only and is not medical advice. Always consult a qualified healthcare professional before making treatment decisions.