Immune Checkpoint Blockade Combined with AbnobaViscum® Therapy Is Linked to Improved Survival in Advanced or Metastatic Non-Small-Cell Lung Cancer Patients: A Registry Study in Accordance with the ESMO Guidance for Reporting Real-World Evidence
2024

Improved Survival in Lung Cancer with Combined Therapy

Sample size: 300 publication 10 minutes Evidence: moderate

Author Information

Author(s): Schad Friedemann, Thronicke Anja, Hofheinz Ralf-Dieter, Klein Reinhild, Grabowski Patricia, Oei Shiao Li, Wüstefeld Hannah, Grah Christian

Primary Institution: Network Oncology Registry, Research Institute Havelhöhe, Berlin, Germany

Hypothesis

Does the combination of immune checkpoint blockade and abnobaViscum® therapy improve survival in advanced or metastatic non-small-cell lung cancer patients?

Conclusion

The addition of abnobaViscum® to immune checkpoint blockade significantly improves survival in patients with advanced or metastatic non-small-cell lung cancer.

Supporting Evidence

  • Overall survival was significantly prolonged in the COMB group by 7 months compared to CTRL.
  • The survival rate was 16.5% in the COMB group vs. 8.0% in the CTRL group.
  • In PD-L1 positive patients, the addition of abnobaViscum® reduced the adjusted hazard of death by 75%.
  • The study adhered to ESMO-GROW criteria with ethics approval.

Takeaway

This study found that patients with lung cancer lived longer when they received a special mistletoe therapy along with their regular cancer treatment.

Methodology

Patients with advanced or metastatic NSCLC were analyzed using real-world data from a registry, comparing survival outcomes between those receiving immune checkpoint blockade alone and those receiving it with abnobaViscum® therapy.

Potential Biases

Potential for selection bias due to non-randomized patient assignment.

Limitations

The non-randomized nature of the study may introduce selection bias.

Participant Demographics

Median age of participants was 68 years, with a male/female ratio of 1.19.

Statistical Information

P-Value

0.005

Confidence Interval

95%CI: 9.2–22 months

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.3390/ph17121713

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