Please click the links above or the images below to download resources and view support materials to help manage patients taking Imfinzi.

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Be IN the know with Imfinzi’s PACIFIC OS data

PACIFIC: Primary OS analysis
(full analysis set; median duration of follow-up 25.2 [0.2–43.1] months [all patients])1,2*

Imfinzi DEMONSTRATED A STATISTICALLY SIGNIFICANT AND CLINICALLY MEANINGFUL IMPROVEMENT IN OS VS. PLACEBO1 Imfinzi demonstrated a statistically significant and clinically meaningful improvement in OS vs. placebo (HR: 0.68; 95% CI: 0.53, 0.87; p=0.00251); 183/476 (38.4%) events with Imfinzi vs. 116/237 (48.9%) events with placebo1

See study parameters below.
Adapted from Imfinzi Product Monograph.1
CI, confidence interval; HR, hazard ratio; mOS, median overall survival.
* Compared with allocated α of 0.00274 (Lan DeMets spending function approximating O’Brien Fleming boundary) for interim analysis. Compared with α of 0.05 following statistically significant progression-free survival and OS at interim analyses.

Consider Imfinzi: The only immunotherapy available for the treatment of patients with locally advanced, stage III, unresectable NSCLC without disease progression following platinum-based CRT.

CRT, chemoradiation therapy.

‡ Comparative clinical significance is unknown.

PACIFIC: 5-year updated OS analysis
(planned exploratory analysis; median duration of follow-up of 34.2 [0.2–74.7] months [all patients], 61.6 [0.4–74.7] months [censored patients])

OS DATA WITH Imfinzi
VS. PLACEBO3

See study parameters below.

See study parameters below.
Adapted from Spigel DR, et al. 2022.3
CI, confidence interval; HR, hazard ratio; mOS, median overall survival.
§ Not formally statistically tested.

Click here to download the full study and learn more.

PACIFIC 5-Year Updated Exploratory OS Analysis Publication
PACIFIC 5-Year Updated Exploratory OS Analysis Publication

‖ PACIFIC was a randomized, double-blind, placebo-controlled, multicentre Phase III study comparing Imfinzi vs. placebo in patients with locally advanced, Stage III, unresectable NSCLC with no disease progression after platinum-based CRT. Patients with World Health Organization performance status 0 or 1 (any tumour programmed cell death-ligand 1 status) were randomly assigned (2:1) to Imfinzi (10 mg/kg IV Q2W for 12 months) or placebo, stratified by age, sex, and smoking history. Time-to-event end point analyses were performed using stratified log-rank tests. Medians and landmark survival rates were estimated using the Kaplan-Meier method. The primary analyses of OS and progression-free survival (RECIST v1.1; assessed by blinded independent central review [BICR]) with Imfinzi vs. placebo was updated in the intent-to-treat population approximately 5 years after the last patient was randomized.3

Overall, 34 of 476 (7.1%) patients in the durvalumab arm received retreatment. Retreatment is not recommended. The recommended dose of Imfinzi is 10 mg/kg Q2W or 1,500 mg Q4W, which should continue for one year or until disease progression or unacceptable toxicity.1,3

CRT, chemoradiation therapy; Q2W, every other week; Q4W, every 4 weeks.

 

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HCP Resources
PACIFIC 5-Year Updated Exploratory OS Analysis Publication
PACIFIC 5-Year Updated Exploratory OS Analysis Publication

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PACIFIC 5-Year Updated Exploratory OS Analysis Publication

NSCLC

Imfinzi's 5-year updated exploratory OS data in Stage III, unresectable NSCLC patients who have not progressed post-CRT.

Spigel DR, Faivre-Finn C, et al. Five-Year Survival Outcomes from the PACIFIC Trial: Durvalumab After Chemoradiotherapy in Stage III Non–Small-Cell Lung Cancer. J Clin Oncol. 2022; 40(12): 1301-1311.

PACIFIC 5-Year Updated Exploratory OS Analysis Publication
PACIFIC 5-Year Updated Exploratory OS Analysis Publication

Download

PACIFIC OS Data Summary

NSCLC

An overview of the primary and 5-year updated exploratory OS data.

IMFINZI Product Monograph
IMFINZI Product Monograph

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Dosing Guide

NSCLC

A guide for Imfinzi’s recommended dosage, dosage adjustments, and administration.

PACIFIC Primary OS Analysis Publication
PACIFIC Primary OS Analysis Publication

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Immune-Mediated Adverse Reactions (imARs) Handbook

NSCLC

A guide for recognizing and managing imARs associated with Imfinzi.

IMFINZI Product Monograph
IMFINZI Product Monograph

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Imfinzi Product Monograph

NSCLC

Complete details on Imfinzi’s properties, indications, dosing, contraindications, warnings, adverse events, and clinical pharmacology.

CRT, chemoradiation therapy; HCP, healthcare professional; imARs, immune-mediated adverse reactions; NSCLC, non-small cell lung cancer; OS, overall survival.

Patient Resources

Watch video

IMFINZI & Me App video

NSCLC

ES-SCLC

Watch this video to learn more about how the IMFINZI & Me App can help support your patients.

Download

IMFINZI & Me App Brochure

NSCLC

ES-SCLC

Download the brochure for patients to learn how to join the IMFINZI & Me App.

IMFINZI Patient Brochure
IMFINZI Patient Brochure

Download

Patient Information and Side
Effects Brochure

NSCLC

A guide for patients with important information about Imfinzi treatment and how to recognize possible side effects.

Caregiver Brochure
Caregiver Brochure

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Caregiver Brochure

NSCLC

Guidance for Imfinzi patients’ loved ones to help them through the treatment process.

IMFINZI Side Effects Tracker
IMFINZI Side Effects Tracker

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Side Effects Tracker

NSCLC

A tool for patients to track any side effects they may experience during Imfinzi treatment.

References:

1.Imfinzi Product Monograph. AstraZeneca Canada Inc. January 17, 2025.

2.Antonia SJ, et al. Overall Survival with Durvalumab after chemoradiotherapy in Stage III NSCLC. N Engl J Med. 2018;379(24):2342-2350.

3.Spigel DR, et al. Five-Year Survival Outcomes from the PACIFIC Trial: Durvalumab After Chemoradiotherapy in Stage III Non-Small-Cell Lung Cancer. J Clin Oncol. 2022;40(12):1301-1311.