NSCLC AND

BIOMARKER TESTING

ALK+ NSCLC is a unique subset of lung cancer

with a distinct pathology and characteristics1-3

Approximately 3–5% of patients with NSCLC are ALK+1–3

 

Patients with ALK+ NSCLC often have more advanced disease upon diagnosis compared with those with ALK-negative disease, and as many as 2 out of 3 will eventually develop CNS metastases1–3

The importance of biomarker testing


in ALK+ NSCLC

Overall, more than 50% of patients with advanced NSCLC have an actionable oncogenic driver.4

 

In advanced NSCLC, targeted therapies for these oncogenic drivers have revolutionize the treatment paradigm and led to significant improvements in response and survival rates.5

Testing for oncogenic drivers, including ALK rearrangements in metastatic NSCLC is important for the identification of potentially efficacious targeted therapies, as well as avoidance of therapies unlikely to provide clinical benefit.6

Biomarker testing is also important in early-stage NSCLC. Following surgery, the risk of recurrence for some patients with early NSCLC remains high7,8; patients with ALK+ NSCLC face a greater risk of recurrence compared with patients with ALK-negative disease.8,9

Approximate 5-year recurrence rate
in resected NSCLC with/without chemotherapy and/or radiotherapy10,11*

40%

For patients (n=1718)
with Stage I NSCLC

75%

For patients (n=1247)
with Stage III NSCLC

A review of a global database of NSCLC (N=25,911 with pathological staging)

found that 5-year OS was12†

80%

For Stage I NSCLC

30%

For Stage III NSCLC

Testing early for PD-L1 expression, EGFR mutations and ALK rearrangements in resected NSCLC can help identify appropriate treatment regimens and should be performed before initiating systemic therapy6,13

ALECENSA is the first and only TKI recommended by the NCCN as an adjuvant treatment option for patients with completely resected NSCLC, positive for ALK rearrangements (Category 1)14||

Discover

ALECENSA