The antibody–drug conjugate ifinatamab deruxtecan (I-DXd) showed
clinically meaningful responses in pretreated patients with
extensive-stage small cell lung cancer (ES-SCLC), according to an
interim analysis of the Phase 2 IDeate-Lung01 study.
SAN DIEGO, Sept. 7, 2024 /PRNewswire-PRWeb/ -- The
antibody–drug conjugate ifinatamab deruxtecan (I-DXd) showed
clinically meaningful responses in pretreated patients with
extensive-stage small cell lung cancer (ES-SCLC), according to an
interim analysis of the Phase 2 IDeate-Lung01 study. The data was
presented today at the International Association for the Study of
Lung Cancer (IASLC) 2024 World Conference on Lung Cancer.
"I-DXd at both doses showed clinically
meaningful efficacy in heavily pretreated patients with ES-SCLC,
with the 12-mg/kg dose demonstrating approximately twice the
confirmed ORR of the 8-mg/kg dose." -- Dr. C.M. Rudin of Memorial
Sloan Kettering Cancer Center in New York
City
Patients with ES-SCLC face poor outcomes and have limited
treatment options. B7 homolog 3 (B7-H3 [CD276]) is part of the B7
family, which includes immune checkpoint proteins such as PD-L1.
B7-H3 is highly expressed in many solid tumors but is absent or
expressed at low levels in normal tissues. High and consistent
expression of B7-H3 has been shown across all molecular subtypes of
SCLC and has been linked to poor prognosis. I-DXd, a B7-H3–directed
antibody–drug conjugate, demonstrated promising efficacy in the
ongoing Phase 1/2 IDeate-Pantumor01 study, with a confirmed
objective response rate (ORR) of 52.4% and a median duration of
response (DOR) of 5.9 months in the SCLC cohort (n=21).
In the dose optimization part of the ongoing Phase 2
IDeate-Lung01 study (NCT05280470), two doses of I-DXd (8 mg/kg and
12 mg/kg IV every 3 weeks) were evaluated in patients with ES-SCLC
who had received at least one prior line of platinum-based
chemotherapy and no more than three prior lines of systemic
treatment in total. Patients with asymptomatic brain metastases
could participate in the study. The primary endpoint was ORR by
blinded independent central review, with secondary endpoints
including DOR, progression-free survival, overall survival, disease
control rate, time to response (TTR), and overall safety
profile.
As of April 25, 2024, 88 patients
had received at least one dose of I-DXd; 46 patients received I-DXd
8 mg/kg and 42 patients I-DXd 12 mg/kg, with a median follow-up of
14.6 and 15.3 months, respectively. I-DXd demonstrated promising
efficacy, with a confirmed ORR of 54.8% in the 12-mg/kg cohort and
of 26.1% in the 8-mg/kg cohort. A rapid response (TTR: 1.4 months)
was observed at both doses, while median DOR was 7.9 months in the
8-mg/kg cohort and 4.2 months in the 12-mg/kg cohort. In a subgroup
analysis of 16 patients with brain target lesions at baseline, the
intracranial response was 66.7% among 6 patients who received I-DXd
8 mg/kg, and 50.0% among 10 patients treated with I DXd 12 mg/kg.
During the study, a higher frequency of treatment-emergent adverse
events was reported in the 12-mg/kg cohort than in the 8 mg/kg
cohort; the most common TEAEs were gastrointestinal or hematologic
in nature, or fatigue. The incidence of adjudicated interstitial
lung disease was similar between cohorts, consistent with previous
reports.
"I-DXd at both doses showed clinically meaningful efficacy in
heavily pretreated patients with ES-SCLC, with the 12-mg/kg dose
demonstrating approximately twice the confirmed ORR of the 8-mg/kg
dose," according to Dr. C.M. Rudin of Memorial Sloan Kettering
Cancer Center in New York City.
Dr. Rudin added that the safety profile was generally consistent
across the two doses and while no new safety signals were observed,
TEAEs were more frequent at the higher dose. Based on these
findings, the 12-mg/kg dose has been selected as the optimal dose
for monotherapy in SCLC and will be further studied in the
extension part of IDeate-Lung01 and in the Phase 3 IDeate-Lung02
study.
About the IASLC:
The International Association for the Study of Lung Cancer (IASLC)
is the only global organization dedicated solely to the study of
lung cancer and other thoracic malignancies. Founded in 1974, the
association's membership includes more than 10,000 lung cancer
specialists across all disciplines in over 100 countries, forming a
global network working together to conquer lung and thoracic
cancers worldwide. The association also publishes the Journal of
Thoracic Oncology, the primary educational and informational
publication for topics relevant to the prevention, detection,
diagnosis, and treatment of all thoracic malignancies. Visit
http://www.iaslc.org for more information.
About the WCLC:
The World Conference on Lung Cancer (WCLC) is the world's largest
meeting dedicated to lung cancer and other thoracic malignancies,
attracting nearly 7,000 researchers, physicians and specialists
from more than 100 countries. The goal is to increase awareness,
collaboration and understanding of lung cancer, and to help
participants implement the latest developments across the globe.
The conference will cover a wide range of disciplines and unveil
several research studies and clinical trial results. For more
information, visit https://wclc2024.iaslc.org.
Media Contact
Chris Martin, The David James
Group, 6306702745, cmartin@davidjamesgroup.com, www.iaslc.org
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