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Association details:
Biomarker:KRAS G12C
Cancer:Solid Tumor
Drug:glecirasib (JAB-21822) (KRAS G12C inhibitor)
Direction:Sensitive
Evidence:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
Title:

A Study of JAB-21822 in Patients With KRAS p.G12C Mutated Pancreatic Cancer

Excerpt:
...- Histopathologically or cytologically confirmed pancreatic cancer with KRAS p.G12C mutation identified through molecular testing....
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
Title:

JAB-21822 Activity in Adult Patients With Advanced Solid Tumors Harboring KRAS G12C Mutation

Excerpt:
...- Histologically or cytologically confirmed solid tumors with KRAS G12C mutation...
Trial ID:
More C2 evidence
Evidence Level:
Sensitive: C2 – Inclusion Criteria
Title:

JAB-21822 in Combination With Cetuximab in Patients With Advanced CRC and Other Solid Tumors With KRAS G12C Mutation

Excerpt:
...- Histologically or cytologically confirmed advanced colorectal cancer, advanced small intestinal cancer and advanced appendiceal cancer with KRAS p.G12C mutation...
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
Title:

A Study of JAB-21822 in Advanced or Metastatic NSCLC With KRAS p.G12C and STK11 Co-mutation and Wild-type KEAP1

Excerpt:
...Pathologically documented, locally-advanced or metastatic NSCLC with KRAS p.G12C mutation identified through molecular testing....
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
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Title:

FIH Study of JAB-21822 in Adult Patients With Advanced Solid Tumors Harboring KRAS G12C Mutation in China

Excerpt:
...Advanced (metastatic or unresectable) KRAS G12C mutant solid tumors, with failure or absence of standard treatment 3....
Trial ID:
Less C2 evidence
Evidence Level:
Sensitive: C3 – Early Trials
Source:
Title:

A phase I/II study of first-in-human trial of JAB-21822 (KRAS G12C inhibitor) in advanced solid tumors.

Published date:
05/26/2022
Excerpt:
A total of 33 patients (22 NSCLC, 9 CRC and 2 pancreatic cancer) had at least 1 post-baseline tumor assessment; in the 800mg QD cohort, overall response rate (ORR) and disease control rate (DCR) were 50% (5/10) and 100% (10/10), respectively, including 4 non-confirmed partial response (PR); in the 400mg QD cohort had an ORR and DCR of 80% (4/5) and 100% (5/5) respectively, including 2 non-confirmed PR. Patients with NSCLC (400mg QD and 800mg QD), the ORR and DCR were 70% (7/10) and 100% (10/10), respectively, including 5 non-confirmed PR. JAB-21822 was well tolerated with impressive preliminary efficacy in patients with heavily treated solid tumors harboring KRAS G12C mutation.
DOI:
10.1200/JCO.2022.40.16_suppl.3089
Trial ID: