PO.CL01.03 · 临床研究
Prognostic and predictive effects of TP53 co-mutations and RET fusion partners in RET -rearranged advanced NSCLC
作者与单位
摘要 Abstract
Background: RET fusions occur in ~1-2% of advanced NSCLC (aNSCLC). Selective RET inhibitors (SRIs) significantly improve outcomes, yet ~10% of patients progress by 6 months and ~30% by 12 months. Predictors of response or early progression remain poorly defined.
Methods: A multicenter retrospective analysis (RET-MAP) of RET+ aNSCLC from 47 international centers evaluated clinical/genomic correlates of SRI outcomes. Multivariable Cox models estimated progression-free (PFS) and overall survival (OS) and tested interactions with first-line (1L) SRI versus chemotherapy ± immune checkpoint inhibitor (CH±ICI). In parallel, genomic/transcriptomic features were characterized in an external Caris Life Sciences (CLS) RET+ aNSCLC cohort.
Results: Among 510 RET-MAP patients (median age 63; 59% female; 36% ever-smokers; 92% adenocarcinoma), 401 received an SRI (1L n=151; later lines n=250). Median PFS on SRI (any line) was 17.1 months (95% CI, 14.5-21.1), median OS 30.4 months (95% CI, 27.0-41.1). TP53 co-mutation was present in 27% (78/292 tested) and was associated with shorter PFS (8.9 vs 19.2 months; p<0.001) and OS (22.7 vs 30.9 months; p=0.002), without a significant treatment-by- TP53 interaction for 1L SRI versus CH±ICI (p=0.22). Fusion partner contributed with additional signal: KIF5B (73%, 274/373) had inferior PFS (13.4 vs 60.2 months; p<0.001) and OS (26.6 vs 73.0 months; p=0.002) compared with CCDC6 (17%, 65/373), and a significant treatment-by-fusion interaction favored SRI over CH±ICI in CCDC6 versus KIF5B (p=0.007). On multivariate analysis, shorter PFS and OS were independently associated with TP53 mutation (HR 1.74, p<0.001; HR 1.77, p=0.001), KIF5B fusion (HR 1.98, p=0.002; HR 1.64, p=0.040), ECOG ≥2 (HR 2.20, p<0.001; HR 3.06, p<0.001), and brain metastases (HR 1.59, p=0.003; HR 1.88, p<0.001); worse OS was associated with non-adenocarcinoma histology (HR 1.74, p=0.049) and smoking (HR 1.42, p=0.034). Notably, KIF5B fusions were enriched for TP53 mutations versus CCDC6 (40% vs 19.6%, p=0.011), suggesting partially overlapping biology. In the CLS cohort (N=211), TP53 -mutant tumors (74/211) were enriched for RB1 mutations, had higher PD-L1 expression and tumor mutational burden, and demonstrated increased M1 macrophage/B-cell infiltration with reduced neutrophils; by fusion partner, CCDC6 showed higher PD-L1, while global transcriptomes were otherwise similar to KIF5B .
Conclusions: In RET+ aNSCLC, TP53 mutation is prognostic for inferior outcomes on SRIs but not predictive of differential benefit versus CH±ICI. Fusion partner carries both prognostic and predictive relevance; CCDC6 is associated with a more indolent course and greater relative benefit from SRI. External profiling supports an inflammatory microenvironment in TP53 -mutant disease, reinforcing biologically distinct-and clinically meaningful-subsets within RET -driven lung cancer.
利益披露 Disclosure
D. Miliziano, None.
J. Rotow,
Amgen consulting fees or honoraria.
AstraZeneca consulting fees or honoraria.
BioAtla consulting fees or honoraria.
BMS consulting fees or honoraria.
Boehringer Ingelheim consulting fees or honoraria.
M. Lomibao, None.
T. Adeyelu,
Caris Life Sciences Employment, Stock.
A. Marinello, None..
H. Bote-de Cabo, None.
J. Feng,
AstraZeneca Other, Speaker’s honoraria and advisory board.
Merck Other, Speaker’s honoraria and advisory board.
Pfizer Other, Speaker’s honoraria and advisory board.
Amgen Other, Speaker’s honoraria and advisory board.
Roche Other, Speaker’s honoraria.
CPD Network (Oncology Education) Other, Speaker’s honoraria.
DAVA Oncology Travel.
Boehringer-Ingelheim Travel.
Eli Lilly Other, PI in sponsored trials.
Black Diamond Therapeutics Other, PI in sponsored trials.
A. De Giglio, None..
M. Brandão, None..
F. Guisier, None.
M. Duruisseaux,
Takeda Other, Institutional research funding, advisory board.
Astra-Zeneca Travel, Other, Institutional research funding, advisory board.
Roche Travel, Other, advisory board.
MSD Travel, Other, advisory board.
Amgen Travel, Other, advisory board.
Pfizer Other, advisory board.
Boehringer Ingelheim Other, advisory board.
BMS Other, advisory board.
Abbvie Other, advisory board.
Guardant Other, advisory board.
Novartis Other, advisory board.
Gamamabs Pharma Other, advisory board.
GSK Other, advisory board.
Sanofi Other, advisory board.
Lilly Other, advisory board.
Merus Other, advisory board.
C. Falcon, None..
M. Cani, None..
F. Colamartini, None..
B. Waissengrin, None.
I. Monnet,
Regeneron Other, Honoraria.
Takeda Other, Financial support.
MSD Other, Financial support.
Pfizer Other, Financial support.
Oxyvie Other, Financial support.
A. Eisert, None..
E. Bria, None.
A. H. Nassar,
Korean Society of Medical Oncology Travel, Other, Honoraria.
TEMPUS Other, Honoraria.
OncLive Other, Honoraria.
Oklahoma University Other, Honoraria.
Targeted Oncology Other, Honoraria.
American Association for Cancer Research Travel.
Guidepoint global Other, Consultation fees.
Putnam associates Other, Consultation fees.
Capvision Other, Consultation fees.
Revolution Medicine Other, Equity.
Summit Therapeutics Other, Equity.
A. Aijaz, None..
P. Iranzo, None.
C. R. Lindsay,
Revolution Medicines Other, research funding (Institutional), participation in advisory boards or educational sessions.
Boehringer Ingelheim Other, research funding (Institutional).
Qiagen Other, research funding (Institutional).
Amgen Other, participation in advisory boards or educational sessions.
Eli Lilly Other, participation in advisory boards or educational sessions.
E. Fabre, None.
V. Cordeiro de Lima,
BMS Other, institutional research funding.
J. Raimbourg, None..
L. Mezquita, None.
N. Minatta,
BMS Consulting/advisory board.
S. Cousin, None..
K. Szymczak, None.
V. Fallet,
Amgen Travel.
C. Audigier-Valette, None.
H. Doubre,
Pfizer Travel, accommodation, congress registration expenses.
P. Rochigneux,
GSK Other, Investigator in clinical trials.
A. Avanzo, None.
A. Calles,
AstraZeneca Honoraria.
M. Tagliamento, None..
D. Cortinovis, None..
B. Halmos, None..
N. Girard, None..
A. Elliott, None..
J. Bar, None..
A. Cortellini, None..
D. Ionescu, None..
F. Shepherd, None.
F. Barlesi,
Roche Other, Consulting.
Genentech Other, Consulting.
Novartis Other, Consulting.
Bristol Myers Squibb Other, Consulting.
AstraZeneca Consulting.
MedImmune Other, Consulting.
Boehringer Ingelheim Consulting.
Lilly Consulting.
Merck Serono Other, Consulting.
MSD Oncology Other, Consulting.
Takeda Other, Consulting.
Bayer Other, Consulting.
Amgen Other, Consulting.
Eisai Europe Other, Consulting.
K. L. Reckamp, None..
D. Planchard, None.
B. Besse,
Abbvie Other, Honoraria, conseils.
Biontech SE Other, Honoraria.
BristolMyerSqibb Other, Honoraria.
Chugai pharmaceutical Other, Honoraria.
CureVac AG Other, Honoraria.
Daiichi Sankyo Honoraria.
F. Hoffmann-La Roche Ltd Honoraria.
Pharmamar Honoraria.
Regeneron Honoraria.
Sanofi aventis Honoraria.
Turning Point Therapeutics Honoraria.
Eli Lilly Conseils.
Astrazeneca steering committee.
Janssen steering committee.
MSD Other, steering committee.
Ose Immunotherapeutics Other, steering committee.
Pharmamar Other, steering committee.
Roche-Genentech Other, steering committee.
Sanofi Other, steering committee.
Takeda Other, steering committee.
A. Drilon,
14ner/Elevation Oncology Other, Honoraria.
Amgen Other, Honoraria.
Abbvie Other, Honoraria.
AnHeart Therapeutics Other, Honoraria.
ArcherDX Other, Honoraria.
AstraZeneca Other, Honoraria.
Beigene Other, Honoraria.
BergenBio Other, Honoraria.
Blueprint Medicines Other, Honoraria.
Bristol Myers Squibb Other, Honoraria.
Boehringer Ingelheim Other, Honoraria.
Chugai Pharmaceutical Other, Honoraria.
EcoR1 Other, Honoraria.
EMD Serono Other, Honoraria.
Entos Other, Honoraria.
Exelixis Other, Honoraria.
Helsinn Other, Honoraria.
Hengrui Therapeutics Other, Honoraria.
Ignyta/Genentech/Roche Other, Honoraria.
Janssen Other, Honoraria.
M. Aldea,
Amgen ).
AstraZeneca ).
Sandoz ).
Owkin ).
Lifen ).
OncLive Honoraria.