Survival outcomes of first-line anti-EGFR antibody versus anti-VEGF therapy stratified by DNA methylation status in right-sided metastatic colorectal cancer: A propensity score weighting analysis.

T Takeshi Suto (Yamagata Prefectural Central Hospital, Yamagata-Shi, Japan) K Kozo Kataoka (Division of Lower GI, Department of Gastroenterological Surgery, Hyogo Medical University, Nishinomiya-Shi, Japan) K Keita Mori K Kunihiro Fushiki (Division of Gastrointestinal Oncology, Shizuoka Cancer Center, Sunto-Gun, Japan) M Manabu Shiozawa M Mitsuru Yokota (Department of General Surgery, Kurashiki Central Hospital, Okayama, Japan) J Junichi Mazaki (Tokyo Medical University, Shinjyuku-Ku, Japan) N Nobuhisa Matsuhashi (Department of Gastroenterological Surgery, Gifu University Graduate School of Medicine, Gifu, Japan) H Hironaga Satake T Toshihiro Kudo (Department of Medical Oncology, Osaka International Cancer Institute, Osaka, Osaka, Japan) H Hiroki Osumi N Naoya Akazawa (Department of Gastroenterological Surgery, Sendai City Medical Center Sendai Open Hospital, Sendai, Japan) T Toshifumi Yamaguchi Y Yusuke Suwa (Department of Surgery, Gastroenterogical Centre, Yokohama City University Medical Center, Yokohama, Japan) T Takashi Ohta (Department of Gastroenterology, Kansai Rosai Hospital, Amagasaki, Japan) K Kiichi Sugimoto (Department of Coloproctological Surgery, Juntendo University Faculty of Medicine, Bunkyo-Ku, Japan) N Naoto Takase (Department of Medical Oncology, Takarazuka City Hospital, Takarazuka, Japan) T Tatsuki Ikoma T Tamotsu Sagawa (Hokkaido Cancer Center, Sapporo, Japan) T Takeshi Yamada (Neutron Science and Technology Center, Comprehensive Research Organization for Science and Society, Tokai, Naka, Ibaraki 319-1106, Japan)

Abstract

156 Background: The clinical benefit of anti-EGFR antibodies (anti-EGFR ab) is generally limited in right-sided metastatic colorectal cancer (mCRC). Recent evidence suggests genome-wide DNA methylation may influence anti-EGFR efficacy (Cancer Sci, 2022). We evaluated whether DNA methylation could identify patients deriving comparable benefit from anti-EGFR ab and anti-VEGF therapy. Methods: We retrospectively analyzed unresectable right-sided RAS wild-type mCRC patients treated first-line with anti-EGFR ab or anti-VEGF therapy. DNA methylation was assessed using OncoGuide EpiLight and classified as high (HM) or low (LM). Endpoints were response rate (RR), depth of response (DpR), PFS, and OS, analyzed by methylation status and molecular subtype. Propensity score weighting (PSW) balanced baseline characteristics. Results: Among 198 patients, 85 and 59 RAS/BRAF wild-type received anti-EGFR (Group E) and anti-VEGF (Group V), respectively. LM proportion was 78.8% (67/85) in Group E and 59.3% (35/59) in Group V. After PSW, RR, DpR, PFS and OS by DNA methylation and molecular subtype are shown in the Table. LM patients in Group E tended to have higher RR and markedly better DpR than those in Group V, while PFS and OS were comparable. Conclusions: Low methylation may identify a subset of right-sided mCRC patients who benefit similarly from anti-EGFR and anti-VEGF therapy. These findings support prospective validation of DNA methylation as a predictive biomarker. DNA methylation status Group RAS wild RAS/BRAF wild RAS/BRF wild/MSS/HER2 (-) RR (event/N;%) All E 69/125=55.2% 48/85=56.5% 47/76=61.8% V 33/73=45.2% 29/59=49.2% 26/54=48.1% P value 0.19 0.40 0.15 LM E 50/75=66.7% 43/67=64.2% 43/61=70.5% V 21/36=58.3% 20/35=57.1% 19/34=55.9% P value 0.41 0.53 0.18 DpR (N;median (range)) All E 115, 26.0(-85.2 - 100) 80, 39.5(-74 - 100) 71, 42.1(-51.4 – 100) V 62, 17.4(43 – 61.6) 51, 21(-43 – 61.6) 46, 21(-43 – 61.6) P value 0.0041 0.012 0.0030 LM E 72, 44.5(-44 – 100) 64, 44(-44 – 100) 58, 45.5(-44 – 100) V 32, 30.5(-41 – 61.6) 31, 30(41 – 61.6) 30, 29(-41 – 61.6) P value 0.0086 0.014 0.0025 PFSmedian months (95% CI) All E 9.95(8.64 -12.0 ) 11.5(9.17 - 16.3) 11.5(9.17 - 18.6) V 11.7(10.6 - 17.8) 12.7(10.9 - 18.2) 12.7 (10.6 - 18.0) HR (95% CI) 0.83 (0.61-1.13) 0.96 (0.67-1.38) 1.03 (0.71-1.5) LM E 13.6(10.4 - 19.1) 13.6(9.95 - 19.1 ) 13.5 (9.46-20.7) V 10.6(9.0 - 15.9) 11.4 (8.87 - 15.9) 11.4 (8.87-18.0) HR (95% CI) 0.83 (0.61-1.13) 0.96 (0.67-1.38) 1.03 (0.71-1.5) OS median months (95% CI) All E 21.7(17.5 - 29.5) 29.5 (21.0 - 36.4) 29.5(21.0 - 36.4) V 31.6 (26.9 - 40.1) 32.0(27.7 - 42.9) 34.4 (27.7 - 50.6) HR (95% CI) 0.77(0.56-1.04) 0.96(0.67 - 1.38) 0.90(0.61 - 1.33) LM E 30.1(25.0 - 38.2) 29.5 (21.6-38.2) 30.1(21.6-39.1) V 38.8 (27.9 - 60.6 ) 38.8 (27.9-60.6) 38.8(27.9 -60.6) HR (95% CI) 0.88(0.56 - 1.37) 0.93(0.59 - 1.46) 0.94(0.59 - 1.50)

Article Details

Volume / Issue Vol. 44, Issue 2_suppl
Published January 10, 2026
Pages 156-156
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (20)

T

Takeshi Suto

Yamagata Prefectural Central Hospital, Yamagata-Shi, Japan

K

Kozo Kataoka

Division of Lower GI, Department of Gastroenterological Surgery, Hyogo Medical University, Nishinomiya-Shi, Japan

K

Keita Mori

K

Kunihiro Fushiki

Division of Gastrointestinal Oncology, Shizuoka Cancer Center, Sunto-Gun, Japan

M

Manabu Shiozawa

M

Mitsuru Yokota

Department of General Surgery, Kurashiki Central Hospital, Okayama, Japan

J

Junichi Mazaki

Tokyo Medical University, Shinjyuku-Ku, Japan

N

Nobuhisa Matsuhashi

Department of Gastroenterological Surgery, Gifu University Graduate School of Medicine, Gifu, Japan

H

Hironaga Satake

T

Toshihiro Kudo

Department of Medical Oncology, Osaka International Cancer Institute, Osaka, Osaka, Japan

H

Hiroki Osumi

N

Naoya Akazawa

Department of Gastroenterological Surgery, Sendai City Medical Center Sendai Open Hospital, Sendai, Japan

T

Toshifumi Yamaguchi

Y

Yusuke Suwa

Department of Surgery, Gastroenterogical Centre, Yokohama City University Medical Center, Yokohama, Japan

T

Takashi Ohta

Department of Gastroenterology, Kansai Rosai Hospital, Amagasaki, Japan

K

Kiichi Sugimoto

Department of Coloproctological Surgery, Juntendo University Faculty of Medicine, Bunkyo-Ku, Japan

N

Naoto Takase

Department of Medical Oncology, Takarazuka City Hospital, Takarazuka, Japan

T

Tatsuki Ikoma

T

Tamotsu Sagawa

Hokkaido Cancer Center, Sapporo, Japan

T

Takeshi Yamada

Neutron Science and Technology Center, Comprehensive Research Organization for Science and Society, Tokai, Naka, Ibaraki 319-1106, Japan