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Poster session 16

1434P - Impact of subsequent anti-tumor therapies in patients (pts) with advanced gastric or gastroesophageal junction (G/GEJ) adenocarcinoma receiving fruquintinib (F) plus paclitaxel (PTX) or placebo plus PTX in FRUTIGA study

Date

14 Sep 2024

Session

Poster session 16

Topics

Cancer Research

Tumour Site

Gastric Cancer;  Gastro-Oesophageal Junction Cancer

Presenters

Rui-Hua Xu

Citation

Annals of Oncology (2024) 35 (suppl_2): S878-S912. 10.1016/annonc/annonc1603

Authors

R. Xu1, F. Wang2, L. Shen3, W. Guo4, T. Liu5, J. Li6, S. Qin7, Y. Bai8, Z. Chen9, J. Wang10, Y. Pan11, Y. Shu12, F. Zhao13, Y. Cheng14, F. Ye15, K. Gu16, T. Zhang17, H. Pan18, P. Tan19, W. Su19

Author affiliations

  • 1 Medical Oncology Dept, Sun Yat-sen University Cancer Center, 510060 - Guangzhou/CN
  • 2 Medical Oncology Dept, Sun Yat-sen University Cancer Center, 510060 - Guangzhou/CN
  • 3 Department Of Gastrointestinal Oncology, Key Laboratory Of Carcinogenesis And Translational Research (ministry Of Education/beijing), Peking University Cancer Hospital & Institute, 100142 - Beijing/CN
  • 4 Medical Oncology, Fudan University Shanghai Cancer Center, 200032 - Shanghai/CN
  • 5 Oncology Dept., Zhongshan Hospital of Fudan University, 200032 - Shanghai/CN
  • 6 Oncology Department, Tongji University Shanghai East Hospital, 200120 - Shanghai/CN
  • 7 Oncology Dept., Chinese People's Liberation Army Cancer Center of Nanjing Bayi Hospital, 210002 - Nanjing/CN
  • 8 Oncology Dept., Harbin Medical University Cancer Hospital, 150081 - Harbin/CN
  • 9 Oncology Dept., The Second Hospital of Anhui Medical University, 230601 - Hefei/CN
  • 10 Internal Medicine-digestive Oncology Dept, Henan Cancer Hospital/Affiliated Cancer Hospital of Zhengzhou University, 450008 - Zhengzhou/CN
  • 11 Oncology Department, The First Affiliated Hospital of USTC/ Anhui Provincial Hospital, 230001 - Hefei/CN
  • 12 Department Of Oncology, Jiangsu Province Hospital/The First Affiliated Hospital of Nanjing Medical University, 210029 - Nanjing/CN
  • 13 Oncology Dept., The First Affiliated Hospital of Bengbu Medical College, 233004 - Bengbu/CN
  • 14 Medical Oncology, Jilin Cancer Hospital, 130000 - Changchun/CN
  • 15 Medical Oncology Dept., The First Affiliated Hospital of Xiamen University, 361003 - Xiamen/CN
  • 16 Oncology Dept., The First Affiliated Hospital of Anhui Medical University, 230032 - Hefei/CN
  • 17 Oncology Department, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology/ Cancer Center Union Hospital, 430022 - Wuhan/CN
  • 18 Medical Oncology Department, Sir Run Run Shaw Hospital, Zhejiang University, School of Medicine, 310016 - Hangzhou/CN
  • 19 C&r, HUTCHMED Limited, 201203 - Shanghai/CN

Resources

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Abstract 1434P

Background

FRUTIGA study showed OS improvement but was not statistically significant in the ITT population who had advanced G/GEJ adenocarcinoma receiving F plus PTX over placebo plus PTX (mOS: 9.67 vs 8.41 mo, HR=0.96, p=0.6064; Xu RH, et al, 2024 ASCO #438780). Here we explored the effect of subsequent anti-tumor therapies on OS in this study.

Methods

A post-hoc analysis for the effect of subsequent anti-tumor therapies on OS (randomization to death from any cause) using Kaplan-Meier method was conducted.

Results

A total of 439/703 pts (F+PTX vs placebo + PTX: 185/351 [52.7%] vs 254/352 [72.2%]) received subsequent anti-tumor therapies. There were 33.7% (28.2% vs 39.2%), 16.9% (14.2% vs 19.6%), and 9.1% (7.4% vs 10.8%) of pts received 1, 2 or ≥ 3 subsequent anti-tumor regimens, respectively. Apatinib (23.1% vs 35.2%), irinotecan (20.8% vs 27.8%) and anti PD-1/PD-L1 antibodies (20.8% vs 27.6%) were the most common subsequent regimens; few pts (3.4% vs 5.7%) used anti-HER2/Claudin 18.2 regimens. Detailed results of impact of subsequent anti-tumor therapies on OS are shown in the table below. Table: 1434P

F+PTX (N = 351) n (%) PTX (N = 352) n (%) Median OS, mo (F+PTX vs PTX) HR
Subsequent treatment 185 (52.7) 254 (72.2) 12.22 vs 9.95 0.91 (0.73, 1.12)
Apatinib 81 (23.1) 124 (35.2) 13.01 vs 10.81 0.95 (0.70, 1.30)
Irinotecan 73 (20.8) 98 (27.8) 12.22 vs 10.71 0.92 (0.67, 1.27)
Anti PD-1/PD-L1 – ICI naïve# 68 (19.4) 86 (24.4) 13.90 vs 13.60 1.12 (0.77, 1.62)
Anti PD-1/PD-L1 – ICI pre-treated 5 (1.4) 11 (3.1) 14.52 vs 14.75 0.73 (0.18, 2.94)
Anti HER2/Claudin 18.2& 12 (3.4) 20 (5.7) 13.77 vs 16.10 2.09 (0.82, 5.30)

Pts who had received prior anti PD-1/PD-L1 antibodies treatment.#Pts who had not received prior anti PD-1/PD-L1 antibodies treatment.&Pts who had not received prior HER2.

Conclusions

Pts who received 3L standard regimens (apatinib, irinotecan) for the subsequent anti-tumor therapies had the consistent OS improvement as shown in ITT population. Subsequent anti PD-1/PD-L1 therapies for pts who had received previous anti PD-1/PD-L1 antibodies could have no potential impact on OS benefit in FRUTIGA study.

Clinical trial identification

NCT03223376.

Editorial acknowledgement

Legal entity responsible for the study

Hutchmed Limited.

Funding

The National Science and Technology Major Project (project no. 2019ZX09301012), the Science and Technology Commission of Shanghai Municipality (Science, Technology and Innovation Action Plan, project no. 17431900100) and Hutchmed Limited.

Disclosure

P. Tan, W. Su: Financial Interests, Personal, Full or part-time Employment: Hutchmed Limited. All other authors have declared no conflicts of interest.

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