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Poster session 17

1410P - Efficacy of fruquintinib plus paclitaxel (F+PTX) in patients (pts) with prior immunotherapy (prior-IO): Subgroup analysis from FRUTIGA study

Date

14 Sep 2024

Session

Poster session 17

Topics

Clinical Research

Tumour Site

Gastric Cancer;  Gastro-Oesophageal Junction Cancer

Presenters

Lin Shen

Citation

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

Authors

L. Shen1, R. Xu2, F. Wang3, 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, B. Zhang19, M. Shi19

Author affiliations

  • 1 Department Of Gastrointestinal Oncology, Key Laboratory Of Carcinogenesis And Translational Research (ministry Of Education/beijing), Peking University Cancer Hospital & Institute, 100142 - Beijing/CN
  • 2 Medical Oncology, Sun Yat-sen University Cancer Center, 510060 - Guangzhou/CN
  • 3 Medical Oncology Dept, Sun Yat-sen University Cancer Center, 510060 - Guangzhou/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 Department, 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 1410P

Background

FRUTIGA has previously reported that F+PTX significantly improved PFS, ORR and DCR in 2L treatment of pts with advanced gastric or gastroesophageal junction (G/GEJ) adenocarcinoma. Treatment landscape of gastric cancer has evolved in the past few years. Immunotherapy plus chemotherapy with or without HER2-targeted therapy is the new standard of care for 1L therapy especially in pts with high PD-L1 expression, while the immunotherapy was not accessible in China at the initiation of FRUTIGA in 2017.

Methods

Pre-defined and post hoc analyses were conducted to evaluate the efficacy of F+PTX compared with placebo plus paclitaxel (PBO+PTX) in pts who received prior-IO in FRUTIGA.

Results

Of the 703 pts enrolled in FRUTIGA, 82 had received prior-IO. Of these, 35 were treated with F+PTX and 47 with PBO+PTX. Baseline demographics and disease characteristics were comparable between treatment arms. The most commonly used prior-IO were sintilimab (20.7%) and tislelizumab (19.5%). PFS was longer with F+PTX versus PBO+PTX (mPFS, 6.4 vs 1.8 months, HR 0.38; p=0.0003). Higher ORR and DCR were also observed in F+PTX (57.1% vs 19.1% and 82.9% vs 42.6%, respectively) compared with PBO+PTX. However, OS was not statistically significant (mOS, 12.1 vs 10.3 months, HR 0.99). It showed the same benefit trends of PFS, ORR and DCR in pts with prior-IO, in consistent with ITT population. Pre-defined subgroup analysis showed that pts with prior-IO might further reduce the risk of death or progression (HR 0.38) compared with those received prior chemotherapy only (HR 0.62) or the ITT population (HR 0.57). Detailed information is provided in the table. Table: 1410P

F+PTX (N=35) PBO+PTX (N=47)
Event (PD/Death), n (%) 23 (65.7) 37 (78.7)
Median PFS (95% CI), month 6.4 (3.7, 9.9) 1.8 (1.0, 2.7)
Unstratified HR (95% CI) 0.38 (0.22,0.65)
Unstratified log-rank test p value 0.0003
ORR, n (%) 20 (57.1) 9 (19.1)
95% CI 39.4, 73.7 9.2, 33.3
Fisher’s exact test p value 0.0005
DCR, n (%) 29 (82.9) 20 (42.6)
95% CI 66.4, 93.4 28.3, 57.8
Fisher’s exact test p value 0.0003

Conclusions

F+PTX also demonstrated efficacy benefits and showed great clinical value in prior-IO exposed pts.

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

B. Zhang, M. Shi: Financial Interests, Personal, Full or part-time Employment: Hutchmed Limited. All other authors have declared no conflicts of interest.

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