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Poster session 17

963P - Quality-adjusted time without symptoms or toxicity (Q-TWiST) analysis to assess the impact of treatment with camrelizumab + rivoceranib (cam+rivo) on quality of life vs sorafenib (sora) in patients (pts) with unresectable hepatocellular carcinoma (uHCC): Study CARES-310

Date

14 Sep 2024

Session

Poster session 17

Topics

Tumour Site

Hepatobiliary Cancers

Presenters

Andrew Moon

Citation

Annals of Oncology (2024) 35 (suppl_2): S656-S673. 10.1016/annonc/annonc1595

Authors

A. Moon1, N. Raphael2, S.L. Chan3, A.O. Kaseb4, S.H. Jang5, X. Meng6, A. Cheng7, S. Qin8, A. Vogel9

Author affiliations

  • 1 Gastroenterology And Hepatology, UNC School of Medicine, 27599 - Chapel Hill/US
  • 2 Medical Affairs, Elevar Therapeutics, 07024 - Fort Lee/US
  • 3 Clinical Oncology Department, The Chinese University of Hong Kong - Sino Building, Sha Tin/HK
  • 4 Gi Medical Oncology Dept., The University of Texas M. D. Anderson Cancer Center, 77030 - Houston/US
  • 5 Operation, Elevar Therapeutics, 07024 - Fort Lee/US
  • 6 Statistics, Elevar Therapeutics, 07024 - Fort Lee/US
  • 7 Department Of Oncology, NTUH - National Taiwan University Hospital, 10002 - Taipei/TW
  • 8 Cancer Center Of Jinling Hospital, Nanjing University Of Chinese Medicine, Nanjing Jingdu Hospital, 210002 - Nanjing/CN
  • 9 Mhh Department Of Gastroenterology, Hannover Medical School, 30625 - Hannover/DE

Resources

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Abstract 963P

Background

Study CARES-310 (NCT03764293) evaluated cam, an anti-PD-1 inhibitor, in combination with rivo, a VEGFR tyrosine kinase inhibitor, vs sora in pts with uHCC. As compared with sora, cam+rivo significantly improved median overall survival (22.1 vs 15.2 months, HR 0.62) and median progression-free survival by BIRC assessment (5.6 vs 3.7 months, HR 0.52). Rates of grade 3/4 adverse events (G 3/4 AEs) were higher with cam+rivo arm vs sora (82% vs 53%). We performed a Q-TWiST analysis to assess the impact of treatment with cam+rivo on quality of life as compared with sora.

Methods

All pts were evaluated for: duration of time before disease progression with G3/4 AEs (TOX), duration of time before disease progression without G3/4 AEs (TWiST), and duration of time between disease progression and death or censoring (REL). Utility coefficients (u) of 1 for TWIST, 0.5 for TOX and REL were used to calculate Q-TWiST (Q-TWiST = [uTOX * TOX] + [uTWiST * TWiST] + [uREL * REL]; mean duration in each state was calculated using the method of Restricted Mean Survival Time (RMST).

Results

Duration of TOX and TWiST was longer for pts in the cam+rivo arm vs sora arm; duration of REL was not significantly different between arms (Table). Clinically important relative Q-TWiST gains favored cam+rivo vs sora by 10.6% (= difference 1.61/mOS of sora 15.2). Table: 963P

Mean duration of TOX, TWiST, REL, and Q-TWiST

Mean duration, months (SE) Cam+rivo (n=272) Sora (n=271) Difference Cam+rivo vs Sora P value
TOX 2.18 (0.2) 1.21 (0.14) 0.97 (0.25)

Conclusions

Pts with uHCC treated with cam+rivo had clinically meaningful quality-adjusted survival benefits compared with pts treated with sora, a benefit driven primarily by time before disease progression without toxicity, supporting that the higher incidence of AEs in pts treated with cam+rivo vs sora is likely due to longer treatment duration with cam+rivo.

Clinical trial identification

NCT03764293.

Editorial acknowledgement

Olivia Adams The Phillips Group Oncology Communications, Inc.

Legal entity responsible for the study

Elevar Therapeutics; Jiangsu Hengrui Pharmaceuticals Co., Ltd.

Funding

Elevar Therapeutics; Jiangsu Hengrui Pharmaceuticals Co., Ltd.

Disclosure

A. Moon: Financial Interests, Personal, Speaker, Consultant, Advisor: Target RWE; Financial Interests, Personal, Advisory Board: Intercept Pharmaceuticals. N. Raphael: Financial Interests, Personal, Full or part-time Employment: Elevar Therapeutics; Financial Interests, Personal, Stocks/Shares: Elevar Therapeutics. S.L. Chan: Financial Interests, Personal, Advisory Board: Eisai, AstraZeneca, MSD, Roche; Financial Interests, Personal, Invited Speaker: AstraZeneca, MSD, Eisai, Roche, Ipsen; Financial Interests, Personal, Research Grant: Eisai, MSD. A.O. Kaseb: Financial Interests, Personal, Research Grant: BMS, Roche, Genentech, Merck, Eisai, Exelixis, Hengrui, Adaptimmune, Tyardi; Financial Interests, Personal, Speaker, Consultant, Advisor: BMS, Roche, Genentech, Merck, Eisai, Exelixis, Elevar; Financial Interests, Personal, Speaker’s Bureau: BMS, Roche, Genentech, Merck, Eisai, Exelixis, Elevar. S.H. Jang, X. Meng: Financial Interests, Personal, Full or part-time Employment: Elevar Therapeutics; Financial Interests, Personal, Stocks/Shares: Elevar Therapeutics. A. Cheng: Financial Interests, Personal, Speaker, Consultant, Advisor: AstraZeneca, BMS, Genentech/Roche, Eisai, Sanofi, MSD, Bayer, BeiGene, Ipsen Innovation, Ono Pharmaceutical, Omega Therapeutics; Financial Interests, Personal, Speaker’s Bureau: Amgen Taiwan, Ipsen Innovation, Bayer, Eisai, Sanofi, MSD, Genentech/Roche, AstraZeneca, BMS, Ono Pharmaceutical, Omega Therapeutics; Financial Interests, Personal, Advisory Board: Abbisko Therapeutics. A. Vogel: Financial Interests, Personal, Speaker, Consultant, Advisor: AstraZeneca, Amgen, BeiGene, Boehringer Mannheim, BMS, BTG, Daiichi Sankyo, Eisai, Incyte, Ipsen, MSD, Pierre Fabre, Roche, Servier, Sirtex, Tahio, Terumo; Financial Interests, Personal, Speaker’s Bureau: AstraZeneca, Amgen, BeiGene, Boehringer Mannheim, BMS, BTG, Daiichi Sankyo, Eisai, GSK, Imaging Equipment Ltd. (AAA), Incyte, Ipsen, Jiangsu Hengrui, Medicines MSD, Pierre Fabre, Roche, Servier, Sirtex, Tahio, Terumo; Financial Interests, Personal, Funding, support for attending meetings and/or travel: Roche, MSD, Astellas; Financial Interests, Personal, Advisory Board: AstraZeneca, Amgen, BeiGene, Boehringer Mannheim, BMS, BTG, Daiichi Sankyo, Eisai, Incyte, Ipsen, MSD, Pierre Fabre, Roche, Servier, Sirtex, Tahio, Terumo. All other authors have declared no conflicts of interest.

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