<p>Whether progression-free survival (PFS) is a valid surrogate endpoint for overall survival (OS) in patients who underwent conversion therapy for hepatocellular carcinoma (HCC) remains uncertain. The present study compares the two survival measures in this patient cohort. Data on unresectable HCC patients undergoing conversion therapy from 20 Chinese medical centers (2019–2023) were retrieved. The correlation (ρ) between PFS and OS was assessed using the rank correlation method combined with iterative multiple imputation to account for censoring. As a secondary analysis, the correlation was evaluated according to the conversion regimen and treatment response. The pairwise correlation between PFS and OS was calculated through sensitivity analysis. A total of 1909 patients with unresectable HCC were included. A moderately strong correlation was found between PFS and OS (ρ = 0.74, 95%CI 0.72–0.76). The strength of the correlation was similar regardless of the conversion therapy regimen (interventional therapy plus systemic therapy: ρ = 0.75, 0.72–0.77; systemic therapy alone: ρ = 0.73, 0.57–0.83; interventional therapy alone: ρ = 0.74, 0.70–0.78). The mean (standard deviation) pairwise correlation coefficient between 24-month PFS and 48-month OS was 0.74 (0.08). Those who responded completely (hazard ratio = 0.24, 95%CI 0.21–0.28) or partially (hazard ratio = 0.23, 95%CI 0.20–0.25) to conversion therapy showed significantly better PFS than those who did not. In patients with unresectable HCC undergoing conversion therapy, a moderately strong correlation was observed between PFS and OS, and this correlation was unaffected by the conversion therapy regimen. Better tumor response following conversion therapy could be used to identify patients with improved PFS.</p>

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Progression-free survival as a potential surrogate endpoint for overall survival after conversion therapy for unresectable hepatocellular carcinoma (GUIDANCE008)

  • Jin-Wei Wu,
  • Da-Long Yang,
  • Shu-Chang Chen,
  • Mian-Jing Li,
  • Yong-Rong Liang,
  • Xue-Yao Wang,
  • Hong-Bing Yao,
  • Jie Liu,
  • Pei-Sheng Wu,
  • Ning Peng,
  • Jun-Liang Nong,
  • Ya-Qun Yu,
  • Lin Ye,
  • Ze Su,
  • Chuang Qin,
  • Kang Chen,
  • Yi-He Yan,
  • Fan-Jian Zeng,
  • Shao-Ping Liu,
  • Ming-Song Wu,
  • Fu-Quan Yang,
  • Yong-Cheng Lai,
  • Xiao-Feng Dong,
  • Teng-Meng Zhong,
  • Qing-Qing Pang,
  • Fu-Xin Li,
  • Ai-Qun Liu,
  • Liang Ma,
  • Jian-Hong Zhong,
  • Ping Cen,
  • Jian-Hong Zhong,
  • Liang Ma,
  • Bang-De Xiang,
  • Da-Long Yang,
  • Ai-Qun Liu,
  • Ya-Qun Yu,
  • Lin Ye,
  • Shu-Qun Li,
  • Shao-Ping Liu,
  • Zhen Liu,
  • Chuang Qin,
  • Zhi-Jun Jiang,
  • Ning Peng,
  • Jia-Liang Wei,
  • Ze Su,
  • Jun-Liang Nong,
  • Yi-He Yan,
  • Kang Chen,
  • Xiao-Feng Dong,
  • Yong-Yu Yang,
  • Jun-Jie Ou,
  • Shu-Chang Chen,
  • Ying Xue Wu,
  • Hong-Bing Yao,
  • Xue-Yao Wang,
  • Fan-Jian Zeng,
  • Jie Liu,
  • Mian-Jing Li,
  • Pei-Sheng Wu,
  • Yong-Rong Liang,
  • Yao-Zhi Chen,
  • Yong-Cheng Lai,
  • Ming-Song Wu,
  • Wen-Feng Li,
  • Tian-Man Li,
  • Fu-Quan Yang,
  • Zhi-Yin Liang,
  • Teng-Meng Zhong,
  • Xian-Shuang Mao,
  • Fu-Xin Li,
  • Teng-Xian Zhou,
  • Guang-Cai Zheng,
  • Yao-Ming Wang,
  • Min Luo,
  • Guo-Dong Wang,
  • Qing-Qing Pang,
  • Xiao-Kai Shen,
  • Lei Liu,
  • Si-Cong Lu,
  • Wen-Hai He,
  • Xian-Jian Wu,
  • Lin-Hong Xie,
  • Jian-Yuan Meng,
  • Zhi-Cheng Li,
  • Ting Quan,
  • Jin-Wei Wu,
  • Ping Cen

摘要

Whether progression-free survival (PFS) is a valid surrogate endpoint for overall survival (OS) in patients who underwent conversion therapy for hepatocellular carcinoma (HCC) remains uncertain. The present study compares the two survival measures in this patient cohort. Data on unresectable HCC patients undergoing conversion therapy from 20 Chinese medical centers (2019–2023) were retrieved. The correlation (ρ) between PFS and OS was assessed using the rank correlation method combined with iterative multiple imputation to account for censoring. As a secondary analysis, the correlation was evaluated according to the conversion regimen and treatment response. The pairwise correlation between PFS and OS was calculated through sensitivity analysis. A total of 1909 patients with unresectable HCC were included. A moderately strong correlation was found between PFS and OS (ρ = 0.74, 95%CI 0.72–0.76). The strength of the correlation was similar regardless of the conversion therapy regimen (interventional therapy plus systemic therapy: ρ = 0.75, 0.72–0.77; systemic therapy alone: ρ = 0.73, 0.57–0.83; interventional therapy alone: ρ = 0.74, 0.70–0.78). The mean (standard deviation) pairwise correlation coefficient between 24-month PFS and 48-month OS was 0.74 (0.08). Those who responded completely (hazard ratio = 0.24, 95%CI 0.21–0.28) or partially (hazard ratio = 0.23, 95%CI 0.20–0.25) to conversion therapy showed significantly better PFS than those who did not. In patients with unresectable HCC undergoing conversion therapy, a moderately strong correlation was observed between PFS and OS, and this correlation was unaffected by the conversion therapy regimen. Better tumor response following conversion therapy could be used to identify patients with improved PFS.