Second-line treatment patterns and outcomes in advanced HCC after progression on atezolizumab/bevacizumab

被引:1
|
作者
Wu, Meng [1 ]
Fulgenzi, Claudia A. M. [2 ]
D'Alessio, Antonio [2 ,3 ]
Cortellini, Alessio [2 ,4 ]
Celsa, Ciro [2 ,5 ]
Manfredi, Giulia F. [2 ,3 ]
Stefanini, Bernardo [2 ,6 ]
Wu, Y. Linda [7 ]
Huang, Yi-Hsiang [8 ,9 ,10 ]
Saeed, Anwaar [11 ]
Pirozzi, Angelo [12 ,13 ]
Pressiani, Tiziana [13 ]
Rimassa, Lorenza [12 ,13 ]
Schoenlein, Martin [14 ]
Schulze, Kornelius [15 ]
von Felden, Johann [15 ]
Mohamed, Yehia [16 ]
Kaseb, Ahmed O. [16 ]
Vogel, Arndt [17 ,18 ]
Roehlen, Natascha [19 ,20 ]
Silletta, Marianna [4 ]
Nishida, Naoshi [21 ]
Kudo, Masatoshi [21 ]
Vivaldi, Caterina [22 ,23 ]
Balcar, Lorenz [24 ]
Scheiner, Bernhard [24 ]
Pinter, Matthias [24 ]
Singal, Amit G. [25 ]
Glover, Joshua [26 ]
Ulahannan, Susanna [26 ]
Foerster, Fredrich [27 ]
Weinmann, Arndt [27 ]
Galle, Peter R. [27 ]
Parikh, Neehar D. [28 ]
Hsu, Wei-Fan [29 ]
Parisi, Alessandro [30 ]
Chon, Hong Jae [31 ]
Pinato, David J. [2 ,3 ]
Ang, Celina [1 ]
机构
[1] Mt Sinai Hosp, Tisch Canc Inst, Dept Med, Div Hematol Oncol, New York, NY USA
[2] Imperial Coll London, Dept Surg & Canc, Div Canc, London, England
[3] Univ Piemonte Orientale, Dept Translat Med, Div Oncol, Novara, Italy
[4] Fdn Policlin Univ Campus Biomed, Operat Res Unit Med Oncol, Rome, Italy
[5] Univ Palermo, Sect Gastroenterol & Hepatol, Dept Hlth Promot Mother & Child Care, Internal Med & Med Specialties PROMISE, Palermo, Italy
[6] Univ Bologna, Dept Med & Surg Sci, Bologna, Italy
[7] Columbia Univ, Irving Med Ctr, Herbert Irving Comprehens Canc, Div Hematol Oncol,Dept Med, New York, NY USA
[8] Taipei Vet Gen Hosp, Healthcare & Serv Ctr, Taipei, Taiwan
[9] Taipei Vet Gen Hosp, Dept Med, Div Gastroenterol & Hepatol, Taipei, Taiwan
[10] Natl Yang Ming Chiao Tung Univ, Coll Med, Inst Clin Med, Taipei, Taiwan
[11] Univ Pittsburgh UPMC, Div Hematol Oncol, Dept Med, Pittsburgh, PA USA
[12] Humanitas Univ, Dept Biomed Sci, Milan, Italy
[13] IRCCS Human Res Hosp, Humanitas Canc Ctr, Milan, Italy
[14] Univ Med Ctr Hamburg Eppendorf, Dept Oncol Hematol & Bone Marrow Transplantat, Sect Pneumol, Hamburg, Germany
[15] Univ Med Ctr Hamburg Eppendorf, Dept Med, Hamburg, Germany
[16] Univ Texas MD Anderson Canc Ctr, Dept Gastrointestinal Med Oncol, Houston, TX USA
[17] Univ Toronto, Princess Margaret Canc Ctr, Toronto, ON, Canada
[18] Hannover Med Sch, Dept Gastroenterol Hepatol & Endocrinol, Hannover, Germany
[19] Freiburg Univ Med Ctr, Fac Med, Dept Med Gastroenterol Hepatol Endocrinol & Infect, Freiburg, Germany
[20] Univ Freiburg, Fac Med, Berta Ottenstein Programme, Freiburg, Germany
[21] Kindai Univ, Dept Gastroenterol & Hepatol, Fac Med, Osaka, Japan
[22] Univ Pisa, Dept Translat Res & New Technol Med & Surg, Pisa, Italy
[23] Univ Hosp Pisa, Unit Med Oncol 2, Pisa, Italy
[24] Med Univ Vienna, Dept Med 3, Div Gastroenterol & Hepatol, Vienna, Austria
[25] Univ Texas Southwestern Med Ctr Dallas, Dept Internal Med, Div Digest & Liver Dis, Dallas, TX USA
[26] Univ Oklahoma, Hlth Sci Ctr, Stephenson Canc Ctr, Oklahoma City, OK USA
[27] Univ Med Ctr Mainz, Dept Psychosomat Med, Mainz, Germany
[28] Univ Michigan, Dept Internal Med, Div Gastroenterol & Hepatol, Ann Arbor, MI USA
[29] China Med Univ Hosp, Ctr Digest Med, Dept Internal Med, Taichung, Taiwan
[30] Azienda Osped Univ Marche, Azienda Ospedaliero Universitaria Marche, Azienda Osped Univ Marche, Ancona, Italy
[31] CHA Univ, CHA Bundang Med Ctr, Dept Internal Med, Med Oncol, Seongnam 13497, South Korea
关键词
Hepatocellular carcinoma; atezolizumab; bevacizumab; second-line therapy; immune checkpoint inhibitors; immunotherapy; tyrosine kinase inhibitors; HEPATOCELLULAR-CARCINOMA; PLUS BEVACIZUMAB; PEMBROLIZUMAB; SORAFENIB;
D O I
10.1016/j.jhepr.2024.101232
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Atezolizumab/bevacizumab (A/B) is now a standard first-line treatment for advanced hepatocellular carcinoma (HCC), but the optimal second-line regimen is not known. We evaluated real-world treatment patterns and outcomes to investigate factors associated with post-progression survival (PPS). Methods: In this multicenter, international, retrospective study, we examined clinical characteristics and outcomes of patients with advanced HCC who progressed on first-line A/B. The primary outcome of PPS was defined as time from first radiographic progression on A/B to death. Results: A total of 406 patients alive after progression on first-line A/B were included in the final analysis, of whom 45.3% (n =184) received best supportive treatment (BST) and 54.7% (n = 222) continued active systemic treatment. In the second line, 155 patients were treated with tyrosine kinase inhibitors (TKIs), 45 with immune checkpoint inhibitor (IO)-based regimens, and 3 had missing data. Median PPS of the whole cohort (mPPS) was 6.0 months (95% CI 5.2-7.2). On multivariate Cox regression analysis, absence of portal vein tumor thrombus, ECOG <2, and continued active treatment were predictors of better PPS. mPPS was significantly longer for patients who continued active treatment vs. BST (9.7 vs. 2.6 months; HR 0.41, p <0.001). In the second-line setting, patients treated with TKIs had a numerically shorter mPPS compared to those treated with IO (8.4 vs. 14.9 months; HR 1.37, p = 0.256). Conclusions: Continuation of active therapy after A/B progression was independently associated with better survival even after adjusting for baseline disease characteristics. mPPS with IO-based therapy exceeded a year, suggesting that IO continuation post-progression may retain benefit. The precise sequencing of TKI and IO regimens warrants further investigation. (c) 2024 The Authors. Published by Elsevier B.V. on behalf of European Association for the Study of the Liver (EASL). This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
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