Abstract
Cases with massive (diameter ≥10 cm) hepatocellular carcinomas (HCCs) are uncommon and typically have poor outcomes; however, conversion therapy offers a beacon of hope for remission in patients with massive unresectable HCCs. Recently, immune checkpoint inhibitors (ICIs) have been used in combination with other treatment modalities to improve the response rates to conversion therapies, yet the safety and generalizability of this combination have not been extensively validated. Herein, we report a man with a chief complaint of abdominal pain who was diagnosed with massive unresectable HCC. Notably, the patient successfully underwent curative surgery after quadruple conversion therapy using tislelizumab (an ICI), lenvatinib, transarterial chemoembolization, and hepatic arterial infusion chemotherapy directed by a multidisciplinary team. With a complete response achieved, this case demonstrated the major potential of this combination regimen for HCC, and the remarkable efficacy was also reflected by substantial reductions in both alpha-fetoprotein and des-gamma-carboxy prothrombin overall. Nevertheless, transient increases in both biomarkers (tumor marker pseudoprogression) were observed within the first three weeks after initiating ICI treatment. Furthermore, the patient developed a biliary stricture, which resolved after discontinuing the ICI and was ultimately assessed as an immune-related adverse event. Therefore, in the context of combination therapy, further evaluation of the robustness of tumor markers is warranted, and it is crucial for clinicians to be mindful of potential immune-related adverse events.
Introduction
Hepatocellular carcinoma (HCC) with a single lesion exceeding 10 cm, known as massive HCC, is not only uncommon and challenging to resect but also associated with a less favorable prognosis (1, 2). Conversion therapy, an emerging therapeutic strategy, may improve the prognosis of patients suffering from massive unresectable HCC (3). Recent years have witnessed the emergence of various conversion regimens for HCC, which typically involve tyrosine kinase inhibitors (TKIs) and locoregional therapies—transarterial chemoembolization (TACE) and hepatic arterial infusion chemotherapy (HAIC) (3–5). However, their efficacy and safety remain controversial, and there are currently no well-recognized preferred conversion regimens (3–5).
Immune checkpoint inhibitors (ICIs) have achieved encouraging results since they were approved for systemic therapy for HCC in 2020 (6, 7). Nonetheless, pseudoprogression, albeit infrequent, and immune-related adverse events (irAEs) raise new challenges for clinicians, yet no validated biomarkers are available to guide clinical decisions (6, 8). Furthermore, because of inadequate monitoring, the incidence of hepatobiliary irAEs is underestimated (9). More recently, better efficacy has been reported in combining ICIs with TACE, HAIC, and TKIs as quadruple conversion therapy compared with TACE alone, but the safety of this combination is largely unknown (10, 11). The case reported here underscores these knowledge gaps as our patient exhibited uncommon pseudoprogression of tumor markers and immune-related cholangiopathy during the quadruple conversion therapy.
Case presentation
On 14 February 2023, a 43-year-old man presented to our outpatient department with right upper quadrant abdominal pain. He had been chronically infected with hepatitis B virus (HBV) for more than 20 years but had not taken entecavir regularly. His other medical history was unremarkable. Physical examination and ultrasound suggested a large space-occupying lesion in his right hemiliver; hence, he was admitted to the hospital.
Laboratory workup revealed elevated HBV DNA—3.21×106 IU/mL—and tumor markers, including alpha-fetoprotein (AFP) 32,982 ng/mL and des-gamma-carboxy prothrombin (DCP, also known as PIVKA-II) >30,000 mAU/mL. Subsequent contrast-enhanced computed tomography demonstrated a massive mass—13.8×11.0×13.6 cm—in the right lobe of his liver and several scattered small nodules throughout the liver (Figure 1A), whereas no abnormalities were found in other organs. Additionally, his Eastern Cooperative Oncology Group status was zero, and his Child–Pugh score was six. Taken together, he was diagnosed with intermediate-stage HCC according to the Barcelona Clinic Liver Cancer classification (12).
Figure 1
Due to the high HBV load, he started antiviral treatment immediately with 0.5 mg of oral entecavir once daily (13). He was then evaluated by a multidisciplinary team (MDT) and recommended the quadruple conversion regimen comprising TACE, TKI, ICI, and HAIC (14). Upon consent, he was treated with the conversion regimen, followed by serial imaging and biomarker measurements to track treatment response (Figures 1A, B). The following is a summary description of the treatment process. On 17 February, he underwent the first TACE, for which 5-fluorouracil (250 mg) and epothilone (50 mg) were mixed 1:2 with lipiodol. Lenvatinib (a TKI; 8 mg once daily) was taken orally beginning on 18 February, and tislelizumab (an ICI; 200 mg every 3 weeks) was administered intravenously beginning on 12 March. On 6 April and 10 May, he received two cycles of TACE–HAIC; for TACE, 5-fluorouracil (250 mg) and epothilone (30 mg) were mixed 1:2 with lipiodol; for HAIC, which was performed following TACE, raltitrexed (4 mg/m2 infusion for 1 h) and oxaliplatin (100 mg/m2 infusion for 4 h) were used.
Remarkably, there were sharp increases followed by spontaneous decreases in both AFP and DCP within three weeks after the first dose of the ICI—tislelizumab (Figure 1B). It was ultimately assessed as tumor marker pseudoprogression since follow-up imaging did not reveal disease progression (15). Notwithstanding several adverse events such as aspartate aminotransferase and alkaline phosphatase increase (Figure 2), they were resolved with symptomatic treatment (13, 16). Overall, his vital signs were stable during the conversion therapy.
Figure 2
After five months of treatment, the AFP and DCP decreased substantially to normal levels (Figure 1B), with undetectable levels of HBV DNA. On 19 July, contrast-enhanced magnetic resonance imaging demonstrated not merely tumor shrinkage but also the absence of intratumoral arterial enhancement (Figure 1A), which achieved a radiological complete response according to the modified RECIST (17). Moreover, magnetic resonance cholangiopancreatography revealed a marked stricture of the middle-lower portion of the common bile duct with dilatation of the upper biliary region compared with that observed during the pretreatment period (Figures 3A–D). Nevertheless, he had no clinical symptoms due to it, and thus, it was evaluated as grade 1 as per the Common Terminology Criteria for Adverse Events version 5.0 (18). As discussed by the MDT, he began withdrawing the anticancer medications and preparing for conversion surgery (14, 16).
Figure 3
On 27 July, the patient underwent hepatectomy with microscopically negative surgical margins—an R0 resection. Furthermore, histopathological examination showed large areas of necrosis in the center of the resected mass with fibrosis and intrahepatic biliary hyperplasia in the surrounding hepatic tissues (Figures 4A, B). Of note, there was no residual microscopic tumor—a pathologic complete response. In addition, a biopsy of the middle-lower portion of the common bile duct revealed hyperplasia of the biliary epithelium, fibrosis of the bile duct wall, and severe inflammatory cell infiltration (Figures 4C–F).
Figure 4
After conversion surgery, the patient resumed the administration of lenvatinib and received another TACE procedure on September 11 as adjuvant therapy to prevent recurrence, whereas he no longer took tislelizumab given the risk of irAEs (16, 19). He is satisfied with the treatment and has regular follow-up visits in our outpatient department. According to follow-up examinations, his biliary stricture has resolved after discontinuation of tislelizumab, and no recurrence or other adverse events have been reported thus far.
Discussion
In this report, we present a case in which massive unresectable HCC successfully achieved a complete response and R0 resection after quadruple conversion therapy directed by an MDT. Yet, despite considerable efficacy, this patient exhibited unexpected inflammatory cholangiopathy of the common bile duct and pseudoprogression in the AFP and DCP, which deserve special attention and are discussed below.
Drug-induced liver injury is common during the treatment of HCC, while ICI-induced large-duct cholangiopathy is infrequent (16, 20, 21). Without standard tests for irAEs, diagnosing irAEs remains challenging and largely relies upon the exclusion of alternative etiologies (19, 22). Chemotherapy-induced cholangiopathy occurs predominantly in the intrahepatic or perihilar biliary ducts but rarely in the common bile duct, and lipiodol deposition can be noted in the wall of bile ducts for TACE-induced cholangiopathy (23–25). By contrast, no lipiodol deposition was observed in our case, and the biliary stricture developed only in the middle-lower portion of the common bile duct (Figures 3C, D). Furthermore, anatomical distinction may explain the differential susceptibility of biliary regions to locoregional chemotherapy: upper biliary tree and HCC are primarily supplied by branches of the right/left hepatic arteries, which are selectively targeted during TACE/HAIC, whereas the middle-lower portion of the common bile duct indirectly receives blood from gastroduodenal artery (24–26). Regarding lenvatinib, hardly any similar adverse events were reported in the era when HCC treatment was dominated by TKIs (27, 28). In this study, our patient stopped the administration of tislelizumab because irAEs could not be ruled out (16, 19). Fortunately, his biliary stricture was observed radiologically only—asymptomatic—and resolved after withdrawal from the ICI. Taken together, biopsy, imaging, and resolution of stricture after ICI discontinuation supported the diagnosis of immune-related cholangitis (Figures 3, 4). Moreover, similar observations were made in other types of cancer treated with ICI-based therapeutics, and it is intriguing that these studies suggest that liver enzymes might be predictive biomarkers of irAEs (20, 29, 30). In HCC, however, TACE and HAIC can cause fluctuations in the levels of liver enzymes (25); consequently, this utility of liver enzymes might be difficult to implement. Robust biomarkers to predict irAEs and guide clinical decisions are still needed (19, 22). In previous studies, the incidence of several adverse events—e.g., gastric ulcers—was considerably increased, albeit with better efficacy, in patients receiving quadruple conversion therapy than in those receiving TACE alone; nonetheless, no treatment-related adverse events similar to the present case were reported in these studies (10, 11). In clinical practice, the incidence of adverse hepatobiliary irAEs may be underestimated because of inadequate monitoring (9). Accordingly, adopting an MDT model can be important for patient-tailored therapeutics and the management of irAEs (5, 31, 32). Together, closer attention should be given to potential irAEs in patients receiving combination regimens involving ICIs, and more clinical trials are essential for broadening the basis for clinical decision-making and advancing this field.
On top of irAEs, pseudoprogression poses a growing challenge for patients and clinicians, and ICIs have profoundly revolutionized the management of HCC (6, 33). Pseudoprogression complicates tumor response assessment during ICI treatment, and there is an urgent need to establish reliable biomarkers to track clinical response (33, 34). Conventional radiological assessment criteria (i.e., RECIST) are insufficient to differentiate pseudoprogression from true progression, and the former usually occurs in the first few weeks after initiating ICI treatment and can lead to premature discontinuation of ICIs and underestimation of the efficacy of therapeutics (8, 34). Therefore, several new criteria have been proposed for ICI-based therapeutics, such as immune-related RECIST and immune-modified RECIST (34–36). Most of these criteria are based on imaging, while recent criteria, called RecistTM, are based on tumor markers (15). RecistTM could assess tumor response more efficiently than immune-related RECIST, as tumor markers might have a shorter response time and provide a more accurate prediction of overall survival compared to imaging (15). Interestingly, a total of 4 of the 70 lung cancer patients exhibited rapid increases followed by decreases in tumor marker levels within 3–6 weeks after ICI treatment (15), which is analogous to what our patient experienced (Figure 2). A similar pattern was observed in PIVKA-II (i.e., DCP) of another HCC patient treated with quadruple conversion therapy; nevertheless, this pattern has not received any attention (37). Notably, tumor marker pseudoprogression has also been observed in gastric cancer, in addition to lung cancer and HCC, suggesting it could be a broader phenomenon across cancer types (15, 37–39). Mechanistically, this phenomenon may be associated with inflammatory reactions, considering that benign inflammatory diseases—e.g., colitis and hepatitis—can also present with elevated AFP and DCP (40–42). The last several decades have seen a plethora of studies on the utility of AFP and DCP in the surveillance and management of HCC, whereas there are only limited studies on the predictive and monitoring role of these two biomarkers in ICI-based therapeutics (43). Based on 44 retrospective studies, a pooled analysis revealed that low baseline AFP and DCP levels and early AFP response might be associated with good outcomes in HCC patients treated with ICIs (44). More recently, a retrospective study reported that trends in AFP during the first three weeks after initiation of treatment and baseline DCP levels could be used to predict which patients would benefit from first-line ICI-based therapy (45); however, poor outcomes might be incorrectly predicted in cases with tumor marker pseudoprogression. With high baseline AFP and DCP levels, our patient achieved a complete response, although he presented tumor marker pseudoprogression during the three weeks after the first dose of tislelizumab (Figure 1B). On the other hand, substantially decreased AFP and DCP overall reflected the remarkable efficacy of the quadruple conversion therapy (Figure 1B), which suggests that serial AFP and DCP measurements are promising for monitoring the impact of therapeutic interventions for HCC. Given the lack of prospective evidence, the utility of AFP and DCP in monitoring and predicting clinical benefit from ICIs awaits validation in large-scale carefully designed studies.
In summary, this case demonstrated the great potential of quadruple conversion therapy for HCC, but presented unusual cholangitis and tumor marker pseudoprogression, both of which are associated with ICIs. Further evaluation, therefore, is warranted to assess the safety and generalizability of combination therapy and the feasibility and power of biomarker-guided treatments.
Statements
Data availability statement
The original contributions presented in the study are included in the article. Further inquiries can be directed to the corresponding authors.
Ethics statement
All procedures performed in the present study were conducted in accordance with local legislation and with the Helsinki Declaration. Written informed consent was obtained from the patient for the publication of any potentially identifiable images or data included in this article.
Author contributions
XZ: Conceptualization, Data curation, Investigation, Writing – original draft, Writing – review & editing. LZ: Conceptualization, Supervision, Visualization, Writing – original draft, Writing – review & editing. SZ: Validation, Writing – review & editing. LD: Resources, Writing – review & editing. HL: Resources, Writing – review & editing. XW: Writing – review & editing. HY: Writing – review & editing. RL: Writing – review & editing. KZ: Funding acquisition, Project administration, Writing – review & editing.
Funding
The author(s) declare that financial support was received for the research and/or publication of this article. This work was partially supported by the Zhejiang Provincial Medical and Health Science and Technology Plan (2022513188) and the Health Science and Technology Project of Yinzhou District (2023Y03 and 2023Y06).
Acknowledgments
We are deeply indebted to the patient for his continued trust and support. We would also like to extend thanks to Jianlei Zhang, Wenyi Xu and other members of the MDT for participating in patient management.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Generative AI statement
The author(s) declare that no Generative AI was used in the creation of this manuscript.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Abbreviations
AFP, alpha-fetoprotein; DCP, des-gamma-carboxy prothrombin; HAIC, hepatic arterial infusion chemotherapy; HBV, hepatitis B virus; HCC, hepatocellular carcinomas; ICI, immune checkpoint inhibitor; irAEs, immune-related adverse events; MDT, multidisciplinary team; TACE, transarterial chemoembolization; TKI, Tyrosine kinase inhibitor.
References
1
CarrBIGuerraV. Features of massive hepatocellular carcinomas. Eur J Gastroenterol Hepatol. (2014) 26:101–8. doi: 10.1097/MEG.0b013e3283644c49
2
LeeAJLWuAGRYewKCShelatVG. Does size matter for resection of giant versus non-giant hepatocellular carcinoma? A meta-analysis. World J Gastrointest Surg. (2023) 15:273–86. doi: 10.4240/wjgs.v15.i2.273
3
ZhouZXuXSunMLiuYLiuQChenCet al. Conversion therapy for massive hepatocellular carcinoma: A case report and literature review. Clin Case Rep. (2023) 11:e7533. doi: 10.1002/ccr3.7533
4
ZhangZZhangE. Conversion therapy for advanced hepatocellular carcinoma with vascular invasion: a comprehensive review. Front Immunol. (2023) 14:1073531. doi: 10.3389/fimmu.2023.1073531
5
ChenQChenSChenMLyuNZhaoM. Improving the conversion success rate of hepatocellular carcinoma: focus on the use of combination therapy with a high objective response rate. J Clin Transl Hepato. (2024) 12:298–304. doi: 10.14218/jcth.2023.00403
6
LlovetJMCastetFHeikenwalderMMainiMKMazzaferroVPinatoDJet al. Immunotherapies for hepatocellular carcinoma. Nat Rev Clin Oncol. (2022) 19:151–72. doi: 10.1038/s41571-021-00573-2
7
GamboaACKoobyDAMaithelSKGamblinTC. Immune checkpoint inhibitors in hepatocellular carcinoma: A review of current clinical trials. J Surg Oncol. (2024) 129:63–70. doi: 10.1002/jso.27545
8
PinterMScheinerBPinatoDJ. Immune checkpoint inhibitors in hepatocellular carcinoma: emerging challenges in clinical practice. Lancet Gastroenterol Hepatol. (2023) 8:760–70. doi: 10.1016/S2468-1253(23)00147-4
9
VitaleGLambertiGComitoFDi NunnoVMassariFMorelliMCet al. Anti-programmed cell death-1 and anti-programmed cell death ligand-1 immune-related liver diseases: from clinical pivotal studies to real-life experience. Expert Opin Biol Ther. (2020) 20:1047–59. doi: 10.1080/14712598.2020.1762562
10
LiLHeJXieYHuangXWengXPanXet al. A retrospective controlled study of TACE-HAIC-targeted-immune quadruple therapy for intermediate and advanced-stage hepatocellular carcinoma. Chin J Hepatol. (2022) 30:939–46. doi: 10.3760/cma.j.cn501113-20220823-00432
11
YuanYHeWYangZQiuJHuangZShiYet al. TACE-HAIC combined with targeted therapy and immunotherapy versus TACE alone for hepatocellular carcinoma with portal vein tumour thrombus: a propensity score matching study. Int J Surg. (2023) 109:1222–30. doi: 10.1097/js9.0000000000000256
12
ReigMFornerARimolaJFerrer-FàbregaJBurrelMGarcia-CriadoÁet al. BCLC strategy for prognosis prediction and treatment recommendation: The 2022 update. J Hepatol. (2022) 76:681–93. doi: 10.1016/j.jhep.2021.11.018
13
MengQYangZZhuZLiJBiXChenXet al. Chinese expert consensus on the overall management of liver function in conversion therapy for liver cancer (2022 edition). Chin Med J. (2023) 136:2909–11. doi: 10.1097/cm9.0000000000002950
14
SunHZhouJWangZLiuXXieQJiaWet al. Chinese expert consensus on conversion therapy for hepatocellular carcinoma (2021 edition). Hepatobil Surg Nutr. (2022) 11:227–52. doi: 10.21037/hbsn-21-328
15
YangYJiangXLiuYHuangHXiongYXiaoHet al. Elevated tumor markers for monitoring tumor response to immunotherapy. eClinicalMedicine. (2022) 46:101381. doi: 10.1016/j.eclinm.2022.101381
16
AndradeRJAithalGPBjörnssonESKaplowitzNKullak-UblickGALarreyDet al. EASL Clinical Practice Guidelines: Drug-induced liver injury. J Hepatol. (2019) 70:1222–61. doi: 10.1016/j.jhep.2019.02.014
17
LlovetJMLencioniR. mRECIST for HCC: Performance and novel refinements. J Hepatol. (2020) 72:288–306. doi: 10.1016/j.jhep.2019.09.026
18
Freites-MartinezASantanaNArias-SantiagoSVieraA. Using the common terminology criteria for adverse events (CTCAE – version 5.0) to evaluate the severity of adverse events of anticancer therapies. Actas Dermo-Sifilogr. (2021) 112:90–2. doi: 10.1016/j.adengl.2019.05.021
19
BrahmerJRAbu-SbeihHAsciertoPABrufskyJCappelliLCCortazarFBet al. Society for Immunotherapy of Cancer (SITC) clinical practice guideline on immune checkpoint inhibitor-related adverse events. J Immunother Cancer. (2021) 9:e002435. doi: 10.1136/jitc-2021-002435
20
PiBWangJTongYYangQLvFYuY. Immune-related cholangitis induced by immune checkpoint inhibitors: a systematic review of clinical features and management. Eur J Gastroenterol Hepatol. (2021) 33:e858–67. doi: 10.1097/meg.0000000000002280
21
LeeSKChoiJYJungESKwonJHJangJWBaeSHet al. An immunological perspective on the mechanism of drug induced liver injury: focused on drugs for treatment of hepatocellular carcinoma and liver transplantation. Int J Mol Sci. (2023) 24:5002. doi: 10.3390/ijms24055002
22
SuijkerbuijkKPMvan EijsMJMvan WijkFEggermontAMM. Clinical and translational attributes of immune-related adverse events. Nat Cancer. (2024) 5:557–71. doi: 10.1038/s43018-024-00730-3
23
AlazmiWMMcHenryLWatkinsJLFogelELSchmidtSShermanSet al. Chemotherapy-induced sclerosing cholangitis: long-term response to endoscopic therapy. J Clin Gastroenterol. (2006) 40:353–7. doi: 10.1097/01.mcg.0000210098.28876.66
24
MiyayamaSYamashiroMOkudaMYoshieYNakashimaYIkenoHet al. Main bile duct stricture occurring after transcatheter arterial chemoembolization for hepatocellular carcinoma. Cardiovasc Intervent Radiol. (2010) 33:1168–79. doi: 10.1007/s00270-009-9781-6
25
XuHYuXHuJ. The risk assessment and clinical research of bile duct injury after transcatheter arterial chemoembolization for hepatocellular carcinoma. Cancer Manag Res. (2021) 13:5039–52. doi: 10.2147/cmar.S303172
26
MiyayamaSYamashiroMHashimotoMHashimotoNIkunoMOkumuraKet al. Blood supply of the main bile duct from the caudate artery and medial subsegmental artery of the hepatic artery: Evaluation using images obtained during transcatheter arterial chemoembolization for hepatocellular carcinoma. Hepatol Res. (2013) 43:1175–81. doi: 10.1111/hepr.12071
27
Al-SalamaZTSyedYYScottLJ. Lenvatinib: A review in hepatocellular carcinoma. Drugs. (2019) 79:665–74. doi: 10.1007/s40265-019-01116-x
28
RimassaLDanesiRPressianiTMerleP. Management of adverse events associated with tyrosine kinase inhibitors: Improving outcomes for patients with hepatocellular carcinoma. Cancer Treat Rev. (2019) 77:20–8. doi: 10.1016/j.ctrv.2019.05.004
29
CoukosAVionnetJObeidMBouchaabHPetersSLatifyanSet al. Systematic comparison with autoimmune liver disease identifies specific histological features of immune checkpoint inhibitor-related adverse events. J Immunother Cancer. (2022) 10:e005635. doi: 10.1136/jitc-2022-005635
30
HountondjiLDe MatosCFLebosséFQuantinXLesageCPalassinPet al. Clinical pattern of checkpoint inhibitor-induced liver injury in a multicentre cohort. JHEP Rep. (2023) 5:100719. doi: 10.1016/j.jhepr.2023.100719
31
ItoTMizunoKYamamotoTYasudaTYokoyamaSYamamotoKet al. Outcomes of immune checkpoint inhibitor-induced liver toxicity managed by hepatologists in a multidisciplinary toxicity team. Hepatol Res. (2024) 54:1060–9. doi: 10.1111/hepr.14043
32
WangMXuXWangKDiaoYXuJGuLet al. Conversion therapy for advanced hepatocellular carcinoma in the era of precision medicine: Current status, challenges and opportunities. Cancer Sci. (2024) 115:2159–69. doi: 10.1111/cas.16194
33
HanXSunQXuMZhuGGaoRNiBet al. Unraveling the complexities of immune checkpoint inhibitors in hepatocellular carcinoma. Semin Liver Dis. (2023) 43:383–401. doi: 10.1055/s-0043-1776127
34
MushtiSLMulkeyFTangSSinghHLemerySJGoldbergKBet al. Immune response evaluation and treatment with immune checkpoint inhibitors beyond clinical progression: response assessments for cancer immunotherapy. Curr Oncol Rep. (2020) 22:116. doi: 10.1007/s11912-020-00974-z
35
TazdaitMMezquitaLLahmarJFerraraRBidaultFAmmariSet al. Patterns of responses in metastatic NSCLC during PD-1 or PDL-1 inhibitor therapy: Comparison of RECIST 1.1, irRECIST and iRECIST criteria. Eur J Cancer. (2018) 88:38–47. doi: 10.1016/j.ejca.2017.10.017
36
HodiFSBallingerMLyonsBSoriaJ-CNishinoMTaberneroJet al. Immune-modified response evaluation criteria in solid tumors (imRECIST): refining guidelines to assess the clinical benefit of cancer immunotherapy. J Clin Oncol. (2018) 36:850–8. doi: 10.1200/jco.2017.75.1644
37
WeiYSuHLvZLiaoXZengZJiaYet al. Case Report: A case of hepatocellular carcinoma with aberrant right hepatic artery treated with transarterial chemoembolization and infusion chemotherapy separately to bilobar lesion combining with systemic therapies and sequential hepatectomy. Front Oncol. (2023) 13:1165538. doi: 10.3389/fonc.2023.1165538
38
SatoyoshiRMutoOMasudaAKotanagiKKichirakuTKudohKet al. A case of gastric cancer with delayed onset of tumor reduction effect by nivolumab therapy. Clin J Gastroenterol. (2019) 12:15–9. doi: 10.1007/s12328-018-0902-0
39
ZhangLTianTZhangYYuSChenFQiaoLet al. Pseudoprogression during immunotherapy for gastric adenocarcinoma: A case report and literature review. J Cancer Res Ther. (2023) 19:144–9. doi: 10.4103/jcrt.jcrt_1050_22
40
WongRJAhmedAGishRG. Elevated alpha-fetoprotein: differential diagnosis - hepatocellular carcinoma and other disorders. Clin Liver Dis. (2015) 19:309–23. doi: 10.1016/j.cld.2015.01.005
41
FuCLiJChenZCaoYZhangHSuiHet al. Diagnostic efficacy and possible underlying mechanisms of noninvasive clinical markers in hepatocellular carcinoma. J Clin Transl Hepato. (2023) 11:889–98. doi: 10.14218/jcth.2022.00285
42
YuZChenDZhengYWangXHuangSLinTet al. Development and validation of a diagnostic model for AFP-negative hepatocellular carcinoma. J Cancer Res Clin Oncol. (2023) 149:11295–308. doi: 10.1007/s00432-023-04997-4
43
KimDYToanBNTanC-KHasanISetiawanLYuM-Let al. Utility of combining PIVKA-II and AFP in the surveillance and monitoring of hepatocellular carcinoma in the Asia-Pacific region. Clin Mol Hepatol. (2023) 29:277–92. doi: 10.3350/cmh.2022.0212
44
ZhangLFengJKuangTChaiDQiuZDengWet al. Blood biomarkers predict outcomes in patients with hepatocellular carcinoma treated with immune checkpoint Inhibitors: A pooled analysis of 44 retrospective sudies. Int Immunopharmacol. (2023) 118:110019. doi: 10.1016/j.intimp.2023.110019
45
TanabeNSaekiIAibeYMatsudaTHanazonoTNishiMet al. Early prediction of response focused on tumor markers in atezolizumab plus bevacizumab therapy for hepatocellular carcinoma. Cancers. (2023) 15:2927. doi: 10.3390/cancers15112927
Summary
Keywords
immune checkpoint inhibitor, tislelizumab, immune-related adverse event, tumor marker, pseudoprogression, hepatocellular carcinoma, conversion therapy, case report
Citation
Zhang X, Zhang L, Zhao S, Dai L, Li H, Wu X, Yan H, Lin R and Zhu K (2025) Tumor marker pseudoprogression and immune-related cholangitis during conversion therapy for massive hepatocellular carcinoma: a case report. Front. Immunol. 16:1529016. doi: 10.3389/fimmu.2025.1529016
Received
15 November 2024
Accepted
07 May 2025
Published
04 June 2025
Volume
16 - 2025
Edited by
Alessandro Poggi, San Martino Hospital (IRCCS), Italy
Reviewed by
Mansoor-Ali Vaali-Mohammed, King Saud University, Saudi Arabia
Mohamed Essameldin Abdelgawad, Wake Forest University, United States
Kratika Singh, Centre of Bio-Medical Research (CBMR), India
Updates
Copyright
© 2025 Zhang, Zhang, Zhao, Dai, Li, Wu, Yan, Lin and Zhu.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Kelei Zhu, dr.zkl@163.com; Luyi Zhang, 166001728@nbu.edu.cn
†These authors share first authorship
‡ORCID: Xiaodong Zhang, orcid.org/0009-0001-8664-3810; Luyi Zhang, orcid.org/0009-0007-0078-9223; Kelei Zhu, orcid.org/0000-0001-6497-3379
Disclaimer
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.