Cabibbo G, Craxì A. Needle track seeding following percutaneous procedures for hepatocellular carcinoma. World J Hepatol 2009; 1(1): 62-66 [PMID: 21160966 DOI: 10.4254/wjh.v1.i1.62]
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Giuseppe Cabibbo, MD, Cattedra di Gastroenterologia, Dipartimento Biomedico di Medicina Interna e Specialstica, University of Palermo, Piazza delle Cliniche 2, Palermo 90127, Italy. email@example.com
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Needle track seeding following percutaneous procedures for hepatocellular carcinoma
Giuseppe Cabibbo, Antonio Craxì
Giuseppe Cabibbo, Antonio Craxì, Cattedra di Gastroenterologia, Dipartimento Biomedico di Medicina Interna e Specialstica, University of Palermo, Palermo 90127, Italy
Giuseppe Cabibbo, Dipartimento di Biopatologia e Metodologie Biomediche, University of Palermo, Palermo 90127, Italy
ORCID number: $[AuthorORCIDs]
Author contributions: Cabibbo G has contributed for drafting of the manuscript and critical revision; Craxì A, hepatologist, has contributed for drafting of the manuscript and critical revision.
Correspondence to: Giuseppe Cabibbo, MD, Cattedra di Gastroenterologia, Dipartimento Biomedico di Medicina Interna e Specialstica, University of Palermo, Piazza delle Cliniche 2, Palermo 90127, Italy. firstname.lastname@example.org
Telephone: +39-91-6552280 Fax: +39-91-6552156
Received: March 17, 2009 Revised: September 8, 2009 Accepted: September 15, 2009 Published online: October 31, 2009
Neoplastic seeding may arise after diagnostic or therapeutic percutaneous procedures for hepatocellular carcinoma. The true incidence of seeding with hepatocellular carcinoma is difficult to assess precisely, but a significant risk of seeding exists and is greater when performing diagnostic biopsy as compared to therapeutic percutaneous procedures [radiofrequency ablation, radiofrequency ablation (RFA); percutaneous ethanol injection, Percutaneous ethanol injection (PEI)]. Whenever liver transplantation is feasible, diagnostic needle biopsies should be avoided, but RFA and PEI are often needed as “bridge” treatments. The role of adjuvant treatments in reducing the incidence of seeding following RFA or PEI requires further evaluation.
Hepatocellular carcinoma (HCC) is a challenging malignancy of global importance. It is the sixth most common cancer, and the third most common cause of cancer-related death worldwide. The incidence rates for HCC in the United States and Western Europe have been increasing[2,3].
Cohort studies and cost-efficiency modelling have suggested that ultra-sonographic surveillance of well-defined cirrhotic patients may decrease tumor-related mortality[4,5]. According to EASL and AASLD criteria, a diagnosis of HCC can be made in most cases with a non-invasive strategy. In fact, advances in cross-sectional imaging have led to a drastic limitation in the requirement for biopsy of focal lesions in the cirrhotic liver[6,7]. In this setting, good quality contrast enhanced computed tomography (CT) and magnetic resonance imaging (MRI) are generally highly accurate for the diagnosis of HCC[8,9]. However, biopsy remains very important in patients with a liver nodule without typical radiological features (hypervascularization in arterial phase followed by venous wash-out in portal/venous phase)[5,10], or when α-fetoprotein levels are not diagnostic of HCC (Figure 1).
Figure 1 Suggested algorithm for evaluation of a liver mass detected during hepatocellular carcinoma surveillance in a patient with cirrhosis according to the American Association for the Study of Liver Diseases (AASLD) guidelines.
Although diagnostic biopsy rates have diminished, biopsy is still widely used and is often considered mandatory for patient management by oncologists. Furthermore liver biopsy may give prognostic information[12,13] regarding malignant potential and may be required for allocation systems in liver transplantation programmes.
Despite many efforts to prevent and screen for HCC, only 20%-30% of patients present with early stage disease amenable to curative treatments, including surgical resection and liver transplantation (LTx). Radiofrequency ablation (RFA) was introduced as an alternative locoregional therapy to ethanol injection. It can achieve high local cure without deteriorating background liver function. RFA is now a valid alternative to resection, and can be used as an adjuvant therapy, or as a bridge to transplantation. Percutaneous ablation (PEI, RFA) achieves complete responses in more than 80% of tumors smaller than 3 cm in diameter, but only in 50% of tumors between 3 and 5 cm in size[16,17]. Five-year survival rates reported after PEI or RFA are 40%-70%[18,19] RFA is preferred to PEI in patients with tumors < 4 cm. because of lower recurrence, lower number of sessions, and longer disease-free survival. A recent meta-analysis has shown that RFA ablation is superior to PEI in the treatment of small HCC with respect to overall survival, 1, 2, and 3 year survival rates, 1, 2, and 3 cancer-free survival rates, and tumor response. RFA entails a significantly smaller risk of local recurrence than PEI.
NEEDLE TRACT SEEDING
Percutaneous diagnostic or therapeutic procedures play an important role in the management of patients with hepatocellular carcinoma. These procedures are used to diagnose and/or provide specific therapy. All procedures, whether medical or surgical, have inherent risks, and the risks must always be weighed against the anticipated benefits. Both patients and physicians must assume that there is some risk involved when they undertake any procedure including a percutaneous approach for HCC. Complications of percutaneous procedures are sometimes unavoidable. Nonetheless, strict attention to detail and knowledge of potential complications and their risk factors can minimize their occurrence. The incidence of specific complications is difficult to assess and depends on a number of variables that are not always comparable across studies.
Malignant seeding is a well known complication of both diagnostic and therapeutic procedures in patients with HCC. Needle tract seeding of a liver tumor was previously defined as the development of new neoplastic disease outside the liver capsule, either in the subcutaneous soft tissues of the abdomen, intercostal muscle (Figure 2) or peritoneum. A review identified several suspicious mechanisms that can contribute to seeding after percutaneous procedures: tumor cells may adhere to a biopsy needle or to an electrode during its retraction; tumor cells may also be carried into the track with a little bleeding; furthermore, cells may be forced into the track by sudden increase in intratumoral pressure which is frequently encountered during RFA; finally, cells may be driven in, when saline is injected during or before RFA.
Figure 2 MRI features of HCC seeding following RFA.
A: An arterial phase MRI examination of the liver and an enhancing mass in the intercostal space, indicated by the arrowheads, in the right hemithorax; B: A delayed phase MRI examination that shows the mass in the intercostal space, but this is hypointense compared with the rest of the liver.
The real incidence of seeding with HCC is difficult to assess precisely. Several studies tried to assess critically the seeding rates after diagnostic and therapeutic procedures, but results are very heterogeneous. Rates of seeding after biopsy range greatly. While modest rates of tumor dissemination of 0.003%-0.009% have been described[23-25], a review on the subject has described incidences of 5%. A recent systematic review and a meta-analysis on needle track seeding following biopsy of liver lesions indicative of HCC showed that the incidence is 2.7% overall [95% Confidence Interval (CI), 1.8-4], and 0.9% per year (95% CI, 0.6-1.3). An important issue of this work is that all diagnosed seedings included in the review, were confirmed histologically.
With increasing use, tumor seeding after percutaneous RFA becomes a major concern, particularly in patients who have a chance of a cure. Llovet et al reported a high rate (12.5%) of tumor seeding in 32 patients with HCC treated with RFA which was preceded by a needle biopsy. Neoplastic seeding was associated with subcapsular HCC location, poorly differentiated tumors, and high alpha-fetoprotein levels. Livraghi et al reported a low rate of tumor seeding (0.9%) in 1314 patients with a median follow-up of 37 mo, using the same RFA technology as Llovet et al and showed that only previous biopsy was significantly associated with tumor seeding. The low risk of seeding after RFA (0%-1.4%) has been confirmed in other recent studies. In a recent study from our group, the risk of seeding of hepatocellular carcinoma after radiofrequency ablation was small (1.1% per patient, 95% CI, 0.19-5.84; 0.7% per procedure, 95% CI, 0.12-3.80).
The cause of the high seeding rate reported in the study by Llovet et al, not confirmed in subsequent studies, remains unclear, but could be due to the shallow position of the nodules (in fact all patients presenting seeding after RFA in the Llovet et al cohort had a subcapsular location).
A systematic review of seeding following percutaneous diagnostic and therapeutic approaches for hepatocellular carcinoma, that included studies published as full length papers and as abstracts, founds 179 seeding episodes from January 1983 until February 2007 resulting from diagnostic biopsy or local ablation therapy using percutaneous ethanol injection; acetic acid or hot saline injection; radiofrequency ablation; microwave therapy, laser therapy, or cryotherapy; and combinations of diagnostic biopsy and therapeutic procedures. The mean risk for seeding following diagnostic biopsy was 3.17% (range: 0%-11%). The mean risk for seeding after diagnostic biopsy and percutaneous ethanol injection was 1.4% (range: 1.15%-1.85%). The mean risk for seeding after radiofrequency ablation alone was 1.73% (range: 0%-5.56%). Following biopsy and radiofrequency ablation, the mean risk for seeding was 2.5% (range: 0-12.5) (Table 1).
Table 1 Summary of studies documenting seeding of HCC following biopsy or percutaneous therapeutic techniques in which the cohort size is specified1.
Biopsy + PEI
Biopsy + RFA
Total patients from series
No. seeding from series
Risk of seeding mean
Risk of seeding median
1Modified from Stigliano et al. PEI: Percutaneous ethanol injection of proven HCC; RFA: Radiofrequency ablation of proven HCC.
The time to the diagnosis of seeding ranged from 7 mo for combined percutaneous diagnostic and therapeutic approaches to 13 mo for biopsy alone. From their literature review, the Authors concluded that the risk of the percutaneous approach to HCC is clinically relevant, and that biopsy of HCC in patients with cirrhosis should not be routine clinical practice. Today, there remains no molecular means for classification of HCC. So, we think that suspicious nodule biopsy remains an important research tool to identify new biological variables to achieve a more accurate prognosis of patients with HCC.
RISK FACTORS FOR SEEDING
Numerous factors are related to the risk of neoplastic dissemination after invasive procedures: larger diameter needles; more passes; perpendicular approach; subcapsular tumor location; biopsy prior RFA; intrinsic metastatic properties of the tumor related to either or both tumor size or aggressivity, and patient immunodepression.
Poor differentiation of the tumor is a known risk factor for seeding after fine needle aspiration biopsy, and PEI, and is also associated with a higher risk of seeding after RFA. This correlation between seeding and the differentiation of HCC is not clearly evident in the review of Stigliano et al. However, a recent study of Imamura et al confirms that poor differentiation degree was a risk factor for neoplastic seeding after RFA of HCC and shows that surrogate markers of poor differentiation degree are larger tumor size (> 5 cm) and elevated tumor marker levels (AFP > 100 ng/mL, DCP > 100 mAU/mL, and aAFP-L3 > 15%).
OUTCOME OF SEEDING
In none of the cases of seeding reported in the meta-analyses of Silva et al did the seeding event impact on the patient’s survival when the lesion was treated successfully by resection and local ablation. Moreover, Livraghi et al have reported successful treatment of tumor seeding after RFA by a combination of surgical resection, PEI and RFA and concluded that in no patient did the presence of tumor seeding have a negative impact on survival. Similarly, in the study of Imamura et al the cumulative survival rates in HCC patients with neoplastic seeding were 81% at 1 year and 45% at 2 years. The Authors concluded that, taking into consideration the relatively low incidence of neoplastic seeding, the risk of neoplastic seeding after RFA would be considered an acceptable clinical risk.
We have found only one report on malignant seeding after orthotopic liver transplantation, secondary just to pre transplant biopsy. No information about the patient’s survival are given.
RFA and PEI are associated with a low risk of neoplastic seeding, although the risk of seeding is significantly increased if needle biopsy has been performed before treatment.
Seeding does not have a major negative impact on survival. However, if liver transplantation is a feasible option in the patient’s management needle biopsy should be avoided. In fact, assuming a role of the host immune response or of tumor aggressiveness for the low rate of needle seeding, an immunosuppressed condition, as in the post transplant status, could lead to a worsening of survival with a rapid extrahepatic diffusion.
Other strategies, apart from biopsy, such as evaluating new imaging techniques for more precise pre-transplant diagnosis (against explant histology), or simply waiting for a defined period with repeated imaging, may also be effective.
By the same token RFA and PEI, which are often needed as “bridge” treatments for patients on the transplant list, can be used safely without unneeded fears of disseminating the tumor outside of the liver. Additional studies with an adequate duration and quality of follow-up will be paramount to exclude late-onset seeding.
As a future field of research, the incidence of seeding after percutaneous treatments of HCC with new adjuvant treatments such as the antiangiogenic drugs will need to be evaluated.
Peer reviewers: Tian-Quan Han, Professor, Department of Surgery, Shanghai Institute of Digestive Surgery, Ruijin Hospital, Shanhai Jiaotong University Medical College, 197 Ruijin 2nd Road, Shanghai 200025, China; Xin Wei Wang, PhD, Senior Investigator, Chief, Liver Carcinogenesis Section, LHC, NCI, NIH, 37 Convent Drive, MSC 4258, Building 37, Room 3044A, Bethesda, MD 20892, United States
Parkin DM, Bray F, Ferlay J, Pisani P. Global cancer statistics, 2002.CA Cancer J Clin. 2005;55:74-108.
El-Serag HB, Mason AC. Rising incidence of hepatocellular carcinoma in the United States.N Engl J Med. 1999;340:745-750.
El-Serag HB, Davila JA, Petersen NJ, McGlynn KA. The continuing increase in the incidence of hepatocellular carcinoma in the United States: an update.Ann Intern Med. 2003;139:817-823.
Sangiovanni A, Del Ninno E, Fasani P, De Fazio C, Ronchi G, Romeo R, Morabito A, De Franchis R, Colombo M. Increased survival of cirrhotic patients with a hepatocellular carcinoma detected during surveillance.Gastroenterology. 2004;126:1005-1014.
Bruix J, Sherman M. Management of hepatocellular carcinoma.Hepatology. 2005;42:1208-1236.
Lim JH, Cho JM, Kim EY, Park CK. Dysplastic nodules in liver cirrhosis: evaluation of hemodynamics with CT during arterial portography and CT hepatic arteriography.Radiology. 2000;214:869-874.
Rode A, Bancel B, Douek P, Chevallier M, Vilgrain V, Picaud G, Henry L, Berger F, Bizollon T, Gaudin JL. Small nodule detection in cirrhotic livers: evaluation with US, spiral CT, and MRI and correlation with pathologic examination of explanted liver.J Comput Assist Tomogr. 2001;25:327-336.
Monzawa S, Ichikawa T, Nakajima H, Kitanaka Y, Omata K, Araki T. Dynamic CT for detecting small hepatocellular carcinoma: usefulness of delayed phase imaging.AJR Am J Roentgenol. 2007;188:147-153.
Hecht EM, Holland AE, Israel GM, Hahn WY, Kim DC, West AB, Babb JS, Taouli B, Lee VS, Krinsky GA. Hepatocellular carcinoma in the cirrhotic liver: gadolinium-enhanced 3D T1-weighted MR imaging as a stand-alone sequence for diagnosis.Radiology. 2006;239:438-447.
Piscaglia F, Bolondi L. Recent advances in the diagnosis of hepatocellular carcinoma.Hepatol Res. 2007;37 Suppl 2:S178-S192.
Parikh P, Malhotra H, Jelic S. Hepatocellular carcinoma: ESMO clinical recommendations for diagnosis, treatment and follow-up.Ann Oncol. 2008;19 Suppl 2:ii27-ii28.
Chignard N, Beretta L. Proteomics for hepatocellular carcinoma marker discovery.Gastroenterology. 2004;127:S120-S125.
Lee JS, Chu IS, Heo J, Calvisi DF, Sun Z, Roskams T, Durnez A, Demetris AJ, Thorgeirsson SS. Classification and prediction of survival in hepatocellular carcinoma by gene expression profiling.Hepatology. 2004;40:667-676.
Schwartz M, Roayaie S, Konstadoulakis M. Strategies for the management of hepatocellular carcinoma.Nat Clin Pract Oncol. 2007;4:424-432.
Cabibbo G, Latteri F, Antonucci M, Craxi A. Multimodal approaches to the treatment of hepatocellular carcinoma.Nat Clin Pract Gastroenterol Hepatol. 2009;6:159-169.
Sala M, Llovet JM, Vilana R, Bianchi L, Sole M, Ayuso C, Bru C, Bruix J. Initial response to percutaneous ablation predicts survival in patients with hepatocellular carcinoma.Hepatology. 2004;40:1352-1360.
Camme C, Di Marco V, Orlando A, Sandonato L, Casaril A, Parisi P, Alizzi S, Sciarrino E, Virdone R, Pardo S. Treatment of hepatocellular carcinoma in compensated cirrhosis with radio-frequency thermal ablation (RFTA): a prospective study.J Hepatol. 2005;42:535-540.
Omata M, Tateishi R, Yoshida H, Shiina S. Treatment of hepatocellular carcinoma by percutaneous tumor ablation methods: Ethanol injection therapy and radiofrequency ablation.Gastroenterology. 2004;127:S159-S166.
Lencioni R, Cioni D, Crocetti L, Franchini C, Pina CD, Lera J, Bartolozzi C. Early-stage hepatocellular carcinoma in patients with cirrhosis: long-term results of percutaneous image-guided radiofrequency ablation.Radiology. 2005;234:961-967.
Orlando A, Leandro G, Olivo M, Andriulli A, Cottone M. Radiofrequency thermal ablation vs. percutaneous ethanol injection for small hepatocellular carcinoma in cirrhosis: meta-analysis of randomized controlled trials.Am J Gastroenterol. 2009;104:514-524.
Jaskolka JD, Asch MR, Kachura JR, Ho CS, Ossip M, Wong F, Sherman M, Grant DR, Greig PD, Gallinger S. Needle tract seeding after radiofrequency ablation of hepatic tumors.J Vasc Interv Radiol. 2005;16:485-491.
Mulier S, Mulier P, Ni Y, Miao Y, Dupas B, Marchal G, De Wever I, Michel L. Complications of radiofrequency coagulation of liver tumours.Br J Surg. 2002;89:1206-1222.
Giorgio A, Tarantino L, de Stefano G, Francica G, Esposito F, Perrotta A, Aloisio V, Farella N, Mariniello N, Coppola C. Complications after interventional sonography of focal liver lesions: a 22-year single-center experience.J Ultrasound Med. 2003;22:193-205.
Smith EH. Complications of percutaneous abdominal fine-needle biopsy. Review.Radiology. 1991;178:253-258.
Weiss H, Duntsch U, Weiss A. [Risks of fine needle puncture--results of a survey in West Germany(German Society of Ultrasound in Medicine survey)].Ultraschall Med. 1988;9:121-127.
Pelloni A, Gertsch P. [Risks and consequences of tumor seeding after percutaneous fine needle biopsy four diagnosis of hepatocellular carcinoma].Schweiz Med Wochenschr. 2000;130:871-877.
Silva MA, Hegab B, Hyde C, Guo B, Buckels JA, Mirza DF. Needle track seeding following biopsy of liver lesions in the diagnosis of hepatocellular cancer: a systematic review and meta-analysis.Gut. 2008;57:1592-1596.
Llovet JM, Vilana R, Bru C, Bianchi L, Salmeron JM, Boix L, Ganau S, Sala M, Pages M, Ayuso C. Increased risk of tumor seeding after percutaneous radiofrequency ablation for single hepatocellular carcinoma.Hepatology. 2001;33:1124-1129.
Livraghi T, Lazzaroni S, Meloni F, Solbiati L. Risk of tumour seeding after percutaneous radiofrequency ablation for hepatocellular carcinoma.Br J Surg. 2005;92:856-858.
Poon RT, Ng KK, Lam CM, Ai V, Yuen J, Fan ST. Radiofrequency ablation for subcapsular hepatocellular carcinoma.Ann Surg Oncol. 2004;11:281-289.
Latteri F, Sandonato L, Di Marco V, Parisi P, Cabibbo G, Lombardo G, Galia M, Midiri M, Latteri MA, Craxi A. Seeding after radiofrequency ablation of hepatocellular carcinoma in patients with cirrhosis: a prospective study.Dig Liver Dis. 2008;40:684-689.
Stigliano R, Marelli L, Yu D, Davies N, Patch D, Burroughs AK. Seeding following percutaneous diagnostic and therapeutic approaches for hepatocellular carcinoma. What is the risk and the outcome? Seeding risk for percutaneous approach of HCC.Cancer Treat Rev. 2007;33:437-447.
Smith EH. The hazards of fine-needle aspiration biopsy.Ultrasound Med Biol. 1984;10:629-634.
Bolondi L, Gaiani S, Celli N, Piscaglia F. Tumor dissemination after radiofrequency ablation of hepatocellular carcinoma.Hepatology. 2001;34:608; author reply 610-611.
Goletti O, Chiarugi M, Buccianti P, Macchiarini P. Subcutaneous implantation of liver metastasis after fine needle biopsy.Eur J Surg Oncol. 1992;18:636-637.
Shimada M, Maeda T, Saitoh A, Morotomi I, Kano T. Needle track seeding after percutaneous ethanol injection therapy for small hepatocellular carcinoma.J Surg Oncol. 1995;58:278-281.
Imamura J, Tateishi R, Shiina S, Goto E, Sato T, Ohki T, Masuzaki R, Goto T, Yoshida H, Kanai F. Neoplastic seeding after radiofrequency ablation for hepatocellular carcinoma.Am J Gastroenterol. 2008;103:3057-3062.
Dumortier J, Lombard-Bohas C, Valette PJ, Boillot O, Scoazec JY, Berger F, Claudel-Bonvoisin S. Needle tract recurrence of hepatocellular carcinoma after liver transplantation.Gut. 2000;47:301.