Minimally invasive liver resections for malignancies: where is the limit?
Review Article

Minimally invasive liver resections for malignancies: where is the limit?

Yusuke Ome, Goro Honda, Yusuke Kawamoto, Naoki Yoshida

Department of Gastroenterological Surgery, New Tokyo Hospital, Matsudo, Chiba, Japan

Contributions: (I) Conception and design: Y Ome, G Honda; (II) Administrative support: None; (III) Provision of study materials or patients: Y Ome, G Honda; (IV) Collection and assembly of data: Y Ome, G Honda; (V) Data analysis and interpretation: Y Ome, G Honda; (VI) Manuscript writing: All authors; (VII) Final approval of manuscript: All authors.

Correspondence to: Goro Honda. Department of Gastroenterological Surgery, New Tokyo Hospital, 1271, Wanagaya, Matsudo, Chiba 270-2232, Japan. Email: ghon67@outlook.jp.

Abstract: Laparoscopic liver resection (LLR) has been disseminated in the last two decades because of the development of devices and improvement of techniques. Its effectiveness and safety have already been reported. In addition, oncological outcomes in LLR for hepatocellular carcinoma and colorectal liver metastases were reported to be similar to those of open surgery in selected cases. The indications for LLR have gradually expanded, and currently, highly challenging procedures including major hepatectomy are applied. However, there are several limitations to LLR in terms of technical aspects, tumor characteristics, and so on because much prolongation of the operation time and increase in the risks should not be permitted. For hepatectomy in which severe complications easily develop, it is most significant to minimize the operative complications. The indication criteria for LLR should be rigorously determined with an understanding of the limitations of laparoscopic surgery.

Keywords: Laparoscopic liver resection (LLR); minimally invasive liver resection; indication


Received: 31 March 2020; Accepted: 07 July 2020; Published: 25 July 2021.

doi: 10.21037/ls-20-59


Introduction

Laparoscopic liver resection (LLR) was first reported in 1991 (1). Since then, LLR has been gradually prevalent, and its efficacy and feasibility have already been reported (2-5). The indications for LLR have been expanded according to the development of laparoscopic instruments, devices, and technical refinements.

The First and Second International Consensus Conference on Laparoscopic Liver Surgery held in Louisville (in 2009) (6) and Morioka (in 2014) (7) showed the evolution of LLR and numerous recommendations. LLR has several superior advantages to open liver resection (OLR) other than cosmetic benefits. A laparoscopic magnified caudo-dorsal view provides excellent visibility of structures including the vessels and enables more meticulous procedures and unique approaches that are different from open surgery (8-13). Additionally, pneumoperitoneal pressure potentially reduces bleeding from the hepatic veins during liver parenchymal transection. However, LLR may have some disadvantages, such as direction misidentification, lack of tactile sense, device movement restriction, risk of tumor exposure, and less controllability for emergency bleeding. The optimal indications for LLR are mandatory to obtain the true benefit of minimally invasive surgery.


Type of procedure

The Second International Consensus Conference concluded that the minor LLR was a standard practice; however, the major LLR, defined as trisectionectomy, bisectionectomy, hemihepatectomy, and resection of the posterosuperior segments, remains an innovative procedure and is still in the exploratory learning phase (7). Laparoscopic partial resection and left lateral sectionectomy already have widespread use and are commonly performed. In experienced institutes, various laparoscopic anatomic resections, including hemihepatectomy, sectionectomy, segmentectomy, and smaller anatomic resections, so-called cone unit resection (14), have been performed successfully (4,15-21). Although many types of laparoscopic anatomic hepatectomy procedures without resection of the hilar vessels or extrahepatic bile duct resection have been standardized (9-13), the indications for these should be well discussed, considering malignant potential such as tumor type and vascular invasion.


Liver function

In terms of liver function, the indication criteria for LLR are basically the same as those for OLR. The Makuuchi criteria (22) are widely used as the indication criteria according to an estimated volume of resected liver, which were categorized using the hepatectomy types, including limited resection. The most common malignancies treated by liver resection are hepatocellular carcinoma (HCC) and colorectal liver metastasis (CRLM). HCC usually develops in patients with chronic liver diseases, such as hepatitis B and C viral infection, alcoholic liver injury, or steatohepatitis, while the liver of patients with CRLM has often been damaged by chemotherapy (23,24). The LLR feasibility and efficacy for patients with liver cirrhosis (LC) have been reported (25-31). A systemic review and meta-analysis showed that LLR for patients with HCC and chronic liver disease achieved fewer postoperative complications and comparable oncological long-term outcomes (32). In this study, it was concluded that postoperative ascites and liver failure were reduced with LLR.

During LLR, the abdominal wall destruction is minimized, and liver mobilization can often be minimized (13). In cases with LC, by avoiding the destruction of the collateral veins and lymphatic vessels around the liver, postoperative ascites can be decreased, and consequently, the liver function can be maintained. LLR may expand the indications for liver resection in patients with LC. The surgical indications for LLR must be considered more carefully than those for OLR in patients with LC because there are risks for intraoperative bleeding due to coagulopathy disorders and portal hypertension and postoperative complications, such as refractory ascites, hemorrhage, and liver failure (33). Further experiences and studies are required to address this issue.


Tumor characteristics

The indication for LLR is decided by referring to tumor type, location, size, number, vascular invasion, and so forth. Acceptable indication criteria for LLR recommended in the First International Consensus Conference were solitary lesions, a size of 5 cm or less, and location in liver segments 2 to 6 (6). Since then, these criteria have been extended with the remarkable development of LLR.

Tumor type

LLR is most commonly performed for HCC, followed by CRLM. Several large studies, including systematic reviews and meta-analyses, have already been conducted. They all reported that LLR for HCC or CRLM was associated with better short-term outcomes such as less blood loss, shorter hospital stays, and less morbidity than OLR and comparable oncological and long-term outcomes (34-42). Based on these results, HCC and CRLM are both good indications for LLR. The following are mainly described for other tumor types.

Metastatic tumors

The indication criteria for liver resection for metastatic tumors depend on their original malignancies. Currently, liver resections for various kinds of metastatic tumors other than CRLM, such as neuroendocrine neoplasm (NEN) (43-47), gastric cancer (48-50), and other tumors (51), have been reported to have better prognoses. The number of liver resections for metastatic tumors is increasing as a part of the multidisciplinary treatment because of the development of chemotherapy and interventional radiology. Particularly for NEN, LLR was associated with better short-term outcomes than OLR and comparable oncological and long-term outcomes, similar to CRLM (43,52-56).

Partial liver resection, which is familiar to LLR, is usually employed for metastatic liver tumors as a parenchyma-sparing liver resection (57,58). LLR is often feasible even in repeat hepatectomy (55); however, it takes a much longer operation time for multiple resections than OLR. LLR is sometimes performed simultaneously with resection of the primary site (59). Synchronous liver and colorectal resection usually require complex procedures and long operation times. In particular, major hepatectomy with low anterior rectal resection not only takes a long operation time but also leads to increased surgical risks. The timing of liver resection should be carefully decided, considering surgical risks and oncological efficacy.

Intrahepatic cholangiocarcinoma (ICC)

ICC is the second most common primary liver tumor (60). Regarding LLR for ICC, there are a few reports that showed better short-term outcomes than OLR and comparable oncological and long-term outcomes in selected patients (61-65). Most reports excluded tumors that had invaded into the blood vessels or bile duct in the hepatic hilum (hilar invasion). However, ICC had a higher malignant potential, and lymph node metastasis developed in 30–40% of patients (66). Although the necessity of routine lymphadenectomy is controversial, especially for tumors without hilar invasion (66) because there are some technical problems with lymphadenectomy in laparoscopic surgery, inadequate nodal evaluation can hinder accurate staging (67). LLR should be carefully performed for ICC, paying attention to the surgical margin.

Perihilar cholangiocarcinoma

For perihilar cholangiocarcinoma, a few reports described LLR (68-71). In general, perihilar cholangiocarcinoma requires major hepatectomy combined with caudate lobe resection, extrahepatic bile duct resection, regional lymphadenectomy, and biliary reconstruction (72). In most cases, the surgical margin in the dissection planes cannot be secured without tactile sensation, and it is difficult to determine an appropriate portion to cut the bile duct on the remnant liver side. Even if each procedure is technically available via a laparoscopic approach in some limited cases, it takes a much longer time to secure the surgical margin as well as complete biliary reconstruction precisely. The surgeon who does not know how difficult it is to secure the surgical margin in the dissection planes and bile duct stumps or how significant it is to prevent stenosis and leakage of the biliary anastomosis in this surgery may attempt to perform via a laparoscopic approach.

Gallbladder cancer (GBC)

For advanced GBC, laparoscopic extended cholecystectomy, in which the gallbladder is removed with gallbladder bed regional lymph nodes and, sometimes, common bile duct, followed by biliary reconstruction, may be an option in expert centers (70,73-77). Similar to patients with perihilar cholangiocarcinoma, patients with GBC involving the hepatoduodenal ligament should not undergo laparoscopic surgery.

Location

Currently, the tumor locations, even difficult ones like segments 1, 7, and 8, do not limit the indications for LLR in expert institutes (78). Liver resection of segments 1 and 7 have been standardized by utilizing the laparoscopic unique approach in the caudo-dorsal view (10,79), and that of segment 8 has been standardized by using intercostal trocars (13).

Size

A large tumor may obstruct the laparoscopic view, making it difficult to handle, as well as increase the risk of tumor exposure and rupture. Previous reports described that large tumors >5 cm could be approached laparoscopically without increased complications compared with OLR, but tumors >10 cm in size showed greater blood loss and longer operative time (80-82). Additionally, the conversion rate to OLR was slightly higher (9.3% to 15.4%). In patients with large tumors, especially those over 10 cm, LLR should be carefully selected.

Number

To remove several lesions, sparing the liver parenchyma and major blood vessels as much as possible, multiple resections with careful parenchymal dissection are required. If it is performed via a laparoscopic approach, it requires a longer operation time. Furthermore, to identify and remove all lesions without tumor exposure, detailed intraoperative ultrasonography and palpation, which are difficult to provide in LLR, are helpful. The limited number of tumors for LLR should be judged in each case referring to the patient’s condition, such as cardiac or renal function, as well as the surgeon’s skill. Hand-assisted laparoscopic surgery (HALS) or hybrid techniques may be useful for managing these intraoperative difficulties (83).

Vascular invasion

Similar to perihilar cholangiocarcinoma or GBC, the tumor suspected to invade the hepatic hilum should not be applicable for LLR.


Repeat hepatectomy

Recently, repeat hepatectomy has been aggressively performed to improve prognosis, and the results regarding HCC and CRLM have been reported (84-88). Repeat hepatectomy has also been increasingly performed via a laparoscopic approach. Wakabayashi et al. (89) reported in a systematic review and meta-analysis that laparoscopic repeat hepatectomy showed favorable short-term outcomes without mortality in highly selected patients although the rate of conversion to open surgery, HALS, or tumor ablation was relatively high (11%). As a previous hepatectomy, OLR was associated with longer operation time and greater blood loss than LLR. Another meta-analysis regarding repeat hepatectomy reported by Peng et al. (90) showed that LLR had similar operation time, less blood loss, fewer major complications, and shorter hospital stays compared with OLR. However, compared with LLR as a first hepatectomy, laparoscopic repeat hepatectomy took longer operation time, while the blood loss amount and transfusion rates, R0 resection, conversion, postoperative complications, and mortality were similar between the two groups.

The technical difficulty of repeat hepatectomy is caused by not only postoperative adhesion but also by the difficulty in recognizing anatomic landmarks due to a deformation of the liver derived from the previous hepatectomy, which increases during LLR because of easy disorientation in a laparoscopic narrow field. Particularly in cases that have been dissected around the hepatic hilum or have undergone mobilization of the right liver with exposure of the inferior vena cava in previous hepatectomy, if the portion around the hepatic hilum is dissected again, the risk of injury of important structures is higher in LLR than in OLR. Around the hepatic hilum, even to apply the Pringle maneuver is sometimes difficult. However, in general, adhesions after laparoscopic surgery are mild and easier to dissect. In addition, by utilizing some unique laparoscopic approaches, the hepatic hilum can remain untouched, and liver mobilization can be minimized in LLR (10,13). The indication for LLR in repeat hepatectomy should be determined by considering the estimated operation time and surgical risk associated with the tumor location and previous hepatectomy.


Conclusions

Recently, LLRs requiring highly difficult and complicated procedures have been increasingly performed in cases of malignant disorders. Although LLR is useful for properly selected cases, its indication criteria should not be expanded immoderately. The true goal of laparoscopic surgery is to provide minimal invasiveness to the patient. For hepatectomy in which severe complications easily develop, it is most significant to minimize the operative complications but not surgical incisions.

The indication criteria for LLR should be rigorously determined with an understanding of the limitations of laparoscopic surgery.


Acknowledgments

Funding: None.


Footnote

Provenance and Peer Review: This article was commissioned by the Guest Editor (Giammauro Berardi) for the series “Minimally Invasive Resections for Liver Malignancies: Among Certainties and Controversies” published in Laparoscopic Surgery. The article has undergone external peer review.

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/ls-20-59). The series “Minimally Invasive Resections for Liver Malignancies: Among Certainties and Controversies” was commissioned by the editorial office without any funding or sponsorship. The authors have no other conflicts of interest to declare.

Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.


References

  1. Reich H, McGlynn F, DeCaprio J, et al. Laparoscopic excision of benign liver lesions. Obstet Gynecol 1991;78:956-8. [PubMed]
  2. Buell JF, Thomas MT, Rudich S, et al. Experience with more than 500 minimally invasive hepatic procedures. Ann Surg 2008;248:475-86. [Crossref] [PubMed]
  3. Kaneko H, Takagi S, Otsuka Y, et al. Laparoscopic liver resection of hepatocellular carcinoma. Am J Surg 2005;189:190-4. [Crossref] [PubMed]
  4. Nguyen KT, Gamblin TC, Geller DA. World review of laparoscopic liver resection-2,804 patients. Ann Surg 2009;250:831-41. [Crossref] [PubMed]
  5. Sasaki A, Nitta H, Otsuka K, et al. Ten-year experience of totally laparoscopic liver resection in a single institution. Br J Surg 2009;96:274-9. [Crossref] [PubMed]
  6. Buell JF, Cherqui D, Geller DA, et al. The international position on laparoscopic liver surgery: The Louisville Statement, 2008. Ann Surg 2009;250:825-30. [Crossref] [PubMed]
  7. Wakabayashi G, Cherqui D, Geller DA, et al. Recommendations for laparoscopic liver resection: a report from the second international consensus conference held in Morioka. Ann Surg 2015;261:619-29. [PubMed]
  8. Tomishige H, Morise Z, Kawabe N, et al. Caudal approach to pure laparoscopic posterior sectionectomy under the laparoscopy-specific view. World J Gastrointest Surg 2013;5:173-7. [Crossref] [PubMed]
  9. Okuda Y, Honda G, Kurata M, et al. Dorsal approach to the middle hepatic vein in laparoscopic left hemihepatectomy. J Am Coll Surg 2014;219:e1-4. [Crossref] [PubMed]
  10. Okuda Y, Honda G, Kobayashi S, et al. Intrahepatic Glissonean pedicle approach to segment 7 from the dorsal side during laparoscopic anatomic hepatectomy of the cranial part of the right liver. J Am Coll Surg 2018;226:e1-6. [Crossref] [PubMed]
  11. Maeda K, Honda G, Kurata M, et al. Pure laparoscopic right hemihepatectomy using the caudodorsal side approach (with videos). J Hepatobiliary Pancreat Sci 2018;25:335-41. [Crossref] [PubMed]
  12. Homma Y, Honda G, Kurata M, et al. Pure laparoscopic right posterior sectionectomy using the caudate lobe-first approach. Surg Endosc 2019;33:3851-7. [Crossref] [PubMed]
  13. Ome Y, Honda G, Doi M, et al. Laparoscopic anatomic liver resection of segment 8 using intrahepatic Glissonean approach. J Am Coll Surg 2020;230:e13-20. [Crossref] [PubMed]
  14. Takasaki K. Glissonean pedicle transection method for hepatic resection: a new concept of liver segmentation. J Hepatobiliary Pancreat Surg 1998;5:286-91. [Crossref] [PubMed]
  15. Dagher I, O'Rourke N, Geller DA, et al. Laparoscopic major hepatectomy: an evolution in standard of care. Ann Surg 2009;250:856-60. [Crossref] [PubMed]
  16. Ishizawa T, Gumbs AA, Kokudo N, et al. Laparoscopic segmentectomy of the liver: from segment I to VIII. Ann Surg 2012;256:959-64. [Crossref] [PubMed]
  17. Tranchart H, Dagher I. Laparoscopic liver resection: a review. J Visc Surg 2014;151:107-15. [Crossref] [PubMed]
  18. Takahara T, Wakabayashi G, Konno H, et al. Comparison of laparoscopic major hepatectomy with propensity score matched open cases from the National Clinical Database in Japan. J Hepatobiliary Pancreat Sci 2016;23:721-34. [Crossref] [PubMed]
  19. Ciria R, Cherqui D, Geller DA, et al. Comparative short-term benefits of laparoscopic liver resection: 9000 cases and climbing. Ann Surg 2016;263:761-77. [Crossref] [PubMed]
  20. Xu H, Liu F, Li H, et al. Outcomes following laparoscopic versus open major hepatectomy: a meta-analysis. Scand J Gastroenterol 2017;52:1307-14. [Crossref] [PubMed]
  21. Jia C, Li H, Wen N, et al. Laparoscopic liver resection: a review of current indications and surgical techniques. Hepatobiliary Surg Nutr 2018;7:277-88. [Crossref] [PubMed]
  22. Makuuchi M, Kosuge T, Takayama T, et al. Surgery for small liver cancers. Semin Surg Oncol 1993;9:298-304. [Crossref] [PubMed]
  23. Rubbia-Brandt L, Audard V, Sartoretti P, et al. Severe hepatic sinusoidal obstruction associated with oxaliplatin-based chemotherapy in patients with metastatic colorectal cancer. Ann Oncol 2004;15:460-6. [Crossref] [PubMed]
  24. Fernandez FG, Ritter J, Goodwin JW, et al. Effect of steatohepatitis associated with irinotecan or oxaliplatin pretreatment on resectability of hepatic colorectal metastases. J Am Coll Surg 2005;200:845-53. [Crossref] [PubMed]
  25. Belli G, Limongelli P, Fantini C, et al. Laparoscopic and open treatment of hepatocellular carcinoma in patients with cirrhosis. Br J Surg 2009;96:1041-8. [Crossref] [PubMed]
  26. Kanazawa A, Tsukamoto T, Shimizu S, et al. Impact of laparoscopic liver resection for hepatocellular carcinoma with F4-liver cirrhosis. Surg Endosc 2013;27:2592-7. [Crossref] [PubMed]
  27. Yamashita Y, Ikeda T, Kurihara T, et al. Long-term favorable surgical results of laparoscopic hepatic resection for hepatocellular carcinoma in patients with cirrhosis: a single-center experience over a 10-year period. J Am Coll Surg 2014;219:1117-23. [Crossref] [PubMed]
  28. Memeo R, de'Angelis N, Compagnon P, et al. Laparoscopic vs. open liver resection for hepatocellular carcinoma of cirrhotic liver: a case-control study. World J Surg 2014;38:2919-26. [Crossref] [PubMed]
  29. Cheung TT, Dai WC, Tsang SH, et al. Pure laparoscopic hepatectomy versus open hepatectomy for hepatocellular carcinoma in 110 patients with liver cirrhosis: apropensity analysis at a single center. Ann Surg 2016;264:612-20. [Crossref] [PubMed]
  30. Yoon YI, Kim KH, Kang SH, et al. Pure laparoscopic versus open right hepatectomy for hepatocellular carcinoma in patients with cirrhosis: a propensity score matched analysis. Ann Surg 2017;265:856-63. [Crossref] [PubMed]
  31. Xu HW, Liu F, Li HY, et al. Outcomes following laparoscopic versus open major hepatectomy for hepatocellular carcinoma in patients with cirrhosis: a propensity score-matched analysis. Surg Endosc 2018;32:712-9. [Crossref] [PubMed]
  32. Morise Z, Ciria R, Cherqui D, et al. Can we expand the indications for laparoscopic liver resection? A systematic review and meta-analysis of laparoscopic liver resection for patients with hepatocellular carcinoma and chronic liver disease. J Hepatobiliary Pancreat Sci 2015;22:342-52. [Crossref] [PubMed]
  33. Farges O, Malassagne B, Flejou JF, et al. Risk of major liver resection in patients with underlying chronic liver disease: a reappraisal. Ann Surg 1999;229:210-5. [Crossref] [PubMed]
  34. Fancellu A, Rosman AS, Sanna V, et al. Meta-analysis of trials comparing minimally-invasive and open liver resections for hepatocellular carcinoma. J Surg Res 2011;171:e33-45. [Crossref] [PubMed]
  35. Xiong JJ, Altaf K, Javed MA, et al. Meta-analysis of laparoscopic vs. open liver resection for hepatocellular carcinoma. World J Gastroenterol 2012;18:6657-68. [Crossref] [PubMed]
  36. Yin Z, Fan X, Ye H, et al. Short- and long-term outcomes after laparoscopic and open hepatectomy for hepatocellular carcinoma: a global systematic review and meta-analysis. Ann Surg Oncol 2013;20:1203-15. [Crossref] [PubMed]
  37. Takahara T, Wakabayashi G, Beppu T, et al. Long-term and perioperative outcomes of laparoscopic versus open liver resection for hepatocellular carcinoma with propensity score matching: a multi-institutional Japanese study. J Hepatobiliary Pancreat Sci 2015;22:721-7. [Crossref] [PubMed]
  38. Wang ZY, Chen QL, Sun LL, et al. Laparoscopic versus open major liver resection for hepatocellular carcinoma: systematic review and meta-analysis of comparative cohort studies. BMC Cancer 2019;19:1047. [Crossref] [PubMed]
  39. Luo LX, Yu ZY, Bai YN. Laparoscopic hepatectomy for liver metastases from colorectal cancer: a meta-analysis. J Laparoendosc Adv Surg Tech A 2014;24:213-22. [Crossref] [PubMed]
  40. Beppu T, Wakabayashi G, Hasegawa K, et al. Long-term and perioperative outcomes of laparoscopic versus open liver resection for colorectal liver metastases with propensity score matching: a multi-institutional Japanese study. J Hepatobiliary Pancreat Sci 2015;22:711-20. [Crossref] [PubMed]
  41. Allard MA, Cunha AS, Gayet B, et al. Early and long-term oncological outcomes after laparoscopic resection for colorectal liver metastases: a propensity score-based analysis. Ann Surg 2015;262:794-802. [Crossref] [PubMed]
  42. Cipriani F, Rawashdeh M, Stanton L, et al. Propensity score-based analysis of outcomes of laparoscopic versus open liver resection for colorectal metastases. Br J Surg 2016;103:1504-12. [Crossref] [PubMed]
  43. Mayo SC, de Jong MC, Bloomston M, et al. Surgery versus intra-arterial therapy for neuroendocrine liver metastasis: a multicenter international analysis. Ann Surg Oncol 2011;18:3657-65. [Crossref] [PubMed]
  44. Saxena A, Chua TC, Perera M, et al. Surgical resection of hepatic metastases from neuroendocrine neoplasms: a systematic review. Surg Oncol 2012;21:e131-41. [Crossref] [PubMed]
  45. Fairweather M, Swanson R, Wang J, et al. Management of neuroendocrine tumor liver metastases: long-term outcomes and prognostic factors from a large prospective database. Ann Surg Oncol 2017;24:2319-25. [Crossref] [PubMed]
  46. Watzka FM, Fottner C, Miederer M, et al. Surgical therapy of neuroendocrine neoplasm with hepatic metastasis: patient selection and prognosis. Langenbecks Arch Surg 2015;400:349-58. [Crossref] [PubMed]
  47. Nigri G, Petrucciani N, Debs T, et al. Treatment options for PNET liver metastases: a systematic review. World J Surg Oncol 2018;16:142. [Crossref] [PubMed]
  48. Kodera Y, Fujitani K, Fukushima N, et al. Surgical resection of hepatic metastasis from gastric cancer: a review and new recommendation in the Japanese gastric cancer treatment guidelines. Gastric Cancer 2014;17:206-12. [Crossref] [PubMed]
  49. Kinoshita T, Kinoshita T, Saiura A, et al. Multicentre analysis of long-term outcome after surgical resection for gastric cancer liver metastases. Br J Surg 2015;102:102-107. [Crossref] [PubMed]
  50. Oki E, Tokunaga S, Emi Y, et al. Surgical treatment of liver metastasis of gastric cancer: a retrospective multicenter cohort study (KSCC1302). Gastric Cancer 2016;19:968-76. [Crossref] [PubMed]
  51. Schiergens TS, Lüning J, Renz BW, et al. Liver resection for non-colorectal non-neuroendocrine metastases: where do we stand today compared to colorectal cancer? J Gastrointest Surg 2016;20:1163-72. [Crossref] [PubMed]
  52. Triantafyllidis I, Gayet B, Tsiakyroudi S, et al. Perioperative and long-term outcomes of laparoscopic liver resections for non-colorectal liver metastases. Surg Endosc 2020;34:3833-44. [Crossref] [PubMed]
  53. Thomaschewski M, Neeff H, Keck T, et al. Is there any role for minimally invasive surgery in NET? Rev Endocr Metab Disord 2017;18:443-57. [Crossref] [PubMed]
  54. Kandil E, Noureldine SI, Koffron A, et al. Outcomes of Laparoscopic and Open Resection for Neuroendocrine Liver Metastases. Surgery 2012;152:1225-31. [Crossref] [PubMed]
  55. Kiritani S, Arita J, Matsumura M, et al. Repeat hepatectomy for patients with recurrent neuroendocrine liver metastasis: Comparison with first hepatectomy. Surgery 2020;167:404-9. [Crossref] [PubMed]
  56. Spolverato G, Bagante F, Aldrighetti L, et al. Management and outcomes of patients with recurrent neuroendocrine liver metastasis after curative surgery: An international multi-institutional analysis. J Surg Oncol 2017;116:298-306. [Crossref] [PubMed]
  57. Postriganova N, Kazaryan AM, Røsok BI, et al. Margin status after laparoscopic resection of colorectal liver metastases: does a narrow resection margin have an influence on survival and local recurrence? HPB (Oxford) 2014;16:822-9. [Crossref] [PubMed]
  58. Montalti R, Tomassini F, Laurent S, et al. Impact of surgical margins on overall and recurrence-free survival in parenchymal-sparing laparoscopic liver resections of colorectal metastases. Surg Endosc 2015;29:2736-47. [Crossref] [PubMed]
  59. Lupinacci RM, Andraus W, De Paiva Haddad LB, et al. Simultaneous laparoscopic resection of primary colorectal cancer and associated liver metastases: a systematic review. Tech Coloproctol 2014;18:129-35. [Crossref] [PubMed]
  60. Razumilava N, Gores GJ. Cholangiocarcinoma. Lancet 2014;383:2168-79. [Crossref] [PubMed]
  61. Uy BJ, Han HS, Yoon YS, et al. Laparoscopic liver resection for intrahepatic cholangiocarcinoma. J Laparoendosc Adv Surg Tech A 2015;25:272-7. [Crossref] [PubMed]
  62. Ratti F, Cipriani F, Ariotti R, et al. Safety and feasibility of laparoscopic liver resection with associated lymphadenectomy for intrahepatic cholangiocarcinoma: a propensity score-based case-matched analysis from a single institution. Surg Endosc 2016;30:1999-2010. [Crossref] [PubMed]
  63. Lee W, Park JH, Kim JY, et al. Comparison of perioperative and oncologic outcomes between open and laparoscopic liver resection for intrahepatic cholangiocarcinoma. Surg Endosc 2016;30:4835-40. [Crossref] [PubMed]
  64. Wei F, Lu C, Cai L, et al. Can laparoscopic liver resection provide a favorable option for patients with large or multiple intrahepatic cholangiocarcinomas? Surg Endosc 2017;31:3646-55. [Crossref] [PubMed]
  65. Zhu Y, Song J, Xu X, et al. Safety and feasibility of laparoscopic liver resection for patients with large or multiple intrahepatic cholangiocarcinomas: a propensity score based case-matched analysis from a single institute. Medicine (Baltimore) 2019;98:e18307 [Crossref] [PubMed]
  66. Weber SM, Ribero D, O'Reilly EM, et al. Intrahepatic cholangiocarcinoma: expert consensus statement. HPB (Oxford) 2015;17:669-80. [Crossref] [PubMed]
  67. Martin SP, Drake J, Wach MM, et al. Laparoscopic approach to intrahepatic cholangiocarcinoma is associated with an exacerbation of inadequate nodal staging. Ann Surg Oncol 2019;26:1851-7. [Crossref] [PubMed]
  68. Machado MA, Makdissi FF, Surjan RC, et al. Laparoscopic resection of hilar cholangiocarcinoma. J Laparoendosc Adv Surg Tech A 2012;22:954-6. [Crossref] [PubMed]
  69. Yu H, Wu SD, Chen DX, et al. Laparoscopic resection of Bismuth type I and II hilar cholangiocarcinoma: an audit of 14 cases from two institutions. Dig Surg 2011;28:44-9. [Crossref] [PubMed]
  70. Gumbs AA, Jarufe N, Gayet B. Minimally invasive approaches to extrapancreatic cholangiocarcinoma. Surg Endosc 2013;27:406-14. [Crossref] [PubMed]
  71. Cho A, Yamamoto H, Kainuma O, et al. Laparoscopy in the management of hilar cholangiocarcinoma. World J Gastroenterol 2014;20:15153-7. [Crossref] [PubMed]
  72. Nimura Y, Hayakawa N, Kamiya J, et al. Hepatic segmentectomy with caudate lobe resection for bile duct carcinoma of the hepatic hilus. World J Surg 1990;14:535-43 discussion 544.
  73. Itano O, Oshima G, Minagawa T, et al. Novel strategy for laparoscopic treatment of pT2 gallbladder carcinoma. Surg Endosc 2015;29:3600-7. [Crossref] [PubMed]
  74. Agarwal AK, Javed A, Kalayarasan R, et al. Minimally invasive versus the conventional open surgical approach of a radical cholecystectomy for gallbladder cancer: a retrospective comparative study. HPB (Oxford) 2015;17:536-41. [Crossref] [PubMed]
  75. Shirobe T, Maruyama S. Laparoscopic radical cholecystectomy with lymph node dissection for gallbladder carcinoma. Surg Endosc 2015;29:2244-50. [Crossref] [PubMed]
  76. Yoon YS, Han HS, Cho JY, et al. Is laparoscopy contraindicated for gallbladder cancer? A 10-year prospective cohort study. J Am Coll Surg 2015;221:847-53. [Crossref] [PubMed]
  77. Han HS, Yoon YS, Agarwal AK, et al. Laparoscopic surgery for gallbladder cancer: an expert consensus statement. Dig Surg 2019;36:1-6. [Crossref] [PubMed]
  78. Zheng B, Zhao R, Li X, et al. Comparison of laparoscopic liver resection for lesions located in anterolateral and posterosuperior segments: a meta-analysis. Surg Endosc 2017;31:4641-8. [Crossref] [PubMed]
  79. Li H, Honda G, Ome Y, et al. Laparoscopic Extended Anatomical Resection of Segment 7 by the Caudate Lobe First Approach: A Video Case Report. J Gastrointest Surg 2019;23:1084-5. [Crossref] [PubMed]
  80. Ai JH, Li JW, Chen J, et al. Feasibility and safety of laparoscopic liver resection for hepatocellular carcinoma with a tumor size of 5-10 cm. PLoS One 2013;8:e72328 [Crossref] [PubMed]
  81. Kwon Y, Han HS, Yoon YS, et al. Are large hepatocellular carcinomas still a contraindication for laparoscopic liver resection? J Laparoendosc Adv Surg Tech A 2015;25:98-102. [Crossref] [PubMed]
  82. Shelat VG, Cipriani F, Basseres T, et al. Pure laparoscopic liver resection for large malignant tumors: does size matter? Ann Surg Oncol 2015;22:1288-93. [Crossref] [PubMed]
  83. Kaneko H, Otsuka Y, Kubota Y, et al. Evolution and revolution of laparoscopic liver resection in Japan. Ann Gastroenterol Surg 2017;1:33-43. [Crossref] [PubMed]
  84. Wanebo HJ, Chu QD, Avradopoulos KA, et al. Current perspectives on repeat hepatic resection for colorectal carcinoma: a review. Surgery 1996;119:361-71. [Crossref] [PubMed]
  85. Itamoto T, Nakahara H, Amano H, et al. Repeat hepatectomy for recurrent hepatocellular carcinoma. Surgery 2007;141:589-97. [Crossref] [PubMed]
  86. Saiura A, Yamamoto J, Koga R, et al. Favorable outcome after repeat resection for colorectal liver metastases. Ann Surg Oncol 2014;21:4293-9. [Crossref] [PubMed]
  87. Petrowsky H, Gonen M, Jarnagin W, et al. Second liver resections are safe and effective treatment for recurrent hepatic metastases from colorectal cancer: a bi-institutional analysis. Ann Surg 2002;235:863-71. [Crossref] [PubMed]
  88. Chan DL, Morris DL, Chua TC. Clinical efficacy and predictors of outcomes of repeat hepatectomy for recurrent hepatocellular carcinoma - a systematic review. Surg Oncol 2013;22:e23-e30. [Crossref] [PubMed]
  89. Wakabayashi T, Felli E, Memeo R, et al. Short-term outcomes of laparoscopic repeat liver resection after open liver resection: a systematic review. Surg Endosc 2019;33:2083-92. [Crossref] [PubMed]
  90. Peng Y, Liu F, Wei Y, et al. Outcomes of laparoscopic repeat liver resection for recurrent liver cancer: A system review and meta-analysis. Medicine (Baltimore) 2019;98:e17533 [Crossref] [PubMed]
doi: 10.21037/ls-20-59
Cite this article as: Ome Y, Honda G, Kawamoto Y, Yoshida N. Minimally invasive liver resections for malignancies: where is the limit? Laparosc Surg 2021;5:37.

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