Endoscopy 2000; 32(8): 591-597
DOI: 10.1055/s-2000-9014
Original Article
Georg Thieme Verlag Stuttgart · New York

Laparoscopic Microwave Coagulation Therapy for Hepatocellular Carcinoma

S. Seki, H. Sakaguchi, H. Kadoya, H. Morikawa, D. Habu, S. Nishiguchi, S. Shiomi, T. Kitada, T. Kuroki
  • Third Dept. of Internal Medicine, Osaka City University Medical School, Osaka, Japan
Further Information

Publication History

Publication Date:
31 December 2000 (online)

Background and Study Aims: Several different effective forms of treatment are available, singly or in combination, for patients with hepatocellular carcinoma (HCC). These include surgical resection, transcatheter arterial embolization, percutaneous ethanol injection, and percutaneous microwave coagulation therapy. In this study, we carried out laparoscopic microwave coagulation therapy (LMCT), using laparoscopic microwave electrodes to treat HCC.

Patients and Methods: Under local anesthesia, 24 patients with HCCs located on or near the liver surface underwent LMCT under direct laparoscopic vision, with ultrasound guidance. LMCT was performed using microwave electrodes with tips ranging from 15 - 45 mm in length, and the effectiveness of the treatment was confirmed using contrast-enhanced computed tomography (CT) within two weeks of the LMCT procedure.

Results: The mean longest axis of the 26 HCC nodules in 24 patients was 20 mm, and that of the coagulated areas including the nodules was 40 mm, with additional therapy being required in two patients. Complete efficacy of the treatment was observed in 21 patients (87.5 %), but local recurrences were seen in three of them one year after LMCT. The three-year survival rate was 92 %, but the number of patients included in the study was small. Hemostasis was complete, but mild pneumothorax occurred in three patients.

Conclusions: LMCT under local anesthesia is a minimally invasive and effective therapy when carried out on a single occasion to treat HCCs located near the liver surface, and it can be safely performed under direct visual guidance.

References

  • 1 Steiner PE. Cancer of the liver and cirrhosis in trans-Sahara Africa and the United States of America.  Cancer. 1960;  13 1085-1066
  • 2 Liaw YF, Chu CM, Lin DY, et al. Age-specific prevalence and significance of hepatitis B e antigen and antibody in chronic hepatitis B virus infection in Taiwan: a comparison among asymptomatic carriers, chronic hepatitis, liver cirrhosis, and hepatocellular carcinoma.  J Med Virol. 1984;  13 385-391
  • 3 Nishioka K, Watanabe J, Furuta S, et al. A high prevalence of antibody to the hepatitis C virus in patients with hepatocellular carcinoma.  Cancer. 1991;  67 429-433
  • 4 Arii S, Tanaka J, Yamazoe Y, et al. Predictive factors for intrahepatic recurrence of hepatocellular carcinoma after partial hepatectomy.  Cancer. 1992;  69 913-919
  • 5 Makuuchi M, Hasegawa H, Yamazaki S. Ultrasonically guided subsegmentectomy.  Surg Gynecol Obstet. 1985;  161 346-350
  • 6 Kinoshita H, Hirohashi K, Kubo S, et al. Diagnosis and treatment for small hepatocellular carcinoma.  Asian Med J. 1993;  36 51-54
  • 7 Ebara M, Ohto M, Sugiura N, et al. Percutaneous ethanol injection for the treatment of small hepatocellular carcinoma: study of 95 patients.  J Gastrol Hepatol. 1990;  5 616-626
  • 8 Shina S, Tagawa K, Niwa Y, et al. Percutaneous ethanol injection for hepatocellular carcinoma: results in 146 patients.  Am J Roentgenol. 1993;  160 1023-1028
  • 9 Yamada R, Sato M, Kawabata M, et al. Hepatic arterial embolization in 120 patients with unresectable hepatoma.  Radiology. 1983;  148 397-401
  • 10 Takayasu K, Wakao F, Moriyama N, et al. Response of early-stage hepatocellular carcinoma and borderline lesions to therapeutic arterial embolization.  Am J Roentgenol. 1993;  160 301-306
  • 11 Seki T, Wakabayashi M, Nakagawa T, et al. Ultrasonically guided percutaneous microwave coagulation therapy for small hepatocellular carcinoma.  Cancer. 1994;  74 817-825
  • 12 Ido K, Isoda N, Kawamoto C, et al. Laparoscopic microwave coagulation therapy for solitary hepatocellular carcinoma performed under laparoscopic ultrasonography.  Gastrointest Endosc. 1997;  45 415-420
  • 13 Tabuse K, Katsumi M, Kobayashi Y, et al. Microwave surgery: hepatectomy using microwave tissue coagulator.  World J Surg. 1985;  9 136-143
  • 14 Hamazoe R, Hirooka Y, Ohtani S, et al. Intraoperative microwave tissue coagulation as treatment for patients with non-resectable hepatocellular carcinoma.  Cancer. 1995;  75 794-800
  • 15 Itai Y, Ohtomo K, Kokubo T, et al. CT of hepatic masses: significant of prolonged and delayed enhancement.  Am J Roentgenol. 1986;  146 729-733
  • 16 Hollett MD, Jeffrey RB Jr, Nino-Murcia M, et al. Dual-phase helical CT of the liver: value of arterial phase scans in the detection of small (< 1.5 cm) malignant hepatic neoplasms.  Am J Roentgenol. 1995;  164 879-884
  • 17 Takayasu K, Furukawa H, Wakao F, et al. CT diagnosis of early hepatocellular carcinoma: sensitivity, findings, and CT-pathologic correlation.  Am J Roentgenol. 1995;  164 885-890
  • 18 Oliver JM III, Baron RL. Helical biphasic contrast-enhanced CT of the liver: technique, indications, interpretation, and pitfalls.  Radiology. 1996;  201 1-14
  • 19 Kobayashi K, Sugimoto T, Makino T, et al. Screening methods for early detection of hepatocellular carcinoma.  Hepatology. 1985;  5 1100-1105
  • 20 Nagasue N, Uchida M, Makino Y, et al. Incidence and factors associated with intrahepatic recurrence following resection of hepatocellular carcinoma.  Gastroenterology. 1993;  105 488-494
  • 21 Nagasue N, Yukaya H, Chang YC, et al. Assessment of pattern and treatment of intrahepatic recurrence after resection of hepatocellular carcinoma.  Surg Gynecol Obstet. 1990;  171 217-222
  • 22 Ngao, T, Inoue S, Yoshimi F, et al. Postoperative recurrence of hepatocellular carcinoma.  Ann Surg. 1990;  211 28-33
  • 23 Tobe T, Kameda H, Okudaira M, et al. Summary of the data from a follow-up study by the Liver Cancer Study Group of Japan. In: Tobe T, Kameda H, Okudaira M, Ohto M, Endo Y, Mito M, Okamoto E, Tanikawa K, Kojiro M (eds). Primary liver cancer in Japan.  Tokyo; Springer, 1992: 31-37
  • 24 Okamoto E, Liver Cancer Study Group of Japan. Survey and follow-up study of primary liver cancer in Japan: report 12 [in Japanese with English abstract].  Acta Hepatol Jpn. 1997;  38 12-33
  • 25 Eguchi A, Nakashima O, Okudaira S, et al. Adenomatous hyperplasia in the vicinity of small hepatocellular carcinoma.  Hepatology. 1992;  15 843-848
  • 26 Shibata M, Morizane T, Uchida T, et al. Irregular regeneration of hepatocytes and risk of hepatocellular carcinoma in chronic hepatitis and cirrhosis with hepatitis-C virus infection.  Lancet. 1998;  351 1773-1777
  • 27 Terasaki S, Kaneko S, Kobayashi K, et al. Histological features predicting malignant transformation of nonmalignant hepatocellular nodules: a prospective study.  Gastroenterology. 1998;  115 1216-1222
  • 28 Kumada T, Nakano S, Takeda I, et al. Patterns of recurrence after initial treatment in patients with small hepatocellular carcinoma.  Hepatology. 1997;  25 87-92
  • 29 Ebara M, Kita K, Sugiura N, et al. Therapeutic effect of percutaneous ethanol injection on small hepatocellular carcinoma: evaluation with CT.  Radiology. 1995;  195 371-377
  • 30 Nishiguchi S, Kuroki T, Nakatani S, et al. Randomised trial of effects of interferon-α on incidence of hepatocellular carcinoma in chronic active hepatitis C with cirrhosis.  Lancet. 1995;  346 1051-1055
  • 31 Muto Y, Moriwaki H, Ninomiya M, et al. Prevention of second primary tumors by an acyclic retinoid, polyprenoic acid, in patients with hepatocellular carcinoma.  N Engl J Med. 1996;  334 1561-1567

M.D. S. Seki

Third Dept. of Internal Medicine Osaka City University Medical School

1-4-3 Asahimach, Abenoku

Osaka 545-8585

Japan

Phone: +81-6-6645-3813

Email: s.seki@med.osaka-cu.ac.jp

    >