Stereotactic body radiation therapy using the CyberKnife(®) system for patients with liver metastases

Zhi-Yong Yuan, Mao-Bin Meng, Chun-Lei Liu, Huan-Huan Wang, Chao Jiang, Yong-Chun Song, Hong-Qing Zhuang, Dong Yang, Jing-Sheng Wang, Wang Wei, Feng-Tong Li, Lu-Jun Zhao, Ping Wang, Zhi-Yong Yuan, Mao-Bin Meng, Chun-Lei Liu, Huan-Huan Wang, Chao Jiang, Yong-Chun Song, Hong-Qing Zhuang, Dong Yang, Jing-Sheng Wang, Wang Wei, Feng-Tong Li, Lu-Jun Zhao, Ping Wang

Abstract

The aim of this study was to evaluate the efficacy and toxicity of stereotactic body radiation therapy (SBRT) in the treatment of patients with liver metastases. Between August 2006 and July 2011, patients with 1-4 liver metastases were enrolled and treated with SBRT using the CyberKnife(®) system at Tianjin Medical University Cancer Institute and Hospital. The metastases were from different primary tumors, with a maximum tumor diameter of less than 6 cm. The primary endpoint was local control. Secondary endpoints were overall survival, progression-free survival, distant progression-free survival, and adverse events. Fifty-seven patients with 80 lesions were treated with SBRT. The 1-year and 2-year local control rates were 94.4% and 89.7%, respectively. The difference in local control between patients who received adjuvant treatment before SBRT and those who did not reached statistical significance (P=0.049). The median overall survival for the entire cohort was 37.5 months. According to the primary tumor sites, the median overall survival was not reached. The 2-year overall survival rate was 72.2% in the favorable group (primary tumors originating from the colon, breast, or stomach, as well as sarcomas); however, in the unfavorable group (primary tumors originating from the pancreas, lung, ovary, gallbladder, uterus, hepatocellular carcinoma, as well as olfactory neuroblastoma), the median overall survival and 2-year overall survival rates were 37.5 months and 55.9%, respectively (P=0.0001). Grade 1-2 fatigue, nausea, and vomiting were the most common adverse events, and no grade 3 and higher adverse events were observed. With excellent local control in the absence of severe toxicity, SBRT provides an alternative for patients with 1-4 liver metastases who cannot undergo surgery or other treatments.

Keywords: liver metastasis; local control; stereotactic body radiotherapy.

Figures

Figure 1
Figure 1
Representative planning CT and isodose distributions with SBRT for patients with 1–3 LM. Notes: Each representative patient had axial, sagittal, and coronal images taken, and red and purple lines indicate GTV and PTV, respectively. (A) A 38-year-old woman treated for a solitary LM from breast carcinoma. SBRT was performed using three fractions of 12 Gy prescribed to the 78% isodose line. (B) A 54-year-old man treated for two LM from rectal carcinoma. SBRT was performed using five fractions of 9 Gy to the 77% isodose line. (C) An 18-year-old man treated for three LM from pancreatic carcinoma. SBRT was performed in three fractions of 12 Gy to the 77% isodose line. Abbreviations: LM, liver metastasis; CT, computer tomography; GTV, gross tumor volume; PTV, planning target volume; Gy, Gray; SBRT, stereotactic body radiation therapy.
Figure 2
Figure 2
Analysis of initial planning CT and PET/CT as well as follow-up MRI images for a representative patient (a 23-year-old woman treated for a solitary LM from breast carcinoma). Notes: SBRT was delivered in three fractions of 14 Gy to the 81% isodose line. (A) Initial planning CT and PET/CT images showing a 3.2 cm lesion. (BG) T1-weighted and T2-weighted MRI images showing a complete response, with decreased attenuation in the surrounding region 6 months after completion of SBRT. The red arrows indicate changes in the liver metastasis after treatment. Abbreviations: CT, computer tomography; PET/CT, positron emission tomography/computer tomography; MRI, magnetic resonance imaging; LM, liver metastasis; Gy, Gray; PTV, planning target volume; SBRT, stereotactic body radiation therapy.
Figure 3
Figure 3
Actuarial local control, PFS, and DPFS of patients with LM. Notes: (A) Overall local control, (B) local control depending on tumor-based or patient-based analyses, (C) local control depending on primary tumor, (D) local control depending on LM site, (E) local control depending on time between first LM and SBRT, (F) local control depending on prior systematic treatment or lack thereof, (G) local control depending on BED, and (H) PFS and DPFS of patients with LM. Abbreviations: PFS, progression-free survival; DPFS, distant progression-free survival; LM, liver metastases; BED, biologically equivalent dose; IT, interval time; SBRT, stereotactic body radiation therapy; Gy, Gray; Cum, cumulative.
Figure 4
Figure 4
Actuarial overall survival in patients with LM. Notes: (A) OS in general, (B) OS depending on patient age, (C) OS depending on patient gender, (D) OS depending on primary tumor, (E) OS depending on number of LM, (F) OS depending on extrahepatic metastasis or lack thereof, (G) OS depending on time between first LM and SBRT, and (H) OS depending on prior systematic treatment or no such history. Abbreviations: OS, overall survival; LM, liver metastasis; IT, interval time; SBRT, stereotactic body radiation therapy; Cum, cumulative; Y, year.

References

    1. Siegel R, Naishadham D, Jemal A. Cancer Statistics, 2012. CA Cancer J Clin. 2012;62:10–29.
    1. Hess KR, Varadhachary GR, Taylor SH, et al. Metastatic patterns in adenocarcinoma. Cancer. 2006;106:1624–1633.
    1. Poston GJ. Surgical strategies for colorectal liver metastases. Surg Oncol. 2004;13:125–136.
    1. Yoon SS, Tanabe KK. Surgical treatment and other regional treatments for colorectal cancer liver metastases. Oncologist. 1999;4:197–208.
    1. Robertson DJ, Stukel TA, Gottlieb DJ, Sutherland JM, Fisher ES. Survival after hepatic resection of colorectal cancer metastases: a national experience. Cancer. 2009;115:752–759.
    1. Reddy SK, Barbas AS, Marroquin CE, et al. Resection of non-colorectal non-neuroendocrine liver metastases: a comparative analysis. J Am Coll Surg. 2007;204:372–382.
    1. Adam R. Chemotherapy and surgery: new perspectives on the treatment of unresectable liver metastases. Ann Oncol. 2003;14(Suppl 2):ii13–ii16.
    1. Albert SR, Horvath WL, Sternfeld WC, et al. Oxaliplatin, fluorouracil, and leucovorin for patients with unresectable liver only metastases from colorectal cancer: a North Central Cancer Treatment Group phase II study. J Clin Oncol. 2005;23:9243–9249.
    1. Garden OJ, Rees M, Poston GJ, et al. Guidelines for resection of colorectal cancer liver metastases. Gut. 2006;55(Suppl 3):iii1–iii8.
    1. Pawlik TM, Schulick RD, Choti MA. Expanding criteria for respectability of colorectal liver metastases. Oncologist. 2008;13:51–64.
    1. Khatri VP, Petrelli NJ, Belghiti J. Extending the frontiers of surgical therapy for hepatic colorectal metastases: is there a limit? J Clin Oncol. 2005;23:8490–8499.
    1. Lawrence TS, Ten Haken RK, Kessler ML, et al. The use of 3-D dose volume analysis to predict radiation hepatitis. Int J Radiat Oncol Biol Phys. 1992;23:781–788.
    1. Cheng JC, Wu JK, Huang CM, et al. Radiation induced liver disease after three-dimensional conformal radiotherapy for patients with hepatocellular carcinoma: dosimetric analysis and implication. Int J Radiat Oncol Biol Phys. 2002;54:156–162.
    1. Katz W, Carey-Sampson M, Muhs AG, Milano MT, Schell MC, Okunieff P. Hypofractionated stereotactic body radiation therapy (SBRT) for limited hepatic metastases. Int J Radiat Oncol Biol Phys. 2007;67:793–798.
    1. Mendez Romero A, Wunderink W, Hussain SM, et al. Stereotactic body radiation therapy for primary and metastatic liver tumors: a single institution phase I–II study. Acta Oncol. 2006;45:831–837.
    1. Adler JR, Jr, Chang SD, Murphy MJ, Doty J, Geis P, Hancock SL. SBRT: a frameless robotic system for radiosurgery. Stereotact Funct Neurosurg. 1997;69:124–128.
    1. Goodman KA, Wiegner EA, Maturen KE, et al. Dose-escalation study of single-fraction stereotactic body radiotherapy for liver malignancies. Int J Radiat Oncol Biol Phys. 2010;78:486–493.
    1. Rule W, Timmerman R, Tong L, et al. Phase I dose-escalation study of stereotactic body radiotherapy in patients with hepatic metastases. Ann Surg Oncol. 2011;18:1081–1087.
    1. Chang DT, Swaminath A, Kozak M, et al. Stereotactic body radiotherapy for colorectal liver metastases. A pooled analysis. Cancer. 2011;117:4060–4069.
    1. Rusthoven KE, Kavanagh BD, Cardenes H, et al. Multi-institutional phase I/II trial of stereotactic body radiation therapy for liver metastases. J Clin Oncol. 2009;27:1572–1578.
    1. Yuan Z, Tian L, Wang P, Song Y, Dong Y, Zhuang H. Comparative research on the efficacy of CyberKnife® and surgical excision for stage I hepatocellular carcinoma. Onco Targets Ther. 2013;6:1527–1532.
    1. Tian LJ, Zhuang HQ, Yuan ZY. A comparison between CyberKnife® and neurosurgery in solitary brain metastases from non-small cell lung cancer. Clin Neurol Neurosurg. 2013;115:2009–2014.
    1. Wang Q, Song Y, Zhuang H, et al. Robotic stereotactic irradiation and reirradiation for spinal metastases: safety and efficacy assessment. Chin Med J (Engl) 2014;127:232–238.
    1. Fowler JF. The linear-quadratic formula and progress in fractionated radiotherapy. Br J Radiol. 1989;62:679–694.
    1. Bogaerts J, Ford R, Sargent D, et al. RECIST Working Party Individual patients data analysis to assess modifications to the RECIST criteria. Eur J Cancer. 2009;45:248–260.
    1. Department of Health and Human Services Common terminology criteria for adverse events (CTCAE), version 4.0. [Accessed March 31, 2014]. Available from: .
    1. Hoyer M, Swaminath A, Bydder S, et al. Radiotherapy for liver metastases: a review of evidence. Int J Radiat Oncol Biol Phys. 2012;82:1047–1057.
    1. Vautravers-Dewas C, Dewas S, Bonodeau F, et al. Image-guided robotic stereotactic body radiation therapy for liver metastases: is there a dose response relationship? Int J Radiat Oncol Biol Phys. 2011;81:e39–e47.
    1. Lee MT, Kim JJ, Dinniwell R, et al. Phase I study of individualized stereotactic body radiotherapy of liver metastases. J Clin Oncol. 2009;27:1585–1591.
    1. Stintzing S, Hoffmann RT, Heinemann V, Kufeld M, Rentsch M, Muacevic A. Radiosurgery of liver tumors: value of robotic radiosurgical devise to treat liver tumors. Ann Surg Oncol. 2010;17:2877–2883.

Source: PubMed

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