The Role of Staged Resection in Management of Hepatic Metastatic Nodules

Document Type : Original Article

Authors

1 General Surgery Department, Zagazig University, Egypt.

2 Medical Oncology Department, Zagazig University, Egypt.

Abstract

Background: Metastatic nodules are the most common malignancy affecting the liver. Colo- rectal cancer is the most common primary tumor sending metastases to liver, less commonly neuro-endocrine tumors and others.
Aim: To study the effect of staged resection (resecting the malignant primary site, neo- adjuvant chemotherapy for 1-3months, liver metastasectomy then chemotherapy completion).
Patients and methods: Eighteen patients were admitted to Zagazig University hospitals with hepatic metastases from different primary sites (mostly colorectal cancer) from June 2012 to September 2015. All patients were assessed clinically and radiologically. Neo-adjuvant chemotherapy was given to synchronous colorectal liver metastases.
Results: This study included 10 (55.5%) females and 8 (44.5%) males with mean age 43 years old. Thirteen patients had hepatic metastases from colorectal cancer. Classical approach was done in 16 patients. 14 patients had anatomical resection while the remaining 4 patients had non-anatomical resection. Postoperative complications occurred in nine patients while recurrence was only in 4 patients (two of them died during the follow-up period).
Conclusion: Liver resection for liver metastases from different primary sites improved the 5 years survival when used combination with neo-adjuvant chemotherapy

Keywords


 

The Role of Staged Resection in Management of Hepatic

Metastatic Nodules

 

 

Wael Mansy,1 MD; Morsi Mohamed,1 MD; Ahmed El-Nagar,2 MD; Mohamed Riad,1 MD.

 

 

1) General Surgery Department, Zagazig University, Egypt.

2) Medical Oncology Department, Zagazig University, Egypt.

 

 

Background: Metastatic nodules are the most common malignancy affecting the liver. Colo- rectal cancer is the most common primary tumor sending metastases to liver, less commonly neuro-endocrine tumors and others.

Aim: To study the effect of staged resection (resecting the malignant primary site, neo- adjuvant chemotherapy for 1-3months, liver metastasectomy then chemotherapy completion).

Patients and methods: Eighteen patients were admitted to Zagazig University hospitals with hepatic metastases from different primary sites (mostly colorectal cancer) from June 2012 to September 2015. All patients were assessed clinically and radiologically. Neo-adjuvant chemotherapy was given to synchronous colorectal liver metastases.

Results: This study included 10 (55.5%) females and 8 (44.5%) males with mean age 43 years old. Thirteen patients had hepatic metastases from colorectal cancer. Classical approach was done in 16 patients. 14 patients had anatomical resection while the remaining 4 patients had non-anatomical resection. Postoperative complications occurred in nine patients while recurrence was only in 4 patients (two of them died during the follow-up period).

Conclusion: Liver resection for liver metastases from different primary sites improved the 5 years survival when used combination with neo-adjuvant chemotherapy.

Key words: Hepatic metastases, liver resection, neo-adjuvant, chemotherapy.

 

 

 

 

 

 

Introduction:

Although the liver is the most common site of metastasis from a variety of tumor types, isolated hepatic metastases mostly occur from colorectal cancer and, less frequently, from neuro-endocrine tumors, gastro-intestinal sarcoma, and others.1  Complete evaluation of  the  extent  of  metastatic  disease,  both intra & extra-hepatically, is important before considering treatment options.2

Approximately 50% to 60% of diagnosed colorectal cancer patients develop colorectal metastases.3, 4 And unfortunately 80% to 90% of these patients have unresectable metastatic liver disease.5,6 Metastatic disease mostly develops metachronously after treatment for loco- regional colorectal cancer, with the liver being the most common site of involvement.7

However, 20% to 34% of colorectal cancer


patients present with synchronous liver metastases.8     Some    evidence    postulated that synchronous metastatic colorectal liver disease is associated with more disseminated disease state and worse prognosis than metastatic colorectal liver disease that develops metachronously.9

Surgical treatment is considered the corner-stone of therapeutic approach to liver metastases, as curative resection of liver metastases increases survival, with 5-year survival rates of 30%-40%.10 Patients with a resectable primary colon tumor and resectable synchronous metastases can be treated with a staged or simultaneous resection.11

 

Patients and methods:

Eighteen patients presenting with liver metastases  from  different  primary  sites  as

 

 

 

colorectal cancer, neuro- endocrine GIT tumors; ovarian cancer and breast cancer were managed and followed-up at the advanced center of liver diseases, Zagazig University in the period from June 2012 to September

2015. All patients were assessed clinically by multidisciplinary team including (surgery, oncology,  hepatology  and  radiology) doctors. All data regarding demographic data, radiology data, chemotherapy, operative data, postoperative complications and follow-up data were recorded.

Preoperative preparations: Assessment of the general performance of the patients was done to determine the ability of the patient to tolerate hepatic resection. Special attention was to cardiopulmonary status (pulmonary function  tests  and  Echo).  Assessment  of the  functional  capacity  of  the  liver  was done  by  liver  function  tests  and  Child- Pugh classification. All patients were given prophylactic dose of low molecular weight heparin and preparation of pack RBCs (PRBCs) and fresh frozen plasma (FFP) if needed.

Assessment of site of the primary tumors was done by tumor markers (CEA, CA 125 and CA15-3), breast examination, rectal examination and colonoscopy (to eliminate anastomotic recurrence or new colic cancer). Also CT abdomen and pelvis was done to verify the absence of loco-regional spread in case of colorectal cancer, neuro-endocrine GIT tumors and ovarian cancer. Metastatic workup was completed by CT chest, brain and bone scans. Pre-operative assessment of hepatic involvement was done by triphasic CT and in some cases by triphasic MRI and PET scan in large metastatic nodules to detect small micro-metastases Figure (1).

Our  protocol  of  management  of colorectal liver metastases was resection of the primary tumors first, followed by 4-6 cycles of chemotherapy for 2-3months, then


•      Leucovorin  400  mg/m2  IV  over  2 hours, day 1.

•       5-FU  400  mg/m2  IV bolus  on  day

1,  then  1200  mg/m2/day  for  2  days  (total

2400 mg/m2 over 46–48 hours) continuous infusion. Repeat every 2 weeks 12.

Regarding staged resection cases, neo- adjuvant  chemotherapy  was  for  3  months then completion chemotherapy for another 3 months. In the other cases where we discover liver metastases after primary resection in the follow up period, chemotherapy was for 6 months after resection.

Surgical  procedures:  J  shaped  incision was done for good exploration. First, intra- operative assessment of the primary tumor site was done to determine any recurrence. Then carful exploration of the abdominal cavity was performed to assess the presence of metastatic lymph nodes in the porta- hepatis,   coeliac   and   para-aortic   regions. Intra-operative ultra-sound (IOUS) was done in every case. It could provided data about the  anatomical  relations  of  the  metastases to main vessels, also to detect small intra- parenchymatous lesions and thereby modify the extent of initially planned operation. Different types of liver resections were done (anatomical and non-anatomical) with safety margin more than 1cm. The specimens were sent for histopathology. Follow-up of the patients for 1year was done by liver triphasic CT to assess any recurrence.

Statistical analysis:

•      The collected data were computerized and statistically analyzed using SPSS program (Statistical Package for Social Science) version 18.0.

•      Qualitative data were represented as frequencies and relative percentages.

•      Quantitative data were expressed as mean ±SD (Standard deviation).

I-Arithmetic Mean:

| x

 

hepatic  resection  and  lastly  completion  of

chemotherapy.


xr =      n


Where:

 

The protocols used for neo-adjuvant is (m

FOLFOX 6):

•       Oxaliplatin 85 mg/m2 IV over 2 hours, day 1.


| x = sum of individual data.

 

n = number of individual data. II-Standard deviation (SD):

 

 

 

 

 

 

Figure (1): Laparoscopic hepatectomy: marking of tumor, excision of the tumor, homeostasis, liver after excision.

 

 

 

 

2

 

| x2 -


| x i


tumors.     While      metachronous      hepatic metastatic nodules occurred in six (33.3%)

 

SD =


n

n - 1


Where


patients  (two  right  lobe  liver  metastatic

nodules  after  modified radical  mastectomy

 

| x = sum of data

 

| x2  = sum of squares of data. n = number of data.

 

Results:

In our work we found that, the most common primary tumors were colorectal tumors that presented in 13 patients. The most common pathology was adeno-carcinoma grade II. Patient’s demographic data and site of primary tumor are shown in Table (1).

The most common site of liver metastases was the right lobe presented in 14 patients (77.8%). 12 (66.7%) patients had synchronous metastatic nodules presented at the same time with the primary colo- rectal and carcinoid


 

for cancer breast, one left lobe after right hemi-colectomy for right sided cancer colon, one right lobe after pan-hysterectomy for cancer right ovary, bi-lobar liver metastatic nodules  after  abdomino-perineal  operation for cancer lower rectum and one right lobe after abdomino-perineal operation for cancer lower rectum) Figures (2,3). Characters of liver metastatic nodules regarding (site, size, number & time of presentation) are shown in Table (2).

The  operative  time  was  210  min., increased in patients with right hepatectomy with an estimated blood loss 800 ml. Blood transfusions using PRBCs occurred in 14 patients with 1-3 units and FFP in 12 patients with 2-4 units. ICU stay length was about two days for three patients with right hepatectomy.

 

 

 

 

 

 

 

 

Figure (2): Right posterior sector metastasis & simultaneous primary colon cancer and liver metastases resection. A. Resection plane with the umblicated appearance. B. Cut surface after resection. C. Mass after excision. D. Opening of the mass after excision. E. Site of liver metastases after primary colon cancer excision. F. Cut surface after liver metastases excision.

 

 

 

Hospital length of stay for all patients was 9 days Table (3).

Complications occurred in nine patients. Three patients suffered from pleural effusion,


in two of them ascites was found postoperative; all these patients were managed by diuretics and human albumin. Another three patients complained  of  wound  infection  that  was

 

 

 

 

 

 

 

 

Figure (3): Bilobar liver metastases resection, right hepatectomy & left liver metastases. A. Demarcation of left liver metastases excision. B. Demarcation of right liver metastases excision. C. Right lobe hepatectomy. D. CT Abdomen showed left liver metastases. E. Left lateral segment hilum dissection. F. Opening of the liver metastases.

 

 

 

managed by drainage and strong antibiotics. Dyspnea and chest pain was the complaint from one patient diagnosed to have pulmonary embolism, and was managed by therapeutic doses  of  anticoagulant  and  stayed  in  ICU for two days. Last two patients complained of chest infection, which was managed by conservative measures.

Recurrence occurred in four patients during the follow-up period, two of them died. The first patient was male, 32years old with past-history  of  low  anterior  resection then


right hepatectomy for right hepatic metastatic nodule. The pathology was mucinous adeno- carcinoma grad III. He developed multiple liver and lung metastases after 9 months and died from respiratory failure after that by 6 months.

2nd  patient was 40 years old male with

bilobar colorectal metastatic nodules who underwent left lateral hepatectomy plus non anatomical resection of 3 right nodules. He developed multiple right nodules after one year. TACE by 5FU was done but the patient

 

 

Table (1): Patient’s demographic data.

 

Type

Number

Sex:

•   Female

 

 

10 (55.5%)

•   Male

8 (45.5%)

Age (in years):

•   Range

 

 

32-60 yrs.

•   Mean ± SD

50.6 ± 8.2

Site Of 1ry Tumor:

•   Cancer Ovary:

 

 

1case (5.5%)

•   Cancer Breast:

2cases (11.1%)

•   Colorectal Cancer:

13 cases (72.3%)

Lower Rectum

3

Recto-Sigmoid

3

Left Colon

3

Right Colon

3

Transverse Colon

1

•   Carcinoid Tumor:

2 cases (1.1%)

Terminal Ileum

1

Jejunum

1

 

Table (2):Characters of liver metastatic nodules.

 

Type

Number

Site of Liver Mets:

•   Right Lobe

 

 

12 (66.7%)

•   Left Lobe

4 (22.2%)

•   Bi-lobar

2 (11.1%)

Size of Liver Mets (cm):

•   Range

 

 

4-8cm

•   Mean ± SD

5.3 ± 1.5

Number of Liver Mets:

•   Solitary

 

 

14 (77.8%)

•   Two

3 (16.7%)

•   >two1

1(5.5%)

•   Mean ± SD

1.33± 0.77

Time of Presentation:

•   Synchronous

 

 

12 (66.7%)

•   Metachronuous

6 (33.3%)

1 four nodules were presented in one case (male with past history of low anterior resection for

colorectal mass.

 

 

 

died after that by one year from liver cell failure.

3rd  patient was 35 years old female who


underwent right hepatectomy for metastatic carcinoid tumor after right hemicolectomy for terminal ileum mass. She developed recurrent

 

 

Table (3): Patients’ operative data.

 

Type

Number

Range

Mean ± SD

Operative time :

18 (100%)

110 - 320

199.4± 65.1

Blood loss (ml):

18 (100%)

400-1300

805.5 ± 329.8

Blood transfusion :

•   PRBCs (1-3 units)

 

 

14 (77.7%)

 

 

•   FFP (2-4units)

12 (66.6%)

 

 

Hospital stay (days):

18 (100%)

7 - 12

8.4 ± 1.6

ICU stay (days):

3 (16.6%)

1-2

 

Time of operation:

•   Simultaneous

 

 

2 (33.3%)

 

 

•   Classic approach

16 (66.7%)

 

 

Type of operations:

•   Right hepatectomy

 

 

1 (5.5%)

 

 

•   Left lateral hepatectomy

4 (22.2%)

 

 

•   Segment 6,7

2 (11.1%)

 

 

•   Segment 5,6

2 (11.1%)

 

 

•   Segment 6

2 (11.1%)

 

 

•   Segment 7

2 (11.1%)

 

 

•   Segment 8

1 (5.5%)

 

 

•   Non-anatomical

4 (22.2%)

 

 

 

 

 

metastatic nodules in the liver and lung after one and half years, systemic chemotherapy was taken. She is still alive till now.

The last patient was 56 years old male who underwent simultaneous resection of transverse colon with non-anatomical liver resection and removal of coeliac LNs. After one year he developed two small liver nodules with para-aortic LNs and two small lung nodules. Repeated cycles of chemotherapy were taken. He is still alive till now.

 

Discussion:

The liver is most commonly involved organ in metastatic colorectal cancer patients. About 20% of these patients have clinically recognizable liver metastases at the time of their primary diagnosis. After resection of a primary colorectal cancer in the absence of apparent  metastatic  disease,  approximately

50% of the patients will subsequently manifest metastatic liver disease. In our study three patients (3/14) of colorectal cancer developed metachronous metastatic nodules.13


The potential for developing liver metastases from neuro-endocrine tumors depends on the tumor type. Appendiceal carcinoid tumors and insulinomas rarely develop liver metastases, while small bowel carcinoid tumors and other islet cell tumors (including gastrinoma and glucagonoma) develop  hepatic  metastatic  disease  in  up to 40% of the cases.14 Other tumor types including   (renal   cell   carcinoma,   Wilm’s tumor  and  breast  cancer),  although,  they do not metastasize principally to the liver, can occasionally develop isolated liver metastases.1

The   majority   of   patients   diagnosed with metastatic colorectal disease have unresectable  disease.  However,  for  those with    liver-limited    unresectable    disease that cannot be resected unless regression is done, chemotherapy is being considered in highly selected patients trying to downsize colorectal metastases and convert them to a resectable status.15

Surgical    resection    remains    the    only

 

 

 

treatment that can, ensure long-term survival and cure in some patients. However, only a minority of patients with liver metastases is able to surgery. Recent progress including (new chemotherapeutic regimens, ablative techniques and interventional radiology) may allow an increase in the number of patients that can be treated with curative intent.16

Patients with resectable disease may undergo   liver   resection   first,   followed by postoperative adjuvant chemotherapy. Alternatively,  perioperative  (neo-adjuvant plus postoperative) chemotherapy can be used.17 In our study we used the staged resection (resecting of the primary malignant site,     neo-adjuvant     chemotherapy     then liver resection followed by postoperative chemotherapy).

Advantages of preoperative chemotherapy include: earlier treatment of micro-metastatic disease, determination of responsiveness to chemotherapy (which can be prognostic and help in planning postoperative management), and avoidance of local therapy for those patients with early disease progression.18,19 A recent meta-analysis of 27 studies including greater than 7200 patients found that patients with longer disease-free intervals; those, whose recurrences were solitary, smaller, or unilobular; and those lacking extra-hepatic disease derived more benefit from repeat hepatectomy.20 An important point to keep in mind is that irinotecan- and oxaliplatin-based chemotherapeutic regimens may cause liver steato-hepatitis and sinusoidal liver injury, respectively.21,22

To limit the development of hepatotoxicity in patients with initially unresectable disease when chemotherapy is planned, a surgical re- evaluation planned 2 months after initiation of chemotherapy, surgery performed as soon as possible after the patient becomes resectable, and that those patients who continue to receive chemotherapy, surgical re-evaluation every 2 months thereafter.23

In most recent studies, in-hospital mortality varies from 0–5% and is strongly affected by peri-operative blood loss, pre-operative liver function and extent of liver resection. Postoperative  complications  are  observed


in 25% of patients. Morbidity is usually due to transient liver failure, hemorrhage, sub- phrenic abscesses or biliary fistula. The mean hospital stay after liver surgery averages 10–

15 days in the absence of complications.24

We had no major complications, only minor ones which occurred in 9 patients.

Liver resection of colorectal metastases is associated with 3- and 5-year survival rates close to 40% and 25%, respectively. After resection, recurrences are observed in two- thirds of the patients and involve the liver in 50% of the cases. In a large retrospective study, 5- year survival was 28% in 1588 patients who had a resection of isolated colorectal liver metastases and 15% in 250 patients who had resected liver and extra- hepatic metastases.25

To improve prognosis and provide a potential selection of the patients before surgery or for postoperative adjuvant treatment, many studies looked at factors affecting  survival.  The  sex  and  the  site of the primary tumor don›t influence the outcome. Prognosis seems better in cases of metachronous metastases, small lesions, and less than 4 lesions, but the involvement of one or both lobes didn›t influence the outcome. The CEA level is strongly correlated with recurrence-free   survival.   A   free   margin of at least 1 cm offers the best chance of avoiding  recurrence.16  We  had  recurrence in four patients (22.2%). We attributed them to, presence of extra-hepatic LNs, large size tumor in case of carcinoid and aggressive tumor (mucinous adenocarcinoma grade III in case of low anterior resection).

 

Conclusion:

Surgery is the cornerstone of therapeutic approach to patients with hepatic metastases especially colorectal cancer. Liver resection for liver metastases from different primary sites improved 5 years survival when used with the combination with neo-adjuvant chemotherapy. However, with the progress in chemotherapy and local ablative treatments, we can expand the resectable definition in the treatment of liver metastatic disease.

 

 

 

Reference:

1-   Michael  A,  Gregory  B:  Management  of hepatic metastases. Liver Transpl And Surg

1999; 5(1): 65–80.

2-   Tosulfas   G,   Georgios   M,   Kanellos   I: Surgical  treatment  of  hepatic  metastases from colorectal cancer. World J Gastrointest Oncol 2011; 3(1): 1–9.

3-   Van  Cutsem  E,  Nordlinger  B,  Adam  R: Towards   a   pan-European   consensus   on the  treatment  of  patients  with  colorectal liver  metastases.  Eur  J  Cancer  2006;  42:

2212–2222.

4-   Kemeny N: Management of liver metastases from colorectal cancer. Oncology (Williston Park). 2006; 20: 1161–1176.

5-   Alberts    S,    Horvath    W,    Sternfeld    W: 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.

6-   Dawood O, Mahadevan A, Goodman KA: Stereotactic   body   radiation   therapy   for liver  metastases.  Eur  J  Cancer  2009;  45:

2947–2959.

7-   Fong Y, Cohen A, Fortner JG: Liver resection for colorectal metastases. J Clin Oncol 1997;

15: 938–946.

8-   Hayashi    M,    Inoue    Y,    Komeda    K: Clinicopathological analysis of recurrence patterns and prognostic factors for survival after    hepatectomy   for    colorectal   liver metastasis. BMC Surg 2010; 10: 27.

9-   Tsai M, Su Y, Ho M: Clinicopathological features        and    prognosis    in    resectable synchronous and metachronous colorectal liver metastasis. Ann Surg Oncol 2007; 14:

786–794.

10-  Kemeny N, Kemeny M, Lawrence T: Liver Metastases. In: Abeloff M, Armitage J, Niederhuber J, Kastan M, McKenna W, editors. Clinical Oncology. 3rd ed Elsevier Philadelphia 2004: 1141–1178.

11-  Poultsides G, Servais E, Saltz L: Outcome of primary tumor in patients with synchronous stage            IV    colorectal    cancer    receiving combination chemotherapy without surgery as initial treatment. J Clin Oncol 2009; 27:

3379–3384.

12- Andre T, Boni C, Mounedji-Boudiaf L: Oxaliplatin, fluorouracil, and leucovorin as adjuvant treatment for colon cancer. N Engl J Med 2004; 350: 2343–2351.

13-  Landis S, Murray T, Bolden S, Wihgo P:

 

Cancer statistics, 1998. CA Cancer J Clin

1998; 48: 6–29.

14-  Ihse I, Persson B, Tibblin S: Neuro-endocrine metastases of the liver. World J Surg 1995;

19: 76–82.

15- Abdalla E: Commentary: Radiofrequency ablation   for   colorectal   liver   metastases: do not blame the biology when it is the technology. Am J Surg 2009; 197: 737–739.

16- Christophe P, Bernard N: Surgery of liver metastases from colorectal cancer: New promises.  British  Med  Bulletin  2002;  64:

127–140

17-  Araujo R, Gonen M, Allen P: Comparison between perioperative and postoperative chemotherapy  after   potentially   curative hepatic resection for metastatic colorectal cancer. Ann Surg Oncol 2013; 20: 4312–4321.

18-  Bischof D, Clary B, Maithel S, Pawl: Surgical management of disappearing colorectal liver metastases. Br J Surg 2013; 100: 1414–1420.

19- van Vledder M, de Jong M, Pawlik T: Disappearing colorectal liver metastases after chemotherapy: should we be concerned? J Gastrointest Surg 2010; 14: 1691–1700.

20- Luo L, Yu Z, Huang J, Wu H: Selecting patients for a second hepatectomy for colorectal metastases: An systemic review and meta analysis. Eur J Surg Oncol 2014;

40: 1036–1048.

21- Sugarbaker P and Ryan D: Cyto-reductive surgery plus hyper- thermic peri-operative chemotherapy to treats peritoneal metastases from colorectal cancer: Standard of care or an  experimental  approach?  Lancet  Oncol

2012; 13: 362–369.

22- Kishi Y, Zorzi D, Contreras C: Extended preoperative     chemotherapy     does     not improve pathologic response and increases postoperative liver insufficiency after hepatic resection for colorectal liver metastases. Ann Surg Oncol 2010; 17: 2870–2876.

23- Ciliberto D, Prati U, Roveda L: Role of systemic chemotherapy in the management of resected or resectable colorectal liver metastases: A systematic review and meta- analysis of randomized controlled trials. Oncol Rep 2012; 27: 1849–1856.

24- Scheele  J,  Stang  R,  Altendorf-Hofmann A: Resection of colorectal liver metastases. World J Surg 1995; 19: 59–71.

25- Andreou A, Brouquet A, Abdalla E: Repeat hepatectomy for recurrent colorectal liver metastases is associated with a high survival rate. HPB (Oxford). 2011; 13: 774–782.