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Research Article
Risk Factors for Early Recurrence after Liver
Resection for Colorectal Liver Metastases -
Badriya Alaraimi*, Alexia Farrugia, Soulat S Raza, Majid Ali, For Tai Lam,
Saboor Khan, Jawad Ahmad and Gabriele Marangoni
University Hospital Coventry and Warwickshire NHS Trust, Coventry, UK
*Address for Correspondence: Badriya Alaraimi, University Hospital Coventry and Warwickshire,
Clifford Bridge Road Coventry CV2 2DX, Coventry, UK, ORCID ID: 0000-0001-5100-0631;
E-mail:
Submitted: 13 June 2019; Approved: 16 July 2019; Published: 18 July 2019
Cite this article: Alaraimi B, Farrugia A, Raza SS, Ali M, Lam FT, et al. Risk Factors for Early Recurrence
after Liver Resection for Colorectal Liver Metastases. Open J Surg. 2019;3(1): 019-023.
Copyright: © 2019 Alaraimi B, et al. This is an open access article distributed under the Creative
Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any
medium, provided the original work is properly cited.
Open Journal of Surgery
Open Journal of Surgery
SCIRES Literature - Volume 3 Issue 1- www.scireslit.com Page - 020
ABSTRACT
Background: Resectability Criteria for Colorectal Liver Metastases (CRLM) have expanded, and advances in liver surgery have increased the number
of patients eligible for resection. Identifying risk factors for early recurrence to help stratify CRLM patients will contribute to targeted management of these
patients, including surveillance follow-up.
Objectives: To identify risk factors for early recurrence post-resection for CRLM in a contemporary cohort of patients. Early recurrence was defined
based on unit protocol as evidence of recurrent disease on follow-up imaging within one year of surgery.
Methods: From January 2012 to December 2016, 133 patients with CRLM underwent liver resection in our Unit; 115 patients followed up for at least
a year were eligible. We analysed pre-operative variables (sex, age, BMI, comorbidities, CEA and Liver function tests (LFTs), lesion number, size of
largest liver lesion, neoadjuvant chemotherapy), operative variables (anatomical vs non-anatomical, major vs minor, redo liver surgery, concomitant use of
ablation techniques, blood loss, blood transfusions, Pringle’s manoeuvre), and post-operative variables (complications, length of hospital stay, histological
parameters) were analysed.
Results: Sixty-seven early recurrences, including 26 intrahepatic recurrences, were observed. Risk factors for early liver recurrence were number of
metastases > 3 (P = 0.03), intra-operative blood loss > 200 ml (P = 0.02), deployment of ablation techniques (P = 0.008), hospital stay >10 days (P = 0.03),
and capsular invasion (P = 0.04).
Conclusion: Stratification of CRLM patients can help identifying the cohort of patients at high risk of early recurrence, thus helping clinicians counselling
patients appropriately. Accordingly; these high-risk patients might benefit from a more intensive follow-up, although further studies are required.
Keywords: Colorectal liver metastasis; Liver resection; Early recurrence
INTRODUCTION
The liver is the most common site for Colorectal Metastasis
(CRLM), and resection offers the best chance of cure in suitable
patients [1]. The purpose of liver resection is to remove all neoplastic
disease with a negative margin and leave adequately functioning liver
parenchyma [2]. Repeated hepatectomies to prolong survival and
benefits are not uncommon among patients [3]. Over the last decades’
new developments such as high-definition cross-sectional imaging,
better neoadjuvant chemotherapy, and improved peri-operative care,
have increased survival after liver resection [4]. However, about 60%
of patients who undergo resection for CRLM will still experience
recurrence of disease [5]. Resectability criteria have expanded, and
advances in liver surgery have increased the number of patients
eligible for resection. As such patients previously deemed inoperable
are now offered resectional surgery, with the potential consequence
of increase rate of recurrence. Only few studies have assessed the
factors leading to early recurrence in CRLM. Identifying these factors
will help stratify CRLM patients for targeted management [6] as well
as surveillance protocols. Intensive follow-up can result in earlier
detection of recurrences and an increased detection rate of isolated
local recurrences [5]. The definition of early recurrence varies in the
literature from one unit to another, and it can range from 6 to 24
months [4,6,7]. Recurrence is defined as recurrent disease in follow-
up imaging after surgery [8].
The aim of this study is to analyse pre-operative, operative and
post-operative parameters to identify factors that contribute to early
recurrence and to establish a scoring system that will enable patient
stratification according to the risk of early recurrence after resection.
METHODS
Study cohort
From January 2012 to December 2016, 133 patients with CRLM
underwent liver resection in our unit. All subjects involved in the
study consented via written consent when they come for their
intervention in line with the trust policy and clinical governance. Only
those who agreed their data to be used in research/publication were
involved. Throughout the data analysis the data set was anonymized
and no breach in confidentiality was reassured. We did not obtain
ethical approval as it is not necessary; as in this occasion we did not
do any clinical trial to the study population. This was an observational
study for those cohort of patients and data was obtained from the unit
prospectively collected database for analysis.
Inclusion criteria were patients who underwent liver resection
for CRLM, who were followed-up for at least one year. We identified
115 patients who were eligible for the study. Early recurrence was
defined as evidence of recurrent disease on CT or Liver MRI within a
year from liver surgery.
Pre-operative, intra-operative, post-operative and follow-up data
were collected from the prospectively maintained Unit database.
Pre-operative and post-operative investigations/analysis
There is a well-maintained unit database for CRLM cases where all
patients’ information and pre-operative/ post-operative parameters
were collected. Those cases were discussed in multidisciplinary team
meetingsometimemorethanonce.Theyhadfullassessmentincluding
fitness for resection; clinically and via cardiopulmonary exercise tests.
Patients who received pre-operative neoadjuvant chemotherapy had
surgery, on average, 6 weeks later. Intra-operative ultrasound was
used when the tumour was not obvious or to clarify the anatomy and
relation to vascular structures. Accompanying ablation techniques
were performed in some patients. All operations performed either by
two consultants or a consultant and senior fellow.
Clinico-pathological parameters
The parameters analysed included pre-operative variables
(sex, age, BMI, comorbidities, CEA and LFTs, lesion number,
size of largest liver lesion, neoadjuvant chemotherapy), operative
variables (anatomical vs non-anatomical, major vs minor, redo liver
surgery, concomitant use of ablation techniques, blood loss, blood
transfusions, Pringle’s manoeuvre), and post-operative variables
(complications, length of hospital stay, histology parameters). This
work has been reported in line with the STROCSS criteria [9].
Statistical analysis
Statistical analysis was performed using IBM SPSS version 22, and
the significance level was set at p < 0.05. Descriptive statistics were
reported, and summary statistics were constructed for the baseline
Open Journal of Surgery
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variables, using frequencies and proportions for categorical data and
medians and ranges for continuous variables. Categorical outcomes
were analysed using the chi‐squared test, and continuous variables
were compared using Student’s t-test and the Mann–Whitney U test
accordingly.
Univariate and multivariate analyses were performed to identify
risk factors contributing to early recurrence. A multiple regression
model was also performed to detect simultaneous significant variables
in predicting recurrence within one year.
RESULTS
133 patients were included in the study, of which 81 (60.9%) were
male. The median age was 66 (SD +/- 10.81), with an age range of 25
to 84. Mean ASA grade was 2.23 and mean WHO performance status
was 0.7. Mean BMI was 27.16 (range 16-42).
Mean liver function test results pre-operatively, on day one and
on day five post-operatively are shown in table 1.
The mean Pringle manoeuvre duration of 10.85 minutes and the
mean length of stay in hospital was 7.5 days (SD = 3.8).
There were 67 (58.2%) early recurrences, of which 26 (22.6%)
were intrahepatic. Descriptive statistics are displayed as the mean ±
SD and median for various variables.
Analyses of the pre-operative, operative and post-operative
factors were performed to determine which factors could predict
CRLM recurrence within one year (Table 2). Risk factors for early
liver recurrence were number of metastases > 3 (OR 0.103; p =
0.03), intra-operative blood loss > 200 ml (OR 0.244 p = 0.02), use of
ablation techniques (OR 0.292 p = 0.008), hospital stay > 10 days (OR
0.295 p = 0.03) and capsular invasion (OR 0.434 p = 0.04).
A multiple regression model was generated (Table 3), and it
showed that these simultaneous significant variables were significant
in predicting recurrence within one year:
• Anatomical resection
• Ablation
• Microvascular infiltration
• Longer length of hospital stay
• Post-op packed Red Blood Cell (RBC) transfusions
DISCUSSION
This study demonstrated that the factors influencing early
recurrence in CRLM are major hepatectomies, presence of more
than three hepatic lesions, use of ablation, microvascular invasion,
prolonged hospital stay and post-operative blood transfusions. Early
hepatic recurrence was 22%, comparable to published studies that
quote figures between 20% and 56.7% [10,11]. Several studies have
been carried out to investigate risks of recurrence.
Shin et al. (2012) used Fong’s clinical risk score to predict
recurrence, employed to predict survival, and found that patients
with a higher clinical risk score were indeed more likely to develop
recurrence. [12] However, most studies focused on overall tumour-
free survival rather than early recurrence [13].
Some studies identify the number of liver lesions as a predictive
factor of overall recurrence and early recurrence [12-14]. However,
timelines used to define early recurrence range between 6 and 18
months due to lack of a standardised definition [7,11,15,16], making
it difficult to predict exactly what constitutes early recurrence.
Imai et al (2017) found that concurrent radiofrequency ablation
with hepatectomies did not increase recurrence rate. However, our
data suggested that radiofrequency ablation is both an independent
predictor of early recurrence as well as a predictor when combined
with other factors [17]. This agrees with results from other published
work in the literature [10,16,18]. Ablation patients might have
increased recurrence rates because it is likely that they have more
advanced disease that cannot be cleared by surgery alone.
Furthermore, we found that postoperative blood transfusion was
predictive of earlier recurrence, as also reported by Postlewait et al.
(2016). In this study, the authors showed that more than 3 units of
blood transfusion was significantly related to early recurrences [19].
The relationship between transfusion and recurrence of cancer can
be explained by the immunosuppressive effect of blood transfusion;
where there is persistent post-operative inflammatory response which
contribute to both growth in cancer cells and reduced cell-mediated
immunity collectively leading to increase chances of recurrence of
CRLM [20]. From our data, it also appears that more than 200mls
of blood loss intraoperatively was associated with earlier recurrence.
The number of chemotherapy cycles has been shown to be of
value when it comes to predicting early recurrence [7]. However,
in our study we could not demonstrate the effect of neoadjuvant
chemotherapy in reducing recurrence rates. Although statistically
not significant the overall number of cycles of chemotherapy before
surgery shows some association with increased early recurrence
which can be justified by disease aggressiveness.
Other tumour characteristics associated with early recurrence
in some studies include bilobar metastases and larger tumour size
[11,12], as well as a timeframe of less than 30 months between
colorectal tumour and initial liver metastases [13]. Our data did not
reveal these factors to be significant [10].
We found that a hospital stay of more than 10 days increases
the risk of early recurrence, and this has also been suggested by
previous studies [21]. Those patients who needed to stay longer had
either a more complex resection due to disease extent or increased
complication rates with consequent negative effect on the immune
system.
While our study found no significant earlier recurrence
with smaller resection margins, several studies states differently.
Intrahepatic recurrence may be associated with microsatellite
metastases around the main tumour [22], and a positive surgical
margin influences surgical site recurrence [14]. We did find that
capsular and microvascular infiltration may be an indication for early
recurrence.
Thus, we can conclude that patients with certain characteristics,
namely higher number of tumours, intraoperative blood loss,
concurrent intraoperative ablation and with longer hospital stay are
Table 1: Liver function test pre-and post-operative
ALT Bilirubin INR
Pre-op 23.6 8.3 0.97
Post-op day 1 373.24 19.4 1.2
Post-op day 5 138.65 12.3 0.85
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Table 2: Analysis of variables
Variables OR (P-value) Analysis
Gender M vs F 1.5 (0.321)
No effect of Gender on recurrence. More females are affected but not
significantly
Age > 65yrs old or < 65yrs old 0.98 (0.96) No effect of Age on recurrence
Body mass index (BMI) 0.91 (0.069)
No effect of BMI on recurrence. Less recurrence for lower BMI but not
significantly
Diabetes mellitus (NIDDM/IDDM)
1.833 (0.662) IDDM to NIDDM
1.96 (0.397) N to NIDDM
No effect of NIDDM/IDDM on recurrence. Less recurrence for NIDDM but
not significantly.
Pre-op ALT (< 20, 20-40, > 40)
1.89 (0.44) < 20 to > 40
1.18 (0.844) 2-40 to > 40
No effect of PreOp ALT on recurrence. Less recurrence for more than 40
but not significantly.
Pre-op Bilirubin 0.968 (0.496)
No effect of Bilirubin on recurrence. Less recurrence for higher bilirubin but
not significantly.
Pre-op Carcinoembryonic Antigen
(CEA)
1.000 (0.958) No effect of CEA on recurrence.
ASA status
000 (.999) 1 to 3
0.906 (0.824) 2 to 3
No effect of ASA on recurrence. Not enough data for status 1
Number of liver lesions (1-3, 3 lesions,
> 3 lesions)
0.328 (0.012) 1-2 to > 3
0.103 (0.037) 3 to > 3
Lower risk for 1-3 as compare to > 3 lesions.
Lower risk for 3 as compare to > 3 lesions.
3 lesions has the lowest risk
Size of largest lesion 1.048 (0.624) No effect of Size of largest lesion on recurrence.
Segments involved (Segments 1,2,3,4
or Segments 5,6,7,8)
.625 (,424) 1-4 to both
.614 (.270) 5-8 to both
No effect
Neoadjuvant chemotherapy 0.565 (0.175)
No effect of Neoadjuvant chemotherapy on recurrence. Lower risk with No
but not significantly
Number of cycles of chemotherapy ( <
6,6, 8, > 8)
1.13 (.055) More risk is associated with more cycle
Liver surgery (anatomical, non-
anatomical)
2.14 (.102) A to NA
2.54 (.083) A + NA to NA
No effect
Surgical approach (laparoscopic or
open)
0.422 (0.273)
No effect of Surgical approach on recurrence. Lower risk with laparoscopic
but not significantly
Major hepatectomy (yes or no) 0.44 (0.053) Major hepatectomies has a higher risk of recurrence
Redo hepatectomy (yes or no) 0.813 (0.697)
No effect of Redo hepatectomy on recurrence. Lower risk with No but not
significantly
IOUS (yes or no) .938 (,89) No effect
Ablation techniques (yes or no) 0.292 (0.008) Use of ablation techniques increase risk of recurrence
Blood loss (< 200ml, 20-500ml, >
500ml)
0.244 (0.021); 200 to > 500
0.28 (.046) 200-500 to > 500
Less blood loss is significantly associated to lower recurrence risk
Post-op blood transfusion (RBC
transfusion)
2.44 (0.11) No effect, more blood transfusion more risk but not significantly
Pringle’s time (nil, < 15 minutes, 15-30
minutes, 30-45minutes, > 45 minutes)
.880 (.85) 0 to > 30
.875 (.87) 0-15 to > 30
.375 (.37) 15 -30 to > 30
No effect
POD1 ALT 1.00 (0.569) No effect
POD1 Bilirubin 1.002 (0.807) No effect
POD 1 INR 0.912 (.836) No effect
POD5 ALT 1.001 (.225) No effect
POD5 Bilirubin 1.01 (.501) No effect
POD 5 INR 2.37 (.738) No effect
Complication (bile leak, intra-
abdominal collection)
1.56 (.379) No effect
Length of stay (5 days, 6-10 days, >
10 days)
.55 (.33) 5 comp. to > 10
.295 (.037) 6-10 com. to > 10
6 to10 days has significantly less risk compare to > 10 days
Distance from resection margin (mm)
(Positive margin = 0, 1-5mm, 6-10 mm,
> 10mm)
1.650 (.433) 0 to > 10
1.000 (1.000) 1-5 to > 10
.529 (.433) 6-10 > 10
No effect
Histology grading Not enough data No Effect
Microvascular infiltration .347 (0.12) No has significantly lower risk
Capsular invasion .434 (.045) No has significantly lower risk
Hepatic Steatosis (yes or no) No effect
Open Journal of Surgery
SCIRES Literature - Volume 3 Issue 1- www.scireslit.com Page - 023
at a higher risk for early recurrence and will need a more intensive
follow up postoperatively.
Further studies might help to further delineate the risk factors for
early colorectal liver metastases recurrence.
ACKNOWLEDGEMENT
The assistance of Mr. William Turner and his team from All Stats
for their contribution in the data analysis.
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early recurrence after curative hepatectomy for colorectal liver metastases.
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Table 3: Multiple regression analysis of factors related to early recurrence of CRLM.
Variables associated with early recurrence Standard error Odds ratio P-value
Anatomical resection 0.796 6.06 0.024
Ablation 0.768 1.62 0.018
Presence of microvascular infiltration 0.606 1.69 0.003
Longer length of stay 0.953 1.16 0.024
Post-op blood transfusions 1.429 37.39 0.011

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Open Journal of Surgery

  • 1. Research Article Risk Factors for Early Recurrence after Liver Resection for Colorectal Liver Metastases - Badriya Alaraimi*, Alexia Farrugia, Soulat S Raza, Majid Ali, For Tai Lam, Saboor Khan, Jawad Ahmad and Gabriele Marangoni University Hospital Coventry and Warwickshire NHS Trust, Coventry, UK *Address for Correspondence: Badriya Alaraimi, University Hospital Coventry and Warwickshire, Clifford Bridge Road Coventry CV2 2DX, Coventry, UK, ORCID ID: 0000-0001-5100-0631; E-mail: Submitted: 13 June 2019; Approved: 16 July 2019; Published: 18 July 2019 Cite this article: Alaraimi B, Farrugia A, Raza SS, Ali M, Lam FT, et al. Risk Factors for Early Recurrence after Liver Resection for Colorectal Liver Metastases. Open J Surg. 2019;3(1): 019-023. Copyright: © 2019 Alaraimi B, et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Open Journal of Surgery
  • 2. Open Journal of Surgery SCIRES Literature - Volume 3 Issue 1- www.scireslit.com Page - 020 ABSTRACT Background: Resectability Criteria for Colorectal Liver Metastases (CRLM) have expanded, and advances in liver surgery have increased the number of patients eligible for resection. Identifying risk factors for early recurrence to help stratify CRLM patients will contribute to targeted management of these patients, including surveillance follow-up. Objectives: To identify risk factors for early recurrence post-resection for CRLM in a contemporary cohort of patients. Early recurrence was defined based on unit protocol as evidence of recurrent disease on follow-up imaging within one year of surgery. Methods: From January 2012 to December 2016, 133 patients with CRLM underwent liver resection in our Unit; 115 patients followed up for at least a year were eligible. We analysed pre-operative variables (sex, age, BMI, comorbidities, CEA and Liver function tests (LFTs), lesion number, size of largest liver lesion, neoadjuvant chemotherapy), operative variables (anatomical vs non-anatomical, major vs minor, redo liver surgery, concomitant use of ablation techniques, blood loss, blood transfusions, Pringle’s manoeuvre), and post-operative variables (complications, length of hospital stay, histological parameters) were analysed. Results: Sixty-seven early recurrences, including 26 intrahepatic recurrences, were observed. Risk factors for early liver recurrence were number of metastases > 3 (P = 0.03), intra-operative blood loss > 200 ml (P = 0.02), deployment of ablation techniques (P = 0.008), hospital stay >10 days (P = 0.03), and capsular invasion (P = 0.04). Conclusion: Stratification of CRLM patients can help identifying the cohort of patients at high risk of early recurrence, thus helping clinicians counselling patients appropriately. Accordingly; these high-risk patients might benefit from a more intensive follow-up, although further studies are required. Keywords: Colorectal liver metastasis; Liver resection; Early recurrence INTRODUCTION The liver is the most common site for Colorectal Metastasis (CRLM), and resection offers the best chance of cure in suitable patients [1]. The purpose of liver resection is to remove all neoplastic disease with a negative margin and leave adequately functioning liver parenchyma [2]. Repeated hepatectomies to prolong survival and benefits are not uncommon among patients [3]. Over the last decades’ new developments such as high-definition cross-sectional imaging, better neoadjuvant chemotherapy, and improved peri-operative care, have increased survival after liver resection [4]. However, about 60% of patients who undergo resection for CRLM will still experience recurrence of disease [5]. Resectability criteria have expanded, and advances in liver surgery have increased the number of patients eligible for resection. As such patients previously deemed inoperable are now offered resectional surgery, with the potential consequence of increase rate of recurrence. Only few studies have assessed the factors leading to early recurrence in CRLM. Identifying these factors will help stratify CRLM patients for targeted management [6] as well as surveillance protocols. Intensive follow-up can result in earlier detection of recurrences and an increased detection rate of isolated local recurrences [5]. The definition of early recurrence varies in the literature from one unit to another, and it can range from 6 to 24 months [4,6,7]. Recurrence is defined as recurrent disease in follow- up imaging after surgery [8]. The aim of this study is to analyse pre-operative, operative and post-operative parameters to identify factors that contribute to early recurrence and to establish a scoring system that will enable patient stratification according to the risk of early recurrence after resection. METHODS Study cohort From January 2012 to December 2016, 133 patients with CRLM underwent liver resection in our unit. All subjects involved in the study consented via written consent when they come for their intervention in line with the trust policy and clinical governance. Only those who agreed their data to be used in research/publication were involved. Throughout the data analysis the data set was anonymized and no breach in confidentiality was reassured. We did not obtain ethical approval as it is not necessary; as in this occasion we did not do any clinical trial to the study population. This was an observational study for those cohort of patients and data was obtained from the unit prospectively collected database for analysis. Inclusion criteria were patients who underwent liver resection for CRLM, who were followed-up for at least one year. We identified 115 patients who were eligible for the study. Early recurrence was defined as evidence of recurrent disease on CT or Liver MRI within a year from liver surgery. Pre-operative, intra-operative, post-operative and follow-up data were collected from the prospectively maintained Unit database. Pre-operative and post-operative investigations/analysis There is a well-maintained unit database for CRLM cases where all patients’ information and pre-operative/ post-operative parameters were collected. Those cases were discussed in multidisciplinary team meetingsometimemorethanonce.Theyhadfullassessmentincluding fitness for resection; clinically and via cardiopulmonary exercise tests. Patients who received pre-operative neoadjuvant chemotherapy had surgery, on average, 6 weeks later. Intra-operative ultrasound was used when the tumour was not obvious or to clarify the anatomy and relation to vascular structures. Accompanying ablation techniques were performed in some patients. All operations performed either by two consultants or a consultant and senior fellow. Clinico-pathological parameters The parameters analysed included pre-operative variables (sex, age, BMI, comorbidities, CEA and LFTs, lesion number, size of largest liver lesion, neoadjuvant chemotherapy), operative variables (anatomical vs non-anatomical, major vs minor, redo liver surgery, concomitant use of ablation techniques, blood loss, blood transfusions, Pringle’s manoeuvre), and post-operative variables (complications, length of hospital stay, histology parameters). This work has been reported in line with the STROCSS criteria [9]. Statistical analysis Statistical analysis was performed using IBM SPSS version 22, and the significance level was set at p < 0.05. Descriptive statistics were reported, and summary statistics were constructed for the baseline
  • 3. Open Journal of Surgery SCIRES Literature - Volume 3 Issue 1- www.scireslit.com Page - 021 variables, using frequencies and proportions for categorical data and medians and ranges for continuous variables. Categorical outcomes were analysed using the chi‐squared test, and continuous variables were compared using Student’s t-test and the Mann–Whitney U test accordingly. Univariate and multivariate analyses were performed to identify risk factors contributing to early recurrence. A multiple regression model was also performed to detect simultaneous significant variables in predicting recurrence within one year. RESULTS 133 patients were included in the study, of which 81 (60.9%) were male. The median age was 66 (SD +/- 10.81), with an age range of 25 to 84. Mean ASA grade was 2.23 and mean WHO performance status was 0.7. Mean BMI was 27.16 (range 16-42). Mean liver function test results pre-operatively, on day one and on day five post-operatively are shown in table 1. The mean Pringle manoeuvre duration of 10.85 minutes and the mean length of stay in hospital was 7.5 days (SD = 3.8). There were 67 (58.2%) early recurrences, of which 26 (22.6%) were intrahepatic. Descriptive statistics are displayed as the mean ± SD and median for various variables. Analyses of the pre-operative, operative and post-operative factors were performed to determine which factors could predict CRLM recurrence within one year (Table 2). Risk factors for early liver recurrence were number of metastases > 3 (OR 0.103; p = 0.03), intra-operative blood loss > 200 ml (OR 0.244 p = 0.02), use of ablation techniques (OR 0.292 p = 0.008), hospital stay > 10 days (OR 0.295 p = 0.03) and capsular invasion (OR 0.434 p = 0.04). A multiple regression model was generated (Table 3), and it showed that these simultaneous significant variables were significant in predicting recurrence within one year: • Anatomical resection • Ablation • Microvascular infiltration • Longer length of hospital stay • Post-op packed Red Blood Cell (RBC) transfusions DISCUSSION This study demonstrated that the factors influencing early recurrence in CRLM are major hepatectomies, presence of more than three hepatic lesions, use of ablation, microvascular invasion, prolonged hospital stay and post-operative blood transfusions. Early hepatic recurrence was 22%, comparable to published studies that quote figures between 20% and 56.7% [10,11]. Several studies have been carried out to investigate risks of recurrence. Shin et al. (2012) used Fong’s clinical risk score to predict recurrence, employed to predict survival, and found that patients with a higher clinical risk score were indeed more likely to develop recurrence. [12] However, most studies focused on overall tumour- free survival rather than early recurrence [13]. Some studies identify the number of liver lesions as a predictive factor of overall recurrence and early recurrence [12-14]. However, timelines used to define early recurrence range between 6 and 18 months due to lack of a standardised definition [7,11,15,16], making it difficult to predict exactly what constitutes early recurrence. Imai et al (2017) found that concurrent radiofrequency ablation with hepatectomies did not increase recurrence rate. However, our data suggested that radiofrequency ablation is both an independent predictor of early recurrence as well as a predictor when combined with other factors [17]. This agrees with results from other published work in the literature [10,16,18]. Ablation patients might have increased recurrence rates because it is likely that they have more advanced disease that cannot be cleared by surgery alone. Furthermore, we found that postoperative blood transfusion was predictive of earlier recurrence, as also reported by Postlewait et al. (2016). In this study, the authors showed that more than 3 units of blood transfusion was significantly related to early recurrences [19]. The relationship between transfusion and recurrence of cancer can be explained by the immunosuppressive effect of blood transfusion; where there is persistent post-operative inflammatory response which contribute to both growth in cancer cells and reduced cell-mediated immunity collectively leading to increase chances of recurrence of CRLM [20]. From our data, it also appears that more than 200mls of blood loss intraoperatively was associated with earlier recurrence. The number of chemotherapy cycles has been shown to be of value when it comes to predicting early recurrence [7]. However, in our study we could not demonstrate the effect of neoadjuvant chemotherapy in reducing recurrence rates. Although statistically not significant the overall number of cycles of chemotherapy before surgery shows some association with increased early recurrence which can be justified by disease aggressiveness. Other tumour characteristics associated with early recurrence in some studies include bilobar metastases and larger tumour size [11,12], as well as a timeframe of less than 30 months between colorectal tumour and initial liver metastases [13]. Our data did not reveal these factors to be significant [10]. We found that a hospital stay of more than 10 days increases the risk of early recurrence, and this has also been suggested by previous studies [21]. Those patients who needed to stay longer had either a more complex resection due to disease extent or increased complication rates with consequent negative effect on the immune system. While our study found no significant earlier recurrence with smaller resection margins, several studies states differently. Intrahepatic recurrence may be associated with microsatellite metastases around the main tumour [22], and a positive surgical margin influences surgical site recurrence [14]. We did find that capsular and microvascular infiltration may be an indication for early recurrence. Thus, we can conclude that patients with certain characteristics, namely higher number of tumours, intraoperative blood loss, concurrent intraoperative ablation and with longer hospital stay are Table 1: Liver function test pre-and post-operative ALT Bilirubin INR Pre-op 23.6 8.3 0.97 Post-op day 1 373.24 19.4 1.2 Post-op day 5 138.65 12.3 0.85
  • 4. Open Journal of Surgery SCIRES Literature - Volume 3 Issue 1- www.scireslit.com Page - 022 Table 2: Analysis of variables Variables OR (P-value) Analysis Gender M vs F 1.5 (0.321) No effect of Gender on recurrence. More females are affected but not significantly Age > 65yrs old or < 65yrs old 0.98 (0.96) No effect of Age on recurrence Body mass index (BMI) 0.91 (0.069) No effect of BMI on recurrence. Less recurrence for lower BMI but not significantly Diabetes mellitus (NIDDM/IDDM) 1.833 (0.662) IDDM to NIDDM 1.96 (0.397) N to NIDDM No effect of NIDDM/IDDM on recurrence. Less recurrence for NIDDM but not significantly. Pre-op ALT (< 20, 20-40, > 40) 1.89 (0.44) < 20 to > 40 1.18 (0.844) 2-40 to > 40 No effect of PreOp ALT on recurrence. Less recurrence for more than 40 but not significantly. Pre-op Bilirubin 0.968 (0.496) No effect of Bilirubin on recurrence. Less recurrence for higher bilirubin but not significantly. Pre-op Carcinoembryonic Antigen (CEA) 1.000 (0.958) No effect of CEA on recurrence. ASA status 000 (.999) 1 to 3 0.906 (0.824) 2 to 3 No effect of ASA on recurrence. Not enough data for status 1 Number of liver lesions (1-3, 3 lesions, > 3 lesions) 0.328 (0.012) 1-2 to > 3 0.103 (0.037) 3 to > 3 Lower risk for 1-3 as compare to > 3 lesions. Lower risk for 3 as compare to > 3 lesions. 3 lesions has the lowest risk Size of largest lesion 1.048 (0.624) No effect of Size of largest lesion on recurrence. Segments involved (Segments 1,2,3,4 or Segments 5,6,7,8) .625 (,424) 1-4 to both .614 (.270) 5-8 to both No effect Neoadjuvant chemotherapy 0.565 (0.175) No effect of Neoadjuvant chemotherapy on recurrence. Lower risk with No but not significantly Number of cycles of chemotherapy ( < 6,6, 8, > 8) 1.13 (.055) More risk is associated with more cycle Liver surgery (anatomical, non- anatomical) 2.14 (.102) A to NA 2.54 (.083) A + NA to NA No effect Surgical approach (laparoscopic or open) 0.422 (0.273) No effect of Surgical approach on recurrence. Lower risk with laparoscopic but not significantly Major hepatectomy (yes or no) 0.44 (0.053) Major hepatectomies has a higher risk of recurrence Redo hepatectomy (yes or no) 0.813 (0.697) No effect of Redo hepatectomy on recurrence. Lower risk with No but not significantly IOUS (yes or no) .938 (,89) No effect Ablation techniques (yes or no) 0.292 (0.008) Use of ablation techniques increase risk of recurrence Blood loss (< 200ml, 20-500ml, > 500ml) 0.244 (0.021); 200 to > 500 0.28 (.046) 200-500 to > 500 Less blood loss is significantly associated to lower recurrence risk Post-op blood transfusion (RBC transfusion) 2.44 (0.11) No effect, more blood transfusion more risk but not significantly Pringle’s time (nil, < 15 minutes, 15-30 minutes, 30-45minutes, > 45 minutes) .880 (.85) 0 to > 30 .875 (.87) 0-15 to > 30 .375 (.37) 15 -30 to > 30 No effect POD1 ALT 1.00 (0.569) No effect POD1 Bilirubin 1.002 (0.807) No effect POD 1 INR 0.912 (.836) No effect POD5 ALT 1.001 (.225) No effect POD5 Bilirubin 1.01 (.501) No effect POD 5 INR 2.37 (.738) No effect Complication (bile leak, intra- abdominal collection) 1.56 (.379) No effect Length of stay (5 days, 6-10 days, > 10 days) .55 (.33) 5 comp. to > 10 .295 (.037) 6-10 com. to > 10 6 to10 days has significantly less risk compare to > 10 days Distance from resection margin (mm) (Positive margin = 0, 1-5mm, 6-10 mm, > 10mm) 1.650 (.433) 0 to > 10 1.000 (1.000) 1-5 to > 10 .529 (.433) 6-10 > 10 No effect Histology grading Not enough data No Effect Microvascular infiltration .347 (0.12) No has significantly lower risk Capsular invasion .434 (.045) No has significantly lower risk Hepatic Steatosis (yes or no) No effect
  • 5. Open Journal of Surgery SCIRES Literature - Volume 3 Issue 1- www.scireslit.com Page - 023 at a higher risk for early recurrence and will need a more intensive follow up postoperatively. Further studies might help to further delineate the risk factors for early colorectal liver metastases recurrence. ACKNOWLEDGEMENT The assistance of Mr. William Turner and his team from All Stats for their contribution in the data analysis. REFERENCES 1. McNally SJ, Parks RW. Surgery for colorectal liver metastases. Dig Surg. 2013; 30: 337-347. https://bit.ly/2SiszJH 2. Garden OJ, Rees M, Poston GJ, Mirza D, Saunders M, Ledermann J, et al. Guidelines for resection of colorectal cancer liver metastases. Gut. 2006; 55 Suppl 3: iii1-8. https://bit.ly/2NUxsKA 3. Yang KH, Ryu JH, Moon KM, Chu CW. More than 7-year survival of a patient following repeat hepatectomy for total 20 colon cancer liver metastases. J Korean Surg Soc. 2012; 82: 128-133. https://bit.ly/2XHRRak 4. 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Presence of microsatellite lesions with colorectal liver metastases correlate with intrahepatic recurrence after surgical resection. Oncol Rep. 2009; 21: 601-607. https://bit.ly/2XMag0M Table 3: Multiple regression analysis of factors related to early recurrence of CRLM. Variables associated with early recurrence Standard error Odds ratio P-value Anatomical resection 0.796 6.06 0.024 Ablation 0.768 1.62 0.018 Presence of microvascular infiltration 0.606 1.69 0.003 Longer length of stay 0.953 1.16 0.024 Post-op blood transfusions 1.429 37.39 0.011