J Cancer 2024; 15(3):610-614. doi:10.7150/jca.90519 This issue Cite
Research Paper
1. 3 rd Department of Surgery, ``AHEPA`` University Hospital, Aristotle University of Thessaloniki, Medical School, Thessaloniki, Greece.
2. Surgery Department, General Clinic Private Hospital, Thessaloniki, Greece.
3. Oncology Department, General Hospital of Kavala, Greece.
4. Oncology Department, General Hospital of Volos, Greece.
5. Oncology Department, General Hospital of Serres, Greece.
6. Surgery Department, Genesis Private Clinic, Thessaloniki, Greece.
7. Oncology Department, General Hospital of Rhodes, Rhodes, Greece.
8. Second Department of Surgery, University Hospital of Alexandroupolis, Medical School, Democritus University of Thrace, Alexandroupolis, Greece.
9. Gastroenterologist, Private Cabinet, Thessaloniki, Greece.
10. Pathology Department, University of Cyprus, Cyprus.
11. Third Department of Obstetrics and Gynecology, University General Hospital “ATTIKON”, Medical School of the National and Kapodistrian University of Athens, Athens, Greece.
12. Oncology Department, University General Hospital of Larissa, University of Thessaly, Greece.
Nowadays we perform synchronous colorectal cancer resection along with synchronous liver metastases. We investigated whether colon resection first is safer than liver resection first and if simultaneous surgeries are in general safe.
Patients and Methods: Twenty patients were included in our multicenter study. In our study patients had simultaneous laparoscopic resection of primary colorectal cancer and liver metastases. The patients included were divided into two groups based on their first surgery. Group A had colon resection first (n = 10) and group B had liver resection first (n = 10). All adverse effects and outcomes were compared after the first day of hospitalization.
Results: The only difference between the two groups was the operative blood loss. It was observed to be less in group B.
Conclusion: In our study we did not observe any significant difference regarding the order of the operation.
Keywords: colon cancer, liver metastasis, simultaneous liver metastasis surgery
Colorectal cancer is a very common type of cancer. Colorectal liver metastases (CRLMs) are observed upon diagnosis in up to 50% of patients with colorectal [1, 2]. Nowadays we have the diagnostic tools and treatment techniques to treat both liver metastases (SLMs) and colon cancer. Liver metastases is an independent prognostic factor for the survival of colon cancer patients [3-5]. In the case of unresectable liver metastases then we can use chemotherapy along with local ablation techniques and then perform hepatectomy with excellent results [6, 7]. It has been previously published that simultaneous resection of primary colon cancer and liver metastases is associated with similar oncological outcomes [8]. In any case when unresectable liver matastasis are diagnosed chemotherapy is administered first along with local therapy when applicable. In the case were both colon cancer and liver metastases are resectable then silmutaneous surgical resection is an option. Simultaneous resection is possible in a single operation. Although it was considered until recently that simultaneous resection might increase postoperative complications, recent published data elucidated that postoperative complications rates were very low due to novel diagnostic and surgical equipment [9],[10], and moreover the length of hospital stay and cost was lower [11] (Figure 1). Until recently the safety of simultaneous resection was unclear. Moreover; the best surgical order regarding complications (colon first or liver-first approach) was not been evaluated. Simultaneous laparoscopic resection of primary tumor and liver metastases is definitely feasible and it has been previously performed [12]. Furthermore; previously published data reported fewer postoperative complications [12, 13]. However; we still need more studies to elucidate the proper order in silmutaneous primary colon cancer with liver metastasis.
In our multicenter retrospective study we recruited twenty patients who had simultaneous resection of primary colon cancer and liver metastasis. We divided the patients into two groups, group A and B based on the operative order. In group A; there was Colon-first operation and in group B liver-first operation. All clinical, operative and postoperative complications were recorded and compared. The study was approved by the investigational review board of 3rd Department of Surgery, ``AHEPA`` University Hospital, Aristotle University of Thessaloniki, Medical School, Thessaloniki, Greece study protocol (January 2020-March 2022) IRB approval number 12/2019 and the study was carried out in accordance with the Declaration of Helsinki.
We collected data regarding the: sex, age, body mass index (BMI), primary tumor site (right/left/rectal), primary tumor diameter, number of involved hepatic segments American Society of Anesthetists-physical status, number of metastatic liver lesions, largest diameter of liver metastases. Moreover; we recorded the presence or absence of preoperative chemotherapy, and chemotherapy regimen along with lobar surgical resection. The surgical approach was categorized as; right colon, left colon and rectal colon. The operative order was left to the surgeon's opinion.
Main characteristics are presented in Table I. In our study we had 10 patients in group A and 10 in group B. No significant differences were observed in demographics. The position of the primary colorectal cancer was right/left/rectum in 8/8/4. We observed in group B a significantly higher rates of rectal cancer compared to that of the group A. The mean primary tumor diameter was 39±13 mm.
'Antisel' new laparoscopic equipment.
Demographic, clinical, and surgical characteristics of study patients
APPROACH | |||||
---|---|---|---|---|---|
Demographic | Total (N=20) | Primary first (N=10) | Liver first (N=10) | p-Value | |
Age, years | Mean±SD | 62±12 | 62±12 | 59±12 | 0.86 |
Gender, n | Male/female | 12/8 | 3/7 | 2/6 | 0.16 |
BMI kg/m2 | Mean±SD | 20.2±3.6 | 24.7±2.1 | 20.5±2.3 | 0.12 |
ASA-PS, n (%) | 1 | 11 (32.3%) | 4 (8.1%) | 7 (45%) | 0.156 |
2 | 7 (64.0%) | 4 (61.8%) | 3 (45%) | ||
3 | 2 (2.7%) | 2 (9.1%) | 0 | ||
Primary site, n (%) | Right | 9 | 6 | 3 | 0.025 |
Left | 10 | 4 | 6 | ||
Rectum | 1 | 0 | 1 | ||
Primary tumor diameter, mm | Mean±SD | 40±12 | 49±11 | 38±12 | 0.056 |
SLM, n (%) | Median no. (range) | 2 (1-10) | 2 (1-6) | 2 (1-10) | 0.85 |
1 SLM | 10 | 5 | 5 | ||
2 SLM | 4 | 2 | 2 | ||
≥ 3 SLM | 6 | 2 | 4 | ||
Segments involved, n | Median (range) | 2 (1-5) | 1 (1-5) | 2 (1-4) | |
Unilobar | 10 | 5 | 5 | 0.53 | |
Bilobar | 10 | 5 | 5 | 0.52 | |
Largest LM diameter, mm | Mean±SD | 20±18 | 19±14 | 22±21 | 0.20 |
Preoperative chemotherapy, n (%) | FOLFOX +mAb | 2 (11.8%) | 3 (16.2%) | 1 (10.5%) | 0.66 |
SOX +mAb | 0 | 0 | 0 | ||
FOLFIRI +mAb | 1 | 1 | 0 | ||
XELOX +mAb | 0 | 0 | 0 | ||
FOLFOXIRI +mAb | 1 | 0 | 1 | ||
IRIS +mAb | 1 | 0 | 1 | ||
FOLFOX +mAb | 1 | 1 | 0 |
Operative methods.
Total (N=20) | Primary first (N=10) | Liver first (N=10) | |
---|---|---|---|
Primar Laparoscopic | 20 | 10 | 10 |
Liver Laparoscopic | 20 | 10 | 10 |
Hand-assist | 5 | 5 | 0 |
Hybrid | 6 | 4 | 2 |
Pure laparoscopic | 20 | 2 | 10 |
Colectomy | |||
Ileocecal resection | 3 | 2 | 1 |
Right hemicolectomy | 5 | 3 | 2 |
Sigmoid colectomy | 7 | 3 | 4 |
Left hemicolectomy | 1 | 1 | 0 |
Partial colectomy | 3 | 2 | 2 |
High anterior resection | 2 | 0 | 2 |
Low anterior resection | 4 | 0 | 4 |
Intersphincteric resection | 2 | 0 | 2 |
Hepatectomy Anatomical resection | 6 | 2 | 4 |
Parenchymal resection | 17 | 7 | 10 |
Both | 4 | 2 | 2 |
In 11 patients we observed one silmutaneous liver matastasis (SLMs), in 7 patients there were two SLMs, and in 2 patients there were ≥2. The median number of hepatic segments involved were 2. Silmutaneous liver matastasis was unilobar in eleven patients, and bilobar for nine. The largest diameter of liver metastases was 19mm. In seven patients chemotherapy was administered preoperatably (Table 2).
However; there was no significant between the operative time, for the two groups. Postoperative complications were observed in eight patients (Table 3). Furthermore; no difference was observed for both groups regarding the nutrition status after surgery and postoperative hospital stay. No fatal event or adverse effect was observed within the next 30 days for patients in both groups.
We reevaluated in our department the clinical impact of laparoscopic simultaneous resection for SLMs with colon cancer. We observed again as in previous studies that the operative order had no effect on the perioperative outcome. In group B which was the liver-first approach we observed lower blood loss as in previous studies. No significant difference in the anastomotic leakage was observed between the two groups in our study. We believe that the main reason for less blood loss in group B are technical and anatomical reasons of the procedure during hepatectomy. A technical and anatomical aspect is the low central venous pressure. This anatomy provides easy control of the hepatic [14]. Laparoscopic technique has improved in the past twelve years and there is less blood loss. There was no statistical difference between the two groups regarding the operative time. Although in group B the operating time was slightly less. Based on previously published studies the positional difference of the patient's body between primary resection and during the resection of metastatic lesions has an impact in the operating time. All centers included in our multicenter study used different positions such as; right upper limb elevation, and semi-lateral decubitus position and use of the intercostal ports where necessary [15]. In laparoscopic colectomy we use the normal position such as a supine or lithotomy position and therefore the operating time is less.
Operative and postoperative results.
Parameter | Total (N=20) | Primary first (N=10) | Liver first (N=10) | p-Value | |
---|---|---|---|---|---|
Operative time, min | Median (range) | 560 (374-879) | 542 (450-724) | 593 (374-837) | 0.21 |
Time in the operating room, min | Median (range) | 686 (551-1,152) | 841 (551-1,183) | 731 (531-1,162) | 0.24 |
Blood loss, ml | Median (range) | 435 (5-2,066) | 490 (94-2,086) | 154 (7-670) | 0.04 |
Complications, n | Surgical site infection | ||||
Abdominal abscess | 1 | 1 | 0 | ||
Biloma | 1 | 0 | 1 | ||
Biliary fistula | 1 | 1 | 0 | ||
Anastomosis leakage | 2 | 2 | 0 | ||
Paralytic ileus | 0 | 0 | 0 | ||
Pneumothorax1 | 0 | 0 | 0 | ||
Pleuraleffusion/ascites | 0 | 0 | 0 | ||
Pneumonia/urinary | 1 | 0 | 1 | ||
Tract infection | 0 | 0 | 0 | ||
None | 20 | 6 | 5 | ||
Clavien-Dindo classification, n (%) | ≥II | 6 (15.5%) | 2 (24.2%) | 1 (11.3%) | 0.33 |
≥III | 4 (13.7%) | 3 (25.2%) | 1 (6.2%) | 0.12 | |
Start of oral intake, days | Median (range) | 3 (2-6) | 3(2-6) | 4 (2-7) | 0.24 |
Postoperative hospital stay, days | Median (range) | 13 (10-50) | 14 (10-50) | 12 (10-25) | 0.21 |
Re-operation within 30 days | Yes | 0 | 0 | 0 | |
Death within 30 days | Yes | 0 | 0 | 0 |
In group B were hepatectomy is performed the rearrangement of the patient's position takes less time. We use the Pringle maneuver to control liver inflow [16-21]. Although, sometimes lower volume may is observed which causes circulatory disorders in organs, and therefore performing the Pringle should be used only when necessary. In our study no significant difference in postoperative complication rates were observed for group A and B. We were not able to assess operative time and blood loss during colectomy and hepatectomy separately. Moreover; the long-term outcome has not been evaluated after 30 days. In previous studies when simultaneous laparoscopic resection for CRLM, was correlated with open surgery it the long-term outcomes observed were similar [22, 23]. In these studies simultaneous and staged resection for CRLM did not provide any difference for [24] disease-free nor overall survival [25, 26]. In our retrospective study there were significant differences in the number of liver metastases, surgical procedures for resection, the number of affected hepatic segments, and the number of patients were insufficient to compare two groups with similar backgrounds. We do not have any additional data whether local treatment plays any significant role in the disease free or survival rates. Major limitation of our study is the small number of patients, which was mostly attributed to the fear of the patients since simultaneous surgeries are not the gold standard in these situations. Moreover; we included in our study only patients that were fit to undergo such a surgery either in group A, or B. A larger study is needed to clarify several perioperative issues such as blood loss, or the technical experience that the operations much have.
In conclusion the order simultaneous resection of primary and liver metastatic lesions, does not affect the short-term surgical outcomes and adverse effects. However; increased operative blood loss is observed in colon-first resections. Based on previous references-studies, our new equipment used, had similar results to the other studies, similar adverse effects and positive results with less than 5 days of hospitilisation.
The authors have declared that no competing interest exists.
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Corresponding author: Paul Zarogoulidis, M.D., Ph.D., 3rd Department of Surgery, ``AHEPA`` University Hospital, Aristotle University of Thessaloniki, Medical School, Thessaloniki, Greece. Mobile: 00306977271974; E-mail: pzarogcom.
Received 2023-9-26
Accepted 2023-11-14
Published 2024-1-1