Evidence - Sigmoid resection, oncological, robotically assisted with medial-to-lateral approach

  1. Summary of the literature

    Staging Diagnostics:

    • Complete Colonoscopy

    - Gold standard in the diagnosis of colorectal carcinoma

    - For localization diagnostics and histological confirmation and to exclude a second carcinoma (approx. 5% of cases)

    - If the entire colon is not visible colonoscopically, a CT or MR colonography can be used

    - After emergency surgery (ileus, tumor perforation, colonoscopically uncontrollable bleeding): postoperative colonoscopy after anastomosis healing and patient recovery to exclude synchronous double carcinoma

    • Histological Confirmation
    • Laboratory examination with determination of the CEA value

    Note: At the time of initial diagnosis, the tumor marker CEA is elevated in about 30% of all colorectal carcinomas and should therefore be determined preoperatively. In tumor follow-up´s, CEA is a reliable indicator of recurrence in marker-expressing tumors and is also an independent prognostic factor in the case of liver metastases. The significance of CA 125 as a parameter for further treatment of a proven peritoneal carcinomatosis is currently unclear (1, 2). CA 19-9 is recurrently discussed as another tumor marker, but does not increase the predictive value regarding the presence of a recurrence compared to a sole determination of the CEA value.

    • Chest X-ray in 2 planes
    • Abdominal sonography
    • Possibly CEUS (contrast-enhanced ultrasound) in case of suspected hepatic dissemination
    • Possibly MRI liver in case of suspected hepatic dissemination

    Note: Although a CT abdomen or CT thorax-abdomen is not considered necessary in the S3 guideline, it is performed in most clinics. It serves not only to detect hepatic metastases but also to assess the primary tumor, possibly enlarged lymph nodes, and to evaluate the positional relationship of the tumor-bearing colon to other structures, such as the ureters and their course.

    From (3): Körber et al.: S3 guideline colorectal carcinoma, Oncology Guidelines Program of the AWMF, German Cancer Society e.V. and German Cancer Aid. Status: 2019. Retrieved on: 03.07.2019.

    Interdisciplinary Tumor Conference:

    All patients with colorectal carcinomas should be presented in an interdisciplinary tumor conference after completion of primary therapy (e.g., surgery, chemotherapy). A study from the UK showed that this approach significantly increased patient survival (4).

    Mandatory pre-therapeutically, patients should be presented in the following constellations (3):

    • any rectal carcinoma
    • any colon carcinoma in stage IV
    • distant metastases
    • local recurrences
    • before any local ablative measure

    TNM Classification:

    The TNM system for colorectal carcinoma is defined as follows (5):


     

    T1


     


     

    Submucosa


     

     


     


     

    T2


     


     

    Muscularis propria


     


     

    T3


     


     

    Perirectal tissue: Mesorectum


     


     

    T4


     


     

    T4a Visceral peritoneum


     

    T4b Other organs/structures


     

     


     


     

    N1/2


     


     

    N1a 1 regional lymph node metastasis


     

    N1b 2–3 regional lymph node metastases


     

    N1c Satellites/tumor nodules in the mesorectum


     

    N2a 4–6 regional lymph nodes


     

    N2b >6 regional lymph nodes


     

     


     


     

    M1


     


     

    M1a Metastases confined to one organ (liver, lung, ovary, non-regional lymph nodes, no peritoneal metastases)


     

    M1b Metastases in more than one organ


     

    M1c Metastases in the peritoneum with/without metastases in other organs


     

    The UICC stages are then as follows:


     

    UICC Stage


     


     

    TNM


     


     

    0


     


     

    Tis (Carcinoma in situ)


     


     

    I


     


     

    Up to T2, N0, M0


     


     

    II


     


     

     


     


     

    IIA


     


     

    T3, N0, M0


     


     

    IIB


     


     

    T4a, N0, M0


     


     

    IIC


     


     

    T4b, N0, M0


     


     

    III


     


     

     


     


     

    IIIA


     


     

    Up to T2, N1, M0 or T1, N2a, M0


     


     

    IIIB


     


     

    T3/T4, N1, M0 or T2/T3, N2a, M0 or T1/T2, N2b, M0


     


     

    IIIC


     


     

    T4a, N2a, M0 or T3/T4a, N2b, M0 or T4b, N1/N2, M0


     


     

    IV


     


     

     


     


     

    IVA


     


     

    Any T, any N, M1a


     


     

    IVB


     


     

    Any T, any N, M1b


     


     

    IVC


     


     

    Any T, any N, M1c


     

    Therapy Planning

    The therapy of colon carcinoma is derived from the TNM and UICC stages determined in diagnostics (3):


     

    UICC Stage


     


     

    TNM


     


     

    Therapy Recommendation


     


     

    0–I


     


     

    Tis to T1


     


     

    Endoscopic resection


     


     

    Further procedure based on histopathology:


     


     

    - Low-risk situation (G1/G2) and


     


     

    Complete resection (R0): No re-resection


     


     

    - Low-risk and incomplete resection: Complete endoscopic/local surgical re-resection


     


     

    - High-risk situation (G3/G4): Radical surgical resection


     


     

    No adjuvant chemotherapy


     


     

    I


     


     

    T2, N0, M0


     


     

    Radical surgical resection


     


     

     


     


     

    No adjuvant chemotherapy


     


     

    II


     


     

    Up to T4, N0, M0


     


     

    Radical surgical resection


     


     

    Consider adjuvant chemotherapy individually/patient counseling


     


     

    III


     


     

    Any T, N+, M0


     


     

    Radical surgical resection


     


     

    Adjuvant chemotherapy


     


     

    IV


     


     

    Any T, N+, M+


     


     

    Individual approach depending on findings


     

     

    Surgical Approach:

    The progress in the treatment of colon carcinoma over the past 30 years is due to increasing individualization of therapy, consistent implementation of surgical-oncological principles, more aggressive therapy regimens in the metastatic stage, and the use of minimally invasive surgical techniques. Standardized treatment concepts in multimodal tumor therapy have led to an increase in the average five-year survival rate from 65% to over 85% and a reduction in the locoregional recurrence rate from an average of over 13% to under 2% in non-metastatic colon carcinoma in UICC stages II and III (6).

    In the metastatic stage, five-year survival rates of over 40% are now achieved in 20% of patients (7).

    The sigmoid carcinoma metastasizes via the Aa. sigmoideae to the trunk of the A. mes. inf. The resection should be performed with sufficient safety margins orally and aborally. The proximal colon transection is located in the C. descendens with central transection of the A. mes. inf. about 1 cm distal to its origin from the aorta, to spare the neural structures located there. (Plexus mesentericus inferior (Ganglion mesentericum inferius) (Autonomic Nervous System).

    CAVE: In 2 - 4% of patients, lymph node metastases are located near the origin of the inferior mesenteric artery (8, 9).

    Proximally, as is usual in the colon, one should aim for a distance of 10 cm from the tumor. Regarding the distal bowel transection, the guidelines for rectal carcinoma in the upper third apply. Here, an aboral safety margin of at least 5 cm should be maintained. When transecting the mesorectum in the upper part, "coning" (thinning) should be avoided.

    The surgical therapy of sigmoid carcinoma should include complete mesocolic excision (CME). In addition to systematic lymphadenectomy, the CME concept also aims to maximize the reduction of the number of local recurrences by increasing the radicality and quality of the resection. Analogous to the mesorectum, there is a mesocolon, which as a bilateral sheath contains the lymph nodes at the supplying arteries and is therefore considered an anatomical guide structure for oncological surgery. The technique was published by Hohenberger et al. in 2009 (10).

    The three basic principles of preparation in CME are adherence to the specified anatomical layers during preparation while preserving the two mesocolic fasciae, central resection of the supplying vessels, and sufficient length of the specimen. The goal is maximum local radicality with maximum lymph node yield. CME leads to higher quality specimens without increasing complication rates (10-12). The previous data also suggest an improvement in survival rates with consistent implementation of CME (10).

    Data from Denmark, Sweden, and Germany show that the CME technique is associated with better disease-free survival in patients with colon carcinoma in UICC stage I – III than conventional colon resection (12-14).

    At least 12 or more lymph nodes should be removed and examined. Although the study quality regarding the number of lymph nodes is low, it is considered that patients with a larger number of removed and examined lymph nodes have an improved prognosis in UICC stage II and III. This correlation was shown in 3411 patients in stage II and III in the so-called Intergroup Trials and in the INTACC study (15, 16).

    Not only the number of lymph node metastases is relevant, but also the general number of removed lymph nodes. Thus, a prognostic effect can also be demonstrated in nodal-negative tumors, which correlates with the number of removed or examined lymph nodes (17).

    The number of lymph nodes can thus be considered a surrogate marker for the quality of treatment and diagnosis for both surgery and pathology. Finally, the pathologist should categorize the specimen into grade 1 (good, preservation of the mesocolic layer) to grade 3 (poor with tears to the muscularis propria or to the tumor).

    Special Surgical Cases:

    · For large polypoid, especially villous tumors and fundamentally possible segmental and tubular resection, where a carcinoma diagnosis could not be confirmed pre-therapeutically, a dignity assessment in frozen section is often not possible for examination technical reasons (examination of multiple tissue blocks!). Therefore, an oncological operation should be considered primarily (3).

    · In cases of tumor adherence to surrounding structures and neighboring organs, it is often not possible to clarify intraoperatively macroscopically whether it is an infiltration of the carcinoma in the sense of an organ-transcending T4 situation or just a peritumoral inflammatory reaction. In such cases, intraoperative tissue samples and frozen section examinations should be strictly avoided to prevent the risk of tumor cell dissemination, which is associated with a significant deterioration in prognosis (18). Therefore, in these cases, an en bloc resection involving adjacent structures is justified.

    · In cases where no clear diagnostic assignment of unclear liver lesions can be made through imaging, histological confirmation should be performed (3).

    Laparoscopic and Robotic Surgery in Colon Carcinoma

    Mono- and multicenter RCTs (KOLOR, COST, CLASSIC-Trail) showed no differences between laparoscopic and open techniques in colon carcinoma surgery in terms of surgical-oncological quality indicators (R-status, number of lymph nodes) and long-term results (tumor recurrences, survival) with appropriate expertise of the surgeon (19-21).

    As an advantage of minimally invasive surgery, a relatively low perioperative morbidity with unchanged overall morbidity and mortality could be demonstrated in the short-term course (22).

    In the long-term course, no differences were found between laparoscopic and conventional surgery in terms of the rate of incisional hernias and adhesion-related relaparotomies or tumor recurrences (23, 24). The British CLASSIC study also confirms the oncological safety of laparoscopic surgery in colorectal carcinomas (25).

    According to the current S3 guideline "Colorectal Carcinoma," a laparoscopic resection of colon carcinoma can be performed in suitable cases with appropriate experience of the surgeon (3).

    Robotic surgery, as a further development of laparoscopic surgery, offers great optimization potential compared to simple laparoscopy, especially in terms of oncological abdominal surgery, with its higher precision of instrument guidance and improved visualization.

    Studies show that robotics can be safely applied in colon carcinoma and has advantages in terms of tissue preservation and reduction of postoperative functional disorders (26-30).

    The best data on robot-assisted versus conventional laparoscopic colorectal oncological surgery with early postoperative results and also oncological long-term results are available for right hemicolectomy and rectal resections.

    Solaini et al. compared in a meta-analysis with an RCT among the total of 11 studies considered 869 robot-assisted with 7388 conventionally laparoscopic operated right hemicolectomies (31). A significantly longer operation time was found for robotic procedures, but with a significantly reduced conversion rate. An intracorporeal anastomosis could be performed significantly more frequently in robot-assisted resected patients. The early postoperative course between robot-assisted and conventionally laparoscopic operated patients did not differ with the same morbidity and mortality in the groups.

    Lorenzon et al. included in their meta-analysis, in addition to 18 case-control studies, 3 RCTs (32). The aim was to compare the early postoperative results between robot-assisted and conventionally laparoscopic colorectal resections. The results from the RCTs showed no differences between robot-assisted and conventionally laparoscopic resected patients in terms of operation time, hospital stay, or postoperative morbidity. Considering all studies and all colorectal resections, lower costs and shorter operation times were found on the side of laparoscopically operated patients, whereas robotically operated patients had slightly lower morbidity (Odds-Ratio=0.6-0.9). In isolated consideration of the subgroup of left-sided hemicolectomies, only one significant difference was found: conventionally laparoscopic operated patients showed a shorter operation time.

    In terms of oncological radicality, the available studies show heterogeneous results, from which no clear advantage of robotics over laparoscopic procedures can currently be derived. Two studies comparing robotic colon procedures with laparoscopic colon procedures showed advantages on the side of robotics in terms of the number of resected lymph nodes (33, 34). However, historical collectives were used as a control group for robotics, which could represent a strong bias, as the radicality and consistency of CME have certainly increased in recent years.

    In the above-cited meta-analysis by Soleini from 2018 and also in another work comparing two collectives, no significant difference was found in terms of the number of lymph nodes (31, 35).

    In terms of 5-year survival after oncological colorectal procedures, no significant differences were found by Spignoglio et al. in the comparison of robotic with conventional laparoscopic surgery (35). Long-term results with larger, also multicenter studies are still pending.

    At the time of guideline development, the evidence for robotic surgery had to be rated as insufficient. At the time of creation, no meaningful prospective randomized studies on the value of robotics in sigmoid colon carcinoma were available. Due to the lack of short- and especially oncological long-term results at the time of guideline development, robot-assisted surgery in colon carcinoma is currently not recommended outside of studies (3).

    Finally, it can be added here that in intestinal centers that enter into the DGAV register, it is evident in the benchmark that robotics has led to an improvement in perioperative results and contributed to excellent oncological results (36). Furthermore, it is shown that the proportion of successfully minimally invasively operated patients without conversion is higher in robotics than in conventional laparoscopy and that significantly fewer contraindications exist.

    The cost aspect of robotics also plays a significant role in the discussion. For example, in the meta-analysis by Solaini, the robot-assisted procedures were associated with significantly higher costs. However, it should not be neglected that after the successful establishment of the robotic system, there are potential savings beyond the acquisition and material costs. It is shown in the German centers that have established robotics for colorectal carcinoma that the length of stay of robotically operated patients is generally reduced compared to conventionally laparoscopic operated patients and that it is generally no longer necessary to provide a monitoring bed, except for multimorbid patients.

    Multimodal Tumor Therapy

    Numerous studies demonstrate the importance of drug tumor therapy in non-metastatic colon carcinoma. An adjuvant chemotherapy in UICC stage III is associated with a significant improvement in prognosis of about 20% overall survival (37). In stage II, patients with risk factors (T4 tumor, tumor perforation, emergency interventions, number of examined/excised lymph nodes < 12) have a significantly worse prognosis than patients in the same stage without risk factors and should therefore receive adjuvant chemotherapy (3).

    Adjuvant Therapy in Sigmoid Carcinoma

    Indications

    • Adjuvant chemotherapy is not recommended in UICC stage I.
    • In UICC stage II, it is a so-called "can situation," i.e., depending on risk factors and microsatellite status, it can certainly be recommended. In the case of microsatellite instability, no adjuvant chemotherapy is recommended. If risk factors are present, adjuvant chemotherapy should be considered. Selected risk situations include: T4 tumor, tumor perforation/tear, emergency surgery, number of examined lymph nodes too low (<12))
    • In UICC stage III, adjuvant therapy is always recommended.

    Prerequisites

    The prerequisite for adjuvant therapy is the R0 resection of the primary tumor. The basis for the indication for adjuvant therapy after quality-assured tumor resection [861] is the pathohistological staging, especially the determination of the pN status. To establish pN0, 12 or more regional lymph nodes should be examined (UICC 2002). Immunocytological findings of isolated tumor cells in bone marrow biopsies or lymph nodes as well as cytological tumor cell findings in peritoneal washings are not an indication for adjuvant therapy outside of studies.

    Contraindications

    • Poor general condition (ECOG >2),
    • severe infection
    • limited life expectancy due to comorbidities
    • liver cirrhosis in Child B or C stage
    • severe coronary heart disease or heart failure (NYHA III and IV)
    • advanced renal insufficiency ((pre-)terminal)
    • blood disorders, impaired bone marrow function
    • inability to participate in regular follow-up examinations

    Therapy Modalities

    • Start: Postoperatively as soon as possible
    • In randomized studies, adjuvant chemotherapy was initiated within 8 weeks.

    Note: RCTs to determine the ideal timing do not exist. In a retrospective analysis of cohort studies, an inverse correlation between the timing of the start of adjuvant chemotherapy and survival was calculated(38). This was also confirmed in another retrospective analysis of cohort studies(39) and in a retrospective registry analysis(39, 40).

    • Duration: 3–6 months, depending on risk-benefit assessment
    • UICC stage II: Monotherapy with fluoropyrimidines
    • UICC stage III: Combination therapy with oxaliplatin
    • FOLFOX: Folinic acid + 5-FU in combination with oxaliplatin
    • XELOX (CAPOX®): Capecitabine + oxaliplatin
    • In patients >70 years, no therapy with oxaliplatin should be performed
    • In case of contraindications to oxaliplatin, monotherapy with fluoropyrimidines should be performed

    Note: Adjuvant chemotherapy should not be omitted solely due to age. However, there is insufficient evidence for adjuvant chemotherapy in patients over 75 years of age.

    Neoadjuvant Chemotherapy in Sigmoid Carcinoma

    The role of neoadjuvant chemotherapy in the treatment of locally advanced colon carcinomas has been investigated in recent years. A randomized study from the UK showed that combined neoadjuvant/adjuvant chemotherapy (oxaliplatin, folinic acid, and 5-FU) vs. adjuvant chemotherapy alone in locally advanced colon carcinomas resulted in a lower rate of R1 resections and significant downstaging. Tumor progression under ongoing neoadjuvant chemotherapy could not be observed [2, 12]. Studies have shown that computed tomography is suitable for identifying locally advanced colon carcinomas in terms of the T category and thus selecting them for neoadjuvant chemotherapy or preoperatively assessing the response to chemotherapy [1, 20]. Oncological long-term results are still pending, and it is currently not recommended in the guidelines.

    Multivisceral Resection

    In cases of tumor adherence to neighboring organs, it is not possible for the surgeon to macroscopically clarify whether it is an infiltration of the carcinoma into the neighboring organ or just a peritumoral inflammatory reaction. In such cases, biopsies and frozen section examinations should be strictly avoided, as there is always the risk of local tumor cell dissemination. This is always associated with a significant deterioration in prognosis. Therefore, if technically feasible, an en bloc resection of the tumor with the infiltrated structures is recommended (multivisceral resection). In the case of rectal carcinoma, a complete pelvic exenteration may be required.

    Metastatic Situation

    At the time of diagnosis, distant metastases are present in about 25% of patients. In the metastatic situation, there is generally a significant reduction in the five-year survival rate.

    If distant metastases are present, it must be clarified whether a purely palliative concept should be pursued or whether a cure is possible through primary or secondary resection of metastases (especially liver metastases). With an increased presentation of patients in UICC stage IV in the tumor conference, the rate of metastasis surgery increased (41).

    In recent years, the prognosis in stage IV has also been significantly improved through both more radical surgical action and drug tumor therapy (combination of dual therapy and antibodies), so that with a five-year survival rate of up to 50%, the prognosis for about 20% of metastatic patients has been significantly improved (42).

    In the literature, response rates of up to 60% and an R0 resection rate of up to 15% are achieved through the application of various chemotherapy protocols (43).

    A distinction should always be made between patients with synchronous and metachronous metastasis (44-46). The synchronous must be considered prognostically unfavorable compared to metachronous metastasis. In addition, information on disease dynamics is lacking here. The benefit of primary resection is therefore more uncertain in this patient group than in patients with metachronous metastasis. Other prognostic factors that can be considered in decision-making include the number of metastatic lesions, the presence of extrahepatic metastasis (47).

    The simultaneous resection of liver metastases probably does not affect long-term survival compared to a two-stage approach with appropriate patient selection.

    Patients in good general condition can be subjected to intensive treatment, i.e., surgery or chemotherapy. In the case of resectable tumor manifestations and favorable risk constellation, primary metastasis resection should be aimed for. Those patients for whom no surgical intervention is possible primarily should receive the most effective systemic chemotherapy possible. The primary therapeutic goal is maximum tumor reduction. The choice of chemotherapy regimen depends significantly on the molecular pathological profile of the tumor. In patients with RAS wild-type tumors, the localization of the primary tumor is also an additional decision-making basis.

    However, simultaneous liver metastasis resection can lead to higher mortality in the presence of comorbidity or older age (>70 years). Especially in the case of multiple synchronous liver metastases, a two-stage and multimodal approach should be chosen (3).

    The assessment should be made by a tumor board with the involvement of a surgeon experienced in metastasis surgery. In the case of extensive hepatic dissemination in stage IV and an asymptomatic primary tumor without stenosis and without bleeding, chemotherapy can also be started without resection of the primary tumor (3).

    Peritoneal Carcinomatosis

    If an isolated and limited peritoneal carcinomatosis is present in colon carcinoma, the indication for cytoreductive surgery followed by hyperthermic intraperitoneal chemotherapy (HIPEC) can be reviewed. The use of this combination therapy has shown a significant survival advantage in terms of extending median survival from 12.6 to 22.3 months (48).

    The Peritoneal Cancer Index (PCI) is used to determine the extent of peritoneal carcinomatosis. The following prerequisites should be met:

    • PCI<20
    • No extra-abdominal metastases
    • Possibility of macroscopic resection or destruction of all tumor manifestations

    If the PCI value is below 20 in patients without additional extra-abdominal metastases, and an R0 resection is possible, operative cytoreduction with HIPEC can be performed in specialized centers. Here, implementation within the framework of studies should be preferred (3).

    Perioperative Concept

    The ERAS concept ("enhanced recovery after surgery") of multimodal postoperative rehabilitation in gastrointestinal surgery is implemented in most clinics in this country in a partially modified form. The goal of the concept is to quickly manage the pathophysiological changes triggered by the surgical intervention, such as fatigue, bowel atony, and insulin resistance. The concept includes, among other things, the early removal of gastric tubes and intra-abdominal drains, early oral nutrition, stimulation of bowel motility, sufficient analgesia (epi-/peridural), and early mobilization. Numerous studies have shown that the ERAS concept can significantly shorten the length of stay, reduce perioperative morbidity, and accelerate recovery (49, 50).

  2. Reviews

    Essani R, Bergamaschi R. Robotic Colorectal Surgery: Advance or Expense? Adv Surg. 2016 Sep;50(1):157-71.

    Fabozzi M, Cirillo P, Corcione F. Surgical approach to right colon cancer: From open technique to robot. State of art. World J Gastrointest Surg. 2016 Aug 27;8(8):564-73.

    Karcz WK, von Braun W. Minimally Invasive Surgery for the Treatment of Colorectal Cancer. Visc Med. 2016 Jun;32(3):192-8.

    Wilder FG, Burnett A, Oliver J, Demyen MF, Chokshi RJ. A Review of the Long-Term Oncologic Outcomes of Robotic Surgery Versus Laparoscopic Surgery for Colorectal Cancer. Indian J Surg. 2016 Jun;78(3):214-9.

  3. Guidelines

    S3 Guideline Colorectal Carcinoma (Guideline Program Oncology (German Cancer Society, German Cancer Aid, AWMF): S3 Guideline Colorectal Carcinoma. Status: 30.11.2017. valid until 29.11.2022): https://www.awmf.org/uploads/tx_szleitlinien/021-007OLl_S3_Kolorektales-Karzinom-KRK_2019-01.pdf

    International Guidelines

    European Society for Medical Oncology (ESMO):

    Management of Patients with Metastatic Colorectal Cancer 2016

    Metastatic Colorectal Cancer 2014

    Early Colon Cancer

    Management of Patients with Colon and Rectal Cancer. A personalized approach to clinical decision making

    American Society of Colon and Rectal Surgeons (ASCRS):

    Practice Parameters for the Management of Colon Cancer

    Practice Guideline for the Surveillance of Patients After Curative Treatment of Colon and Rectal Cancer

Currently ongoing studies

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