Peritoneal metastases (PM) are diagnosed in 10–25% of colorectal cancer (CRC) patients
1‐
3 and severely jeopardize survival. Patients with colorectal PM have a median overall survival of 4 months without treatment
4 and 12–16 months after treatment with systemic chemotherapy.
5,6 Currently, the only potentially curative option for patients with colorectal PM consists of cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC). In carefully selected patients with limited peritoneal disease, a median overall survival of 45 months can be reached, resembling the survival rates of stage 3 CRC patients.
5,7,8
Treatment with cytoreduction and HIPEC is associated with relatively high morbidity and mortality rates of 16–64% and 5%, respectively
9‐
11 warranting careful selection of potential HIPEC candidates. Consequently, much of the current literature focuses on the identification of prognostic factors. Two major prognosticators associated with poor oncologic outcome are a high intraperitoneal tumor load and, inherently, an incomplete cytoreduction (R2).
1,12,13 Accordingly, an earlier diagnosis of PM is key to further improving prognosis, warranting enhanced detection of PM during primary tumor resection. Second, it is crucial to achieve a complete cytoreduction to improve oncologic outcomes. Nevertheless, visualization of PM and quantification of the peritoneal tumor burden are challenging. The value of current preoperative imaging by positron emission tomography/computed tomography (PET/CT) is limited by its low sensitivity for detection of PM (72%),
14 which decreases further to 11% for nodules smaller than 5 mm.
15 Accordingly, intraperitoneal tumor detection and a complete cytoreduction rely on intraoperative staging based on visual detection of tumor nodules and palpation of the abdominal surface.
Advanced imaging techniques are increasingly used for visualization of several cancer types, in addition to white-light imaging, the conventional imaging technique, and could improve the detection of PM. Promising methods include narrow-band imaging (NBI), near-infrared imaging with indocyanine green (NIR-ICG), and spray-dye chromoendoscopy (SDCE) with indigo carmine blue. NBI consists of 415 and 540 nm wavelengths, and highlights microvascular architecture,
16,17 thereby accentuating deviating patterns and demarking peritoneal nodules.
18,19 Near-infrared imaging depends on intravenously administered indocyanine green (ICG) that accumulates in tumor tissue, resulting in fluorescence using near-infrared light.
20‐
22 A third method is SDCE with the indigo carmine blue dye that accentuates the malignant architecture of tumor lesions and is mainly described for its use during gastroendoscopy and colonoscopy.
23,24
The modalities NBI, NIR-ICG, and SDCE have been shown to improve the detection of lesions in different medical fields of specialty. However, to date, NBI and SDCE have never been studied for the the detection of colorectal PM, and studies on NIR-ICG report contradictory results. Therefore, the present study aims to investigate the feasibility and safety of NBI, NIR-ICG, and SDCE for the detection of colorectal PM.
Methods
Surgery and Imaging Modalities
Patients with colorectal PM scheduled for CRS and HIPEC were prospectively enrolled in this clinical feasibility study. All included patients underwent a diagnostic laparoscopy prior to CRS and HIPEC, during which NBI, NIR-ICG, and SDCE were compared with white-light imaging. Details on study design, patients, and surgical procedures are provided in the electronic supplementary methods.
Per imaging modality, two predefined scoring systems were used: (1) lesions were scored as benign or malignant; and (2) lesions were scored using a visual analog scale (VAS) ranging from 1 (certainly benign) to 10 (certainly malignant). Benign lesions were scored as VAS 1–4, dubiously malignant lesions were scored as VAS 5–6, and malignant lesions were scored as VAS 7–10. The VAS indicated whether surgeons were more likely to classify a lesion as benign (low VAS) or malignant (high VAS). Guidelines for the assessment of lesions are provided per imaging modality in the electronic supplementary methods. Biopsies of all potentially malignant lesions and negative control biopsies within 2 cm proximity of these lesions were taken. Two independent gastrointestinal surgeons reviewed the photographs of all lesions in order to assess interrater variability, and a pathologist inspected all biopsies in a blinded fashion.
Statistics
According to the sample size calculation (electronic supplementary methods), a sample size of 25–30 patients was required. Primary (sensitivity, specificity) and secondary outcomes (positive [PPV] and negative predictive values [NPV], positive [LR +] and negative likelihood ratios [LR −]) were calculated for each imaging modality, using pathological examination of the biopsies as the golden standard. Differences in sensitivity and specificity between the advanced imaging techniques and white-light imaging were compared using McNemar’s test, and differences in VAS for certainty of malignancy or benignancy were calculated using the Wilcoxon signed rank test. Statistical significance was assumed at a p value of < 0.05 for two-sided testing. Interrater variability was assessed using Cohen’s weighted kappa value (Kw) with 95% confidence intervals (CIs). Statistical analyses were performed using SPSS version 22 (IBM Corporation, Armonk, NY, USA).
Discussion
This clinical feasibility study clearly demonstrates NBI to be superior to white-light imaging, NIR-ICG, and SDCE for the detection of colorectal PM. These results encourage the use of NBI for enhanced visualization of PM during inspection of the peritoneum at the time of primary tumor resection and realization of a complete CRS prior to HIPEC treatment. In 28 patients with colorectal PM, NBI improved sensitivity for the detection of PM from 80.0% with white-light imaging to 96.0% (p = 0.008). The use of NBI alone did not significantly impair specificity (74.8% vs. 73.1%; p = 0.804), although the combined use of NBI and white light did. Using NBI, lesions were identified that would have been missed with white-light imaging. Thereby, this technique provided guidance to categorize lesions that were dubiously positive with white light.
NBI is available on most laparoscopic systems and is a practical method not requiring extra costs or significant additional time. This method has already been widely studied for its use during colonoscopy
26 and the detection of other primary tumors,
18,19,27 but its use for the detection of PM has been reported less frequently. Although NBI enhanced sensitivity for the detection of PM in 26 gastric cancer patients, from 48 to 91%,
18 its additional value was not shown in 20 patients with gastrointestinal and gynecological malignancies.
28 The latter study did not provide clear alignments for classification of lesions and did not assess interrater variability, making these results subject to individual variation in interpretation. More importantly, only one patient in this heterogeneous cohort had colorectal PM, severely hampering the conclusions of this study. Furthermore, a recent study including 124 patients with gynecological cancer did not find NBI to be superior to white-light imaging for the detection of PM.
29 However, it is questionable whether the conclusions on PM of mucinous ovarian cancers can be extrapolated to PM of colorectal origin. The present prospective evaluation of three advanced imaging techniques in a computer-randomized order does suggest a role for NBI in the detection of colorectal PM. Notably, combining white light with NBI resulted in a higher false positive rate, potentially leading to unnecessary resections. In addition, the slightly higher VAS assigned to both benign and malignant lesions using NBI suggests that not only pathologically confirmed malignant lesions but also benign lesions are more likely to be scored as malignant. Nevertheless, the oncologic benefits of a better tumor resection are expected to outweigh the potential risks of a more extensive surgical resection.
In the present study, SDCE with indigo carmine blue was not considered suitable for application onto the whole abdominal cavity and intraperitoneal organs, even impairing visualization of intra-abdominal organs, while assessment of the complete peritoneal lining is crucial to achieving a complete cytoreduction. In particular, abdominal regions less easily approachable by laparoscopy cannot be properly evaluated using this technique. To date, only one case report has described the intraperitoneal use of SDCE, and found this method to be of potential benefit for the identification of endometriotic lesions.
30 Considering the lack of visualization of all potentially affected surfaces, which may impair oncologic outcome, its application in terms of cancer detection will probably be limited to characterization of previously identified and localized lesions, such as early gastric cancer lesions,
31 and to its use during colonoscopy.
23
No fluorescence was detected in the present study using NIR-ICG. The timing of ICG administration may be an explanation for the lack of fluorescence in the present study. The optimal timing of ICG administration is highly debated, ranging from intraoperative administration
20 to 1–24 h preoperatively.
21,22,32 These contradictory recommendations are in line with the conflicting results on NIR-ICG for the detection of PM. Although two small studies (
n = 10) reported relatively low sensitivities of 65% and 76%,
22,32 the ex vivo use of tumor-to-background ratios after intraoperative ICG administration resulted in a relatively high sensitivity (88%). Unfortunately, the value of NIR-ICG was limited for the detection of mucinous tumors and in areas with high physiological ICG accumulation, such as the liver, as well as areas with a high peritoneal tumor load.
20 In our institution, ICG is routinely administrated intraoperatively during laparoscopic segment resections to assess anastomotic vascular sufficiency. However, in patients with PM, no peritoneal deposits have been visualized using this technique, which may be partly explained by high background fluorescence. Therefore, the time interval in the present study was based on the enhanced permeability and retention principles.
32,33 Currently, fluorescence with antibody-coupled ICG is an emerging technique that shows promise. Both the use of fluorescent monoclonal carcinoembryonic antigen antibodies
34 and ICG-coupled antibodies targeting vascular endothelial growth factor
35 are promising methods, revealing tumor tissue that has been missed with white light. A comparative study evaluating promising dyes should determine the optimal target for this imaging modality. Until now, these techniques are not widely available in clinical practice and their implementation will require substantial investment in time and money.
The main potential clinical implication of NBI is the detection of PM during evaluation of the peritoneum at the time of laparoscopic primary tumor resection. Early detection of PM and subsequent treatment is crucial for the successful treatment of patients with PM. In particular, patients with T4 tumors deserve a dedicated inspection since T4 CRC is a major risk factor for PM, with up to 20% of these patients presenting with synchronous PM.
36‐
38 NBI could help detect peritoneal disease in an early stage, resulting in early referral to specialized HIPEC centers and, consequently, improved outcome. A second implication is determination of the feasibility of a complete CRS at the time of diagnostic laparoscopy. Currently, 25–44% of CRC patients considered eligible for CRS and HIPEC based on preoperative imaging undergo unnecessary explorative procedures.
39,40 This number was shown to be reduced by 25–35% with prior laparoscopic assessment in colorectal, ovarian, and gastric cancer patients.
40‐
45 However, it should be noted that the Peritoneal Cancer Index (PCI) is often underestimated during diagnostic laparoscopy,
46 and a relatively disappointing PPV of 83% for prediction of complete cytoreduction has been reported.
47 A third implication is the optimization of a radical resection at the time of CRS, although the NBI system is less practical for use during open surgery. Notably, improved detection of PM may reveal higher PCI scores. The mean size of the lesions missed with white light was > 5 mm, implying that proper visualization of these lesions would impact PCI scores and that patients who would have been treated with curative intent based on white-light imaging might have received palliative treatment based on advanced imaging. Therefore, it is of utmost importance to investigate whether the visual advantages indeed translate into therapeutic benefit for patients in terms of tumor staging and oncologic outcomes, warranting randomization between imaging techniques and a long-term follow-up.
This prospective clinical study is the first to demonstrate that NBI improves the detection of colorectal PM. However, some limitations should be taken into account. First, we could not compensate for a potential learning curve regarding assessment of the lesions. This problem was encountered by providing photographs of all lesions, clear scoring guidelines, and evaluation of all lesions by two independent surgeons. Second, we did not use ex vivo evaluation systems, such as tumor-to-background ratios, that could have resulted in higher sensitivities. Nevertheless, real-life assessment of imaging techniques provides a better indication for their use in clinical practice. The risk of taking non-representative biopsies should also be noted. This issue was addressed by careful documentation of the locations of scored and biopsied lesions and by recording all surgical procedures.