Introduction

Colorectal cancer (CRC) is a leading cause of cancer death with an estimated 95,520 new cases and 50,260 deaths in 20171. Laparoscopic colectomy (LC) has gained widespread acceptance for resection of CRC, with better short term complication rates and similar long-term outcomes relative to open colectomy (OC) in stage I-III patients2,3,4. However, about ten percent of patients are diagnosed with locally advanced cancer (T4) with locoregional invasion, who may have worse outcomes5. Such tumors have a reasonable chance of a cure when accompanied by an en bloc multivisceral resection6,7,8, but a landmark randomized study excluded locally advanced colon cancer when comparing LC versus OC9.

The safety and effectiveness of LC in T4 colon cancer patients is still unresolved because of technical difficulties with en-bloc dissection of large tumors. The American Society of Colon & Rectal Surgeons recommends that “laparoscopic resection of T4 colon cancer may be performed safely and effectively with long-term oncologic outcomes that do not differ in comparison with open surgery.”10 In contrast, the National Comprehensive Cancer Network guidelines for colon cancer surgery recommend against LC when locally advanced disease is present11. The European Association of Endoscopic Surgery (EAES) also failed to recommend LC in locally advanced colon cancer12. While recent studies have compared LC with OC in locally advanced colon cancer13,14,15,16,17, many of those studies used small sample sizes or studied only patients from single institutions, while others were performed outside the United States.

There is also a major need to determine which T4 patients are appropriate candidates for LC18. For example, T4b tumors (invade and/or adhere to other organs or structures) are technically more demanding than T4a tumors (penetrate to the surface of the visceral peritoneum), depending on the nature of the multivisceral resection required to achieve negative margins. Resection of locally advanced tumors is difficult to perform laparoscopically because of the need to perform an extended resection and obtaining negative margins is more challenging19. The effectiveness of LC versus OC across different locations in locally advanced tumors in the colon is unknown. The advantages of LC have prompted its application to a wider range of patients with colon cancer such as those who are obese, have locally advanced tumors or require more extended resections. Older studies have argued that LC in obese patients is technically more difficult and could be a contraindication20,21. Additionally, observational studies with small patient samples examining transverse colon cancers have found that laparoscopic resection resulted in acceptable outcomes, but such studies may have been underpowered22,23,24. Studies to compare directly the effectiveness of LC versus OC across different locations in locally advanced tumors in the colon are not available, and transverse colon cancers were excluded from the landmark Clinical Outcomes of Surgical Therapy (COST) trial9.

We examined differences in 30 day outcomes of LC versus OC and also compared subgroups of patients: (1) T4a and T4b patients, (2) those with tumors located in the left, right, or transverse colon, and (3) obese and nonobese patients. Our findings should help guide the use of LC in minimally invasive surgery in T4 colon cancer patients.

Materials and methods

Data source

Data for our cohort was constructed using the 2013–2015 American College of Surgeons’ National Surgical Quality Improvement Program (ACS-NSQIP) Participant Use File and Targeted Colectomy File. Preoperative patient comorbidities, preoperative laboratory results, intraoperative procedures, 30-day postoperative mortality rates, and complications were abstracted by trained reviewers. Additional details are described here (https://www.facs.org/quality-programs/acs-nsqip). All methods were carried out in accordance with relevant guidelines and regulations. The Saint Louis University Institutional Review Board deemed this protocol to be exempt from oversight since it was nonhuman subjects research.

Patient selection

All patients who underwent colectomy (with or without obstruction) and were diagnosed with pT4 colon cancer (and nonmetastatic disease M0 or Mx) were included. Patients who underwent LC, including robotic, or OC were included; patients with other types of surgery were excluded. We included patient in the LC groups that resulted in conversion to OC based on intention to treat13,25. Patients who underwent emergency surgery were excluded since they are much more likely to receive open surgery26, which may lead to difficulty creating comparable groups of OC and LC patients. To test the robustness of our findings, we performed a sensitivity analysis by including LC performed with open or hand assistance in the LC group. Hand or open assistance may be used as a bridge between a straight LC and an OC in cases where straight LC may be difficult because of the size of tumor, local advancement, or intra-abdominal adhesions16. There were no participants who were younger than 18 years of age.

Patient outcomes

Outcomes included operation time, anastomotic leakage, mortality, readmission, re-operation, length of stay, wound infection, transfusion, prolonged postoperative ileus, sepsis, myocardial infarction, deep vein thrombosis, and pulmonary embolism. Conversion occurred when LC was converted to an unplanned OC. Re-operation was defined as any unplanned return to the operating room for a surgical procedure, for any reason, within 30 days of the colectomy at any hospital or surgical facility. All-cause mortality was defined as deaths within 30 days following surgery. Readmission was defined as any readmission (to the same or another hospital), for any reason, within 30 days of the colectomy. A wound infection included superficial or deep incisional surgical site infection or any other wound infection. Postoperative bleeding occurrence was defined as any transfusion given from the start of the colectomy to 72 h post operation. Because of the infrequent occurrence for some of the postoperative outcomes, we constructed a composite outcome of mortality, readmission, re-operation, wound infection, bleeding occurrence, and prolonged postoperative ileus. Patients with at least one adverse outcome were contrasted to those without any such adverse outcomes27, recognizing the variability in the severity of its components but summarizing information across several quality dimensions.

Covariates

Based on previous studies28,29, we included patient sex, age, Hispanic ethnicity, race, ASA grouping, smoking status, chronic comorbid conditions (congestive heart failure, hypertension, chronic obstructive pulmonary disease, chronic kidney disease, anemia, weight loss > 10%, bleeding disorder, transfusion), patient functional status prior to surgery, chemotherapy, and mechanical bowel preparation.

T4a and T4b colon cancers were determined based on AJCC TNM staging. Tumor location was based on post-operative diagnosis using ICD-9 or ICD-10 codes. The patient’s most recent height and weight documented in the medical record within the 30 days prior to the colectomy or at the time the patient was being considered a candidate for surgery was used to calculate BMI. Patients were classified as obese (BMI ≥ 30 kg/m2) or nonobese (BMI < 30 kg/m2).

Statistical analysis

We used 1:1 propensity score matching to obtain patient groups with comparable characteristics to assess the effect of LC on patient outcomes with all covariates. We calculated standardized differences for all covariates before and after matching. A standardized difference of less than − 0.1 or greater than 0.1 was used as a marker for imbalance30. We also compared the means and variances of the covariates after matching to determine the balance between the LC and OC groups. We calculated the average treatment effect among the treated (ATT) and associated 95% confidence intervals to describe the effectiveness of LC versus OC, focusing on absolute differences.

To assess potential heterogeneous treatment effects of LC by T4 type, we first matched patients who received LC to those who received OC. Matching was done in a 2:1 ratio using optimal matching on the propensity score, e(x), with a caliper of 0.25 × sd(e[x])31. Once patients were matched, we ran separate regressions in the LC and OC groups to predict respective outcomes. The coefficients for T4 type were compared between the two models to assess treatment heterogeneity due to these factors32. A similar approach was used to assess treatment heterogeneity due to tumor location (left, right, transverse) and obesity.

We conducted sensitivity analyses to challenge the robustness of the findings. We examined the ATT using inverse probability weighting and nearest neighbor propensity score matching. P < 0.05 was considered to be statistically significant.

Results

Patients

Data were collected on 29,922 patients with colectomies for colon cancer with or without obstruction (any stage) in the 2013–2015 NSQIP data with ASA class < 5. Of those, 1370 patients were diagnosed with locally advanced colon cancer (T4) non-emergently with ASA class 0-IV, 563 patients underwent LC and 807 patients underwent OC, and these together comprised the study population (Table 1). Patients were predominantly white (71.1%) and non-Hispanic (84.0%). Twenty-nine percent of patients were obese. Most patients had ASA class three (56.0%), and were nonsmokers (82.1%).

Table 1 Patient characteristics by laparoscopic versus open surgery, NSQIP 2013–2015.

Unmatched outcomes

Of all patients, 45.1% experienced at least one adverse postoperative outcome (Table 2), which was higher in OC (52.2%) versus LC patients (35.0%) (p < 0.05). Mortality was 3.1%, which was higher in OC (4.1%) versus LC patients (1.8%) (p < 0.05). Ileus was prolonged in OC patients (26.9%) versus LC patients (14.4%) (p < 0.05). Blood transfusions were more frequent in OC (22.2%) versus LC patients (11.9%) (p < 0.05). Length of stay was an average of 3 days shorter for LC versus OC patients (p < 0.05). In LC patients, 31.3% of patients were converted to open surgery. No other differences existed between OC and LC patients (p > 0.05).

Table 2 Patient outcomes of laparoscopic versus open colectomy, NSQIP 2013–2015.

Propensity-score matched outcomes

The percentage of patients who experienced at least one of the adverse postoperative outcomes was 10.7% (95% CI − 16.7; − 4.7) lower in LC versus OC patients (Table 2). For every nine patients treated with LC, there was one fewer adverse postoperative outcome compared to OC. Prolonged ileus was 11.0% (95% CI − 15.7; − 6.2) lower in LC versus OC patients. The percentage of LC patients requiring blood transfusion was 4.3% (95% CI − 8.7; 0.0) lower in LC versus OC patients. Length of stay was an average of 2 days (95% CI − 3.1; − 1.1) shorter for LC versus OC patients. However, LC patients were in the operating room an average of 14.3 min longer (95% CI 2.2; 26.5). Mortality was similar in both patient groups. No other statistical differences existed between OC and LC patients. For all comparisons, LC and OC patients were well balanced after matching based on the standardized differences as well as the means and variances of the covariates.

Heterogeneity in LC effectiveness

Postoperative outcomes were similar for both LC and OC among patients with T4a and those with T4b colon cancer (p = 0.976) (Table 3). There were no significant differences in length of stay between both types of surgery among T4a and T4b colon cancer patients (p = 0.989). Mean length of operation was longer among T4b patients regardless of the type of surgery, and LC resulted in longer average operation time among T4a patients (p = 0.005).

Table 3 Effect of laparoscopic versus open colectomy by type of T4 tumor, NSQIP 2013–2015.

Composite adverse postoperative outcomes between LC and OC were similar regardless of where the tumor was located (ascending, descending, transverse colon) (p = 0.397) (Table 4). Mean length of stay was consistently lower for LC versus OC patient, but this was irrespective of where the tumor was located (p = 0.930). Mean length of operation was lower among tumors located in the ascending colon versus those located in the descending or transverse colon. Additionally, the difference in operation time between LC and OC differed by location, with LC associated with an increase in operation time for tumors located in the descending colon, a slight reduction in operation time for tumors in the transverse and ascending colon (p = 0.001).

Table 4 Effect of laparoscopic versus open colectomy by type of tumor location, NSQIP 2013–2015.

The composite outcome, length of stay, and length of operation were all similar between OC and LC among obese and nonobese patients (Table 5). While 45.2% of obese patients who underwent OC experienced at least one of the composite outcomes compared to 35.5% of obese patients who underwent LC, this same of pattern of worse composite outcomes when undergoing OC was seen among nonobese patients. Thus, LC was similarly effective compared to OC among obese versus nonobese patients with T4 colon cancer (p = 0.295). Mean length of stay was about two days shorter for LC versus OC, but that difference existed for both obese and nonobese patients (p = 0.589). The mean length of operation was about 20 min longer in LC versus OC patients, but this difference was similar for both obese and nonobese T4 colon cancer patients (p = 0.357).

Table 5 Effect of laparoscopic versus open colectomy by obesity, NSQIP 2013–2015.*

Our findings were generally robust with respect to different methods of propensity score matching and inclusion of hand-assisted approach in LC (online Tables 14).

Discussion

This is the first and largest study to examine differences in effectiveness of LC in various types of locally advanced (T4) colon cancer patients. In matched analysis, LC patients had better overall outcomes and shorter lengths of stay compared with OC patients. Studies to date comparing LC and OC in T4 colon cancer patients consist predominantly of single-institution studies and one meta-analysis of five small studies, resulting in unstable estimates of many patient outcomes13,14,15,16,17.

T4b tumors are technically more demanding than T4a colon tumors. Our results show that LC is less likely to be used in T4b than T4a cancers, due to possible involvement of other organs requiring multi-visceral resection. We also observed no statistical difference in outcomes using data of over 900 T4a and T4b colon cancer patients, suggesting that LC can be used safely in T4b patients. Only two studies15,26 were identified as part of a recent meta-analysis focused on patient outcomes using LC in T4b colon cancers18. Neither study observed differences in overall survival between the LC and OC groups, but the power to detect clinically important differences was low because there were fewer than 100 T4b patients in both studies combined.

LC of transverse colon cancers is more challenging than cancers at other locations in the colon because of anatomical constraints24. Small studies that excluded locally advanced colon cancers showed few differences between LC and OC in transverse colon cancers22,23,24. Our results extend these findings to suggest that LC can be used safely and effectively in locally advanced cancer, even those located in the transverse colon.

Older studies have argued that obesity could be a contra-indication to LC because of technically difficulties20,21. However, our results show that obese patients were more likely to receive LC than nonobese patients during 2013–2015. While LC appears to result in similar patient outcomes in obese and nonobese colon cancer patients33, T4 colon cancer patients were not included. Small studies with fewer than 50 patients showed similar outcomes of LC in obese and nonobese patients who receive colon resection for various reasons34. Our finding based on 1370 patients now confirm these results to show similar outcomes of LC in obese and nonobese T4 patients, suggesting that there is no reason for obese T4 colon cancer patients not to undergo LC.

A strength of our study is its inclusion of patient outcomes from multiple hospitals reporting on many different types of outcomes. Our matched propensity-score analysis maximized causal inferences35. High-quality observational studies can provide information on treatment effectiveness in subpopulations36, because it is unlikely that a randomized trial will be conducted to determine which patients benefit from LC.

We also recognize some limitations of our findings. Some patient outcomes were relatively infrequent. Therefore, we constructed a composite outcome, which is less likely to reflect this limitation. In addition, we were unable to control for characteristics of hospitals (e.g., enhanced recovery after surgery), surgeons (e.g., volume), or tumors (e.g., resection margins, lymph nodes reported) in the propensity score because of confidentiality concerns with releasing this data. In addition, the similarity in patient outcomes between LC and OC may be due to more skilled laparoscopists at facilities with higher volume. Thus, the potential for selection bias remains present. Furthermore, we recognize that the NSQIP typically includes data from larger hospitals and is not a nationally representative sample. Finally, we recognize that the effectiveness of LC may vary within the large range of BMIs that is included in our definition of obesity (BMI ≥ 30 kg/m2)37, but the sample size was insufficient to examine LC effectiveness in patients with BMI ≥ 40 kg/m2.

Thus, T4 colon cancer patients, including obese patients, those with T4b colon cancer, and those with cancer located in the transverse colon, can safely receive LC based on their lower rates of adverse outcomes.