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Outcomes of abdominoperineal resection for management of anal cancer in HIV-positive patients: a national case review
© The Author(s). 2016
Received: 13 February 2016
Accepted: 2 August 2016
Published: 5 August 2016
The incidence of anal cancer in human immunodeficiency virus (HIV)-positive individuals is increasing, and how co-infection affects outcomes is not fully understood. This study sought to describe the current outcome disparities between anal cancer patients with and without HIV undergoing abdominoperineal resection (APR).
A retrospective review of all US patients diagnosed with anal squamous cell carcinoma, undergoing an APR, was performed. Cases were identified using a weighted derivative of the Healthcare Utilization Project’s National Inpatient Sample (2000–2011). Patients greater than 60 years old were excluded after finding a skewed population distribution between those with and without HIV infection. Multivariable logistic regression and generalized linear modeling analysis examined factors associated with postoperative outcomes and cost. Perioperative complications, in-hospital mortality, length of hospital stay, and hospital costs were compared for those undergoing APR with and without HIV infection.
A total of 1725 patients diagnosed with anal squamous cell cancer undergoing APR were identified, of whom 308 (17.9 %) were HIV-positive. HIV-positive patients were younger than HIV-negative patients undergoing APR for anal cancer (median age 47 years old versus 51 years old, p < 0.001) and were more likely to be male (95.1 versus 30.6 %, p < 0.001). Postoperative hemorrhage was more frequent in the HIV-positive group (5.1 versus 1.5 %, p = 0.05). Mortality was low in both groups (0 % in HIV-positive versus 1.49 % in HIV-negative, p = 0.355), and length of stay (LOS) (10+ days; 75th percentile of patient data) was similar (36.9 % with HIV versus 29.8 % without HIV, p = 0.262).
Greater hospitalization costs were associated with patients who experienced a complication. However, there was no difference in hospitalization costs seen between HIV-positive and HIV-negative patients (p = 0.66).
HIV status is not associated with worse postoperative recovery after APR for anal cancer as measured by length of stay or hospitalization cost. Further study may support APRs to be used more aggressively in HIV-positive patients with anal cancer.
The incidence of squamous cell anal cancer in the last decade has been increasing , and the disease disproportionately affects HIV-positive individuals . In non-elderly populations, anal cancer affects approximately 46 in 100,000 HIV-positive men and 10 in 100,000 HIV-positive women compared to 2 in 100,000 HIV-negative men and negligible rates for HIV-negative women . Increasing evidence suggests that the HIV-positive population with anal cancer is distinctly different from the historical squamous cell anal cancer population . Amongst HIV-positive individuals, the risk of anal cancer diagnosis is 25 times higher [2, 5], and HIV infection increases the risk of death from anal cancer by one to four times [4, 6, 7]. HIV-positive patients with anal cancer are more likely to die of anal cancer than those without HIV, and prior studies have suggested a less effective initial treatment response in the HIV-positive population to first-line anal cancer therapy [4, 8–12].
The National Comprehensive Cancer Network (NCCN) Clinical Practice Guidelines in Oncology for anal carcinoma recommends chemoradiation therapy as the primary treatment . This recommendation arises from historical findings that the majority of patients who underwent surgical resection had a complete pathological response with no evidence of residual tumor in the pathological specimen after neoadjuvant chemoradiation therapy was administered. Chemoradiation rivals abdominoperineal resection in that it preserves anal sphincter function [14, 15]. For progressive and persistent disease, abdominoperineal resection is recommended.
Anal cancer is rare with less than 8000 reported cases in the USA annually [1, 16], and recurrent anal cancer eligible for salvage surgery is less than 5 % of total cases [17, 18]. All studies of recurrent squamous cell anal cancer that go beyond observational survival statistics are typically based on small case series usually reporting a single institution’s experience of only 100 or fewer cases [19, 20]. Moreover, the vast majority of these studies do not examine the relationship between HIV infection and anal cancer surgery outcomes even though the virus has been implicated in the rise of anal cancer and its worsening outcomes in recent years [1, 2, 4, 21]. Without larger case populations with good-quality data, the risk factors, trajectories, and subgroup disparities have been difficult to describe. This study aims to describe differences between anal cancer patients with and without HIV undergoing abdominoperineal resection (APR).
Under Institutional Review Board approval, selection criteria for this study included all patients diagnosed with squamous cell anal cancer undergoing APRs from January 1, 2000 through December 31, 2011 using the Agency for Healthcare Research and Quality’s (AHRQ) Healthcare Utilization Project’s (HCUP) National Inpatient Sample (NIS). The NIS is the largest all-payer inpatient healthcare database in the USA and, with weighting, represents approximately 95 % (~20 % unweighted) of all hospitalized patients in the USA. Patients with anal cancer requiring an APR were identified by the International Classification of Diseases, 9th Revision (ICD-9) codes (anal cancer 154.2, 154.3; APR 48.5×), which were also used for comorbidity and complication reporting (Additional file 1: Table S1). ICD-9 coding was also used to group patients with (042) and without HIV as well as those with (86.7×) and without perineal closure tissue flaps.
Study variables were selected through a consensus-driven selection process using the available variables in the National Inpatient Sample and excluding those that five experienced colorectal surgeons found to be unlikely to be predictive of outcomes following abdominoperineal resection. Patient demographics were included in the study (e.g., age, sex, race) with age categorized into decades. Hospital characteristics (e.g., teaching vs. non-teaching hospital, urban vs. rural hospital) were included. Categories of comorbidities (e.g., diabetes; cardiovascular, liver, pulmonary, and renal) and postoperative complications (e.g., renal, cardiac, respiratory, liver, and gastrointestinal; deep venous thrombosis/pulmonary embolism, wound and intra-abdominal infections, sepsis and septic shock, postoperative hemorrhage, re-exploration) were identified using ICD-9 codes from external sources . In-hospital mortality was examined. Using hospital-specific cost-to-charge ratios provided by HCUP, hospitalization costs per patient were derived. All dollar values were adjusted to 2011 equivalents.
HCUP NIS data was obtained with weighting to the size of the US population. Continuous variables were compared using the Mann-Whitney test of medians. Categorical variables were compared using the chi-square test. Logistic regression models were used to examine which factors determined extended length of stay. A generalized linear model examined which factors increased hospitalization costs. A modified Park test was used to determine the appropriate distribution. Both models were built using forward and backward selection methods in which HIV status was forced into the model and variables were retained in the model if their p values were less than 0.20. A p value of <0.05 was considered statistically significant. All analyses were performed using Stata/MP® version 12.1 (StataCorp, College Station, TX).
Patients' demographics and baseline characteristics
HIV− >60 years
98 (6.9 %)
80 (25.9 %)
567 (40.0 %)
119 (38.5 %)
110 (35.6 %)
711 (44.2 %)
900 (55.9 %)
432 (30.6 %)
293 (95.1 %)
649 (44.1 %)
981 (69.4 %)
15 (4.9 %)
956 (55.9 %)
796 (77.9 %)
160 (60.6 %)
1020 (84.7 %)
125 (12.3 %)
55 (20.7 %)
85 (7.0 %)
50 (4.9 %)
29 (10.8 %)
63 (5.2 %)
15 (1.5 %)
11 (0.8 %)
≤10 (<1 %)
30 (2.9 %)
16 (6.0 %)
26 (2.1 %)
144 (10.1 %)
25 (8.2 %)
223 (13.8 %)
9 (0.6 %)
134 (8.3 %)
19 (1.3 %)
≤10 (3 %)
16 (1 %)
180 (12.7 %)
30 (9.7 %)
299 (18.6 %)
20 (1.4 %)
≤10 (3 %)
43 (2.6 %)
≤10 (3 %)
1089 (76.8 %)
252 (81.8 %)
1055 (62.4 %)
Any 1 comorbidity
286 (20.2 %)
47 (15.2 %)
508 (31.6 %)
Any 2 comorbidities
43 (3.0 %)
9 (2.9 %)
88 (5.5 %)
Any 3 comorbidities
≤10 (0.6 %)
329 (23.2 %)
56 (18.1 %)
606 (37.6 %)
Perineal tissue flaps
191 (13.5 %)
49 (16.0 %)
113 (7.0 %)
1226 (86.5 %)
259 (84.0 %)
1497 (93.0 %)
1067 (75.8 %)
239 (77.4 %)
929 (57.9 %)
340 (24.2 %)
70 (22.7 %)
676 (42.1 %)
1321 (93.8 %)
302 (98.1 %)
1469 (91.5 %)
87 (6.2 %)
≤10 (<3 %)
136 (8.48 %)
After excluding elderly patients, a total of 1725 patients diagnosed with anal squamous cell cancer undergoing APR were identified. Three hundred eight patients (17.9 %) were HIV-positive. HIV-positive patients were younger than HIV-negative patients undergoing APR for anal cancer with a median age of 47 versus 51 years (p < 0.001), and HIV-positive patients were also disproportionately male (95.1 versus 30.6 %, p < 0.001). There was no statistical difference in race, comorbidities (diabetes, cardiovascular, liver, pulmonary, renal), use of tissue flaps for perineal closure, whether the surgery was performed at a teaching hospital, and the type of community (urban versus rural). The characteristics of the two populations are presented in Table 1.
Postoperative outcomes following APR for anal cancer, compared by HIV infection status
106 (7.5 %)
28 (9.1 %)
154 (9.6 %)
≤10 (<1 %)
≤10 (<3 %)
68 (4.2 %)
221 (15.6 %)
56 (17.8 %)
258 (16.0 %)
15 (1.0 %)
29 (1.8 %)
16 (1.2 %)
30 (1.8 %)
Wound infection and intra-abdominal infection
200 (14.1 %)
39 (12.5 %)
209 (13.0 %)
40 (2.8 %)
≤10 (<3 %)
71 (4.4 %)
19 (1.4 %)
16 (5.1 %)
46 (2.8 %)
447 (31.5 %)
107 (34.7 %)
613 (38.1 %)
21 (1.5 %)
0 (0 %)
46 (2.9 %)
Length of staya
114 (36.9 %)
Mean (95 % CI)
Multivariable logistic regression model for extended length of stay after APR for anal cancer
Unadjusted OR (95 % CI)
Adjusted OR (95 % CI)
Generalized linear modeling (gamma distribution) of total hospitalization costs after APR for anal cancer
Adjusted exp:coefficienta (95 % CI)
Mean difference in cost (2011$)
This study highlights important differences between those with and without HIV infection undergoing APR for anal cancer. In a weighted, national sample of patients requiring APR for anal cancer, HIV-positive patients were more likely to be male and, on average, younger than HIV-negative patients. However, this study also found important similarities between these two subpopulations with anal cancer requiring APR. Except for postoperative hemorrhage, which was more common in HIV-positive patients, there were no significant differences in complications, inpatient mortality, or length of stay between HIV-positive and HIV-negative patients. For median hospitalization costs, there was borderline significance; however, further analysis adjusting for other factors showed it to be both statistically insignificant.
Multivariable analysis demonstrated that the majority of variance in length of stay is explained by the occurrence of complications, more complex perineal closures, and the tendency for males to remain hospitalized longer than females, rather than a direct association with HIV infection. Gender differences were also found in hospitalization costs with females having lower costs than males. This trend may be driven by the larger number of males in the HIV-positive subset of anal cancer patients and the association of male gender with increased hospital length of stay following APR.
The limitations of our study deserve discussion. Many limitations of this study are inherent to the HCUP NIS database. First, this study was performed retrospectively using a national sample of patients. It is possible that surgeon selection bias of whom was selected for APR versus who was declined surgery may influence these results. The database does not differentiate outcomes based on surgeon experience or techniques for abdominoperineal resection. Long-term oncologic outcomes are also not followed through the NIS. Although the NIS is a sample of hospitalized patients from all US states and with appropriate stratified sampling represents 95 % of US inpatients, it still relies on hospital-reported ICD-9 codes for all the diagnoses and procedures studied here. The database contains administrative-level data and has the potential for coding errors and omissions. Hence, some components of patients’ care may not be recorded in the NIS .
The low prevalence of anal cancer requiring APR further limits this study’s conclusions. There are just over 7000 cases of anal cancer annually in the USA [1, 19], and less than 5 % of these cases require APR (e.g., late-stage disease, recurrent disease) [17, 18]. Furthermore, patients over the age of 60 were excluded to prevent confounding. The findings reported here are suggestive of no difference between patients undergoing APR for anal cancer with or without HIV infection, but the low prevalence limits statistical power. One important question for further exploration is whether the increased incidence of postoperative bleeding seen in HIV-positive patients—a relationship not previously seen—persists across other HIV-positive surgical patients, a potential unrecognized “idiopathic HIV-related functional coagulopathy”. However, it is important to note that this is the largest population of anal cancer patients undergoing APR ever studied, and there is no practical means to increase the size of the population studied in the near term.
Finally, this study is unable to assess long-term results regarding the post-hospital course of patients with anal cancer following APR. The NIS does not have any data following inpatient discharge, and the de-identified nature of the data prevents linking of NIS patient records to cancer databases that could potentially inform the matter. An important question this study is not able to answer is whether HIV infection status affects the long-term course of anal cancer after APR, such as rate of recurrence and overall survival.
Our hypothesis was that HIV-positive patients would do worse following an APR than HIV-negative patients due to recognized risk factors present in HIV-positive patients like atypical disease presentation, poor wound healing, and more expensive medical care [24–26]. However, our findings do not support this hypothesis. Our analysis suggests that HIV infection has no independent effect on perioperative mortality, length of stay, or hospitalization costs after accounting for other factors.
This conclusion is contrary to conventional wisdom. We believe there are two possible explanations for our findings. First, it is possible that the HIV-positive patients in this study were substantially healthier than historical populations previously studied. This study exclusively used data after January 1, 2000, while much of the previous literature examined HIV-associated disease at the height of the AIDS epidemic in an era prior to the introduction of highly active anti-retroviral therapy (HAART). Many studies specifically highlight low CD4 cell counts as a causal link to morbidity [24, 25]. It is also widely understood that CD4 cell counts rise with initiation of HAART . One explanation for the lack of difference in outcomes between HIV-positive and HIV-negative anal cancer patients undergoing APR is that there may be little physiologic difference between these two populations. In the current era, it is possible that HIV-positive patients may no longer represent a unique population when it comes to surgical care if their HIV infection is well controlled on HAART. However, it is likely that there is considerable HIV-related variability within the population. For example, a 2012 study examined CD4 counts amongst HIV-positive patients undergoing chemotherapy for anal cancer and demonstrated median CD4 cell counts <300 suggesting ongoing active HIV infection . Another limitation of the current study is the lack of CD4 counts to stratify patients by degree of immunosuppression.
An alternative explanation for the lack of significant difference between the two subsets studied has more concerning healthcare implications. Is it possible HIV-positive patients are thought to be too high-risk for high morbidity surgery like APRs and therefore being offered less optimal therapies instead? Previous studies have made the argument that APRs should be offered earlier to high-risk patients with anal cancer [29, 30]. One would expect HIV-positive patients to be disproportionately represented amongst those needing an APR and therefore should have worse outcomes. Perhaps the lack of difference in outcomes seen here is indicative of the need for liberalized selection of HIV-positive patients for APR to optimize long-term outcomes. Future prospective studies may need to account for the inherent selection of optimal surgical candidates from the broader population of those patients in which an APR for anal cancer is indicated.
An 11-year retrospective study of the largest HIV population of patients undergoing APR for anal cancer shows that perioperative outcomes and costs are similar to HIV-negative patients undergoing APR. Further study of linked cancer datasets and prospective studies of HIV-positive patients diagnosed with anal cancer are necessary to better understand this phenomenon.
APR, abdominoperineal resection; HIV, human immunodeficiency virus
This research was not supported with outside funding.
Availability of data and materials
All data presented here is obtainable directly from the National Inpatient Sample database.
ILL, HA, ES, JE, EW, SG, BS, and SF contributed to the study concept and design. ILL, HA, JC, ES, SF contributed to the acquisition, analysis, or interpretation of data. ILL, HA, ES, SF contributed to the draft of the manuscript. ILL, HA, JC, ES did the statistical analysis. JE, EW, SG, BS, and SF did the study supervision. All authors performed critical revision of the manuscript for important intellectual content. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
This study was performed using national de-identified hospital-level data. The Johns Hopkins University School of Medicine Institutional Review Board found the study exempt from further review.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
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