ERAS Program Items Adherence, PROMs and RIOT After Colorectal Surgery

Colorectal Surgery Clinical Trial

— iCral3  

Official title:

Enhanced Recovery Pathways, Patient-reported Outcomes and Return to Intended Oncological Therapy After Colorectal Surgery: the Italian ColoRectal Anastomotic Leakage Study Group (iCral 3).

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT04397627
• Other study ID #: iCral3
• Status: Not yet recruiting
• Start date: November 1, 2020
• Est. completion date: October 31, 2021

Study information

• Verified date: May 2020
• Source: Ospedale C & G Mazzoni
• Contact: Marco Catarci, MD, FACS
• Phone: 3298610040
• Email: marco.catarci[@]sanita.marche.it
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Prospective multicenter observational no-profit study evaluating the impact of ERAS program items adherence rates on patient-reported outcomes (PRO) and return to intendend oncologic therapy (RIOT) after colorectal resection.

Prospective enrollment from November 2020 to October 2021 in 60 Italian surgical centers. All patients undergoing elective colorectal surgery with anastomosis will be included in a prospective database after written informed consent. A total of 3,000 patients is expected based on a mean of 50 cases per center.

Description:

BACKGROUND Enhanced Recovery After Surgery (ERAS) is a multimodal and multifactorial approach to the optimization of perioperative management. In order to modify and improve the response to surgery-induced trauma, the program relies on a series of evidence-based items related to pre-, intra- and post-operative care. Several meta-analyses on ERAS showed a significant reduction of morbidity rates and length of stay after colorectal surgery. However, program implementation outside clinical trials is still extremely variable, as the necessary multidisciplinary involvement makes the program vulnerable to various areas of failure, that explain the great variation in adherence rates to program items.

During the early phase of program implementation, adherence rate to program items rarely goes beyond 50%, needing to reach at least 70% in order to significantly improve results (faster recovery and reduced morbidity). Recent cohort studies reported a mean adherence rate to ERAS items between 63 and 75%. In other studies, adherence to ERAS items was higher, reaching up to 90%. Moreover, a clear and significant dose-effect curve between adherence rate to ERAS program items and early outcomes was demonstrated, and recent evidence deriving from retrospective studies suggests that ERAS programs may also offer a definite advantage over long-term survival after colorectal resection for malignancy. While many studies to date have focused on early outcomes (i.e. earlier return of bowel function, lower complication rates, and/or shorter length of inpatient stay), for the majority of oncologic operations, however, postoperative recovery carries the additional demand of returning the patient to adjuvant oncologic therapies. It is still unclear if ERAS program could improve the failure to "return to intended oncologic therapy" (RIOT) after cancer surgery due to complications and lingering poor performance status, that is strongly associated with worse oncologic outcomes, including shortened overall survival. Measuring patient-reported outcomes (PROs) addresses the gap in enhanced recovery assessment by incorporation of patient-centered quality into our global assessment of outcomes. Taken together, these data establish a paradigm for association of perioperative medical care to long-term oncologic outcomes—revealing how the perioperative care team's actions over a relatively short number of days and hours around the time of a cancer surgery can improve cancer-specific survival. The concept is that various perioperative techniques, protocols, and agents will blunt the patient's perioperative stress response, reduce complications, and improve functional recovery after surgery. Together, these effects allow more people to RIOT in a more timely fashion and in a more complete way. To the extent that the combination of preservation of immune competence and more reliable return to adjuvant therapies then reduce recurrence rates, longer and more meaningful survivals may be achieved.

Therefore, the Italian Colorectal Anastomotic Leakage study group planned this study to prospectively evaluate the impact of adherence to ERAS program items after colorectal resections on PRO in the whole population and on failure to RIOT for malignant disease.

Outcome measures

1. Preoperative risk factors (age, gender, obesity, nutritional status, diabetes, cardiovascular disease, chronic liver disease, renal failure, inflammatory bowel disease, perioperative steroid therapy, ASA class I-II vs III, SARS-CoV-2 infection)

2. Operative parameters (approach, procedure, anastomotic technique, length of operation, pTNM stage)

3. Adherence to ERAS program items

Primary Endpoints

1. Patient-related outcomes measures (PROMs):

2. Return to intended oncologic therapy (RIOT)

Secondary Endpoints

3. Anastomotic leakage rate

4. Minor and major complication rates

5. Overall length of postoperative hospital stay (including any readmission)

6. Readmission and reoperation rates

Recorded data and follow-up During the postoperative period, the local attending surgeon will make any decision for complementary exams and imaging according to his own criteria, the only exception being the creation of a proximal diverting stoma at operation, that mandates routine check of anastomotic integrity through an intraluminal contrast exam (standard x-rays or CT scan) three to six weeks after the operation. The rate of any complication will be calculated and graded according to Clavien-Dindo including all anastomotic leaks, wound infection (according to the definitions of the Centers for Disease Control and Prevention and wound culture), pneumonia (clinical symptoms, and physical and radiological examinations), central line infection (positive blood culture), urinary tract infection (positive urine culture with bacterial count). Patients will be followed-up in the outpatient clinic up to 8 weeks after discharge from the hospital.

Anastomotic dehiscence (any deviation from the planned postoperative course related to the anastomosis, or presence of pus or enteric contents within the drains, presence of abdominal or pelvic collection in the area of the anastomosis on postoperative CT scan, leakage of contrast through the anastomosis during enema or evident anastomotic dehiscence at reoperation for postoperative peritonitis) will be defined and graded according to international consensus guidelines. Anastomotic testing will be performed intraoperatively with the air-leak test (ALT) and using ICG-NIR-NBI with a standard protocol [ICG 25 mg diluted in 10 mL saline (2.5 mg/mL); first bolus i.v. injection of 4 mL (10 mg) after vascular control and mesenteric division, just before proximal and/or distal bowel division; second bolus i.v. injection of 4 mL (10 mg) just before joining anastomotic stumps; third (optional) bolus i.v. injection of 2 mL (5 mg) after the anastomosis is completed; NIR-NBI observation within 60-120" after every ICG injection (direct, laparoscopic or endoscopic)].

PROM questionnaires will be administered to all enrolled patients four to one week before the planned operation, on the day of discharge (or POD5), and 6 weeks after the operation.

RIOT rates will be recorded in all patients submitted to surgery for malignancy, according to national guidelines for colorectal cancer.

After anonymization, all data of each single case will be prospectively uploaded by local investigator(s) on a protected web-based database and incorporated into a spreadsheet for data analysis, checking for any discrepancy, that will be addressed and solved through strict cooperation between chief investigator, data manager and participating centers.

This study protocol will be submitted to the coordinating center ethics committee (Comitato Etico Regionale delle Marche - C.E.R.M.) for approval and then registered at ClinicalTrials.gov. Thereafter, all the participating centers will obtain authorization to participate from the local institutional review board. Anonymized participant-level datasets will be available after study completion upon reasonable request by contacting the principal investigator.

Statistical Analysis Quantitative values will be expressed as mean ± standard deviation (SD), median and range; categorical data with percentage frequencies. For categorical data, analysis will include the use of cross tabulation, chi squared or Fisher's exact test where indicated. Continues or discrete variables will be analyzed using Student's two-sided t test (allowing for heterogeneity of variances) or with a non-parametric test (Mann-Whitney U test or Kruskal-Wallis test as indicated). Joint and conditional multivariate association between all variables shown to be significant on univariate analysis will be assessed using binary logistic or multiple linear regression. The odds ratio (OR) will be presented followed by 95% confidence interval (95% CI). Concerning comparison of nutritional status scores, areas under the receiver-operating characteristics curve (AUC-ROC) will be calculated for all endpoints, considering values from 0.7 to 0.8 as acceptable, 0.8 to 0.9 excellent, and above 0.9 as outstanding (40). Differences in AUC-ROC curves will be analyzed with the chi-squared test. Optimal cut-off points will be obtained applying Youden's Index (Sensitivity+Specificity-1), choosing those values of the AUC-ROC curve where this index is maximal. Negative predictive values (NPV) and positive predictive values (PPV) will also be calculated; finally, a logistic regression model will be built using the presence/absence of endpoint as dependent variable, and nutritional scores ≤ or > the cut-off values as explanatory factors; using logistic transformation of the linear predictors, the probabilities of the endpoint related to the different combinations of factors level will be obtained . For all statistical tests the significant level is fixed at p < .05. Statistical analyses will be carried out using STATA software (Stata Corp. College Station, Texas, USA).

Sample size Adherence to at least 70% of the ERAS program items was identified as a cut-off for significant improvement of outcomes , with a 2:1 expected ratio below:above the cut-off. Estimating a reduction of postoperative PRO from preoperative baseline (1.0) at 0.7 for adherence above the cut-off and at 0.64 for adherence below the cut-off, alpha 0.04, beta 0.8, the required sample size is n=2,406 (802 cases above 70% adherence and 1,604 below 70% adherence). Reported rates for failure to RIOT and ERAS program items adherence below or above 70% are 13 and 6.5%, respectively (27); the required sample size for evaluation of failure to RIOT is n=885 (295 cases above 70% adherence and 590 below 70% adherence). Based on previous iCral observational study on colorectal surgery in Italy, the expected ratio of malignant:benign indications to surgery is 70:30 (2,100 resections for malignancy and 900 resections for benign disease on the basis of 3,000 expected cases).

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 3000
• Est. completion date: October 31, 2021
• Est. primary completion date: October 31, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

1. Patients submitted to laparoscopic/robotic/open/converted ileo-colo-rectal resection with anastomosis, including planned Hartmann's reversals.

2. American Society of Anesthesiologists' (ASA) class I, II or III

3. Elective or delayed urgency surgery

4. Patients' written acceptance to be included in the study.

Exclusion Criteria:

1. American Society of Anesthesiologists' (ASA) class IV-V

2. Emergent surgery

3. Pregnancy

4. Hyperthermic intraperitoneal chemotherapy for carcinomatosis.

Related Conditions & MeSH terms

• Colorectal Surgery
• Enhanced Recovery After Surgery
• Patient Reported Outcomes

Intervention

Procedure:
• Colorectal resection
All patients undergoing elective colorectal surgery with anastomosis will be included in a prospective database after written informed consent.

Locations

Country	Name	City	State
Italy	S.C. Chirurgia Generale e Oncologica - Azienda Ospedaliera S. Croce e Carle - Cuneo, Italia	Cuneo	CN
Italy	UOC Chirurgia Generale - Ospedale di Esine (BS) - ASST Valcamonica	Esine	NS
Italy	UOC Chirurgia Generale ad Indirizzo Oncologico - IRCCS San Martino IST - Genova	Genova	GE
Italy	UOC Chirurgia Generale Universitaria - Ospedale San Salvatore - L'Aquila	L'Aquila	AQ
Italy	SOC Chirurgia Colorettale - Istituto Nazionale dei Tumori - IRCCS Fondazione "G.Pascale" - Napoli	Napoli
Italy	UOC Chirurgia Generale - Ospedale Sacro Cuore Don Calabria Negrar Verona	Negrar	VR
Italy	UOC Chirurgia Generale e D'Urgenza . Azienda Ospedaliera San Camillo Forlanini Roma	Roma	RM
Italy	U.O.C. di Chirurgia Generale e dell'Esofago e Stomaco - AOUI di Verona	Verona	VR

Sponsors (1)

Lead Sponsor	Collaborator
Ospedale C & G Mazzoni

Country where clinical trial is conducted

Italy, 

References & Publications (4)

Aloia TA, Zimmitti G, Conrad C, Gottumukalla V, Kopetz S, Vauthey JN. Return to intended oncologic treatment (RIOT): a novel metric for evaluating the quality of oncosurgical therapy for malignancy. J Surg Oncol. 2014 Aug;110(2):107-14. doi: 10.1002/jso.23626. Epub 2014 May 21. — View Citation

Fearon KC, Ljungqvist O, Von Meyenfeldt M, Revhaug A, Dejong CH, Lassen K, Nygren J, Hausel J, Soop M, Andersen J, Kehlet H. Enhanced recovery after surgery: a consensus review of clinical care for patients undergoing colonic resection. Clin Nutr. 2005 Jun;24(3):466-77. Epub 2005 Apr 21. Review. — View Citation

Italian ColoRectal Anastomotic Leakage (iCral) Study Group. Anastomotic leakage after elective colorectal surgery: a prospective multicentre observational study on use of the Dutch leakage score, serum procalcitonin and serum C-reactive protein for diagnosis. BJS Open. 2020 Mar 5. doi: 10.1002/bjs5.50269. [Epub ahead of print] — View Citation

Kehlet H. Fast-track colorectal surgery. Lancet. 2008 Mar 8;371(9615):791-3. doi: 10.1016/S0140-6736(08)60357-8. Review. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in patient-reported outcome measure #1; Health Questionnaire; Euro-QoL Group EQ-5D-5L™;	Quality of life questionnaire based on five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems. Scores ranging from 5 (worst) to 125 (best)	Before the operation, postoperative day 5, 4 to 6 weeks after the operation
Primary	Change in patient-reported outcome measure #2; Health Questionnaire: MD Anderson Symptom Inventory for gastrointestinal surgery patients (MDASI-GI)	Specific quality of life questionnaire for patients submitted to GI surgery: based on 24 questions with scores ranging from 0 (best) to 10 (worst); total score from 0 (best) to 240 (worst)	Before the operation, postoperative day 5, 4 to 6 weeks after the operation
Primary	Change in patient-reported outcome measure #3; Health Questionnaire Functional Assessment of Cancer Therapy - Colorectal® (FACT-C)	Specific quality of life questionnaire for patients with colorectal cancer. Scores ranging form 0 (worst) to 144 (best).	Before the operation, postoperative day 5, 4 to 6 weeks after the operation
Primary	Return to intended oncologic therapy (RIOT)	Number of patients eligible for adjuvant therapy after surgery for colorectal cancer that receive appropriate treatment starting within 8 weeks after the operation	8 weeks after the operation
Secondary	Anastomotic leakage rate	number of anastomotic leakage	within 8 weeks from operation
Secondary	Overall morbidity rate	number of any perioperative adverse event graded according to Clavien-Dindo	within 8 weeks from operation
Secondary	Major morbidity rate	number of Clavien-Dindo grade >II perioperative adverse events	within 8 weeks from operation
Secondary	Length of hospital stay (LOS)	Total number of days spent in the hospital (including any readmission)	within 8 weeks from operation