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Proactive Management of Endoperitoneal Spread in Colonic Cancer (PROMENADE)

Primary Purpose

Colon Cancer, Intraperitoneal Rectal Cancer

Status
Not yet recruiting
Phase
Phase 3
Locations
Italy
Study Type
Interventional
Intervention
Standard surgical treatment
Proactive management
Standard adjuvant systemic chemotherapy
Sponsored by
University of Roma La Sapienza
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Colon Cancer

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with colon cancer or intraperitoneal rectosigmoid cancer with clinical (by CT) high-risk(> 5mm) T3, T4 tumors, any N, M0
  • Performance Status (ECOG) 0, 1 or 2
  • Signed informed consent

Exclusion Criteria:

  • BMI> 30
  • Impossibility of an adequate follow-up
  • Intra and extraabdominal metastatic disease, multiple colorectal cancer or other malignancies
  • Active infections or severe associated medical conditions (ASA IV or V)
  • Abnormal bone marrow or renal and liver function indices

Sites / Locations

  • ASST Nord Milano P.O. Città di Sesto S. Giovanni
  • ASO S. Croce e Carle
  • Azienda Ospedaliera dei Colli
  • Istituto Nazionale Tumori IRCCS Fondazione Pascale di Napoli
  • Ospedale di Rimini
  • University of Rome Sapienza
  • Ospedale Sant'Eugenio
  • Azienda Ospedaliera Universitaria Integrata di Verona

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Standard surgical treatment group

Proactive management group

Arm Description

Colon cancer patients (high-risk T3 and T4) without peritoneal or systemic metastases are resected for cure. Standard adjuvant systemic chemotherapy (FOLFOX or CAPOX regimens for 6 months) will be reserved in pT3 tumors with poor prognostic factors, pT4 tumor and if lymph-nodes metastases are present. Presence or absence of peritoneal recurrence will be evaluated by MDCT.

Colon cancer patients (high-risk T3 and T4) without peritoneal or systemic metastases are resected for cure. Simultaneously patients will undergo infracolic omentectomy, appendectomy, exeresis of the liver round ligament and, in women, a bilateral oophorectomy. At the end of surgical procedure HIPEC will be performed with oxaliplatin 460 mg/m2 and before the beginning of HIPEC an intravenous infusion of 400 mg/m2 of 5-FU and 20 mg/m2 of leucovorin will be administered. Standard adjuvant systemic chemotherapy (FOLFOX or CAPOX regimens for 6 months) will be reserved in pT3 tumors with poor prognostic factors, pT4 tumor and if lymph-nodes metastases are present. Presence or absence of peritoneal recurrence will be evaluated by MDCT.

Outcomes

Primary Outcome Measures

Incidence of endoperitoneal recurrence at 36 months
The primary endpoint is the incidence of endoperitoneal recurrence at 36 months defined as the proportion of subjects with peritoneal metastases at 36 months from randomization.

Secondary Outcome Measures

disease-free survival (DFS)
disease-free survival (DFS)
overall survival (OS)
overall survival (OS)
extraperitoneal (systemic) or liver recurrence rate
morbidity rate
morbidity rate
HIPEC toxicity rate
HIPEC toxicity rate
EORTC QLQ-C30 Summary Score
The EORTC QLQ-C30 Summary Score range from 0 to 100 and is calculated from the mean of 13 of the 15 QLQ-C30 scales (the Global Quality of Life scale and the Financial Impact scale are not included). Prior to calculating the mean, the symptom scales need to be reversed to obtain a uniform direction of all scales. QLQ-C30 Summary Score = (Physical Functioning+ Role Functioning+ Social Functioning+ Emotional Functioning+ Cognitive Functioning+ 100-Fatigue+ 100-Pain+ 100-Nausea_Vomiting+ 100-Dyspnoea+ 100-Sleeping Disturbances+ 100-Appetite Loss+ 100-Constipation+ 100-Diarrhoea)/13
EORTC QLQ-C30 Summary Score
The EORTC QLQ-C30 Summary Score range from 0 to 100 and is calculated from the mean of 13 of the 15 QLQ-C30 scales (the Global Quality of Life scale and the Financial Impact scale are not included). Prior to calculating the mean, the symptom scales need to be reversed to obtain a uniform direction of all scales. QLQ-C30 Summary Score = (Physical Functioning+ Role Functioning+ Social Functioning+ Emotional Functioning+ Cognitive Functioning+ 100-Fatigue+ 100-Pain+ 100-Nausea_Vomiting+ 100-Dyspnoea+ 100-Sleeping Disturbances+ 100-Appetite Loss+ 100-Constipation+ 100-Diarrhoea)/13

Full Information

First Posted
November 9, 2016
Last Updated
May 4, 2023
Sponsor
University of Roma La Sapienza
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1. Study Identification

Unique Protocol Identification Number
NCT02974556
Brief Title
Proactive Management of Endoperitoneal Spread in Colonic Cancer
Acronym
PROMENADE
Official Title
Proactive Management of Endoperitoneal Spread in Colonic Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
March 1, 2024 (Anticipated)
Primary Completion Date
September 1, 2024 (Anticipated)
Study Completion Date
September 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Roma La Sapienza

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study aims to determine the oncological effectiveness, compared to standard surgical treatment, of proactive management including target organs for peritoneal spread resection (omentectomy, bilateral adnexectomy, appendectomy, hepatic round ligament resection) and preventive HIPEC (intraperitoneal oxaliplatin with concomitant i.v. 5-fluorouracil/leucovorin) following a curative resection of high-risk ( >/= 5 mm tumor invasion beyond the muscularis propria) T3 and T4 colon cancer in preventing the development of peritoneal metastases. Adjuvant systemic chemotherapy will be reserved in both groups for patients with poor prognostic factors according to Folinic acid/Fluorouracil/Oxaliplatin (FOLFOX) or to Capecitabine/Oxaliplatin (CAPOX) regimens. Hypothesis: The hypothesis is that compared to the standard treatment proactive management following curative resection of high-risk T3 and T4 colon cancer will reduce the development of endoperitoneal metastases
Detailed Description
Colorectal cancer is one of the leading causes of cancer death in developed countries. Despite recent advances in understanding the molecular pathogenesis and improvements in diagnosis and treatment, more than 1,2 million new cases and 600,000 deaths occur annually worldwide and cure rates remain low for patients with metastatic or recurrent disease. According to reports from the National Cancer Institute, cancer of the colon is a highly treatable and often curable disease when confined to the bowel. Surgery is the primary treatment and results in a cure rate of approximately 50% of the patients; however, recurrence following surgery is a major problem and is often the ultimate cause of death. In colon cancer locoregional recurrence (local recurrence and metachronous peritoneal spread), as the main site of recurrence, is less common (up to 10% of all recurrences) and generally occurs within 3 years of resection. An important concept is the origin of local recurrences and peritoneal metastases that have a common natural history. Specific features of the primary tumor like size and depth of bowel wall invasion (pT3-pT4), which determine a specific clinical evolution (obstruction, perforation with exfoliation of cancer cells) are responsible for endoperitoneal recurrence. Cytoreductive Surgery (CRS) defined as removal of macroscopic abdominal and peritoneal disease combined with Hyperthermic Perioperative Chemotherapy (HIPEC) is the treatment considered standard of care for selected patients with moderate to small volume peritoneal metastases secondary to colorectal cancer. Nevertheless treatment of locoregional recurrence and peritoneal metastases in colon cancer are disappointing first because only 30% of patients can be surgically treated and second because of this 30% only 15- 30% survive 5 years, leaving only 10% of patients with a chance of being cured. Furthermore the economic burden of metastatic colorectal cancer treatment is considerable including the common adverse events associated that increase healthcare resource utilization and considering the addition of biological drugs to standard treatment. An evaluation of CRS combined with HIPEC for peritoneal metastases of colorectal origin in the era of value-based medicine, showed an incremental cost respect to modern chemotherapy regimens of 44,217 US$ for life-year saved, making investment in prevention even more attractive. Despite screening for colorectal cancer in average-risk patients using colonoscopy was associated with a substantially reduced risk of diagnosis with new-onset primary late-stage tumors, colorectal cancer screening remains underused. Analyzing the recent surgical published series, the majority (around 70%), of patients with a diagnosis of colonic cancer operated with curative intent, have a pT3-4 tumor, which is exactly the high-risk class of patients for local recurrence and peritoneal metastases. In this scenario the most effective strategy to combat endoperitoneal recurrence seems prevention. Two previous studies performed in our Institution investigated how a proactive management of peritoneal metastases in colon cancer patients considered at high-risk for peritoneal recurrence according to depth of bowel wall invasion and specific histopathologic features (pT3, pT4 any N, M0, mucinous or signet ring cell pathology) influence outcome. A group of 25 patients for whom inclusion criteria were verified by intraoperative pathologic assessment, were submitted to a "proactive" treatment that included in addition to the standard surgical treatment, a greater omentectomy, appendectomy, exeresis of the liver round ligament and, in post-menopausal women, a bilateral oophorectomy. At the end of the operation, in these patients a HIPEC was performed with oxaliplatin and simultaneous iv infusion of 5-fluorouracil (FU) + leucovorin (LV). Short and long-term results showed that when compared to a control group (50 cases) of similar patients treated only by standard treatment in the same Institution, this group of patients had a statistically significant decreased incidence of peritoneal recurrence (4 vs. 28%) and an increase in overall and disease-free survival rates. These results should obviously validated by larger controlled studies, and this is the aim of the PROMENADE protocol, to verify if the treatment criteria applied in colorectal peritoneal metastases (Surgery combined with HIPEC) could represent a mean of tertiary prevention of endoperitoneal recurrence in high-risk colon cancer. However, simpler application criteria were needed for a large-scale study. For this reason histological typing have not been yet considered an inclusion criteria and will only represent a secondary outcome measure. Furthermore, also considering other experiences, the protocol will use an imaging technique (MDCT) for preoperative selection of high-risk T3 (>/= 5 mm tumor invasion beyond the muscularis propria) and T4 colon cancers, combined in patients with suspected systemic disease after MDCT with functional positron-emission tomography (PET), avoiding the need for an intraoperative frozen-sections pathologic assessment. The results of this study will hopefully confirm the therapeutic rationale that makes microscopic local seeding as the main reason for endoperitoneal recurrence. It will be also important to verify if, as demonstrated in our pilot study, a better loco-regional control of the disease will carry better long-term survival.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colon Cancer, Intraperitoneal Rectal Cancer

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
140 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Standard surgical treatment group
Arm Type
Active Comparator
Arm Description
Colon cancer patients (high-risk T3 and T4) without peritoneal or systemic metastases are resected for cure. Standard adjuvant systemic chemotherapy (FOLFOX or CAPOX regimens for 6 months) will be reserved in pT3 tumors with poor prognostic factors, pT4 tumor and if lymph-nodes metastases are present. Presence or absence of peritoneal recurrence will be evaluated by MDCT.
Arm Title
Proactive management group
Arm Type
Experimental
Arm Description
Colon cancer patients (high-risk T3 and T4) without peritoneal or systemic metastases are resected for cure. Simultaneously patients will undergo infracolic omentectomy, appendectomy, exeresis of the liver round ligament and, in women, a bilateral oophorectomy. At the end of surgical procedure HIPEC will be performed with oxaliplatin 460 mg/m2 and before the beginning of HIPEC an intravenous infusion of 400 mg/m2 of 5-FU and 20 mg/m2 of leucovorin will be administered. Standard adjuvant systemic chemotherapy (FOLFOX or CAPOX regimens for 6 months) will be reserved in pT3 tumors with poor prognostic factors, pT4 tumor and if lymph-nodes metastases are present. Presence or absence of peritoneal recurrence will be evaluated by MDCT.
Intervention Type
Procedure
Intervention Name(s)
Standard surgical treatment
Intervention Description
Standard surgical treatment (open or laparoscopic techniques) containing at least 12 lymph-nodes for accurate pN staging.
Intervention Type
Procedure
Intervention Name(s)
Proactive management
Intervention Description
Colon cancer patients (high-risk T3 and T4) without peritoneal or systemic metastases are resected for cure. Simultaneously patients will undergo infracolic omentectomy, appendectomy, exeresis of the liver round ligament and, in women, a bilateral oophorectomy. After positioning three in- and outflow catheters HIPEC perfusion starts with a minimum of 2 L isotonic dialysis fluid at a flow-rate of 1-2 l min and an inflow temperature of 42-43° C with a total of 30 minutes perfusion time. Before the beginning of HIPEC 5-fluouracil and leucovorin will be administrated intravenously to potentiate oxaliplatin activity.
Intervention Type
Drug
Intervention Name(s)
Standard adjuvant systemic chemotherapy
Other Intervention Name(s)
adjuvant capecitabine and oxaliplatin (CAPOX), adjuvant 5-FU and oxaliplatin (FOLFOX)
Intervention Description
Adjuvant systemic chemotherapy (according CAPOX or FOLFOX regimens for a total of 6 months) will be reserved in patients with pT3 tumors with poor prognostic factors, in patients with pT4 tumors and when lymph-nodes metastases are present. Presence or absence of peritoneal recurrence will be evaluated by MDCT every six months for the first 24 months and later every year for the next three years in both study arms.
Primary Outcome Measure Information:
Title
Incidence of endoperitoneal recurrence at 36 months
Description
The primary endpoint is the incidence of endoperitoneal recurrence at 36 months defined as the proportion of subjects with peritoneal metastases at 36 months from randomization.
Time Frame
36 months
Secondary Outcome Measure Information:
Title
disease-free survival (DFS)
Time Frame
3 years
Title
disease-free survival (DFS)
Time Frame
5 years
Title
overall survival (OS)
Time Frame
3 years
Title
overall survival (OS)
Time Frame
5 years
Title
extraperitoneal (systemic) or liver recurrence rate
Time Frame
3 years
Title
morbidity rate
Time Frame
1 month
Title
morbidity rate
Time Frame
6 months
Title
HIPEC toxicity rate
Time Frame
1 month
Title
HIPEC toxicity rate
Time Frame
6 month
Title
EORTC QLQ-C30 Summary Score
Description
The EORTC QLQ-C30 Summary Score range from 0 to 100 and is calculated from the mean of 13 of the 15 QLQ-C30 scales (the Global Quality of Life scale and the Financial Impact scale are not included). Prior to calculating the mean, the symptom scales need to be reversed to obtain a uniform direction of all scales. QLQ-C30 Summary Score = (Physical Functioning+ Role Functioning+ Social Functioning+ Emotional Functioning+ Cognitive Functioning+ 100-Fatigue+ 100-Pain+ 100-Nausea_Vomiting+ 100-Dyspnoea+ 100-Sleeping Disturbances+ 100-Appetite Loss+ 100-Constipation+ 100-Diarrhoea)/13
Time Frame
6 months
Title
EORTC QLQ-C30 Summary Score
Description
The EORTC QLQ-C30 Summary Score range from 0 to 100 and is calculated from the mean of 13 of the 15 QLQ-C30 scales (the Global Quality of Life scale and the Financial Impact scale are not included). Prior to calculating the mean, the symptom scales need to be reversed to obtain a uniform direction of all scales. QLQ-C30 Summary Score = (Physical Functioning+ Role Functioning+ Social Functioning+ Emotional Functioning+ Cognitive Functioning+ 100-Fatigue+ 100-Pain+ 100-Nausea_Vomiting+ 100-Dyspnoea+ 100-Sleeping Disturbances+ 100-Appetite Loss+ 100-Constipation+ 100-Diarrhoea)/13
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with colon cancer or intraperitoneal rectosigmoid cancer with clinical (by CT) high-risk(> 5mm) T3, T4 tumors, any N, M0 Performance Status (ECOG) 0, 1 or 2 Signed informed consent Exclusion Criteria: BMI> 30 Impossibility of an adequate follow-up Intra and extraabdominal metastatic disease, multiple colorectal cancer or other malignancies Active infections or severe associated medical conditions (ASA IV or V) Abnormal bone marrow or renal and liver function indices
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Paolo Sammartino, MD PhD
Phone
336615632
Ext
+39
Email
paolo.sammartino@uniroma1.it
First Name & Middle Initial & Last Name or Official Title & Degree
Tommaso Cornali, MD
Ext
+39
Email
tommaso.cornali@uniroma1.it
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paolo Sammartino, MD PhD
Organizational Affiliation
University of Roma La Sapienza
Official's Role
Principal Investigator
Facility Information:
Facility Name
ASST Nord Milano P.O. Città di Sesto S. Giovanni
City
Milano
State/Province
PD
ZIP/Postal Code
35031
Country
Italy
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gianandrea Baldazzi, MD
Email
gbaldazzi@hotmail.com
First Name & Middle Initial & Last Name & Degree
Gianandrea Baldazzi, MD
First Name & Middle Initial & Last Name & Degree
Diletta Cassini, MD
Facility Name
ASO S. Croce e Carle
City
Cuneo
ZIP/Postal Code
12100
Country
Italy
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Felice Borghi, MD
Email
borghi.f@ospedale.cuneo.it
First Name & Middle Initial & Last Name & Degree
Felice Borghi, MD
First Name & Middle Initial & Last Name & Degree
Maria Carmela Giuffrida, MD
Facility Name
Azienda Ospedaliera dei Colli
City
Napoli
ZIP/Postal Code
80131
Country
Italy
Facility Name
Istituto Nazionale Tumori IRCCS Fondazione Pascale di Napoli
City
Napoli
ZIP/Postal Code
80131
Country
Italy
Facility Name
Ospedale di Rimini
City
Rimini
ZIP/Postal Code
47923
Country
Italy
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gianluca Garulli, MD
Email
lucagarulli@gmail.com
First Name & Middle Initial & Last Name & Degree
Gialuca Garulli, MD
First Name & Middle Initial & Last Name & Degree
Basilio Pirrera, MD
Facility Name
University of Rome Sapienza
City
Roma
ZIP/Postal Code
00161
Country
Italy
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Paolo Sammartino, MD PhD
Phone
336615632
Ext
+39
Email
paolo.sammartino@uniroma1.it
First Name & Middle Initial & Last Name & Degree
Tommaso Cornali, MD
Ext
+39
Email
tommaso.cornali@uniroma1.it
First Name & Middle Initial & Last Name & Degree
Paolo Sammartino, MD PhD
First Name & Middle Initial & Last Name & Degree
Tommaso Cornali, MD
First Name & Middle Initial & Last Name & Degree
Fabio Accarpio, MD PhD
First Name & Middle Initial & Last Name & Degree
Daniele Biacchi, MD Phd
Facility Name
Ospedale Sant'Eugenio
City
Rome
ZIP/Postal Code
00144
Country
Italy
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Massimo Carlini, MD FACS
Email
maxcarlini@tiscali.it
First Name & Middle Initial & Last Name & Degree
Massimo Carlini, MD
First Name & Middle Initial & Last Name & Degree
Domenico Spoletini, MD
First Name & Middle Initial & Last Name & Degree
Daniela Apa, MD
Facility Name
Azienda Ospedaliera Universitaria Integrata di Verona
City
Verona
ZIP/Postal Code
37126
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
27065712
Citation
Sammartino P, Biacchi D, Cornali T, Cardi M, Accarpio F, Impagnatiello A, Sollazzo BM, Di Giorgio A. Proactive Management for Gastric, Colorectal and Appendiceal Malignancies: Preventing Peritoneal Metastases with Hyperthermic Intraperitoneal Chemotherapy (HIPEC). Indian J Surg Oncol. 2016 Jun;7(2):215-24. doi: 10.1007/s13193-016-0497-1. Epub 2016 Jan 26.
Results Reference
background
PubMed Identifier
24980687
Citation
Sammartino P, Sibio S, Biacchi D, Cardi M, Mingazzini P, Rosati MS, Cornali T, Sollazzo B, Atta JM, Di Giorgio A. Long-term results after proactive management for locoregional control in patients with colonic cancer at high risk of peritoneal metastases. Int J Colorectal Dis. 2014 Sep;29(9):1081-9. doi: 10.1007/s00384-014-1929-4. Epub 2014 Jul 1.
Results Reference
background
PubMed Identifier
24263309
Citation
Sammartino P, Sibio S, Accarpio F, Di Giorgio A. Prevention of peritoneal carcinomatosis from colorectal cancer: a critical issue. Ann Surg. 2014 Mar;259(3):e51. doi: 10.1097/SLA.0000000000000372. No abstract available.
Results Reference
background
PubMed Identifier
22645605
Citation
Sammartino P, Sibio S, Biacchi D, Cardi M, Accarpio F, Mingazzini P, Rosati MS, Cornali T, Di Giorgio A. Prevention of Peritoneal Metastases from Colon Cancer in High-Risk Patients: Preliminary Results of Surgery plus Prophylactic HIPEC. Gastroenterol Res Pract. 2012;2012:141585. doi: 10.1155/2012/141585. Epub 2012 May 8.
Results Reference
background

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Proactive Management of Endoperitoneal Spread in Colonic Cancer

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