Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
CROSCO-1 study is a national, multi-center, prospective observational study presenting patients to the emergency departments of the participating centers with obstructive left colon cancer (in the absence of metastases and peritoneal carcinomatosis) undergoing primary surgical tumor resection with a primary colorectal anastomosis (associated or not with a diverting loop ileostomy) or without a primary anastomosis ("Hartmann's procedure") or staged resection after endoscopic stenting with Self-expandable Metallic Stent (SEMS).
The main questions it aims to answer are:
Researchers will compare: primary surgical tumor resection with a primary colorectal anastomosis (associated or not with a diverting loop ileostomy) or an "Hartmann's procedure" with a staged resection after endoscopic stenting with SEMS.
Since surgical and oncological outcomes of the different treatment strategies for obstructing left colon cancers have not been studied on a large scale globally, we launched the CROSCO-1 study intending to compare the clinical results of all these therapeutic regimens in a cohort of patients treated for obstructive left-sided colorectal cancer (CRC).
The primary aim of the CROSCO-1 (Colonic Resection, stOma or self-expanding metal Stents for obstruCtive left cOlon cancer) study is to describe the outcomes of the management of emergency presentations of obstructive left CRC with colorectal resection with or without primary anastomosis versus the staged approach with SEMS insertion and subsequent colorectal resection. The primary aim of the CROSCO-1 study will be the 1-year stoma rate of patients undergoing primary emergency surgical resection (Hartmann procedure or primary resection and anastomosis) compared with patients undergoing staged resection (emergency endoscopic treatment with SEMS followed by elective resection). Other outcomes will be 30-day and 90-day major morbidity and mortality, 1-year quality of life, and the timing and type of chemotherapy initiation in the two groups.
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| primary surgical tumor resection with anastomosis or only tumor resection without anastomosis | primary surgical tumor resection with a primary colorectal anastomosis (associated or not with a diverting loop ileostomy) or without a primary anastomosis ("Hartmann's procedure") |
| |
| endoscopic stent positioning | staged resection after endoscopic stenting with Self-expandable Metallic Stent (SEMS) |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| primary tumor resection | Procedure | primary surgical tumor resection with a primary colorectal anastomosis (associated or not with a diverting loop ileostomy) or without a primary anastomosis ("Hartmann's procedure") |
| Measure | Description | Time Frame |
|---|---|---|
| Stoma rate at 1 year after tumor resection | the number of stomas after 1 year of primary surgery with tumor resection | 1 year |
| Measure | Description | Time Frame |
|---|---|---|
| 30-day and 90-day major morbidity | morbidity after 30 and 90-days | 30-days; 90-days |
| 30-day and 90-day mortality | mortality (Overall survival) after 30 and 90-days |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
The study population includes all consecutive adult patients (≥18 years of age) presenting acutely ( unplanned and non-elective presentation to hospital for urgent or emergency reasons) at the participating centers with a clinical and radiological diagnosis of (known or unknown descending or sigmoid colon tumor) for 1 year. According to the different management methods, the cohort will be divided into the following categories:
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Alessio Giordano | Contact | +390557949173 | alessio.giordano8@gmail.com | |
| Sfogli Anna | Contact | +39055794111 | sfoglia@aou-careggi.toscana.it |
| Name | Affiliation | Role |
|---|---|---|
| Alessio Giordano | AOU Careggi Firenze | Principal Investigator |
Not provided
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 42236555 | Derived | Giordano A, Mastronardi M, Fugazzola P, Montori G, Agresta F, Martellucci J, Catena F, Coccolini F, Anania G, Costa G, Bottino V, Cillara N, Prosperi P, Bergamini C, Podda M; CROSCO-1 Collaborative Group. Colonic resection or self-expanding metal stents for obstructive left colon cancer: results of a national multicenter prospective cohort study (CROSCO-1). Surg Endosc. 2026 Jun 3. doi: 10.1007/s00464-026-12929-9. Online ahead of print. |
Not provided
Not provided
all individual participant data (IPD) that underlie results in a publication
IPD can be Share for 1 year after follow up closure
by email with colleagues who will be interested
Not provided
Not provided
| ID | Term |
|---|---|
| D003110 | Colonic Neoplasms |
| ID | Term |
|---|---|
| D015179 | Colorectal Neoplasms |
| D007414 | Intestinal Neoplasms |
| D005770 | Gastrointestinal Neoplasms |
| D004067 | Digestive System Neoplasms |
Not provided
Not provided
Not provided
Not provided
Not provided
| 30-days; 90-days |
| 1-year quality of life (The 5-level EQ-5D version (EQ-5D-5L)test) | The EQ-5D-5L is an instrument to describe the quality of life with a state system comprises 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. In this first part, the patient is asked to indicate his/her health state by ticking the box next to the most appropriate statement in each of the five dimensions with graduate answers from 1 (no problem) to 5 (extreme limitations). The aggregation of the responses forms a five-digit number representing the patient's health status. in the second part, the patient is asked to indicate an assessment using a visual analog (VAS) graphically represented by a graduated scale ranging from 0 (the worst possible state of health) to 100 (the best possible state of health) on which the interviewee indicates his or her perceived level of health. | 1-year |
| Timing of chemotherapy initiation | data for chemotherapy initiation in both groups of study | 2-years |
| type of chemotherapy regimen | type of drugs regimen in both groups of study | 2-years |
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
| D004066 | Digestive System Diseases |
| D005767 | Gastrointestinal Diseases |
| D003108 | Colonic Diseases |
| D007410 | Intestinal Diseases |