Health Related Quality of Life Following Hepatectomy for Colorectal Liver Metastasis: Global and Disease Specific Changes Over Time
1 other identifier
observational
219
1 country
7
Brief Summary
This study is being done to learn more about health related quality of life factors in people having surgery for colorectal liver metastasis. The investigators will look at how these factors may change over time. The information gained from this study will help the investigators to understand the long-term effects that cancer treatments have on the health related quality of life of patients. This information is of high value and will help doctors talk to patients about the possible effects of their operations. While many patients live a long time after such operations, the studies that have been done do not tell the full story of what patients go through after surgery. This study will help us to understand cancer treatment from the patient's perspective. It will also help cancer patients make better decisions about their treatment options and will help them know what to expect after the operation.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Mar 2015
Longer than P75 for all trials
7 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2015
CompletedFirst Submitted
Initial submission to the registry
March 23, 2015
CompletedFirst Posted
Study publicly available on registry
March 26, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
March 1, 2027
April 14, 2026
April 1, 2026
12 years
March 23, 2015
April 9, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
changes in the quality of life (QoL)
in patients at high risk of recurrence undergoing hepatectomy to assess health related quality of life (HRQoL) using the EORTC QLQ-C30, QLQ-LMC21 and the EuroQol EQ-5D-5L, in patients at high risk of recurrence undergoing hepatectomy for colorectal liver metastasis and to evaluate global and disease specific changes over time.
3 years
Study Arms (1)
patients following hepatectomy
Interventions
Questionnaires/Forms to be completed preoperatively in clinic with assistance from research study administrator: * Baseline sociodemographic and clinical variable data sheet (RSA) * EORTC QLQ-C30, QLQ-LMC21, EuroQoL EQ-5D-5L/VAS * Baseline disease status and treatment assessment questionnaire Questionnaires/Forms to be completed at first postoperative clinic visit: * EORTC QLQ-C30, QLQ-LMC21, EuroQoL EQ-5D-5L/VAS Questionnaires/Forms to be mailed to patients at ± 2 month window at the following time points 6,12,18,24, and 36 months following hepatectomy: * EORTC QLQ-C30, QLQ-LMC21, EuroQoL EQ-5D-5L/VAS * Post surgical follow up disease status and treatment assessment questionnaire * At 8 weeks following the mailing of the initial questionnaire package if no response has been received, research personnel will attempt to contact participants by phone.
Eligibility Criteria
All patients scheduled to undergo liver resection who meet the established criteria will be approached for participation in this study during their preoperative visit. Should patients not undergo their liver resection surgery within 30 days of consent they will be excluded and replaced. Patients undergoing a two stage resection will have their time point frozen for up to six months after their initial surgery. If the time before the second stage of their resection exceeds six months, these patients will be excluded and replaced. The time point will restart at the completion of the second time point. If the patient has an incomplete resection without mention of a second stage resection, the patient will be made ineligible, taken off study, and replaced.
You may qualify if:
- Diagnosis of Colorectal cancer liver metastases (CRLM)
- \> 18 years of age
- Absence of unresectable extrahepatic disease
- No previous liver surgery for CRLM
- Clinical risk score (CRS) \>/= 3 or \> 4 tumors
- CRS includes the following variables;
- Lymph node positive primary
- Disease free interval \<12 months
- CEA level \>200ng/mL (highest CEA level within 6 months prior to surgery, not including day of surgery)
- Tumor size \> 5cm
- Number of tumors \>1(based on most recent scan or pathology before liver resection)
- Each variable is given a score of one and summed to give final CRS
- Clinical risk score (CRS) \< 3 with pending variables that cannot be determined preoperatively
- If CRS is still \< 3 postoperatively, these patients will be excluded and replaced (inevaluable).
- Ability to read and write in English
- +2 more criteria
You may not qualify if:
- Non-English speaking
- Inability to read and/or write
- International Patients
- Concurrent malignancy (excluding non-melanoma skin cancers)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (7)
Memorial Sloan Kettering Basking Ridge (Consent and Follow up)
Basking Ridge, New Jersey, United States
Memorial Sloan Kettering Monmouth (Consent and Follow up)
Middletown, New Jersey, 07748, United States
Memorial Sloan Kettering Bergen (Consent and Follow up)
Montvale, New Jersey, 07645, United States
Memorial Sloan Kettering Commack (Consent and Follow up)
Commack, New York, 11725, United States
Memorial Sloan Kettering Westchester (Consent and Follow Up)
Harrison, New York, 10604, United States
Memorial Sloan Kettering Cancer Center (All Protocol Activities)
New York, New York, 10065, United States
Memorial Sloan Kettering Nassau (Consent and follow up)
Uniondale, New York, 11553, United States
Related Links
Study Officials
- PRINCIPAL INVESTIGATOR
Michael D'Angelica, MD
Memorial Sloan Kettering Cancer Center
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 23, 2015
First Posted
March 26, 2015
Study Start
March 1, 2015
Primary Completion (Estimated)
March 1, 2027
Study Completion (Estimated)
March 1, 2027
Last Updated
April 14, 2026
Record last verified: 2026-04