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Parenchymal Sparing Hepatectomy in Post-chemotherapy Liver Atrophy

Performance of Parenchymal Sparing Hepatectomy in Patients With CLM and Post-chemotherapy Liver Atrophy

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06329700
Enrollment
74
Registered
2024-03-26
Start date
2010-05-01
Completion date
2022-06-30
Last updated
2024-03-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Cancer Stage IV

Brief summary

Major hepatectomy in patients with colorectal liver metastases (CLM) and post-chemotherapy liver atrophy is associated with increased complications. Whether the performance of parenchymal-sparing hepatectomy (PSH) in those patients can be safer is unknown. The aim of this study was to assess the clinical impact of post-chemotherapy liver atrophy on patients undergoing PSH for CLM. For this purpose, the occurrence of liver atrophy was recorded and then computed against the occurrence of postoperative morbidity and mortality.

Detailed description

Patients affected by CLMs and trated with neoadjuvant systemic chemotherapy and then hepatectomy were reviewed with the intent to assess the occurrence of liver atrophy, which is a sign of liver dysfunction and a source of morbidity expecially in patients treated with major or extended hepatectomy. Whether the performance of parenchymal-sparing hepatectomy (PSH) in those patients can be safer is unknown. Then, we planned to review our cases with the above mentioned endpoint.

Interventions

PROCEDUREHepatectomy

Surgical removal of a part of the liver

Sponsors

Azienda Ospedaliero Universitaria Maggiore della Carita
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Consecutive patients with multiple CLMs treated with preoperative chemotherapy and parenchymal sparing surgery; * Only patients with available volumetry of the pre- and post-chemotherapy abdominal enhanced computed tomography (CT) images;

Exclusion criteria

* Patients who underwent preoperative PVE; * Patients treated by major hepatectomies; Patients treated with thermal ablation alone or in association with hepatic resection.

Design outcomes

Primary

MeasureTime frameDescription
Postoperative complicationsFrom the date of surgery up to 90 daysAny adverse event after surgery

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026