Genomic stratification beyond Ras/B‐Raf in colorectal liver metastasis patients treated with hepatic arterial infusion
Background Resection of colorectal liver metastases (CLM) can cure disease, but many patients with extensive disease cannot be fully resected and others recur following surgery. Hepatic arterial infusion (HAI) chemotherapy can convert extensive liver disease to a resectable state or decrease recurre...
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Published in | Cancer medicine (Malden, MA) Vol. 8; no. 15; pp. 6538 - 6548 |
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Main Authors | , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
John Wiley & Sons, Inc
01.11.2019
John Wiley and Sons Inc Wiley |
Subjects | |
Online Access | Get full text |
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Summary: | Background
Resection of colorectal liver metastases (CLM) can cure disease, but many patients with extensive disease cannot be fully resected and others recur following surgery. Hepatic arterial infusion (HAI) chemotherapy can convert extensive liver disease to a resectable state or decrease recurrence risk, but response varies and no biomarkers currently exist to identify patients most likely to benefit.
Methods
We performed a retrospective cohort study of CLM patients receiving HAI chemotherapy whose tumors underwent MSK‐IMPACT sequencing. The frequency of oncogenic alterations and their association with overall survival (OS) and objective response rate were analyzed at the individual gene and signaling pathway levels.
Results
Three hundred and seventy patients met inclusion criteria: 189 (51.1%) who underwent colorectal liver metastasectomy followed by HAI + systemic therapy (Adjuvant cohort), and 181 (48.9%) with unresectable CLM (Metastatic cohort) who received HAI + systemic therapy, consisting of 63 (34.8%) with extrahepatic disease and 118 (65.2%) with liver‐restricted disease. Genomic alterations were similar in each cohort, and no individual gene or pathway was significantly associated with objective response. Patients in the adjuvant cohort with concurrent Ras/B‐Raf alteration and SMAD4 inactivation had worse prognosis while in the metastatic cohort patients with co‐alteration of Ras/B‐Raf and TP53 had worse OS. Similar findings were observed in a validation cohort.
Conclusions
Concurrently altered Ras/B‐Raf and SMAD4 mutations were associated with worse survival in resectable patients, while concurrent Ras/B‐Raf and TP53 alterations were associated with worse survival in unresectable patients. The mutual exclusivity of Ras/B‐Raf, SMAD4, and TP53 may have prognostic value for CLM patients receiving HAI.
Patients with colorectal liver metastases receiving hepatic arterial infusion chemotherapy who have either resectable disease with concurrently altered Ras/B‐Raf and SMAD4 mutations, or unresectable disease with concurrent Ras/B‐Raf and TP53 alterations had worse survival. Mutual exclusivity of Ras/B‐Raf, SMAD4, and TP53 status may be useful for prognostic stratification in these patients. |
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Bibliography: | Funding information This research was supported by the National Institutes of Health (P30 CA008748 [Memorial Sloan Kettering Cancer Center]) and the Marie‐Josée and Henry R. Kravis Center for Molecular Oncology. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. Support was also provided by the Joel J. Roslyn Faculty Research Award from the Association for Academic Surgery, a Limited Project Grant and a Career Development Grant from the American Society of Colon and Rectal Surgeons, a Research Grant from the Society of MSK, and the Franklin Martin, MD, FACS Faculty Research Fellowship from the American College of Surgeons, the Wasserman Colon and Rectal Cancer Fund, and a Department of Surgery Faculty Research Award from Memorial Sloan Kettering. Further funding was provided through a grant from the Brown Performance Fund for Innovation in Cancer Informatics. This work is also supported by the Robertson Foundation, Stand Up to Cancer Colorectal Cancer Dream Team Translational Research Grant (Grant Number: SU2C‐AACR‐DT22‐17). Stand Up to Cancer is a program of the Entertainment Industry Foundation, and its research grants are administered by the American Association for Cancer Research, the scientific partner of SU2C. One investigator has been supported by Amgen for this work. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 J. Joshua Smith, Walid K. Chatila, and Francisco Sanchez‐Vega contributed equally. |
ISSN: | 2045-7634 2045-7634 |
DOI: | 10.1002/cam4.2415 |