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Associations between AI-Assisted Tumor Amphiregulin and Epiregulin IHC and Outcomes from Anti-EGFR Therapy in the Routine Management of Metastatic Colorectal Cancer.


ABSTRACT:

Purpose

High tumor production of the EGFR ligands, amphiregulin (AREG) and epiregulin (EREG), predicted benefit from anti-EGFR therapy for metastatic colorectal cancer (mCRC) in a retrospective analysis of clinical trial data. Here, AREG/EREG IHC was analyzed in a cohort of patients who received anti-EGFR therapy as part of routine care, including key clinical contexts not investigated in the previous analysis.

Experimental design

Patients who received panitumumab or cetuximab ± chemotherapy for treatment of RAS wild-type mCRC at eight UK cancer centers were eligible. Archival formalin-fixed paraffin-embedded tumor tissue was analyzed for AREG and EREG IHC in six regional laboratories using previously developed artificial intelligence technologies. Primary endpoints were progression-free survival (PFS) and overall survival (OS).

Results

A total of 494 of 541 patients (91.3%) had adequate tissue for analysis. A total of 45 were excluded after central extended RAS testing, leaving 449 patients in the primary analysis population. After adjustment for additional prognostic factors, high AREG/EREG expression (n = 360; 80.2%) was associated with significantly prolonged PFS [median: 8.5 vs. 4.4 months; HR, 0.73; 95% confidence interval (CI), 0.56-0.95; P = 0.02] and OS [median: 16.4 vs. 8.9 months; HR, 0.66 95% CI, 0.50-0.86; P = 0.002]. The significant OS benefit was maintained among patients with right primary tumor location (PTL), those receiving cetuximab or panitumumab, those with an oxaliplatin- or irinotecan-based chemotherapy backbone, and those with tumor tissue obtained by biopsy or surgical resection.

Conclusions

High tumor AREG/EREG expression was associated with superior survival outcomes from anti-EGFR therapy in mCRC, including in right PTL disease. AREG/EREG IHC assessment could aid therapeutic decisions in routine practice. See related commentary by Randon and Pietrantonio, p. 4021.

SUBMITTER: Williams CJM 

PROVIDER: S-EPMC10570673 | biostudies-literature | 2023 Oct

REPOSITORIES: biostudies-literature

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Associations between AI-Assisted Tumor Amphiregulin and Epiregulin IHC and Outcomes from Anti-EGFR Therapy in the Routine Management of Metastatic Colorectal Cancer.

Williams Christopher J M CJM   Elliott Faye F   Sapanara Nancy N   Aghaei Faranak F   Zhang Liping L   Muranyi Andrea A   Yan Dongyao D   Bai Isaac I   Zhao Zuo Z   Shires Michael M   Wood Henry M HM   Richman Susan D SD   Hemmings Gemma G   Hale Michael M   Bottomley Daniel D   Galvin Leanne L   Cartlidge Caroline C   Dance Sarah S   Bacon Chris M CM   Mansfield Laura L   Young-Zvandasara Kathe K   Sudan Ajay A   Lambert Katy K   Bibby Irena I   Coupland Sarah E SE   Montazeri Amir A   Kipling Natalie N   Hughes Kathryn K   Cross Simon S SS   Dewdney Alice A   Pheasey Leanne L   Leng Cathryn C   Gochera Tatenda T   Mangham D Chas DC   Saunders Mark M   Pritchard Martin M   Stott Helen H   Mukherjee Abhik A   Ilyas Mohammad M   Silverman Rafael R   Hyland Georgina G   Sculthorpe Declan D   Thornton Kirsty K   Gould Imogen I   O'Callaghan Ann A   Brown Nicholas N   Turnbull Samantha S   Shaw Lisa L   Seymour Matthew T MT   West Nicholas P NP   Seligmann Jenny F JF   Singh Shalini S   Shanmugam Kandavel K   Quirke Philip P  

Clinical cancer research : an official journal of the American Association for Cancer Research 20231001 20


<h4>Purpose</h4>High tumor production of the EGFR ligands, amphiregulin (AREG) and epiregulin (EREG), predicted benefit from anti-EGFR therapy for metastatic colorectal cancer (mCRC) in a retrospective analysis of clinical trial data. Here, AREG/EREG IHC was analyzed in a cohort of patients who received anti-EGFR therapy as part of routine care, including key clinical contexts not investigated in the previous analysis.<h4>Experimental design</h4>Patients who received panitumumab or cetuximab ± c  ...[more]

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