@article{a88a704d498448a489742ebb340f5e16,
title = "Expression of the DNA repair gene MLH1 correlates with survival in patients who have resected pancreatic cancer and have received adjuvant chemoradiation: NRG Oncology RTOG Study 9704",
abstract = "BACKGROUND: The majority of patients with pancreatic cancer who undergo curative resection experience rapid disease recurrence. In previous small studies, high expression of the mismatch-repair protein mutL protein homolog 1 (MLH1) in pancreatic cancers was associated with better outcomes. The objective of this study was to validate the association between MLH1 expression and survival in patients who underwent resection of pancreatic cancer and received adjuvant chemoradiation. METHODS: Samples were obtained from the NRG Oncology Radiation Therapy Oncology Group 9704 prospective, randomized trial (clinicaltrials.gov identifier NCT00003216), which compared 2 adjuvant protocols in patients with pancreatic cancer who underwent resection. Tissue microarrays were prepared from formalin-fixed, paraffin-embedded, resected tumor tissues. MLH1 expression was quantified using fluorescence immunohistochemistry and automated quantitative analysis, and expression was dichotomized above and below the median value. RESULTS: Immunohistochemical staining was successfully performed on 117 patients for MLH1 (60 and 57 patients from the 2 arms). The characteristics of the participants who had tissue samples available were similar to those of the trial population as a whole. At the time of analysis, 84% of participants had died, with a median survival of 17 months. Elevated MLH1 expression levels in tumor nuclei were significantly correlated with longer disease-free and overall survival in each arm individually and in both arms combined. Two-year overall survival was 16% in patients who had low MLH1 expression levels and 53% in those who had high MLH1 expression levels (P <.0001 for both arms combined). This association remained true on a multivariate analysis that allowed for lymph node status (hazard ratio, 0.41; 95% confidence interval, 0.27-0.63; P <.0001). CONCLUSIONS: In the current sample, MLH1 expression was correlated with long-term survival. Further studies should assess whether MLH1 expression predicts which patients with localized pancreatic cancer may benefit most from aggressive, multimodality treatment. Cancer 2018;124:491-8.",
keywords = "adjuvant, adjuvant, biomarkers, chemotherapy, clinical trial phase 3, mutL protein homolog 1 (MLH1), pancreatic neoplasms, radiotherapy, tumor",
author = "Lawrence, {Yaacov R.} and Jennifer Moughan and Magliocco, {Anthony M.} and Klimowicz, {Alexander C.} and Regine, {William F.} and Mowat, {Rex B.} and DiPetrillo, {Thomas A.} and William Small and Simko, {Jeffry P.} and Talia Golan and Winter, {Kathryn A.} and Chandan Guha and Crane, {Christopher H.} and Dicker, {Adam P.}",
note = "Funding Information: This project was supported by grants U10CA21661 (RTOG-Ops-Stat), U10CA37422 (Community Clinical Oncology Program), U10CA180822 (NRG Oncology Statistics and Data Management Center), U24CA114734 (RTOG Specimen Bank) from the National Cancer Institute and Eli Lilly. Yaacov R. Lawrence is supported by the European Union Seventh Framework Program (FP7) Marie Curie program FP7-MC-CIG 303795 and the Rosetrees Trust. Funding Information: Alexander C. Klimowicz is currently employed by Boehringer Ingelheim Pharmaceuticals, Inc. Jeffrey P. Simko reports grants from the National Cancer Institute during the conduct of the study; nondirected research funds from Genomic Health Inc. and Myriad Inc outside the submitted work; personal fees from 3D Biopsy Inc, GenomeDx Inc, Genomic Health Inc, and 3Scan outside the submitted work; and membership on the Scientific Advisory Boards and equity ownership in 3D Biopsy Inc and 3Scan. Anthony M. Magliocco reports grants from Ventana Medical Systems and BioTheranostics; personal fees from Illumina, Genoptixs, BioTheranostics; Janssen Diagnostics LLC, Bristol-Myers Squibb, Merck, and Johnson & Johnson; travel support from Illumina, Guardant Health, and Definiens International, all outside the submitted work; and travel support and related expenses associated with being the Co-chair of pathology for NRG Oncology. The remaining authors made no disclosures. This project was supported by grants U10CA21661 (RTOG-Ops-Stat), U10CA37422 (Community Clinical Oncology Program), U10CA180822 (NRG Oncology Statistics and Data Management Center), U24CA114734 (RTOG Specimen Bank) from the National Cancer Institute and Eli Lilly. Yaacov R. Lawrence is supported by the European Union Seventh Framework Program (FP7) Marie Curie program FP7-MC-CIG 303795 and the Rosetrees Trust. Publisher Copyright: {\textcopyright} 2017 American Cancer Society",
year = "2018",
month = feb,
day = "1",
doi = "10.1002/cncr.31058",
language = "English (US)",
volume = "124",
pages = "491--498",
journal = "Cancer",
issn = "0008-543X",
publisher = "John Wiley and Sons Inc.",
number = "3",
}