- Letter to the Editor
- Open Access
Favorable outcome of patients with lung adenocarcinoma harboring POLE mutations and expressing high PD-L1
© The Author(s). 2018
- Received: 3 January 2018
- Accepted: 4 April 2018
- Published: 12 April 2018
Mutations in polymerase ε (POLE) confer favorable prognosis and outcomes in various cancer types, but their role in non-small cell lung cancer (NSCLC) is unknown. Utilizing the data of 513 patients with adenocarcinoma (LUAD) and 497 patients with squamous cell carcinoma (LUSC) from The Cancer Genome Atlas (TCGA) cohort, we tested the prognostic value of POLE mutations and programmed cell death ligand 1 (PD-L1) expression in the two main subtypes of NSCLC. POLE mutation is a favorable biomarker for the improved overall survival (OS) of the LUSC patients (P = 0.033, 28 mutant vs. 469 wildtype patients), but not that of the LUAD patients (P = 0.12, 31 mutant vs. 482 wildtype patients). POLE-mutant LUAD patients with high expression of PD-L1 (Mut-High, n = 6) exhibited improved OS (P = 0.024) when compared to POLE-mutant patients with low PD-L1 expression (Mut-Low, n = 24) and other patients without POLE mutation (n = 476). This benefit was not due to the high content of the tumor infiltrating lymphocytes. Instead, the antitumor immune response was activated in Mut-High patients so that these patients were likely responding more effectively to immuno-oncology (IO) treatments; whereas genes involved with metabolic pathways were enriched in Mut-Low group, which may cause the decreased OS of these patients. Our study sheds light on the molecular basis of NSCLC and adds to our understanding of responses to chemotherapy and IO therapy.
- POLE mutation
- PD-L1 expression
- Lung cancer adenocarcinoma
- Lung cancer squamous cell carcinoma
- Overall survival
- Non-small cell lung cancer
Non-small cell lung cancer (NSCLC) accounts for 85% of lung cancers and can be further broadly divided by histology into adenocarcinoma (LUAD), squamous cell carcinoma (LUSC), and large cell carcinoma. Therapies directed against molecular targets in NSCLC, including immuno-oncology (IO) treatments, have improved response rates and overall survival [1, 2]; however, predictive markers for response and patient outcomes are still lacking.
Polymerase ε (POLE) is a DNA polymerase involved in DNA replication and repair. POLE mutation is associated with an ultra-mutated phenotype and a good prognosis in uterine corpus endometrial carcinoma (UCEC)  and a subgroup of colorectal tumors (CRC) . In NSCLC, the mutations of POLE and DNA mismatch repair (MMR) genes result in ultra-mutation in both LUAD and LUSC . Interestingly, this event was also observed in patients who had favorable responses to immunotherapy . Despite these observations, little is known about POLE mutations in NSCLC.
We analyzed the relationship of POLE mutations with programmed cell death ligand 1 (PD-L1) expression in patents with LUAD or LUSC in The Cancer Genome Atlas (TCGA) cohort. PD-L1 expression was not a good prognostic predictor of patient outcomes for the two subtypes. POLE mutation alone could predict the overall survival (OS) for LUSC but not LUAD patients. Both PD-L1 expression and tumor mutation burden (TMB) have exhibited associations with better response to immunotherapies in some but not all studies. Given that POLE mutations were correlated with high mutation rates, we hypothesized that the two predictors may jointly influence response to immunotherapy and survival outcomes. We found that the combination of POLE mutations and PD-L1 expression was a favorable indicator for the improved OS of LUAD patients. Our analyses describe the molecular differences among the LUAD patients with POLE mutations and different levels of PD-L1 expression and patients without POLE mutation, which may suggest distinct responses to chemotherapy and IO treatment.
POLE mutation alone is a good prognostic biomarker for patients with lung squamous cell carcinoma but not lung adenocarcinoma
Analysis using genomic data across multiple types of cancers from the TCGA cohort (Additional file 1: Methods and Materials) showed that LUSC and LUAD are among the cancers with the most frequent POLE mutations (28/497 = 5.6% and 31/513 = 6.0%, respectively), which are close to the rates in UCEC (28/519 = 5.4%) and CRC cancers (32/594 = 5.4%). However, compared to the UCEC cancer patients whose mutations mostly locate in the proofreading domain, the mutations in NSCLC patients are distributed across the POLE gene body (Additional file 2: Figure S1A).
PD-L1 expression level serves as a predictive biomarker to IO therapy response in a number of cancers types [7, 8], including advanced NSCLC [1, 2, 7]. Yet, analysis of TCGA samples with high- (top 20%, n = 102), low- (bottom 20%, n = 102), and intermediate (others, n = 302) PD-L1 expression levels, who had not received IO therapy treatments, did not demonstrate that the LUAD patients with high PD-L1 expression had longer OS (P = 0.13, Fig. 1e).
LUAD patients with POLE mutations and PD-L1 high expression level have the best survival
We performed the same analyses in the LUSC cancer but did not observe similar associations. The Mut-High group of LUSC patients (n = 6) had worse outcomes than the Mut-Low group (n = 22), but both were likely better than POLE-wild patients (n = 469, P = 0.094, Additional file 2: Figure S2C and Additional file 3: Table S4). Similar to LUAD cancer, PD-L1 expression cannot stratify POLE-wild LUSC patients by OS (P = 0.76, 95 High vs. 374 Low, Additional file 2: Figure S2D).
Tumor infiltrating lymphocytes (TILs) have been identified as a good prognostic predictor in several cancer types. For LUAD patients, POLE mutations were moderately associated with higher TIL percentage (P = 0.42, Additional file 2: Figure S2E), but not favorable outcomes (Fig. 1d). We tested whether Mut-High patients had better outcomes as a result of higher numbers of TIL. The results showed that Mut-High patients indeed contained lower TIL (P = 9.0e-4, Fig. 2c) compared to Mut-Low patients, but still experienced a better outcome relative to mortality rate (0/2 = 0% vs. 10/11 = 90.9% at 5.5-year follow-up), although survival curve comparison was not statistically significant probably due to the small sample size (P = 0.35, Additional file 2: Figure S2F). This observation suggests that PD-L1 performs functions in POLE-mutant patients that are not due to the existence of TIL.
Genes promoting tumors are mutated in Mut-high but not Mut-low patients
We compared the mutation landscapes of Mut-High and Mut-Low LUAD patients, and identified multiple genes differentially mutated between the two groups, such as KNDC1, ENOX1 and CACNA1H (P < 0.05, Additional file 2: Figure S3). Gene Set Enrichment Analysis (GSEA) analysis showed that these genes are enriched in olfactory transduction that promote cancer cell invasiveness and metastasis emergence . They also are involved in G-protein coupled receptor activity that stimulates cell proliferation in various cell types, and have a crucial role in many aggressive human cancers, including SCLC, pancreatic cancer, and prostate cancer . The mutation of these genes may cause the loss of function and contribute to improved survivals upon treatment.
Antitumor immune response is activated in Mut-high LUAD patients
LUSC and LUAD, as the two main subtypes of NSCLC, are distinct in disease pathology, smoking associations, metastatic trends, molecular mechanisms, treatment options, and patient outcomes. We demonstrated the distinct prognostic values of POLE mutation and PD-L1 expression in these two subtypes. Importantly, we revealed the combination of POLE mutation and PD-L1 expression as a favorable indicator for improved OS of LUAD patients and the activation of antitumor immune system. Our results identify the molecular signatures associated with POLE mutations and PD-L1 expression in LUAD and LUSC and may reveal a distinct response status to chemotherapy and immunotherapy, which needs further experiments to validate.
We would like to thank Mac Robinson from the Wake Forest Baptist Comprehensive Cancer Center for editing this manuscript.
The work is partially supported by the Cancer Center Support Grant from the National Cancer Institute to the Comprehensive Cancer Center of Wake Forest Baptist Medical Center (P30CA012197). W.Z. is supported by Hanes and Willis Professorship in Cancer and a Fellowship by the National Foundation for Cancer Research. B.P. is supported by Charles L. Spurr Professorship of Medicine.
Availability of data and materials
All data analyzed in the present study are available in the TCGA databases.
WZ conceived and designed the project; LL, MY, UT performed the analysis; LL, JR, SSO, SCG, WJP, KC, BP and WZ interpreted the results and wrote the paper. All authors read, edited and approved the manuscript.
Ethics approval and consent to participate
All studies have been approved by the Institutional Research Board.
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Carbone DP, Reck M, Paz-Ares L, Creelan B, Horn L, Steins M, Felip E, van den Heuvel MM, Ciuleanu TE, Badin F, et al. First-line Nivolumab in stage IV or recurrent non-small-cell lung Cancer. N Engl J Med. 2017;376(25):2415–26.View ArticlePubMedGoogle Scholar
- Gettinger S, Rizvi NA, Chow LQ, Borghaei H, Brahmer J, Ready N, Gerber DE, Shepherd FA, Antonia S, Goldman JW, et al. Nivolumab monotherapy for first-line treatment of advanced non-small-cell lung Cancer. J Clin Oncol. 2016;34(25):2980–7.View ArticlePubMedPubMed CentralGoogle Scholar
- Cancer Genome Atlas Research N, Kandoth C, Schultz N, Cherniack AD, Akbani R, Liu Y, Shen H, Robertson AG, Pashtan I, Shen R, et al. Integrated genomic characterization of endometrial carcinoma. Nature. 2013;497(7447):67–73.View ArticleGoogle Scholar
- Cancer Genome Atlas N. Comprehensive molecular characterization of human colon and rectal cancer. Nature. 2012;487(7407):330–7.View ArticleGoogle Scholar
- Devarakonda SH, Masood A, Johanns TM, Lanc I, Du L, Ganesh B, Maggi LB, Waqar SN, Morgensztern D, Govindan R. Somatic mutations in mismatch repair pathway genes in non-small cell lung cancer. J Clin Oncol. 2016;34(no. 15_suppl):11523-11523.Google Scholar
- Rizvi NA, Hellmann MD, Snyder A, Kvistborg P, Makarov V, Havel JJ, Lee W, Yuan J, Wong P, Ho TS, et al. Cancer immunology. Mutational landscape determines sensitivity to PD-1 blockade in non-small cell lung cancer. Sci. 2015;348(6230):124–8.View ArticleGoogle Scholar
- Aguiar PN Jr, De Mello RA, Hall P, Tadokoro H, Lima Lopes G. PD-L1 expression as a predictive biomarker in advanced non-small-cell lung cancer: updated survival data. Immunotherapy. 2017;9(6):499–506.View ArticlePubMedGoogle Scholar
- Kluger HM, Zito CR, Turcu G, Baine MK, Zhang H, Adeniran A, Sznol M, Rimm DL, Kluger Y, Chen L, et al. PD-L1 studies across tumor types, its differential expression and predictive value in patients treated with immune checkpoint inhibitors. Clin Cancer Res. 2017;23(15):4270–9.View ArticlePubMedGoogle Scholar
- De la Cruz O, Blekhman R, Zhang X, Nicolae D, Firestein S, Gilad Y. A signature of evolutionary constraint on a subset of ectopically expressed olfactory receptor genes. Mol Biol Evol. 2009;26(3):491–4.View ArticlePubMedGoogle Scholar
- Bar-Shavit R, Maoz M, Kancharla A, Nag JK, Agranovich D, Grisaru-Granovsky S, Uziely B. G protein-coupled receptors in Cancer. Int J Mol Sci. 2016;17(8):1320.View ArticlePubMed CentralGoogle Scholar