Clinicopathologic characteristics and therapeutic responses of Chinese patients with non-small cell lung cancer who harbor an anaplastic lymphoma kinase rearrangement
- Sha Fu†1, 4,
- Hai-Yun Wang†2,
- Fang Wang1, 4,
- Ma-Yan Huang3,
- Ling Deng4,
- Xiao Zhang4,
- Zu-Lu Ye4 and
- Jian-Yong Shao1, 4Email author
© Fu et al. 2015
Received: 20 November 2014
Accepted: 8 May 2015
Published: 8 August 2015
The rearrangement of the anaplastic lymphoma kinase (ALK) gene accounts for approximately 1%–6% of lung adenocarcinoma cases and defines a molecular subgroup of tumors characterized by clinical sensitivity to ALK inhibitors such as crizotinib. This study aimed to identify the relationship between ALK rearrangement and the clinicopathologic characteristics of non-small cell lung cancer (NSCLC) and to analyze the therapeutic responses of crizotinib and conventional chemotherapy to ALK rearrangement in NSCLC patients.
A total of 487 lung cancer patients who underwent testing for ALK rearrangement in our department were included in this study. ALK rearrangement was examined by using fluorescence in situ hybridization (FISH) assay.
Among the 487 patients, 44 (9.0%) were diagnosed with ALK rearrangement by using FISH assay. In 123 patients with adenocarcinoma who were non-smokers and of a young age (≤58 years old), the frequency of ALK rearrangement was 20.3% (25/123). Short overall survival (OS) was associated with non-adenocarcinoma tumor type (P = 0.006), poorly differentiated tumors (P = 0.001), advanced-stage tumors (P < 0.001), smoking history (P = 0.008), and wild-type epidermal growth factor receptor (EGFR) (P = 0.008). Moreover, patients with poorly differentiated and advanced-stage tumors had a shorter time to cancer progression compared with those with well differentiated (P = 0.023) and early-stage tumors (P = 0.001), respectively.
ALK-rearranged NSCLC tends to occur in younger individuals who are either non-smokers or light smokers with adenocarcinoma. Patients with ALK rearrangement might benefit from ALK inhibitor therapy.
KeywordsAnaplastic lymphoma kinase rearrangement Non-small cell lung cancer Fluorescence in situ hybridization Pathology
Lung cancer is a lethal but common disease with a 5-year survival rate of approximately 5%–15% . Molecular targeted therapy is emerging as an effective therapeutic strategy for many cancers [2–4]. The following molecularly targeted genes are potentially relevant to oncogenic events and have demonstrated remarkable significance: the v-raf murine sarcoma viral oncogene homolog B1 (BRAF), human epidermal growth factor receptor-2 (HER2), phosphoinositide 3′-kinase (PI3K), v-Ki-ras 2 Kirsten rat sarcoma viral oncogene homolog (KRAS), discoidin domain receptor 2 (DDR2), epidermal growth factor receptor (EGFR), anaplastic lymphoma kinase (ALK), c-ros oncogene 1 (ROS1), and ret proto-oncogene (RET). ALK rearrangement represents a new oncogene driver [5, 6].
The echinoderm microtubule-associated protein like 4 (EML4)-ALK in non-small cell lung cancer (NSCLC) was first discovered as an oncogenic driver gene in 2007; the EML4-ALK fusion gene was generated by an inversion in the short arm of chromosome 2 . According to the breakpoint on EML4 (from exon 2 to exon 20), 13 variants of the EML4-ALK fusion gene have been found . Recently, the TRK-fused gene (TFG), the kinesin family member 5B (KIF5B), and the kinesin light chain 1 (KLC1) were reported to invert and fuse to ALK in NSCLC [5, 8, 9].
Compared with other genetic abnormalities in NSCLC, the frequency of the ALK rearrangement is approximately 1%–6% in unselected NSCLC [10–12]. Patients with ALK rearrangement are highly sensitive to crizotinib, an oral tyrosine kinase inhibitor (TKI) of the c-Met proto-oncogene (c-Met), ALK, and ROS1 genes. The powerful and specific therapeutic efficacy of this drug on ALK-rearranged NSCLC led to the approval by the Food and Drug Administration (FDA) in the United States . Several studies have shown that most of the patients who harbor this chromosomal abnormality have benefited from targeted therapy. A randomized phase III study reported that, in the subgroup of ALK-rearranged NSCLC, patients treated with crizotinib showed higher response rate and longer progression-free survival (PFS) compared with those treated with the standard second-line chemotherapies (docetaxel or pemetrexed) . Other studies showed dramatic clinical benefits associated with crizotinib in patients with ALK-rearranged NSCLC [15, 16].
The tumors from patients with ALK rearrangements are characterized by distinct histologic features including a solid or acinar growth pattern, a cribriform structure, the presence of mucous cells and abundant extracellular mucus, a lack of lepidic growth, and nuclear pleomorphism . Nevertheless, these histologic parameters are of insufficient sensitivity and specificity to detect ALK rearrangements, and therefore, histomorphology should not replace confirmatory molecular or immunohistochemical studies . The histomorphology of ALK-rearranged lung cancer cannot be used as a screening method. Several methods including reverse transcription-polymerase chain reaction (RT-PCR), fluorescence in situ hybridization (FISH), and immunohistochemistry (IHC) are currently used to identify ALK translocations in patients with NSCLC. In the present study, we performed ALK FISH in NSCLC cases at the Sun Yat-sen University Cancer Center (SYSUCC) using the gold standard method, Abbott ALK break-apart probe. We analyzed the clinicopathologic features of the patients, their survival status, and the relationship between the clinicopathologic features and ALK rearrangement. In previous studies, ALK rearrangement represented a unique molecular subset of NSCLC with no overlap with cancers that featured alterations in the EGFR or KRAS genes [18, 19]. According to EGFR and ALK status, we retrospectively studied the responses of patients to traditional therapies compared with targeted therapies.
Patients and methods
We reviewed 1,000 patients with NSCLC who were observed and tested for ALK rearrangement at the Department of Molecular Diagnostics of SYSUCC between February 2012 and November 2013. Patients were involved into this study based on the following criteria: complete clinical data, complete follow-up information, and sufficient paraffin tissue from primary tumors at the time of the initial genetic diagnosis. The patients were excluded if they received any treatment outside of SYSUCC or had a previous history of other cancers that were identified either before or after the NSCLC. Finally, a total of 487 patients were enrolled in this study. All cases were confirmed independently by two experienced pathologists. Pathologic staging was defined according to the International Association for the Study of Lung Cancer (IASLC) TNM staging classification of NSCLC . Histopathologic classification of the cancers was determined according to the 2004 World Health Organization (WHO) histological classification of lung cancer . Patients were classified as non-smokers if they smoked for less than 10 pack-years or smokers if they smoked for 10 pack-years or more in their lifetime. This study was approved by the Institutional Research Medical Ethics Committee of SYSUCC.
Formalin-fixed, paraffin-embedded, 4-μm sections were used for FISH detection. According to the hematoxylin and eosin stain of the same tissue block, the tumor portion on each slide was selected and demarcated by a single pathologist. The FISH assay included the use of the Vysis LSI ALK Dual Color, Break Apart Probe (Abbott Molecular Inc. Des Plaines, IL, USA), which hybridizes to the 2p23 band with 3′-ALK spectrum orange and 5′-ALK spectrum green. The slides were deparaffinized prior to probe application. Detailed FISH staining procedures have been previously described .
FISH signals for each locus-specific FISH probe were assessed under an Olympus BX51 TRF microscope (Olympus, Tokyo, Japan) equipped with a triple-pass filter (DAPI/Green/Orange; Abbott Molecular Inc. Des Plaines, IL, USA). Any tissues with questionable tumor areas were reviewed and noted by a pathologist; the FISH results were evaluated by two independent and experienced pathologists. Cases with ALK rearrangements were determined to exhibit one of two patterns: the first type was a classic pattern with one fusion signal (native ALK) and two separated orange and green signals; the other was an atypical pattern with one fusion signal (native ALK) and an isolated orange signal. By using the signal size as a reference, the tumor cells were considered positive when the probe separation distance in ALK-rearranged tumors was larger than the two signal diameters in normal tissue . When ALK break-apart signals were found in more than 15% of no less than 50 counted tumor cells, the tumor samples were considered ALK rearrangement-positive [23–25]. The tumor samples with a single green signal or an increased copy number of non-rearranged ALK genes with fused signals that corresponded to polysomy of chromosome 2 or ALK amplification were considered ALK rearrangement-negative . For each case, the entire slide was reviewed for possible areas where rearrangements might have been missed.
DNA was extracted by a DNA FFPE tissue kit (Qiagen, Valencia, CA, USA) according to the manufacturer’s instructions. DNA was quantified by a NanoDrop 2000 Spectrophotometer (Thermo Fisher Scientific, Waltham, MA, USA), and a total of 200 ng DNA was used for PCR. Nucleotide sequencing of the kinase domain of EGFR (exons 18, 19, 20, and 21) was performed with PCR amplification and Sanger sequencing. PCR-amplified products were purified with a PCR purification kit (Qiagen, Valencia, CA, USA) and were sequenced with a BigDye Terminator Cycle Sequencing Reaction Kit and an ABI 3500 XL Genetic Analyzer (Hitachi, Tokyo, Japan).
Follow-up and classification of cause of death
The clinical data including follow-up information were obtained from the medical record system as well as by telephone interview. The collection of follow-up data for each case was executed based on a semi-annual schedule. For deceased patients, we classified the underlying cause of death as stated on the death certificate. Local relapse was defined as recurrence of lung cancer as determined by biopsy, whereas distant metastasis was defined according to evidence shown on a chest computed tomography (CT) scan, abdominal ultrasound, or bone scan. The overall survival (OS) was defined as the period from the date of diagnosis to death from any cause or the date of last contact; the PFS was defined as the period from the date of diagnosis to the first regional or distant metastasis. The last follow-up was performed in April 2014, and the median follow-up was 18.8 months (range 0.3–172.2 months). In total, 86 (17.7%) cases died during follow-up.
The relationship between ALK status and the clinicopathologic features was analyzed by using Chi square test and Fisher’s exact test. Kaplan–Meier curves with the log-rank test were applied for OS and PFS analysis. Cox proportional hazards models were used to compare independent predictive factors of each biological and clinicopathologic feature. A two-sided statistical significance was defined as P < 0.05. All analyses were performed with SPSS 16.0 Statistics software (SPSS Inc., Chicago, IL, USA).
Associations between ALK rearrangement and the clinicopathologic characteristics of 487 patients with non-small cell lung cancer (NSCLC)
Number of patients (%)
ALK rearrangement [cases (%)]
I + II
III + IV
EGFR mutation status
Detection of ALK rearrangement by FISH
Of the 487 NSCLC cases, 44 (9.0%) were identified with ALK rearrangements. The percentage of ALK break-apart signals ranged from 16% to 90%. Of the 44 ALK-rearranged cases, 15 (34.1%) showed more than 50% split fluorescence signals, and 29 (65.9%) demonstrated less than 50% split signals. The mean percentage of positive nuclei was 51.7% in the cases with ALK rearrangement. Among the 44 patients with ALK rearrangement, the median age was 49 years (range 25–80 years). We compared the clinicopathologic characteristics between the ALK-fusion-positive group and the ALK-fusion-negative group and found significant differences in age (P = 0.008), histological type (P = 0.001), clinical stage (P = 0.019), smoking history (P = 0.001), and EGFR mutation status (P < 0.001); no significant difference was found in other clinicopathologic parameters between the two groups (Table 1).
Analysis of EGFR mutation status and clinical characteristics in patients with NSCLC
Associations between EGFR mutation status and the clinicopathologic features of patients with NSCLC
EGFR mutation [cases (%)]
I + II
III + IV
Survival analysis of NSCLC patients
Cox regression analysis of OS and PFS in 487 patients with NSCLC
HR (95% CI)
HR (95% CI)
≤58 vs. >58
Male vs. female
Adenocarcinoma vs. others
Well vs. poor
I + II vs. III + IV
Non-smoker vs. smoker
T1–2 vs. T3–4
N0 vs. N1–3
M0 vs. M1
Negative vs. positive
Negative vs. positive
Adenocarcinoma vs. others
T1–2 vs. T3–4
N0 vs. N1–3
M0 vs. M1
Therapeutic responses and clinical outcome of patients with ALK rearrangement
Of the 44 patients with ALK rearrangement, 18 (40.9%) were treated with crizotinib, 4 (9.1%) were treated with an EGFR-TKI, and 22 (50.0%) were treated with conventional chemotherapy. After treated with crizotinib, the tumors in the 18 patients shrank, and both the symptoms and the quality of life were substantially improved. By the last follow-up date, the median OS in the 18 patients with ALK rearrangements who were treated with an ALK-TKI was higher than that in the 22 patients with ALK rearrangements who were treated with conventional chemotherapy, but there was no statistical difference (21.2 vs. 19.1 months, P = 0.587). Because of the short follow-up time, no significant difference was found between the two groups in terms of OS rate (P = 0.773) or PFS rate (P = 0.608).
The identification of ALK rearrangements in NSCLC is pivotal to guide the appropriate treatment with ALK-TKI. In this study, we used an ALK break-apart probe assay to test 487 NSCLC cases and identified 44 (9.0%) with ALK rearrangements, which was in accordance with the results of previous investigations [25–28]. The frequency of ALK rearrangements was 20.3% (25/123) in young patients with the adenocarcinoma subtype who were non-smokers, which was also consistent with the previously reported results [24, 27, 29, 30]. Our study also revealed other characteristics of NSCLC with ALK rearrangements, such as advanced stage (70.5%, 31/44) and wild-type EGFR (97.7%, 43/44). Additionally, patients with advanced-stage tumors and poorly differentiated tumors had a shorter time to cancer progression in comparison with those with early-stage tumors and well differentiated tumors.
Tumors with ALK rearrangement were found to exhibit papillary and acinar growth patterns , mucinous cribriform patterns , and a solid signet-ring cell pattern . In addition, the coexistence of glandular and squamous morphologies was also reported in previous studies [18, 24]. In our study, acinar, papillary, and mucinous adenocarcinomas were found in ALK-rearranged cases. Interestingly, in our study, we also detected ALK rearrangements in a case of squamous cell carcinoma. Furthermore, 4 ALK-rearranged adenocarcinomas were observed in patients with focal squamous differentiation. This suggests that a test for ALK rearrangement should be performed in patients with classical morphologic patterns, mixed squamous and adenocarcinoma patterns as well as in patients with squamous carcinoma in case of a wrong therapeutic decision.
ALK rearrangement was generally reported to be found in tumors with wild-type EGFR and KRAS [7, 19, 27, 31, 32]. However, some investigators also observed the coexistence of ALK rearrangement and EGFR mutations [33–35]. It was reported that patients who harbor a concurrent EGFR mutation and an ALK rearrangement may partially respond to EGFR inhibitors [36–38]. Interestingly, we identified one patient with a concomitant ALK rearrangement and EGFR mutation who had undergone therapy with erlotinib. Nevertheless, this patient experienced disease progression less than 1 month later as confirmed by CT scan. The mechanism of resistance might be affected by different signal transduction pathways. Sasaki et al.  reported that in in vitro studies the co-expression of an EGFR mutation and the EML4-ALK fusion gene might lead to resistance to targeted therapies. It is therefore important to determine the optimal combination of a given EGFR-TKI and ALK inhibitor or other new therapeutic regimens for patients with a concomitant EGFR mutation and an ALK rearrangement.
In an analysis of OS and PFS between ALK rearrangement-positive and ALK rearrangement-negative groups, no statistical significance was observed. The reason might be that the patients with ALK rearrangements, in our study, were not treated with targeted therapy or they were treated for only a short time. Li et al.  reported that EGFR/KRAS mutation status appeared to be significantly associated with neither PFS nor OS if these patients did not receive targeted therapies. This hypothesis is consistent with the results of our study. All evidence supports the hypothesis that gene subtypes could only predict the therapeutic response but not the survival benefit until patients received a given molecular targeted therapy.
Patients with EGFR mutations demonstrated a superior PFS after treatment with molecular targeted therapy compared with those treated with traditional platinum-doublet chemotherapy . However, in our study, disease progression was observed in two patients with ALK rearrangement after they were treated with crizotinib, and the two patients were considered resistant to crizotinib. Presently, the mechanism of resistance to ALK inhibitors is thought to be a compensatory mechanism or the occurrence of drug-resistant gene mutation, such as a mutation in ALK, EGFR, KRAS, or BRAF [41, 42]. Rapid disease progression can deprive the patients of a second chance for survival. Spaans et al.  suggested that a combination targeted therapy that simultaneously inhibits multiple resistance pathways would elicit a better clinical response. However, the toxicity of combination drugs requires further investigation.
There are some limitations in our study. First, this was a retrospective study and all cases were selected within a single hospital. Second, many patients with ALK rearrangement or EGFR mutations could not receive targeted therapy or they had a short medication duration due to budget limitations. Therefore, we were not able to exclude geographic and demographic variations that might have influenced the outcome of the study.
In conclusion, the patients who harbor ALK rearrangements tend to be relatively young, non-smokers or light smokers with the adenocarcinoma subtype. Prior to treatment, it is necessary to assess ALK rearrangement status to determine the appropriate therapeutic regimen. Because the underlying mechanism of the partial response to targeted therapy is unknown, we will continue to investigate this mechanism in patients with NSCLC in the future.
JYS conceived of the study and participated in its design and coordination. SF performed the study and drafted the manuscript. HYW revised the paper. FW performed the statistical analyses. MYH, LD, XZ, and ZLY participated in the collection of the data. All authors read and approved the final manuscript.
This work was supported in part by grants from the National High Technology Research and Development Program of China (863 Program) (No. 2012AA02A502) and a State Key Laboratory Grant at Sun Yat-sen University Cancer Center.
Compliance with ethical guidelines
Competing interests The authors declare that they have no competing interests.
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- Sasaki H, Endo K, Okuda K, Kawano O, Kitahara N, Tanaka H, et al. Epidermal growth factor receptor gene amplification and gefitinib sensitivity in patients with recurrent lung cancer. J Cancer Res Clin Oncol. 2008;134:569–77.View ArticlePubMedGoogle Scholar
- Druker BJ, Talpaz M, Resta DJ, Peng B, Buchdunger E, Ford JM, et al. Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukemia. N Engl J Med. 2001;344:1031–7.View ArticlePubMedGoogle Scholar
- Demetri GD, von Mehren M, Blanke CD, Van den Abbeele AD, Eisenberg B, Roberts PJ, et al. Efficacy and safety of imatinib mesylate in advanced gastrointestinal stromal tumors. N Engl J Med. 2002;347:472–80.View ArticlePubMedGoogle Scholar
- Inoue A, Suzuki T, Fukuhara T, Maemondo M, Kimura Y, Morikawa N, et al. Prospective phase II study of gefitinib for chemotherapy-naive patients with advanced non-small-cell lung cancer with epidermal growth factor receptor gene mutations. J Clin Oncol. 2006;24:3340–6.View ArticlePubMedGoogle Scholar
- Rikova K, Guo A, Zeng Q, Possemato A, Yu J, Haack H, et al. Global survey of phosphotyrosine signaling identifies oncogenic kinases in lung cancer. Cell. 2007;131:1190–203.View ArticlePubMedGoogle Scholar
- Soda M, Choi YL, Enomoto M, Takada S, Yamashita Y, Ishikawa S, et al. Identification of the transforming EML4-ALK fusion gene in non-small-cell lung cancer. Nature. 2007;448:561–6.View ArticlePubMedGoogle Scholar
- Sasaki T, Rodig SJ, Chirieac LR, Janne PA. The biology and treatment of EML4-ALK non-small cell lung cancer. Eur J Cancer. 2010;46:1773–80.PubMed CentralView ArticlePubMedGoogle Scholar
- Takeuchi K, Choi YL, Togashi Y, Soda M, Hatano S, Inamura K, et al. KIF5B-ALK, a novel fusion oncokinase identified by an immunohistochemistry-based diagnostic system for ALK-positive lung cancer. Clin Cancer Res. 2009;15:3143–9.View ArticlePubMedGoogle Scholar
- Togashi Y, Soda M, Sakata S, Sugawara E, Hatano S, Asaka R, et al. KLC1-ALK: a novel fusion in lung cancer identified using a formalin-fixed paraffin-embedded tissue only. PLoS One. 2012;7:e31323.PubMed CentralView ArticlePubMedGoogle Scholar
- Takeuchi K, Choi YL, Soda M, Inamura K, Togashi Y, Hatano S, et al. Multiplex reverse transcription-PCR screening for EML4-ALK fusion transcripts. Clin Cancer Res. 2008;14:6618–24.View ArticlePubMedGoogle Scholar
- Palmer RH, Vernersson E, Grabbe C, Hallberg B. Anaplastic lymphoma kinase: signalling in development and disease. Biochem J. 2009;420:345–61.PubMed CentralView ArticlePubMedGoogle Scholar
- Wong DW, Leung EL, So KK, Tam IY, Sihoe AD, Cheng LC, et al. The EML4-ALK fusion gene is involved in various histologic types of lung cancers from nonsmokers with wild-type EGFR and KRAS. Cancer. 2009;115:1723–33.View ArticlePubMedGoogle Scholar
- Kwak EL, Bang YJ, Camidge DR, Shaw AT, Solomon B, Maki RG, et al. Anaplastic lymphoma kinase inhibition in non-small-cell lung cancer. N Engl J Med. 2010;363:1693–703.PubMed CentralView ArticlePubMedGoogle Scholar
- Shaw AT, Kim DW, Nakagawa K, Seto T, Crino L, Ahn MJ, et al. Crizotinib versus chemotherapy in advanced ALK-positive lung cancer. N Engl J Med. 2013;368:2385–94.View ArticlePubMedGoogle Scholar
- Camidge DR, Bang YJ, Kwak EL, Iafrate AJ, Varella-Garcia M, Fox SB, et al. Activity and safety of crizotinib in patients with ALK-positive non-small-cell lung cancer: updated results from a phase 1 study. Lancet Oncol. 2012;13:1011–9.PubMed CentralView ArticlePubMedGoogle Scholar
- Cao YB, Xiao GL, Qiu XB, Ye S, Lin TY. Efficacy and safety of crizotinib among Chinese EML4-ALK-positive, advanced-stage non-small cell lung cancer patients. PLoS One. 2014;9:e114008.PubMed CentralView ArticlePubMedGoogle Scholar
- Yoshida A, Tsuta K, Nakamura H, Kohno T, Takahashi F, Asamura H, et al. Comprehensive histologic analysis of ALK-rearranged lung carcinomas. Am J Surg Pathol. 2011;35:1226–34.View ArticlePubMedGoogle Scholar
- Inamura K, Takeuchi K, Togashi Y, Nomura K, Ninomiya H, Okui M, et al. EML4-ALK fusion is linked to histological characteristics in a subset of lung cancers. J Thorac Oncol. 2008;3:13–7.View ArticlePubMedGoogle Scholar
- Takahashi T, Sonobe M, Kobayashi M, Yoshizawa A, Menju T, Nakayama E, et al. Clinicopathologic features of non-small-cell lung cancer with EML4-ALK fusion gene. Ann Surg Oncol. 2010;17:889–97.View ArticlePubMedGoogle Scholar
- Goldstraw P. The 7th edition of TNM in lung cancer: what now? J Thorac Oncol. 2009;4:671–3.View ArticlePubMedGoogle Scholar
- Travis W, Brambilla E, Muller-Hermelink H, Harris CC. Pathology and genetics of yumours of the lung, pleura, thymus and heart. 3rd ed. Lyon, France: IARC Press. World Health Organization Classification of Tumours; 2004; vol 10.
- Li YH, Wang F, Shen L, Deng YM, Shao QO, Feng F, et al. EGFR fluorescence in situ hybridization pattern of chromosome 7 disomy predicts resistance to cetuximab in KRAS wild-type metastatic colorectal cancer patients. Clin Cancer Res. 2011;17:382–90.View ArticlePubMedGoogle Scholar
- Conde E, Angulo B, Izquierdo E, Munoz L, Suarez-Gauthier A, Plaza C, et al. The ALK translocation in advanced non-small-cell lung carcinomas: preapproval testing experience at a single cancer centre. Histopathology. 2013;62:609–16.View ArticlePubMedGoogle Scholar
- Rodig SJ, Mino-Kenudson M, Dacic S, Yeap BY, Shaw A, Barletta JA, et al. Unique clinicopathologic features characterize ALK-rearranged lung adenocarcinoma in the western population. Clin Cancer Res. 2009;15:5216–23.PubMed CentralView ArticlePubMedGoogle Scholar
- Camidge DR, Kono SA, Flacco A, Tan AC, Doebele RC, Zhou Q, et al. Optimizing the detection of lung cancer patients harboring anaplastic lymphoma kinase (ALK) gene rearrangements potentially suitable for ALK inhibitor treatment. Clin Cancer Res. 2010;16:5581–90.PubMed CentralView ArticlePubMedGoogle Scholar
- Martelli MP, Sozzi G, Hernandez L, Pettirossi V, Navarro A, Conte D, et al. EML4-ALK rearrangement in non-small cell lung cancer and non-tumor lung tissues. Am J Pathol. 2009;174:661–70.PubMed CentralView ArticlePubMedGoogle Scholar
- Shaw AT, Yeap BY, Mino-Kenudson M, Digumarthy SR, Costa DB, Heist RS, et al. Clinical features and outcome of patients with non-small-cell lung cancer who harbor EML4-ALK. J Clin Oncol. 2009;27:4247–53.PubMed CentralView ArticlePubMedGoogle Scholar
- Wallander ML, Geiersbach KB, Tripp SR, Layfield LJ. Comparison of reverse transcription-polymerase chain reaction, immunohistochemistry, and fluorescence in situ hybridization methodologies for detection of echinoderm microtubule-associated proteinlike 4-anaplastic lymphoma kinase fusion-positive non-small cell lung carcinoma implications for optimal clinical testing. Arch Pathol Lab Med. 2012;136:796–803.View ArticlePubMedGoogle Scholar
- Sequist LV, Heist RS, Shaw AT, Fidias P, Rosovsky R, Temel JS, et al. Implementing multiplexed genotyping of non-small-cell lung cancers into routine clinical practice. Ann Oncol. 2011;22:2616–24.PubMed CentralView ArticlePubMedGoogle Scholar
- Li Y, Pan YJ, Wang R, Sun YH, Hu HC, Shen XX, et al. ALK-rearranged lung cancer in Chinese: a comprehensive assessment of clinicopathology, IHC, FISH and RT-PCR. PLoS One. 2013;8:e69016.PubMed CentralView ArticlePubMedGoogle Scholar
- Soda M, Takada S, Takeuchi K, Choi YL, Enomoto M, Ueno T, et al. A mouse model for EML4-ALK-positive lung cancer. Proc Natl Acad Sci USA. 2008;105:19893–7.PubMed CentralView ArticlePubMedGoogle Scholar
- Inamura K, Takeuchi K, Togashi Y, Hatano S, Ninomiya H, Motoi N, et al. EML4-ALK lung cancers are characterized by rare other mutations, a TTF-1 cell lineage, an acinar histology, and young onset. Mod Pathol. 2009;22:508–15.View ArticlePubMedGoogle Scholar
- Koivunen JP, Mermel C, Zejnullahu K, Murphy C, Lifshits E, Holmes AJ, et al. EML4-ALK fusion gene and efficacy of an ALK kinase inhibitor in lung cancer. Clin Cancer Res. 2008;14:4275–83.PubMed CentralView ArticlePubMedGoogle Scholar
- Zhang X, Zhang S, Yang X, Yang J, Zhou Q, Yin L, et al. Fusion of EML4 and ALK is associated with development of lung adenocarcinomas lacking EGFR and KRAS mutations and is correlated with ALK expression. Mol Cancer. 2010;9:188.PubMed CentralView ArticlePubMedGoogle Scholar
- Wang J, Cai Y, Dong Y, Nong J, Zhou L, Liu G, et al. Clinical characteristics and outcomes of patients with primary lung adenocarcinoma harboring ALK rearrangements detected by FISH, IHC, and RT-PCR. PLoS One. 2014;9:e101551.PubMed CentralView ArticlePubMedGoogle Scholar
- Kuo YW, Wu SG, Ho CC, Shih JY. Good response to gefitinib in lung adenocarcinoma harboring coexisting EML4-ALK fusion gene and EGFR mutation. J Thorac Oncol. 2010;5:2039–40.View ArticlePubMedGoogle Scholar
- Popat S, Vieira de Araujo A, Min T, Swansbury J, Dainton M, Wotherspoon A, et al. Lung adenocarcinoma with concurrent exon 19 EGFR mutation and ALK rearrangement responding to erlotinib. J Thorac Oncol. 2011;6:1962–3.View ArticlePubMedGoogle Scholar
- Sasaki T, Koivunen J, Ogino A, Yanagita M, Nikiforow S, Zheng W, et al. A novel ALK secondary mutation and EGFR signaling cause resistance to ALK kinase inhibitors. Cancer Res. 2011;71:6051–60.PubMed CentralView ArticlePubMedGoogle Scholar
- Li C, Hao L, Li Y, Wang S, Chen H, Zhang L, et al. Prognostic value analysis of mutational and clinicopathological factors in non-small cell lung cancer. PLoS One. 2014;9:e107276.PubMed CentralView ArticlePubMedGoogle Scholar
- Suzuki H, Hirashima T, Okmoto N, Yamadori T, Tamiya M, Morishita N, et al. The relationship between tyrosine kinase inhibitor therapy and overall survival in patients with non-small cell lung cancer carrying EGFR mutations. Chin J Cancer. 2013;32:136–40.PubMed CentralView ArticlePubMedGoogle Scholar
- Zhang S, Wang F, Keats J, Zhu X, Ning Y, Wardwell SD, et al. Crizotinib-resistant mutants of EML4-ALK identified through an accelerated mutagenesis screen. Chem Biol Drug Des. 2011;78:999–1005.PubMed CentralView ArticlePubMedGoogle Scholar
- Spaans JN, Goss GD. Drug resistance to molecular targeted therapy and its consequences for treatment decisions in non-small-cell lung cancer. Front Oncol. 2014;4:190.PubMed CentralPubMedGoogle Scholar