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  1. Article ; Online: Tolvaptan and Number Needed to Harm in Autosomal Dominant Polycystic Kidney Disease.

    Betts, Keith A / Nunna, Sasikiran / Kumar, Retesh / Nie, Xiaoyu / Fernandes, Ancilla W

    Kidney medicine

    2024  Volume 6, Issue 4, Page(s) 100802

    Language English
    Publishing date 2024-02-20
    Publishing country United States
    Document type Journal Article
    ISSN 2590-0595
    ISSN (online) 2590-0595
    DOI 10.1016/j.xkme.2024.100802
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Effects of tolvaptan discontinuation in patients with autosomal dominant polycystic kidney disease: a post hoc pooled analysis.

    Lioudis, Michael / Zhou, Xiaolei / Davenport, Eric / Nunna, Sasikiran / Krasa, Holly B / Oberdhan, Dorothee / Fernandes, Ancilla W

    BMC nephrology

    2023  Volume 24, Issue 1, Page(s) 182

    Abstract: Background: Tolvaptan slows kidney function decline in patients with autosomal dominant polycystic kidney disease (ADPKD) who are at risk of rapid progression. Given that treatment requires commitment to long-term use, we evaluated the effects of ... ...

    Abstract Background: Tolvaptan slows kidney function decline in patients with autosomal dominant polycystic kidney disease (ADPKD) who are at risk of rapid progression. Given that treatment requires commitment to long-term use, we evaluated the effects of tolvaptan discontinuation on the trajectory of ADPKD progression.
    Methods: This was a post hoc analysis of pooled data from two clinical trials of tolvaptan (TEMPO 2:4 [NCT00413777] and TEMPO 3:4 [NCT00428948]), an extension trial (TEMPO 4:4 [NCT01214421]), and an observational study (OVERTURE [NCT01430494]) that enrolled patients from the other trials. Individual subject data were linked longitudinally across trials to construct analysis cohorts of subjects with a tolvaptan treatment duration > 180 days followed by an off-treatment observation period of > 180 days. For inclusion in Cohort 1, subjects were required have ≥ 2 outcome assessments during the tolvaptan treatment period and ≥ 2 assessments during the follow-up period. For Cohort 2, subjects were required to have ≥ 1 assessment during the tolvaptan treatment period and ≥ 1 assessment during the follow-up period. Outcomes were rates of change in estimated glomerular filtration rate (eGFR) and total kidney volume (TKV). Piecewise-mixed models compared changes in eGFR or TKV in the on-treatment and post-treatment periods.
    Results: In the Cohort 1 eGFR population (n = 20), the annual rate of eGFR change (in mL/min/1.73 m
    Conclusions: Although limited by small sample sizes, these analyses showed directionally consistent acceleration in measures of ADPKD progression following the discontinuation of tolvaptan.
    MeSH term(s) Humans ; Tolvaptan/therapeutic use ; Polycystic Kidney, Autosomal Dominant/drug therapy ; Antidiuretic Hormone Receptor Antagonists/adverse effects ; Disease Progression ; Kidney ; Glomerular Filtration Rate
    Chemical Substances Tolvaptan (21G72T1950) ; Antidiuretic Hormone Receptor Antagonists
    Language English
    Publishing date 2023-06-22
    Publishing country England
    Document type Observational Study ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2041348-8
    ISSN 1471-2369 ; 1471-2369
    ISSN (online) 1471-2369
    ISSN 1471-2369
    DOI 10.1186/s12882-023-03247-6
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Validation of a Case-Finding Algorithm for Identifying Patients with Non-small Cell Lung Cancer (NSCLC) in Administrative Claims Databases.

    Turner, Ralph M / Chen, Yen-Wen / Fernandes, Ancilla W

    Frontiers in pharmacology

    2017  Volume 8, Page(s) 883

    Abstract: Objective: ...

    Abstract Objective:
    Language English
    Publishing date 2017-11-30
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2587355-6
    ISSN 1663-9812
    ISSN 1663-9812
    DOI 10.3389/fphar.2017.00883
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Brain metastases in non-small cell lung cancer patients on epidermal growth factor receptor tyrosine kinase inhibitors: symptom and economic burden.

    Fernandes, Ancilla W / Wu, Bingcao / Turner, Ralph M

    Journal of medical economics

    2017  Volume 20, Issue 11, Page(s) 1136–1147

    Abstract: Objective: This study describes the symptom and economic burden associated with brain metastases (BM) in patients with non-small cell lung cancer (NSCLC) receiving epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (EGFR-TKIs).: ... ...

    Abstract Objective: This study describes the symptom and economic burden associated with brain metastases (BM) in patients with non-small cell lung cancer (NSCLC) receiving epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (EGFR-TKIs).
    Methods: This retrospective study included adults with ≥2 medical claims, within 90 days, for lung cancer and ≥1 administration of EGFR-TKIs. Based on ICD-9 codes, patients were stratified into cohorts by type of metastases (BM, other metastases [OM], or no metastases [NM]), and by when the metastasis diagnosis occurred (synchronous or asynchronous).
    Results: The population (synchronous BM [SBM] = 24, synchronous OM [SOM] = 23, asynchronous BM [ASBM] = 15, asynchronous OM [ASOM] = 49, NM = 85) was mostly female (57%), average age 69 years (SD = 11). SBM patients experienced more fatigue and nausea/vomiting compared with SOM and NM patients and more headaches and loss of appetite than NM patients. ASBM was associated with more fatigue, nausea/vomiting, headaches, pain/numbness, altered mental status, and seizures than NM, and more headaches and pain/numbness than ASOM. SBM patients experienced a greater increase in per-member-per-month all-cause total healthcare costs after diagnosis ($20,301) vs SOM ($9,131, p = .001) and NM ($2,493, p = .001). ASBM's cost increase between baseline and follow-up ($7,867) did not differ from ASOM's ($4,947, p = .195); both were larger than NM ($2,493, p = .001 and p = .009, respectively).
    Limitations: EGFR mutation status was inferred based on EGFR-TKI treatment, not by molecular testing. Patients were from US commercial insurance plans; results may not be generalizable to other populations.
    Conclusions: Among patients with EGFR-TKI-treated NSCLC, patients with BM experienced more symptoms and, when diagnosed synchronously, had significant increases in total medical costs vs patients with OM and NM. Therapeutic options with central nervous system activity may offer advantages in symptomatology and costs in EGFR-mutated patients with BM.
    MeSH term(s) Aged ; Aged, 80 and over ; Antineoplastic Agents/therapeutic use ; Brain Neoplasms/economics ; Brain Neoplasms/physiopathology ; Brain Neoplasms/secondary ; Carcinoma, Non-Small-Cell Lung/drug therapy ; Carcinoma, Non-Small-Cell Lung/genetics ; Carcinoma, Non-Small-Cell Lung/pathology ; Female ; Humans ; Lung Neoplasms/drug therapy ; Lung Neoplasms/genetics ; Lung Neoplasms/pathology ; Male ; Middle Aged ; Protein Kinase Inhibitors/therapeutic use ; Receptor, Epidermal Growth Factor/antagonists & inhibitors ; Receptor, Epidermal Growth Factor/genetics ; Retrospective Studies
    Chemical Substances Antineoplastic Agents ; Protein Kinase Inhibitors ; EGFR protein, human (EC 2.7.10.1) ; Receptor, Epidermal Growth Factor (EC 2.7.10.1)
    Language English
    Publishing date 2017-11
    Publishing country England
    Document type Journal Article
    ZDB-ID 2270945-9
    ISSN 1941-837X ; 1369-6998
    ISSN (online) 1941-837X
    ISSN 1369-6998
    DOI 10.1080/13696998.2017.1361960
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Complications and Economic Burden Associated With Obtaining Tissue for Diagnosis and Molecular Analysis in Patients With Non-Small-Cell Lung Cancer in the United States.

    Kelly, Ronan J / Turner, Ralph / Chen, Yen-Wen / Rigas, James R / Fernandes, Ancilla W / Karve, Sudeep

    Journal of oncology practice

    2019  Volume 15, Issue 8, Page(s) e717–e727

    Abstract: Purpose: With an increase in biomarker-directed therapies, tissue biopsy to identify targetable genomic and immunologic alterations has become the mainstay of managing patients with non-small-cell lung cancer (NSCLC); however, little is known about the ... ...

    Abstract Purpose: With an increase in biomarker-directed therapies, tissue biopsy to identify targetable genomic and immunologic alterations has become the mainstay of managing patients with non-small-cell lung cancer (NSCLC); however, little is known about the associated economic impact and complication rate. This study assesses the frequency, complications, and costs of diagnostic and postprogression biopsy.
    Methods: This retrospective, observational study was conducted using administrative claims data from more than 30 million commercially insured individuals in the United States (2006 to 2014). Data were analyzed for the overall population and by time of biopsy (diagnostic or postprogression biopsy).
    Results: Of 20,013 eligible patients, 13,411 (67%) received a diagnostic biopsy, whereas only 2,056 (10%) received a postprogression biopsy (mean cost, $9,977 and $16,806, respectively). Complication rates were similar at diagnosis and after progression, on the day of biopsy (10%
    Conclusion: From 2006 to 2014, postprogression biopsies were not common practice in NSCLC. Complication rates were similar at diagnosis and after progression, with mean costs higher among patients with a complication than those without a complication. With increasing demands for effective novel targeted therapies and safe testing methods, these data may be valuable in determining the budget impact and comparing complication rates with newer, less invasive molecular testing methods, including plasma circulating tumor DNA testing.
    MeSH term(s) Aged ; Biopsy/economics ; Biopsy/methods ; Carcinoma, Non-Small-Cell Lung/economics ; Carcinoma, Non-Small-Cell Lung/surgery ; Cost of Illness ; Female ; Humans ; Lung Neoplasms/economics ; Lung Neoplasms/surgery ; Male ; Retrospective Studies ; United States
    Language English
    Publishing date 2019-06-25
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2236338-5
    ISSN 1935-469X ; 1554-7477
    ISSN (online) 1935-469X
    ISSN 1554-7477
    DOI 10.1200/JOP.18.00762
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: The rate of occurrence, healthcare resource use and costs of adverse events among metastatic non-small cell lung cancer patients treated with first- and second-generation epidermal growth factor receptor tyrosine kinase inhibitors.

    Subramanian, Janakiraman / Fernandes, Ancilla W / Laliberté, François / Pavilack, Melissa / DerSarkissian, Maral / Duh, Mei Sheng

    Lung cancer (Amsterdam, Netherlands)

    2019  Volume 138, Page(s) 131–138

    Abstract: Objectives: Clinical trials with first- and second-generation epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) reported severe adverse events (SAEs) in 6%-49% of patients with EGFR-mutated non-small cell lung cancer. This study ... ...

    Abstract Objectives: Clinical trials with first- and second-generation epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) reported severe adverse events (SAEs) in 6%-49% of patients with EGFR-mutated non-small cell lung cancer. This study describes incremental healthcare resource utilization (HRU) and costs associated with real-world management of AEs in this population, with a focus on SAEs.
    Materials and methods: Patients receiving erlotinib, gefitinib, or afatinib as first-line (1L) monotherapy were identified from IQVIA™ Real-World Data Adjudicated Claims-US database (04/01/2012-03/31/2017). Relevant AEs were selected from corresponding prescribing information; SAEs were identified from hospitalization claims. HRU and cost per-patient-per-month (PPPM) were assessed during 1L treatment and compared for patients with and without each AE using multivariate Poisson and linear regression, respectively, adjusting for baseline characteristics.
    Results: Of 1646 patients, 86.9% were treated with erlotinib, 12.1% with afatinib, and 1.0% with gefitinib. In 1L, 12.2% of patients had ≥1 acute SAE (220.1/1000 patient-years). Patients with any SAE had higher PPPM costs than patients without SAEs (cost difference = $4700, p < 0.001). Incremental costs ranged from $2604 PPPM for diarrhea to $10,143 PPPM for microangiopathic hemolytic anemia (MAHA), and were statistically significant for all SAEs (all p < 0.001) except MAHA (p < 0.0528). Patients with any SAEs had higher rates of HRU relative to patients without SAEs (hospitalization rate ratio = 6.15; outpatient visits rate ratio = 1.21; all p < 0.001).
    Conclusion: More than one-tenth of patients experienced SAEs, resulting in sizeable economic burden with respect to HRU and costs. EGFR-TKIs with more favorable safety profiles may reduce the burden of managing this population.
    MeSH term(s) Afatinib/administration & dosage ; Antineoplastic Combined Chemotherapy Protocols/adverse effects ; Antineoplastic Combined Chemotherapy Protocols/economics ; Antineoplastic Combined Chemotherapy Protocols/therapeutic use ; Carcinoma, Non-Small-Cell Lung/drug therapy ; Carcinoma, Non-Small-Cell Lung/economics ; Carcinoma, Non-Small-Cell Lung/pathology ; Drug-Related Side Effects and Adverse Reactions/economics ; Drug-Related Side Effects and Adverse Reactions/epidemiology ; ErbB Receptors/antagonists & inhibitors ; ErbB Receptors/genetics ; Erlotinib Hydrochloride/administration & dosage ; Female ; Gefitinib/administration & dosage ; Health Resources/statistics & numerical data ; Humans ; Incidence ; Lung Neoplasms/drug therapy ; Lung Neoplasms/economics ; Lung Neoplasms/pathology ; Male ; Middle Aged ; Mutation ; Protein Kinase Inhibitors/administration & dosage ; Protein Kinase Inhibitors/adverse effects ; Protein Kinase Inhibitors/economics ; Retrospective Studies ; Treatment Outcome ; United States/epidemiology
    Chemical Substances Protein Kinase Inhibitors ; Afatinib (41UD74L59M) ; Erlotinib Hydrochloride (DA87705X9K) ; EGFR protein, human (EC 2.7.10.1) ; ErbB Receptors (EC 2.7.10.1) ; Gefitinib (S65743JHBS)
    Language English
    Publishing date 2019-07-24
    Publishing country Ireland
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 632771-0
    ISSN 1872-8332 ; 0169-5002
    ISSN (online) 1872-8332
    ISSN 0169-5002
    DOI 10.1016/j.lungcan.2019.07.021
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Objective response rate is a possible surrogate endpoint for survival in patients with advanced, recurrent ovarian cancer.

    Siddiqui, Mohammed Kashif / Tyczynski, Jerzy / Pahwa, Ankit / Fernandes, Ancilla W

    Gynecologic oncology

    2017  Volume 146, Issue 1, Page(s) 44–51

    Abstract: Objective: Evaluate literature to assess response rate as a surrogate endpoint of survival in ovarian cancer (OC).: Methods: Systematic review consistent with PRISMA criteria, identified randomized, controlled trials reporting overall survival (OS), ... ...

    Abstract Objective: Evaluate literature to assess response rate as a surrogate endpoint of survival in ovarian cancer (OC).
    Methods: Systematic review consistent with PRISMA criteria, identified randomized, controlled trials reporting overall survival (OS), progression-free survival (PFS), and objective response rate (ORR) in recurrent OC. MEDLINE® and Embase® searches (year 2000-March 23, 2015) were augmented by bibliographic screening. Proposed surrogate measures (independent variables) were ORR and disease control rate. True clinical outcomes (dependent variables) were median OS and PFS. Analyses were performed on unweighted and weighted data using correlation analysis, linear regression, and surrogate threshold effect (STE). Smaller STE indicates greater predictive precision with magnitude of STE dependent on variance of prediction.
    Results: Thirty-nine studies were included for review, representing 9223 platinum-sensitive and resistant patients. Objective response rate (r=0.82; P<0.001) was a better predictor than disease control rate (r=0.58; P<0.001) and strongly correlated with PFS (r=0.85; P<0.0001). Weighted-regression analysis demonstrated that for each 10% increase in ORR, PFS increased by 1.20months and OS by 2.83months. Regression analysis of treatment effects (odds ratio of response, hazard ratio of survival) suggests that a 10% increase in odds ratio of ORR would result in 2.5% reduction in the hazard ratio of OS. Based on weighted data, STE indicated that an ORR of ≥1% is needed to achieve nonzero OS benefit.
    Conclusion: This systematic review supports ORR as a possible surrogate clinical trial endpoint for OS in recurrent OC with at least second-line therapy.
    MeSH term(s) Biomarkers ; Female ; Humans ; Neoplasm Recurrence, Local/mortality ; Neoplasm Recurrence, Local/therapy ; Ovarian Neoplasms/mortality ; Ovarian Neoplasms/therapy ; Survival Rate
    Chemical Substances Biomarkers
    Language English
    Publishing date 2017-07
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 801461-9
    ISSN 1095-6859 ; 0090-8258
    ISSN (online) 1095-6859
    ISSN 0090-8258
    DOI 10.1016/j.ygyno.2017.03.515
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: EGFR mutation testing and treatment decisions in patients progressing on first- or second-generation epidermal growth factor receptor tyrosine kinase inhibitors.

    Chiang, Anne C / Fernandes, Ancilla W / Pavilack, Melissa / Wu, Jennifer W / Laliberté, François / Duh, Mei Sheng / Chehab, Nabil / Subramanian, Janakiraman

    BMC cancer

    2020  Volume 20, Issue 1, Page(s) 356

    Abstract: Background: The objective of this study was to investigate real-world EGFR mutation testing in patients with metastatic non-small cell lung cancer (NSCLC) upon progression on first-/second-generation epidermal growth factor receptor (EGFR)-tyrosine ... ...

    Abstract Background: The objective of this study was to investigate real-world EGFR mutation testing in patients with metastatic non-small cell lung cancer (NSCLC) upon progression on first-/second-generation epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKI), and subsequent treatments received.
    Methods: Flatiron Health electronic health records-derived database was used to identify adult patients with metastatic NSCLC treated with first-/second-generation EGFR-TKI from 11/2015-09/2017, with start of first EGFR-TKI defined as the index date. Patients were stratified by receipt of EGFR-TKI as first-line (1 L) or later-line (2 L+) treatment. Mutation testing and subsequent therapies following first-/second-generation EGFR-TKI were described.
    Results: Overall, 782 patients (1 L = 435; 2 L+ =347) were included. Median age was 69.0 years, 63.6% were female, 56.3% were white, 87.1% were treated in community-based practices, and 30.1% of patients died during the study period; median follow-up was 309.0 days. Among the 294 (1 L = 160; 2L+ =134) patients who received subsequent therapies, treatments included chemotherapy only (1 L = 15.6%; 2L+ =21.6%), immunotherapy only (1 L = 13.8%; 2 L+ =41.0%), and targeted therapies (1 L = 70.0%; 2 L+ =36.6%). Specifically, 40 (25.0%) 1 L patients and 7 (5.2%) 2 L+ patients received osimertinib as subsequent therapy. Before the start of subsequent therapy, EGFR T790M resistance mutation testing was performed in 88 (29.9%) patients (1 L = 63 [39.4%]; 2 L+ =25 [18.7%]). Of these patients, 25 (28.4%) were T790M positive, among whom 24 (96.0%) received osimertinib.
    Conclusions: A third of patients received subsequent therapies on disease progression; only 30% of these were tested for EGFR-TKI resistance mutation, prior to receiving subsequent therapies. These results highlight the importance of choosing treatments in the 1 L setting that optimize benefits for patients with EGFR-mutated NSCLC.
    MeSH term(s) Aged ; Biomarkers, Tumor/genetics ; Carcinoma, Non-Small-Cell Lung/drug therapy ; Carcinoma, Non-Small-Cell Lung/genetics ; Carcinoma, Non-Small-Cell Lung/pathology ; Decision Making ; Drug Resistance, Neoplasm ; ErbB Receptors/genetics ; Female ; Follow-Up Studies ; Humans ; Longitudinal Studies ; Lung Neoplasms/drug therapy ; Lung Neoplasms/genetics ; Lung Neoplasms/pathology ; Male ; Mutation ; Prognosis ; Protein Kinase Inhibitors/therapeutic use ; Retrospective Studies ; Survival Rate
    Chemical Substances Biomarkers, Tumor ; Protein Kinase Inhibitors ; EGFR protein, human (EC 2.7.10.1) ; ErbB Receptors (EC 2.7.10.1)
    Language English
    Publishing date 2020-04-28
    Publishing country England
    Document type Journal Article
    ISSN 1471-2407
    ISSN (online) 1471-2407
    DOI 10.1186/s12885-020-06826-0
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Treatment patterns and overall survival among patients with unresectable, stage III non-small-cell lung cancer.

    Bobbili, Priyanka / Ryan, Kellie / Duh, Mei S / Dua, Akanksha / Fernandes, Ancilla W / Pavilack, Melissa / Gomez, Jorge E

    Future oncology (London, England)

    2019  Volume 15, Issue 29, Page(s) 3381–3393

    Abstract: Aim: ...

    Abstract Aim:
    MeSH term(s) Adenocarcinoma of Lung/mortality ; Adenocarcinoma of Lung/pathology ; Adenocarcinoma of Lung/therapy ; Aged ; Carcinoma, Non-Small-Cell Lung/mortality ; Carcinoma, Non-Small-Cell Lung/pathology ; Carcinoma, Non-Small-Cell Lung/therapy ; Carcinoma, Squamous Cell/mortality ; Carcinoma, Squamous Cell/pathology ; Carcinoma, Squamous Cell/therapy ; Chemoradiotherapy/mortality ; Female ; Follow-Up Studies ; Humans ; Lung Neoplasms/mortality ; Lung Neoplasms/pathology ; Lung Neoplasms/therapy ; Male ; Neoplasm Staging ; Retrospective Studies ; SEER Program ; Survival Rate
    Language English
    Publishing date 2019-09-23
    Publishing country England
    Document type Journal Article
    ZDB-ID 2274956-1
    ISSN 1744-8301 ; 1479-6694
    ISSN (online) 1744-8301
    ISSN 1479-6694
    DOI 10.2217/fon-2019-0282
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Real-world treatment patterns among patients with unresected stage III non-small-cell lung cancer.

    Ryan, Kellie J / Skinner, Karen E / Fernandes, Ancilla W / Punekar, Rajeshwari S / Pavilack, Melissa / Walker, Mark S / VanderWalde, Noam A

    Future oncology (London, England)

    2019  Volume 15, Issue 25, Page(s) 2943–2953

    Abstract: Aim: ...

    Abstract Aim:
    MeSH term(s) Adult ; Aged ; Anaplastic Lymphoma Kinase/genetics ; Carcinoma, Non-Small-Cell Lung/drug therapy ; Carcinoma, Non-Small-Cell Lung/genetics ; Carcinoma, Non-Small-Cell Lung/pathology ; Carcinoma, Non-Small-Cell Lung/radiotherapy ; Combined Modality Therapy ; Disease Progression ; Disease-Free Survival ; ErbB Receptors/genetics ; Female ; Humans ; Kaplan-Meier Estimate ; Male ; Middle Aged ; Neoplasm Staging ; Platinum/therapeutic use ; Proto-Oncogene Proteins p21(ras)/genetics
    Chemical Substances KRAS protein, human ; Platinum (49DFR088MY) ; ALK protein, human (EC 2.7.10.1) ; Anaplastic Lymphoma Kinase (EC 2.7.10.1) ; EGFR protein, human (EC 2.7.10.1) ; ErbB Receptors (EC 2.7.10.1) ; Proto-Oncogene Proteins p21(ras) (EC 3.6.5.2)
    Language English
    Publishing date 2019-04-30
    Publishing country England
    Document type Journal Article ; Observational Study
    ZDB-ID 2274956-1
    ISSN 1744-8301 ; 1479-6694
    ISSN (online) 1744-8301
    ISSN 1479-6694
    DOI 10.2217/fon-2018-0939
    Database MEDical Literature Analysis and Retrieval System OnLINE

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