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  1. Article ; Online: Real-world treatment patterns and clinical outcomes in patients treated with eribulin after prior phosphoinositide 3-Kinase inhibitor treatment for metastatic breast cancer.

    Goyal, Ravi K / Zhang, Jingchuan / Davis, Keith L / Sluga-O'Callaghan, Martina / Kaufman, Peter A

    Breast cancer research and treatment

    2024  Volume 205, Issue 1, Page(s) 201–210

    Abstract: Purpose: In 2010, the US Food and Drug Administration approved eribulin for the treatment of metastatic breast cancer (MBC). Since then, the treatment landscape has evolved with many new therapy classes, a more recent one being the small molecule ... ...

    Abstract Purpose: In 2010, the US Food and Drug Administration approved eribulin for the treatment of metastatic breast cancer (MBC). Since then, the treatment landscape has evolved with many new therapy classes, a more recent one being the small molecule inhibitors of phosphoinositide 3 kinase (PI3K). We sought to characterize the treatment patterns and clinical outcomes of patients with MBC who received eribulin following prior treatment with a PI3K inhibitor.
    Methods: A retrospective cohort study based on medical record review included MBC patients who initiated eribulin between March 2019 and September 2020 following prior treatment with a PI3K inhibitor was conducted. Patient demographics, treatment characteristics, and clinical outcomes were analyzed descriptively. Real-world progression-free survival (rwPFS) and overall survival (OS) were estimated from the initiation of eribulin therapy using Kaplan-Meier analyses.
    Results: 82 eligible patients were included. Patients' median age at eribulin initiation was 62 years; 86.5% had hormone receptor-positive, human epidermal growth factor receptor 2-negative tumors. Eribulin was most often administered in the second or third line (82.9%) in the metastatic setting. Best overall response on eribulin was reported as complete or partial response in 72% of the patients. The median rwPFS was 18.9 months (95% confidence interval [CI], 12.4-not estimable); median OS was not reached. The estimated rwPFS and OS rates at 12 months were 63.3% (95% CI, 50.5-73.7) and 82.6% (95% CI, 72.4-89.3), respectively.
    Conclusion: Our real-world study suggests that eribulin may be a potential treatment option for MBC patients who fail a prior PI3K inhibitor.
    MeSH term(s) Humans ; Furans/therapeutic use ; Ketones/therapeutic use ; Female ; Breast Neoplasms/drug therapy ; Breast Neoplasms/pathology ; Breast Neoplasms/mortality ; Middle Aged ; Aged ; Retrospective Studies ; Phosphoinositide-3 Kinase Inhibitors/therapeutic use ; Adult ; Neoplasm Metastasis ; Treatment Outcome ; Aged, 80 and over ; Polyether Polyketides
    Chemical Substances eribulin (LR24G6354G) ; Furans ; Ketones ; Phosphoinositide-3 Kinase Inhibitors ; Polyether Polyketides
    Language English
    Publishing date 2024-02-04
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 604563-7
    ISSN 1573-7217 ; 0167-6806
    ISSN (online) 1573-7217
    ISSN 0167-6806
    DOI 10.1007/s10549-023-07080-1
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Early Real-World Treatment Patterns and Clinical Outcomes in Patients with Metastatic Breast Cancer Treated with Eribulin After Prior Immuno-Oncology or Antibody-Drug Conjugate Therapy.

    Goyal, Ravi K / Zhang, Jingchuan / Davis, Keith L / Sluga-O'Callaghan, Martina / Kaufman, Peter A

    Breast cancer (Dove Medical Press)

    2023  Volume 15, Page(s) 855–865

    Abstract: Introduction: Eribulin was approved by the FDA in 2010 for the treatment of metastatic breast cancer (MBC) in the United States (US). More recently, several immuno-oncology (IO) and antibody-drug conjugate (ADC) regimens have been approved for MBC. We ... ...

    Abstract Introduction: Eribulin was approved by the FDA in 2010 for the treatment of metastatic breast cancer (MBC) in the United States (US). More recently, several immuno-oncology (IO) and antibody-drug conjugate (ADC) regimens have been approved for MBC. We assessed the treatment patterns and clinical outcomes in MBC patients treated with eribulin following treatment with an IO or ADC in US clinical practice.
    Materials and methods: In a retrospective patient medical chart review study, patients with MBC, aged ≥18 years, who initiated eribulin therapy between March 1, 2019, and September 30, 2020, treated with either prior IO or ADC in the metastatic setting were included. Patient demographics, treatment characteristics, and clinical outcomes were analyzed descriptively. Real-world progression-free survival (rwPFS) and overall survival (OS) were estimated using Kaplan-Meier analyses.
    Results: In the study population (N=143), median age at eribulin initiation was 62 years; 64% were Caucasian, and 67% had triple-negative MBC (TNBC). Eribulin therapy was used in the second to fifth line of therapy in the metastatic setting; median treatment duration was 7.2 months. The overall response rate for eribulin was 59.4%. Median rwPFS and OS from eribulin initiation were 21.4 months (95% CI, 12.9-not estimable [NE]) and 24.2 months (95% CI, 17.5-NE), respectively. In patients with TNBC, median rwPFS and OS from eribulin initiation were 12.0 months (95% CI, 8.8-NE) and 18.3 months (95% CI, 14.9-NE), respectively.
    Conclusion: These real-world data provide evidence for the clinical effectiveness outcomes of eribulin treatment among MBC patients previously treated with an IO or ADC.
    Language English
    Publishing date 2023-11-17
    Publishing country New Zealand
    Document type Journal Article
    ZDB-ID 2520722-2
    ISSN 1179-1314
    ISSN 1179-1314
    DOI 10.2147/BCTT.S422025
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Effectiveness of standard treatments in non-small-cell lung cancer with METexon14 skipping mutation: a real-world study.

    Furqan, Muhammad / Karanth, Siddharth / Goyal, Ravi K / Cai, Beilei / Rombi, Julien / Davis, Keith L / Caro, Nydia / Saliba, Teddy

    Future oncology (London, England)

    2024  

    Abstract: Aim: ...

    Abstract Aim:
    Language English
    Publishing date 2024-04-17
    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-2023-1064
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Real-World Treatment Patterns and Clinical Outcomes Among Patients With Advanced Renal Cell Carcinoma.

    Esterberg, Elizabeth / Iyer, Shrividya / Nagar, Saurabh P / Davis, Keith L / Tannir, Nizar M

    Clinical genitourinary cancer

    2023  Volume 22, Issue 2, Page(s) 115–125.e3

    Abstract: Background: Nearly 30% of new renal cell carcinoma (RCC) cases are diagnosed at an advanced or metastatic stage. Recent approvals of immunotherapies (IO) have significantly impacted patient care, but real-world outcomes of these treatments have not been ...

    Abstract Background: Nearly 30% of new renal cell carcinoma (RCC) cases are diagnosed at an advanced or metastatic stage. Recent approvals of immunotherapies (IO) have significantly impacted patient care, but real-world outcomes of these treatments have not been widely evaluated.
    Methods: Eligible physicians abstracted demographic and clinical data from patient medical records for patients with advanced clear and non-clear cell RCC (aRCC) who initiated treatment between January 1, 2018, and December 31, 2020. Overall survival (OS) and progression-free survival (PFS) were estimated by the Kaplan-Meier method. A multivariate Cox regression model was developed to assess the impact of treatment category on clinical outcomes while controlling for International Metastatic RCC Database Consortium (IMDC) risk category, histology, and other patient characteristics.
    Results: A total of 498 patients were included (201 from US, 62 from Canada, 58 from UK, 59 from France, 58 from Germany, 60 from Spain). Of these, 250 received tyrosine kinase inhibitor (TKI) monotherapy, 197 received immunotherapy (IO) combination (119 IO+TKI, 78 IO+IO), and 32 received IO monotherapy as first-line treatment for aRCC; 19 patients received various other regimens. 16% of patients had a favorable IMDC risk score. Based on results of multivariable Cox regression, PFS (hazard ratio [HR] [95% confidence interval (CI)]: 0.50 [0.36-0.72]) (P < .001) and time to next treatment (TTNT) were significantly longer (HR [95% CI]: 0.54 [0.39-0.73]) (P < .001) for patients treated with IO combination versus TKI monotherapy. IO combination had a numerically reduced, but statistically insignificant, risk of death versus TKI monotherapy (HR: 0.66; P = .114). IO+TKI combination was associated with significantly longer PFS and reduced risk of progression (HR: 0.52; P = .04) versus IO+IO combination; similar results were observed for TTNT (HR: 0.57; P = .03).
    Conclusion: Our evaluation of real-world treatment outcomes in aRCC revealed that IO + TKI combination is associated with improved PFS and prolonged TTNT compared with TKI monotherapy and IO+IO combination.
    MeSH term(s) Humans ; Carcinoma, Renal Cell/drug therapy ; Carcinoma, Renal Cell/pathology ; Kidney Neoplasms/drug therapy ; Treatment Outcome ; Protein Kinase Inhibitors/therapeutic use ; Proportional Hazards Models ; Retrospective Studies
    Chemical Substances Protein Kinase Inhibitors
    Language English
    Publishing date 2023-10-06
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2225121-2
    ISSN 1938-0682 ; 1558-7673
    ISSN (online) 1938-0682
    ISSN 1558-7673
    DOI 10.1016/j.clgc.2023.09.009
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Real-world effectiveness of lenvatinib monotherapy in previously treated unresectable hepatocellular carcinoma in US clinical practice.

    Singal, Amit G / Nagar, Saurabh P / Hitchens, Abby / Davis, Keith L / Iyer, Shrividya

    Cancer reports (Hoboken, N.J.)

    2022  Volume 6, Issue 1, Page(s) e1679

    Abstract: Background: Lenvatinib monotherapy was approved in the United States for first-line treatment of patients with unresectable hepatocellular carcinoma (uHCC) in 2018. This study assessed real-world treatment patterns and outcomes of lenvatinib beyond ... ...

    Abstract Background: Lenvatinib monotherapy was approved in the United States for first-line treatment of patients with unresectable hepatocellular carcinoma (uHCC) in 2018. This study assessed real-world treatment patterns and outcomes of lenvatinib beyond first-line systemic treatment in the United States.
    Methods: A retrospective study was conducted among US adults (≥18 years) with uHCC. Eligible patients initiated lenvatinib monotherapy as second- or later-line systemic therapy (2L-plus) from August 2018 to September 2019. Clinical outcomes included physician-reported best response, progression-free survival (PFS), and overall survival (OS).
    Results: Of 164 patients who received lenvatinib in 2L-plus, most (n = 133; 81.1%) received lenvatinib in 2 L. There were 109 patients (66.4%) who initiated lenvatinib after immunotherapy. At lenvatinib initiation, only 31.1% of patients had Child-Pugh class A, while half (49.4%) had Child-Pugh class B. Most patients had Barcelona Clinic Liver Cancer stage B (23.8%) or C (38.4%) uHCC. Median duration of lenvatinib treatment was 6.9 months, with 42.7% of patients still on treatment at the end of follow-up. Physician-reported best response was complete and partial response for 8.5% and 44.5% of patients, respectively. PFS and OS rate estimates from lenvatinib initiation at 12 months were 51.7% and 57.8%, respectively. Among patients treated after immunotherapy, complete and partial responses were 10.1% and 43.1%, respectively, and PFS and OS estimates from lenvatinib initiation at 12 months were 52.8% and 60.0%, respectively.
    Conclusion: This retrospective study suggests clinical effectiveness of lenvatinib monotherapy in a real-world setting among previously treated patients with uHCC, including among those previously treated with immunotherapy.
    MeSH term(s) Adult ; Humans ; Carcinoma, Hepatocellular/drug therapy ; Retrospective Studies ; Liver Neoplasms/drug therapy ; Phenylurea Compounds/therapeutic use
    Chemical Substances lenvatinib (EE083865G2) ; Phenylurea Compounds
    Language English
    Publishing date 2022-07-13
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 2573-8348
    ISSN (online) 2573-8348
    DOI 10.1002/cnr2.1679
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Real-world outcomes in non-small-cell lung cancer patients with MET Exon 14 skipping mutation and brain metastases treated with capmatinib.

    Paik, Paul K / Goyal, Ravi K / Cai, Beilei / Price, Mark A / Davis, Keith L / Ansquer, Valerie Derrien / Caro, Nydia / Saliba, Teddy R

    Future oncology (London, England)

    2023  Volume 19, Issue 3, Page(s) 217–228

    Abstract: Aim: ...

    Abstract Aim:
    MeSH term(s) Humans ; Brain Neoplasms/drug therapy ; Brain Neoplasms/genetics ; Brain Neoplasms/secondary ; Carcinoma, Non-Small-Cell Lung/drug therapy ; Carcinoma, Non-Small-Cell Lung/genetics ; Carcinoma, Non-Small-Cell Lung/pathology ; ErbB Receptors/genetics ; Exons ; Lung Neoplasms/drug therapy ; Lung Neoplasms/genetics ; Lung Neoplasms/pathology ; Mutation ; Retrospective Studies
    Chemical Substances capmatinib (TY34L4F9OZ) ; ErbB Receptors (EC 2.7.10.1) ; MET protein, human (EC 2.7.10.1)
    Language English
    Publishing date 2023-02-07
    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-2022-1133
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Real-World Effectiveness of Lenvatinib in Hepatocellular Carcinoma Patients with Nonalcoholic Steatohepatitis.

    Singal, Amit G / Nagar, Saurabh P / Hitchens, Abby / Davis, Keith L / Iyer, Shrividya

    Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association

    2021  Volume 21, Issue 3, Page(s) 830–831.e1

    Abstract: Hepatocellular (HCC) is the most common type of primary liver cancer and the fourth most common cause of cancer-related deaths globally. ...

    Abstract Hepatocellular (HCC) is the most common type of primary liver cancer and the fourth most common cause of cancer-related deaths globally.
    MeSH term(s) Humans ; Carcinoma, Hepatocellular/pathology ; Non-alcoholic Fatty Liver Disease/complications ; Liver Neoplasms/pathology
    Chemical Substances lenvatinib (EE083865G2)
    Language English
    Publishing date 2021-11-20
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2119789-1
    ISSN 1542-7714 ; 1542-3565
    ISSN (online) 1542-7714
    ISSN 1542-3565
    DOI 10.1016/j.cgh.2021.11.020
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Real-world effectiveness of lenvatinib monotherapy among unresectable hepatocellular carcinoma patients in the USA.

    Singal, Amit G / Nagar, Saurabh P / Hitchens, Abby / Davis, Keith L / Iyer, Shrividya

    Future oncology (London, England)

    2021  Volume 17, Issue 21, Page(s) 2759–2768

    Abstract: Aim: ...

    Abstract Aim:
    MeSH term(s) Adult ; Aged ; Aged, 80 and over ; Carcinoma, Hepatocellular/diagnosis ; Carcinoma, Hepatocellular/drug therapy ; Carcinoma, Hepatocellular/mortality ; Carcinoma, Hepatocellular/pathology ; Female ; Humans ; Liver Neoplasms/diagnosis ; Liver Neoplasms/drug therapy ; Liver Neoplasms/mortality ; Liver Neoplasms/pathology ; Male ; Middle Aged ; Phenylurea Compounds/therapeutic use ; Progression-Free Survival ; Protein Kinase Inhibitors/therapeutic use ; Quinolines/therapeutic use ; Retrospective Studies ; United States/epidemiology
    Chemical Substances Phenylurea Compounds ; Protein Kinase Inhibitors ; Quinolines ; lenvatinib (EE083865G2)
    Language English
    Publishing date 2021-04-09
    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-2021-0242
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Real-world clinical outcomes of patients with myelofibrosis treated with ruxolitinib: a medical record review.

    Passamonti, Francesco / Heidel, Florian H / Parikh, Rohan C / Ajmera, Mayank / Tang, Derek / Nadal, Jose Alberto / Davis, Keith L / Abraham, Pranav

    Future oncology (London, England)

    2022  Volume 18, Issue 18, Page(s) 2217–2231

    Abstract: Aim: ...

    Abstract Aim:
    MeSH term(s) Female ; Humans ; Male ; Medical Records ; Middle Aged ; Nitriles/therapeutic use ; Primary Myelofibrosis/drug therapy ; Pyrazoles/therapeutic use ; Pyrimidines/therapeutic use ; Treatment Outcome
    Chemical Substances Nitriles ; Pyrazoles ; Pyrimidines ; ruxolitinib (82S8X8XX8H)
    Language English
    Publishing date 2022-04-07
    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-2021-1358
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Effect of Combination Vaccines on Hepatitis B Vaccine Compliance in Children in the United States.

    Kurosky, Samantha K / Davis, Keith L / Galindo, Claudia M

    The Pediatric infectious disease journal

    2017  Volume 36, Issue 7, Page(s) e189–e196

    Abstract: Background: An increasingly crowded immunization schedule threatens the completion and compliance of hepatitis B vaccinations (HepB), the primary method of hepatitis B prevention. Combination vaccines have been proposed to alleviate this problem.: ... ...

    Abstract Background: An increasingly crowded immunization schedule threatens the completion and compliance of hepatitis B vaccinations (HepB), the primary method of hepatitis B prevention. Combination vaccines have been proposed to alleviate this problem.
    Methods: Data from the 2011 National Immunization Survey Public-Use Data File were utilized (GSK study identifier: HO-11-770) to compare HepB completion and compliance rates between 3 groups of children: those who received HepB combination vaccine, those who received non-HepB combination vaccine and those who received HepB single-antigen vaccine only. Completion was defined as the accumulation of 3 HepB doses by 18 months. Compliance was defined as the receipt of vaccine doses within the Advisory Committee on Immunization Practices' recommended age ranges.
    Results: Of a sample of 4,040,116 children, 39.4% received a HepB combination vaccine, 43.0% received a non-HepB combination vaccine and 17.5% received a HepB single-antigen vaccine. Overall, 91.2% of children completed all 3 recommended doses, but only 61.8% completed them at age-appropriate times. Those receiving single-antigen only (odds ratio = 0.25, 95% confidence interval: 0.17-0.35) or non-HepB combination vaccines (odds ratio = 0.50, 95% confidence interval: 0.37-0.69) were substantially less likely to complete 3 doses of HepB than those who received the HepB combination vaccine.
    Conclusions: Although completion rates were high, a large proportion of children did not receive HepB doses at age-appropriate times. Combination vaccine was associated with both higher completion and compliance outcomes compared with HepB single-antigen vaccine.
    MeSH term(s) Adult ; Child, Preschool ; Female ; Hepatitis B Vaccines ; Humans ; Male ; Mothers ; Patient Compliance/statistics & numerical data ; Poverty ; United States/epidemiology ; Vaccination/statistics & numerical data ; Vaccines, Combined ; Young Adult
    Chemical Substances Hepatitis B Vaccines ; Vaccines, Combined
    Language English
    Publishing date 2017-01-19
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 392481-6
    ISSN 1532-0987 ; 0891-3668
    ISSN (online) 1532-0987
    ISSN 0891-3668
    DOI 10.1097/INF.0000000000001548
    Database MEDical Literature Analysis and Retrieval System OnLINE

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