Literature DB >> 24435321

Afatinib: a review of its use in the treatment of advanced non-small cell lung cancer.

Gillian M Keating1.   

Abstract

Afatinib (Gilotrif™, Giotrif(®)) is an orally administered, irreversible inhibitor of the ErbB family of tyrosine kinases. Afatinib downregulates ErbB signalling by covalently binding to the kinase domains of epidermal growth factor receptor (EGFR), human epidermal growth factor receptor (HER) 2 and HER4, resulting in irreversible inhibition of tyrosine kinase autophosphorylation; it also inhibits transphosphorylation of HER3. Afatinib is approved as monotherapy for the treatment of EGFR tyrosine kinase inhibitor (TKI)-naïve adults with locally advanced or metastatic non-small cell lung cancer (NSCLC) with activating EGFR mutations in the EU, and for the first-line treatment of patients with metastatic NSCLC whose tumours have EGFR exon 19 deletions or exon 21 (L858R) substitution mutations as detected by a US FDA-approved test in the US. In two randomized, open-label, multinational phase III trials, progression-free survival was significantly prolonged with afatinib compared with pemetrexed plus cisplatin (LUX-Lung 3) or gemcitabine plus cisplatin (LUX-Lung 6) in treatment-naïve patients with advanced NSCLC with activating EGFR mutations. The objective response rate was significantly higher with afatinib than with pemetrexed plus cisplatin or gemcitabine plus cisplatin, and patient-reported outcomes for symptoms such as cough and dyspnoea and certain health-related quality of life measures significantly favoured afatinib versus pemetrexed plus cisplatin or gemcitabine plus cisplatin. Afatinib also showed efficacy in EGFR TKI-naïve patients with advanced lung adenocarcinoma and activating EGFR mutations who had received no more than one prior chemotherapy regimen for advanced disease, according to the results of the noncomparative, multinational, phase II LUX-Lung 2 trial. Oral afatinib had a manageable tolerability profile. EGFR-mediated adverse events (e.g. diarrhoea, rash/acne) were generally managed using dose reduction and delays. In conclusion, afatinib is a valuable new option for use in treatment-naïve or EGFR TKI-naïve patients with advanced lung adenocarcinoma and activating EGFR mutations.

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Year:  2014        PMID: 24435321     DOI: 10.1007/s40265-013-0170-8

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  31 in total

1.  Afatinib pharmacokinetics and metabolism after oral administration to healthy male volunteers.

Authors:  Peter Stopfer; Kristell Marzin; Hans Narjes; Dietmar Gansser; Mehdi Shahidi; Martina Uttereuther-Fischer; Thomas Ebner
Journal:  Cancer Chemother Pharmacol       Date:  2011-12-27       Impact factor: 3.333

2.  Activation of IL-6R/JAK1/STAT3 signaling induces de novo resistance to irreversible EGFR inhibitors in non-small cell lung cancer with T790M resistance mutation.

Authors:  Sun Mi Kim; Oh-Joon Kwon; Yun Kyoung Hong; Joo Hang Kim; Flavio Solca; Sang-Jun Ha; Ross A Soo; James G Christensen; Ji Hyun Lee; Byoung Chul Cho
Journal:  Mol Cancer Ther       Date:  2012-08-13       Impact factor: 6.261

3.  The EGFR T790M mutation in acquired resistance to an irreversible second-generation EGFR inhibitor.

Authors:  Youngwook Kim; Jeonghun Ko; ZhengYun Cui; Amir Abolhoda; Jin Seok Ahn; Sai-Hong Ou; Myung-Ju Ahn; Keunchil Park
Journal:  Mol Cancer Ther       Date:  2012-01-06       Impact factor: 6.261

4.  Afatinib prolongs survival compared with gefitinib in an epidermal growth factor receptor-driven lung cancer model.

Authors:  Takashi Ninomiya; Nagio Takigawa; Eiki Ichihara; Nobuaki Ochi; Toshi Murakami; Yoshihiro Honda; Toshio Kubo; Daisuke Minami; Kenichiro Kudo; Mitsune Tanimoto; Katsuyuki Kiura
Journal:  Mol Cancer Ther       Date:  2013-02-26       Impact factor: 6.261

5.  Target binding properties and cellular activity of afatinib (BIBW 2992), an irreversible ErbB family blocker.

Authors:  Flavio Solca; Goeran Dahl; Andreas Zoephel; Gerd Bader; Michael Sanderson; Christian Klein; Oliver Kraemer; Frank Himmelsbach; Eric Haaksma; Guenther R Adolf
Journal:  J Pharmacol Exp Ther       Date:  2012-08-10       Impact factor: 4.030

6.  Pharmacokinetics of afatinib, a selective irreversible ErbB family blocker, in patients with advanced solid tumours.

Authors:  Sven Wind; Marion Schmid; Julia Erhardt; Rainer-Georg Goeldner; Peter Stopfer
Journal:  Clin Pharmacokinet       Date:  2013-12       Impact factor: 6.447

7.  Phase III study of afatinib or cisplatin plus pemetrexed in patients with metastatic lung adenocarcinoma with EGFR mutations.

Authors:  Lecia V Sequist; James Chih-Hsin Yang; Nobuyuki Yamamoto; Kenneth O'Byrne; Vera Hirsh; Tony Mok; Sarayut Lucien Geater; Sergey Orlov; Chun-Ming Tsai; Michael Boyer; Wu-Chou Su; Jaafar Bennouna; Terufumi Kato; Vera Gorbunova; Ki Hyeong Lee; Riyaz Shah; Dan Massey; Victoria Zazulina; Mehdi Shahidi; Martin Schuler
Journal:  J Clin Oncol       Date:  2013-07-01       Impact factor: 44.544

8.  Symptom control and quality of life in LUX-Lung 3: a phase III study of afatinib or cisplatin/pemetrexed in patients with advanced lung adenocarcinoma with EGFR mutations.

Authors:  James Chih-Hsin Yang; Vera Hirsh; Martin Schuler; Nobuyuki Yamamoto; Kenneth J O'Byrne; Tony S K Mok; Victoria Zazulina; Mehdi Shahidi; Juliane Lungershausen; Dan Massey; Michael Palmer; Lecia V Sequist
Journal:  J Clin Oncol       Date:  2013-07-01       Impact factor: 44.544

Review 9.  Dermatologic adverse events associated with afatinib: an oral ErbB family blocker.

Authors:  Mario E Lacouture; Dirk Schadendorf; Chia-Yu Chu; Martina Uttenreuther-Fischer; Uz Stammberger; Dennis O'Brien; Axel Hauschild
Journal:  Expert Rev Anticancer Ther       Date:  2013-03-18       Impact factor: 4.512

10.  Afatinib: emerging next-generation tyrosine kinase inhibitor for NSCLC.

Authors:  Valerie Nelson; Jacqueline Ziehr; Mark Agulnik; Melissa Johnson
Journal:  Onco Targets Ther       Date:  2013-03-05       Impact factor: 4.147

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  33 in total

Review 1.  Which tyrosine kinase inhibitor should be recommended as initial treatment for non-small cell lung cancer patients with EGFR mutations?

Authors:  Alfredo Tartarone; Rosa Lerose; Chiara Lazzari; Vanesa Gregorc; Michele Aieta
Journal:  Med Oncol       Date:  2014-06-24       Impact factor: 3.064

2.  Structure-Based Design of Selective, Covalent G Protein-Coupled Receptor Kinase 5 Inhibitors.

Authors:  Rachel A Rowlands; M Claire Cato; Helen V Waldschmidt; Renee A Bouley; Qiuyan Chen; Larisa Avramova; Scott D Larsen; John J G Tesmer; Andrew D White
Journal:  ACS Med Chem Lett       Date:  2019-11-12       Impact factor: 4.345

3.  IL-33 increases ST2+ Tregs and promotes metastatic tumour growth in the lungs in an amphiregulin-dependent manner.

Authors:  E C Halvorsen; S E Franks; B J Wadsworth; B T Harbourne; R A Cederberg; C A Steer; I Martinez-Gonzalez; J Calder; W W Lockwood; K L Bennewith
Journal:  Oncoimmunology       Date:  2018-10-16       Impact factor: 8.110

Review 4.  New insights into RAS biology reinvigorate interest in mathematical modeling of RAS signaling.

Authors:  Keesha E Erickson; Oleksii S Rukhlenko; Richard G Posner; William S Hlavacek; Boris N Kholodenko
Journal:  Semin Cancer Biol       Date:  2018-03-05       Impact factor: 15.707

5.  Present and Future Prospect of Small Molecule & Related Targeted Therapy Against Human Cancer.

Authors:  Akshat Pathak; Sanskriti Tanwar; Vivek Kumar; Basu Dev Banarjee
Journal:  Vivechan Int J Res       Date:  2018

6.  Efficacy generated by afatinib in a lung adenocarcinoma patient harboring HER2 S310Y mutation.

Authors:  Jian Wang; Yuxin Wen; Guanggui Ding; Peikun Ding; Lu Zhang; Jing Liu; Tengfei Zhang; Lin Yang
Journal:  Cancer Biol Ther       Date:  2018-04-12       Impact factor: 4.742

7.  ΔFOSB: A Potentially Druggable Master Orchestrator of Activity-Dependent Gene Expression.

Authors:  Alfred J Robison; Eric J Nestler
Journal:  ACS Chem Neurosci       Date:  2022-01-12       Impact factor: 4.418

8.  Reduction in Hepatocyte Growth Factor Serum Levels is Associated with Improved Prognosis in Advanced Lung Adenocarcinoma Patients Treated with Afatinib: a Phase II Trial.

Authors:  Oscar Arrieta; Graciela Cruz-Rico; Enrique Soto-Perez-de-Celis; Laura-Alejandra Ramírez-Tirado; Enrique Caballe-Perez; Jorge-Negueb Martínez-Hernández; Ivan Martinez-Alvarez; Giovanny Soca-Chafre; Eleazar Omar Macedo-Pérez; Horacio Astudillo-de la Vega
Journal:  Target Oncol       Date:  2016-10       Impact factor: 4.493

Review 9.  Targeting transcription factors in cancer - from undruggable to reality.

Authors:  John H Bushweller
Journal:  Nat Rev Cancer       Date:  2019-09-11       Impact factor: 60.716

10.  Acquired Resistance to the Mutant-Selective EGFR Inhibitor AZD9291 Is Associated with Increased Dependence on RAS Signaling in Preclinical Models.

Authors:  Catherine A Eberlein; Daniel Stetson; Aleksandra A Markovets; Katherine J Al-Kadhimi; Zhongwu Lai; Paul R Fisher; Catherine B Meador; Paula Spitzler; Eiki Ichihara; Sarah J Ross; Miika J Ahdesmaki; Ambar Ahmed; Laura E Ratcliffe; Elizabeth L Christey O'Brien; Claire H Barnes; Henry Brown; Paul D Smith; Jonathan R Dry; Garry Beran; Kenneth S Thress; Brian Dougherty; William Pao; Darren A E Cross
Journal:  Cancer Res       Date:  2015-04-13       Impact factor: 12.701

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