Literature DB >> 29650685

Osimertinib: A Novel Dermatologic Adverse Event Profile in Patients with Lung Cancer.

Chia-Yu Chu1, Jennifer Choi2, Beth Eaby-Sandy3, Corey J Langer3, Mario E Lacouture4.   

Abstract

Dermatologic adverse events (dAEs) are common with the use of epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI) therapy. First- and second-generation agents (erlotinib, gefitinib, and afatinib) are frequently associated with acneiform rash, pruritus, xerosis, and paronychia; the incidence and characterization of these dAEs have been well described. However, there is evidence that the dAE profile is different with third-generation EGFR-TKIs. Herein, we describe the dAEs associated with third-generation EGFR-TKIs and our clinical experience with osimertinib, a third-generation EGFR-TKI approved by the U.S. Food and Drug Administration for the treatment of metastatic, EGFR T790M mutation-positive non-small cell lung cancer in patients whose disease has progressed on or after EGFR-TKI therapy. Case summaries of patients from two of our institutions who received osimertinib and were referred to a dermatologist for dAEs are also presented. Overall, the evidence suggests that osimertinib is associated with less severe and less frequent dAEs than first- and second-generation EGFR-TKIs and that therefore a different approach is warranted. Finally, we outline dAE management approaches for osimertinib in the context of those typically employed with first- and second-generation EGFR-TKIs. IMPLICATIONS FOR PRACTICE: Appropriate prevention and management of dermatologic adverse events (dAEs) associated with the use of epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs) may help patients to continue therapy and lessen any negative impact on their quality of life. EGFR-TKIs are frequently associated with acneiform rash, pruritus, xerosis, and paronychia; however, dAEs associated with third-generation EGFR-TKIs are lower in frequency and severity. Before therapy, health care providers should discuss the potential osimertinib-associated dAEs and encourage patients to report their dAEs. Patients should also be educated on prophylactic measures to minimize the severity of dAEs and the importance of adherence to the treatment regimen. © AlphaMed Press 2018.

Entities:  

Keywords:  Dermatologic adverse events; Epidermal growth factor receptor; Non‐small cell lung cancer; T790M; Tyrosine kinase inhibitor

Mesh:

Substances:

Year:  2018        PMID: 29650685      PMCID: PMC6156184          DOI: 10.1634/theoncologist.2017-0582

Source DB:  PubMed          Journal:  Oncologist        ISSN: 1083-7159


  44 in total

Review 1.  Management of egfr tki-induced dermatologic adverse events.

Authors:  B Melosky; N B Leighl; J Rothenstein; R Sangha; D Stewart; K Papp
Journal:  Curr Oncol       Date:  2015-04       Impact factor: 3.677

2.  A pilot quality-of-life instrument for pruritus.

Authors:  Nisha S Desai; Gabriele B Poindexter; Yvette Miller Monthrope; Sandra E Bendeck; Robert A Swerlick; Suephy C Chen
Journal:  J Am Acad Dermatol       Date:  2008-06-11       Impact factor: 11.527

Review 3.  Is there evidence for different effects among EGFR-TKIs? Systematic review and meta-analysis of EGFR tyrosine kinase inhibitors (TKIs) versus chemotherapy as first-line treatment for patients harboring EGFR mutations.

Authors:  Eva Regina Haspinger; Francesco Agustoni; Valter Torri; Francesco Gelsomino; Marco Platania; Nicoletta Zilembo; Rosaria Gallucci; Marina Chiara Garassino; Michela Cinquini
Journal:  Crit Rev Oncol Hematol       Date:  2014-11-22       Impact factor: 6.312

4.  Gefitinib or chemotherapy for non-small-cell lung cancer with mutated EGFR.

Authors:  Makoto Maemondo; Akira Inoue; Kunihiko Kobayashi; Shunichi Sugawara; Satoshi Oizumi; Hiroshi Isobe; Akihiko Gemma; Masao Harada; Hirohisa Yoshizawa; Ichiro Kinoshita; Yuka Fujita; Shoji Okinaga; Haruto Hirano; Kozo Yoshimori; Toshiyuki Harada; Takashi Ogura; Masahiro Ando; Hitoshi Miyazawa; Tomoaki Tanaka; Yasuo Saijo; Koichi Hagiwara; Satoshi Morita; Toshihiro Nukiwa
Journal:  N Engl J Med       Date:  2010-06-24       Impact factor: 91.245

5.  Skin toxicity evaluation protocol with panitumumab (STEPP), a phase II, open-label, randomized trial evaluating the impact of a pre-Emptive Skin treatment regimen on skin toxicities and quality of life in patients with metastatic colorectal cancer.

Authors:  Mario E Lacouture; Edith P Mitchell; Bilal Piperdi; Madhavan V Pillai; Heather Shearer; Nicholas Iannotti; Feng Xu; Mohamed Yassine
Journal:  J Clin Oncol       Date:  2010-02-08       Impact factor: 44.544

6.  Gefitinib and erlotinib in metastatic non-small cell lung cancer: a meta-analysis of toxicity and efficacy of randomized clinical trials.

Authors:  Mauricio Burotto; Elisabet E Manasanch; Julia Wilkerson; Tito Fojo
Journal:  Oncologist       Date:  2015-03-20

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

Review 8.  Clinical practice guidelines for the prevention and treatment of EGFR inhibitor-associated dermatologic toxicities.

Authors:  Mario E Lacouture; Milan J Anadkat; René-Jean Bensadoun; Jane Bryce; Alexandre Chan; Joel B Epstein; Beth Eaby-Sandy; Barbara A Murphy
Journal:  Support Care Cancer       Date:  2011-06-01       Impact factor: 3.603

Review 9.  Management of Common Toxicities in Metastatic NSCLC Related to Anti-Lung Cancer Therapies with EGFR-TKIs.

Authors:  Barbara Melosky; Vera Hirsh
Journal:  Front Oncol       Date:  2014-09-16       Impact factor: 6.244

10.  First-line gefitinib in Caucasian EGFR mutation-positive NSCLC patients: a phase-IV, open-label, single-arm study.

Authors:  J-Y Douillard; G Ostoros; M Cobo; T Ciuleanu; R McCormack; A Webster; T Milenkova
Journal:  Br J Cancer       Date:  2013-11-21       Impact factor: 7.640

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  8 in total

1.  First- and third-generation epidermal growth factor receptor inhibitors mediate distinct phosphoprotein signalling networks: implications for adverse dermatological reactions.

Authors:  C Vasavda; B K Ho; D Y Zhang; K A Williams; B H Kaffenberger; S G Kwatra; M M Kwatra
Journal:  Br J Dermatol       Date:  2020-07-27       Impact factor: 9.302

2.  Association between dermatologic adverse events and quality of life in lung cancer patients treated with epidermal growth factor receptor-tyrosine kinase inhibitors.

Authors:  Hui-Te Hsu; Chu-Chun Yu; Yun-Hsiang Lee; Jui-Chun Chan; Chia-Yu Chu
Journal:  Support Care Cancer       Date:  2022-09-03       Impact factor: 3.359

3.  Osimertinib-associated ashy dermatosis-like hyperpigmentation.

Authors:  Pattamon Lertpichitkul; Jade Wititsuwannakul; Pravit Asawanonda; Pawinee Rerknimitr
Journal:  JAAD Case Rep       Date:  2020-01-17

4.  EGFR inhibitors switch keratinocytes from a proliferative to a differentiative phenotype affecting epidermal development and barrier function.

Authors:  Nicolas Joly-Tonetti; Thomas Ondet; Mario Monshouwer; Georgios N Stamatas
Journal:  BMC Cancer       Date:  2021-01-05       Impact factor: 4.430

5.  Prognostic and predictive impact of creatine kinase level in non-small cell lung cancer treated with tyrosine kinase inhibitors.

Authors:  Yu Jiang; Zixuan Su; Yuechun Lin; Yaming Xiong; Caichen Li; Jianfu Li; Runchen Wang; Ran Zhong; Bo Cheng; Jianxing He; Zhanhong Xie; Wenhua Liang
Journal:  Transl Lung Cancer Res       Date:  2021-09

Review 6.  Challenges in the Use of Targeted Therapies in Non-Small Cell Lung Cancer.

Authors:  Joel Rivera-Concepcion; Dipesh Uprety; Alex A Adjei
Journal:  Cancer Res Treat       Date:  2022-02-18       Impact factor: 5.036

7.  Drug eruptions with novel targeted therapies - immune checkpoint and EGFR inhibitors.

Authors:  Isabella Pospischil; Wolfram Hoetzenecker
Journal:  J Dtsch Dermatol Ges       Date:  2021-11       Impact factor: 5.231

8.  Results of the non-small cell lung cancer part of a phase III, open-label, randomized trial evaluating topical corticosteroid therapy for facial acneiform dermatitis induced by EGFR inhibitors: stepwise rank down from potent corticosteroid (FAEISS study, NCCH-1512).

Authors:  Kazumi Nishino; Yutaka Fujiwara; Yuichiro Ohe; Ryota Saito; Eisaku Miyauchi; Tetsu Kobayashi; Yasuo Nakai; Toshiaki Takahashi; Taro Shibata; Tetsuya Hamaguchi; Katsuko Kikuchi; Naoya Yamazaki; Haruhiko Fukuda; Keiko Nozawa; Yoshio Kiyohara
Journal:  Support Care Cancer       Date:  2020-09-11       Impact factor: 3.603

  8 in total

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