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A Randomized Controlled Trial of Epidermal Growth Factor Ointment for Treating Epidermal Growth Factor Receptor Inhibitor-Induced Skin Toxicities.
Kim, Young Saing; Ji, Jun Ho; Oh, Sung Yong; Lee, Suee; Huh, Seok Jae; Lee, Ji Hyun; Song, Ki-Hoon; Son, Choon Hee; Roh, Mee Sook; Lee, Gyeong Won; Lee, Jeeyun; Kim, Seung Tae; Kim, Chan Kyu; Jang, Joung Soon; Hwang, In Gyu; Ahn, Hee Kyung; Park, Lee Chun; Oh, So Yeon; Kim, Seong-Geun; Lee, Sang-Cheol; Lim, Do-Hyoung; Lee, Soon Il; Kang, Jung Hun.
Afiliação
  • Kim YS; Department of Internal Medicine, Gachon University Gil Medical Center, Incheon, Republic of Korea.
  • Ji JH; Division of Hematology-Oncology, Samsung Changwon Hospital, Sungkyunkwan University School of Medicine, Changwon, Republic of Korea.
  • Oh SY; Department of Internal Medicine, Dong-A University Hospital, Busan, Republic of Korea.
  • Lee S; Department of Internal Medicine, Dong-A University Hospital, Busan, Republic of Korea.
  • Huh SJ; Department of Internal Medicine, Dong-A University Hospital, Busan, Republic of Korea.
  • Lee JH; Department of Internal Medicine, Dong-A University Hospital, Busan, Republic of Korea.
  • Song KH; Department of Dermatology, National Cancer Center, Goyang, Republic of Korea.
  • Son CH; Department of Pulmonology, Dong-A University Hospital, Busan, Republic of Korea.
  • Roh MS; Department of Pathology, Dong-A University College of Medicine, Busan, Republic of Korea.
  • Lee GW; Department of Internal Medicine, Gyeongsang National University Hospital, Jinju, Republic of Korea.
  • Lee J; Department of Medicine, Samsung Medical Center, Seoul, Republic of Korea.
  • Kim ST; Department of Medicine, Samsung Medical Center, Seoul, Republic of Korea.
  • Kim CK; Department of Internal Medicine, Soonchunhyang University Bucheon Hospital, Bucheon, Republic of Korea.
  • Jang JS; Department of Internal Medicine, Chung-Ang University College of Medicine, Seoul, Republic of Korea.
  • Hwang IG; Department of Internal Medicine, Chung-Ang University College of Medicine, Seoul, Republic of Korea.
  • Ahn HK; Department of Internal Medicine, Gachon University Gil Medical Center, Incheon, Republic of Korea.
  • Park LC; Division of Hematology-Oncology, Department of Medicine, Kosin University College of Medicine, Busan, Republic of Korea.
  • Oh SY; Department of Internal Medicine, Pusan National University Yangsan Hospital, Yangsan, Republic of Korea.
  • Kim SG; Department of Internal Medicine, Pusan National University Yangsan Hospital, Yangsan, Republic of Korea.
  • Lee SC; Department of Internal Medicine, Soonchunhyang University Hospital Cheonan, Cheonan, Republic of Korea.
  • Lim DH; Department of Internal Medicine, Dankook University College of Medicine, Cheonan, Republic of Korea.
  • Lee SI; Department of Internal Medicine, Dankook University College of Medicine, Cheonan, Republic of Korea.
  • Kang JH; Department of Internal Medicine, Gyeongsang National University Hospital, Jinju, Republic of Korea.
Oncologist ; 25(1): e186-e193, 2020 01.
Article em En | MEDLINE | ID: mdl-31492766
ABSTRACT

BACKGROUND:

The efficacy of epidermal growth factor (EGF) receptor (EGFR) inhibitors in patients with non-small cell lung cancer (NSCLC), pancreatic cancer (PC), or colorectal cancer (CRC) has been demonstrated. However, dermatological reactions to these inhibitors can cause significant physical and psychosocial discomfort. The objective of the present study was to evaluate the efficacy of EGF ointment for EGFR inhibitor-related skin adverse events (ERSEs). MATERIALS AND

METHODS:

This placebo-controlled, double-blind, multicenter, pilot phase III trial enrolled patients with NSCLC, PC, or CRC treated with EGFR inhibitors. Patients with grade ≥2 ERSEs were included. Patients were randomized to three treatment arms arm 1, placebo; arm 2, 1 ppm of EGF ointment; and arm 3, 20 ppm of EGF ointment. Patients applied ointment to their skin lesions twice daily.

RESULTS:

Efficacy evaluation was available for 80 patients (9 for PC, 28 for NSCLC, and 43 for CRC). Responses were 44.4% in arm 1, 61.5% in arm 2, and 77.8% in arm 3. There was a linear correlation between EGF concentrations and responses (p = .012). Quality of life (QoL) was assessed for 74 patients. Maximum changes in composite scores by Skindex-16 after treatment were significantly different among arms (mean ± SD -5.2 ± 8.6 for arm 1, -11.7 ± 14.2 for arm 2, and - 18.6 ± 17.7 for arm 3; p = .008). EGF arms showed significant improvement in emotions (p = .005) and functioning (p = .044) scores over the placebo arm.

CONCLUSION:

EGF ointment is effective for managing ERSEs. It can also improve patients' QoL compared with placebo. Clinical trial identification number. NCT02284139 IMPLICATIONS FOR PRACTICE Patients with non-small cell lung cancer, pancreatic cancer, or colorectal cancer who are treated with epidermal growth factor (EGF) receptor (EGFR) inhibitors may experience dermatologic reactions to their treatment. This study investigated the benefit of an EGF ointment in the treatment of these adverse events and observed the ointment to be effective in managing EGFR inhibitor-related skin adverse events.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pomadas / Dermatopatias Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Oncologist Assunto da revista: NEOPLASIAS Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pomadas / Dermatopatias Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Oncologist Assunto da revista: NEOPLASIAS Ano de publicação: 2020 Tipo de documento: Article