Literature DB >> 21303791

Interstitial lung disease during chemotherapy combined with oxaliplatin and/or bevacizumab in advanced colorectal cancer patients.

Kazuhiro Usui1, Yuu Katou, Kaoru Furushima, Yoshiaki Tanaka, Chiharu Tanai, Teruo Ishihara.   

Abstract

OBJECTIVE: Interstitial lung disease in patients with colorectal cancer during chemotherapy combined with bevacizumab is rare.
METHODS: We reviewed 104 colorectal cancer patients treated with standard chemotherapy with bevacizumab and examined the incidence of interstitial lung disease and its clinical features.
RESULTS: We identified interstitial lung disease in four patients (3.85%). All patients were male. The median age was 64.5 years. Three of four patients had a history of smoking; median smoking index was 40 pack-years. Except one patient who had asymptomatic pulmonary fibrosis, chest computed tomography before chemotherapy showed no fibrotic changes. Pulmonary function test before chemotherapy showed normal values. All patients had received median 10 cycles (range 10-15 cycles) of FOLFOX before the onset of interstitial lung disease. Interstitial lung disease developed during FOLFOX + bevacizumab in two patients and during FOLFIRI + bevacizumab in two patients. The initial symptom of interstitial lung disease was fever in all patients. The median duration from the last chemotherapy to the onset of interstitial lung disease was 3.5 days (range 2-8 days). Three of four patients showed Grade 3 or more severity of interstitial lung disease according to Common Terminology Criteria for Adverse Events v3.0. High-dose steroid therapy was effective in all patients.
CONCLUSIONS: Interstitial lung disease induced by standard chemotherapy with bevacizumab is rare, but rapidly progressed and were severe in our experience.

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Year:  2011        PMID: 21303791     DOI: 10.1093/jjco/hyr006

Source DB:  PubMed          Journal:  Jpn J Clin Oncol        ISSN: 0368-2811            Impact factor:   3.019


  7 in total

1.  Novel adverse events of bevacizumab in the US FDA adverse event reporting system database: a disproportionality analysis.

Authors:  Behrooz K Shamloo; Pankdeep Chhabra; Andrew N Freedman; Arnold Potosky; Jennifer Malin; Sheila Weiss Smith
Journal:  Drug Saf       Date:  2012-06-01       Impact factor: 5.606

2.  Interstitial pneumonia during bevacizumab-based chemotherapy for colorectal cancer.

Authors:  Shingo Tamura; Hitoshi Kusaba; Naoki Kubo; Kayo Ijichi; Kenji Tsuchihashi; Masato Komoda; Keita Uchino; Hiroshi Ariyama; Koichi Akashi; Eishi Baba
Journal:  Med Oncol       Date:  2014-01-30       Impact factor: 3.064

3.  Carboplatin plus paclitaxel in combination with bevacizumab for the treatment of adenocarcinoma with interstitial lung diseases.

Authors:  Hidekazu Suzuki; Tomonori Hirashima; Masashi Kobayashi; Norio Okamoto; Yuka Matsuura; Motohiro Tamiya; Naoko Morishita; Kohei Okafuji; Takayuki Shiroyama; Osamu Morimura; Satomu Morita; Ichiro Kawase
Journal:  Mol Clin Oncol       Date:  2013-03-01

4.  Interstitial pneumonia in a patient treated with TAS-102 for metastatic colorectal cancer: a case report.

Authors:  Hideki Kamei; Nobuya Ishibashi; Masahiko Tanigawa; Keizo Yamaguchi; Masafumi Uchida; Yoshito Akagi
Journal:  J Med Case Rep       Date:  2016-11-03

5.  Pre-existing interstitial lung disease as a risk factor for pneumonitis associated with ramucirumab and paclitaxel in patients with gastric cancer: The impact of usual interstitial pneumonia.

Authors:  Nobuyuki Koyama; Sou Katayanagi; Shigeyuki Kawachi
Journal:  PLoS One       Date:  2018-06-07       Impact factor: 3.240

6.  Management of hypersensivity pneumonitis.

Authors:  Ioana O Agache; Liliana Rogozea
Journal:  Clin Transl Allergy       Date:  2013-02-04       Impact factor: 5.871

7.  A phase ΙI study of five peptides combination with oxaliplatin-based chemotherapy as a first-line therapy for advanced colorectal cancer (FXV study).

Authors:  Shoichi Hazama; Yusuke Nakamura; Hiroaki Tanaka; Kosei Hirakawa; Ko Tahara; Ryoichi Shimizu; Hiroaki Ozasa; Ryuichi Etoh; Fumiaki Sugiura; Kiyotaka Okuno; Takumi Furuya; Taku Nishimura; Koichiro Sakata; Kazuhiko Yoshimatsu; Hiroko Takenouchi; Ryouichi Tsunedomi; Yuka Inoue; Shinsuke Kanekiyo; Yoshitaro Shindo; Nobuaki Suzuki; Shigefumi Yoshino; Hirokazu Shinozaki; Akira Kamiya; Hiroyuki Furukawa; Takeharu Yamanaka; Tomonobu Fujita; Yutaka Kawakami; Masaaki Oka
Journal:  J Transl Med       Date:  2014-04-30       Impact factor: 5.531

  7 in total

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