Clinical significance of chronic pulmonary aspergillosis in lung cancer patients undergoing anticancer drug therapy

Author:

Morimoto Kenji1ORCID,Hamashima Ryosuke1,Yamada Tadaaki1ORCID,Yokoyama Toshihide2,Kobayashi Takehiko3,Tsuyuguchi Kazunari3,Kanematsu Takanori4,Tamiya Nobuyo5,Tsuji Taisuke6,Nakamura Ryota1,Katayama Yuki1,Nishioka Naoya1,Iwasaku Masahiro1,Tokuda Shinsaku1,Takayama Koichi1

Affiliation:

1. Department of Pulmonary Medicine, Graduate School of Medical Science Kyoto Prefectural University of Medicine Kyoto Japan

2. Department of Respiratory Medicine Ohara Healthcare Foundation, Kurashiki Central Hospital Okayama Japan

3. Clinical Research Center, Kinki‐Chuo Chest Medical Center Osaka Japan

4. Department of Respiratory Medicine Japanese Red Cross Matsuyama Hospital Matsuyama Japan

5. Department of Respiratory Medicine Rakuwakai Otowa Hospital Kyoto Japan

6. Department of Respiratory Medicine Japanese Red Cross Kyoto Daiichi Hospital Kyoto Japan

Abstract

AbstractBackgroundAdvances in anticancer drugs for lung cancer (LC) have improved the prognosis of LC. Chronic pulmonary aspergillosis (CPA) is a progressive and often exacerbating respiratory disease with a poor prognosis. To date, the prognosis of LC complicated by CPA has not been elucidated. This study investigated the clinical implications of concomitant CPA in patients with LC undergoing anticancer drug treatment.MethodsBetween January 2010 and May 2020, we consecutively enrolled patients with LC complicated with CPA at five different institutions in Japan. We analyzed patients with LC complicated by CPA who received anticancer drug treatment.ResultsA total of 10 patients with LC complicated by CPA received anticancer drug treatment. The median overall survival (OS) was 14.57 months (95% confidence interval [CI]: 5.37–21.67). The cause of death in all patients was LC. Six of the seven patients with LC did not show worsening pulmonary aspergillosis lesions during the anticancer drug treatment. Although two patients discontinued anticancer drug treatment due to pneumonitis, CPA complications did not interfere with the continuation of anticancer drug treatment. In univariate analyses, squamous histology (p = 0.01) and body mass index (<18.5 kg/m2) (p = 0.0008) were significantly associated with poorer OS.ConclusionsThis study demonstrated that the cause of death in LC patients with concomitant CPA who received anticancer drug treatments and effective antifungal treatment was LC progression. Further large‐scale studies are needed to identify the effect of CPA in patients with LC.

Publisher

Wiley

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