New risk scoring system for predicting acute exacerbation of interstitial pneumonia after chemotherapy for lung cancer associated with interstitial pneumonia. (November 2018)
- Record Type:
- Journal Article
- Title:
- New risk scoring system for predicting acute exacerbation of interstitial pneumonia after chemotherapy for lung cancer associated with interstitial pneumonia. (November 2018)
- Main Title:
- New risk scoring system for predicting acute exacerbation of interstitial pneumonia after chemotherapy for lung cancer associated with interstitial pneumonia
- Authors:
- Isobe, Kazutoshi
Kaburaki, Kyohei
Kobayashi, Hiroshi
Sano, Go
Sakamoto, Susumu
Takai, Yujiro
Makino, Takashi
Tochigi, Naobumi
Iyoda, Akira
Homma, Sakae - Abstract:
- Highlights: AE developed in 27.5% in lung cancer associated with IP during chemotherapy. The AE risk score was calculated with the formula. The AE incidence rate was 66.7% for a score of ≥11. The present AE score was able to identify high risk for AE after chemotherapy. Abstract: Background: Fatal acute exacerbation (AE) of interstitial pneumonia (IP) sometimes occurs after chemotherapy for lung cancer. We developed and evaluated a scoring system for assessing AE risk after chemotherapy in patients with lung cancer associated with IP. Methods: A review of medical records identified 109 patients with primary lung cancer associated with IP who had received chemotherapy at our center during the period from June 2007 through September 2017. We developed a model to score AE risk after chemotherapy in this patient group, and logistic regression was used to evaluate the model. Results: The anticancer agent score was determined by using AE rates reported in past studies. The risk score was calculated with the following formula: (1 × anticancer agent score) + (3 × smoking history [>70 pack-years]) + (4 × history of steroid use) + (3 × %diffusing capacity of lung carbon monoxide [<50%]). Patients were then classified into three groups. The AE incidence rate was 12% for a risk score of 0–5, 47% for a score of 6–10, and 66.7% for a score of ≥11. The sensitivity of the scoring system was 78.6% and specificity was 67.8%. Conclusions: The present scoring system was able to identify IPHighlights: AE developed in 27.5% in lung cancer associated with IP during chemotherapy. The AE risk score was calculated with the formula. The AE incidence rate was 66.7% for a score of ≥11. The present AE score was able to identify high risk for AE after chemotherapy. Abstract: Background: Fatal acute exacerbation (AE) of interstitial pneumonia (IP) sometimes occurs after chemotherapy for lung cancer. We developed and evaluated a scoring system for assessing AE risk after chemotherapy in patients with lung cancer associated with IP. Methods: A review of medical records identified 109 patients with primary lung cancer associated with IP who had received chemotherapy at our center during the period from June 2007 through September 2017. We developed a model to score AE risk after chemotherapy in this patient group, and logistic regression was used to evaluate the model. Results: The anticancer agent score was determined by using AE rates reported in past studies. The risk score was calculated with the following formula: (1 × anticancer agent score) + (3 × smoking history [>70 pack-years]) + (4 × history of steroid use) + (3 × %diffusing capacity of lung carbon monoxide [<50%]). Patients were then classified into three groups. The AE incidence rate was 12% for a risk score of 0–5, 47% for a score of 6–10, and 66.7% for a score of ≥11. The sensitivity of the scoring system was 78.6% and specificity was 67.8%. Conclusions: The present scoring system was able to identify IP patients at high risk for AE after chemotherapy for lung cancer associated with IP. … (more)
- Is Part Of:
- Lung cancer. Volume 125(2018)
- Journal:
- Lung cancer
- Issue:
- Volume 125(2018)
- Issue Display:
- Volume 125, Issue 2018 (2018)
- Year:
- 2018
- Volume:
- 125
- Issue:
- 2018
- Issue Sort Value:
- 2018-0125-2018-0000
- Page Start:
- 253
- Page End:
- 257
- Publication Date:
- 2018-11
- Subjects:
- IP interstitial pneumonia -- AE acute exacerbation -- IPF idiopathic pulmonary fibrosis -- CVD collagen vascular disease -- UIP usual interstitial pneumonia -- cIPF clinical idiopathic pulmonary fibrosis -- A-aDO2 alveolar–arterial oxygen partial pressure difference -- FVC forced vital capacity -- VC vital capacity -- KL-6 Krebs von den Lungen-6 -- SP-D surfactant protein D -- DLCO diffusing capacity of lung for carbon monoxide -- PaO2 partial pressure of arterial oxygen -- HRCT high-resolution CT -- CPFE combined pulmonary fibrosis and emphysema -- GEM gemcitabine -- CPT-11 irinotecan -- AMR amrubicin -- ACNU nimustine -- PEM pemetrexed -- DOC docetaxel -- VRB vinorelbine -- TOP topotecan -- CBDCA carboplatin -- PAC paclitaxel -- CDDP cisplatin -- VP-16 etoposide -- NAC N-acetylcysteine
Acute exacerbation -- Usual interstitial pneumonia -- Lung cancer -- Idiopathic pulmonary fibrosis -- Collagen vascular disease -- Interstitial pneumonia
Lungs -- Cancer -- Periodicals
Lung Neoplasms -- Abstracts
Lung Neoplasms -- Periodicals
Poumons -- Cancer -- Périodiques
Lungs -- Cancer
Periodicals
Electronic journals
Electronic journals
616.99424 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01695002 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/01695002 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/01695002 ↗
http://www.lungcancerjournal.info/issues ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.lungcan.2018.10.008 ↗
- Languages:
- English
- ISSNs:
- 0169-5002
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5307.245000
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- 8361.xml