Predicting cumulative incidence of adverse events in older patients with cancer undergoing first-line palliative chemotherapy: Korean Cancer Study Group (KCSG) multicentre prospective study

Background Older patients have increased risk of toxicity from chemotherapy. Current prediction tools do not provide information on cumulative risk. Methods Patients aged ≥ 70 years with solid cancer were prospectively enrolled. A prediction model was developed for adverse events (AEs) ≥ Grade 3 (G3...

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Published inBritish journal of cancer Vol. 118; no. 9; pp. 1169 - 1175
Main Authors Kim, Jin Won, Lee, Yun-Gyoo, Hwang, In Gyu, Song, Hong Suk, Koh, Su Jin, Ko, Yoon Ho, Shin, Seong Hoon, Woo, In Sook, Hong, Soojung, Kim, Tae-Yong, Kim, Sun Young, Nam, Byung-Ho, Kim, Hyun Jung, Kim, Hyo Jung, Lee, Myung Ah, Kwon, Jung Hye, Hong, Yong Sang, Bae, Sung Hwa, Koo, Dong-Hoe, Kim, Kwang-Il, Kim, Jee Hyun
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.05.2018
Nature Publishing Group
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ISSN0007-0920
1532-1827
1532-1827
DOI10.1038/s41416-018-0037-6

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Summary:Background Older patients have increased risk of toxicity from chemotherapy. Current prediction tools do not provide information on cumulative risk. Methods Patients aged ≥ 70 years with solid cancer were prospectively enrolled. A prediction model was developed for adverse events (AEs) ≥ Grade 3 (G3), based on geriatric assessment (GA), laboratory, and clinical variables. Results 301 patients were enrolled (median age, 75 years). Median number of chemotherapy cycles was 4. During first-line chemotherapy, 53.8% of patients experienced AEs ≥ G3. Serum protein < 6.7 g/dL, initial full-dose chemotherapy, psychological stress or acute disease in the past 3 months, water consumption < 3 cups/day, unable to obey a simple command, and self-perception of poor health were significantly related with AEs ≥ G3. A predicting model with these six variables ranging 0–8 points was selected with the highest discriminatory ability (c-statistic= 0.646), which could classify patients into four risk groups. Predicted cumulative incidence of AEs ≥ G3 was discriminated according to risk groups. Conclusions This prediction tool could identify the risk of AEs ≥ G3 after chemotherapy and provide information on the cumulative incidence of AEs in each cycle. Clinical Trial Id WHO ICTRP number, KCT0001071
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ISSN:0007-0920
1532-1827
1532-1827
DOI:10.1038/s41416-018-0037-6