Abstract 349P
Background
It is unknown whether proteinuria caused by ramcirumab (RAM) induces renal dysfunction. Thus, this study assessed the relationship between proteinuria and other factors with RAM therapy, and compared estimated glomerular filtration rate (eGFR) with or without proteinuria in long-term treatment.
Methods
Medical records were retrospectively reviewed for 156 patients treated with chemotherapy that included RAM between April 1, 2015 and May 31, 2019 at Kure Medical Center. Forty-eight patients with a performance status of 3 or 4, or not measured for proteinuria among those treated with RAM, or has detected proteinuria before first commencing RAM administration were excluded. Proteinuria and eGFR were measured before treatment with RAM, and compared to minimum eGFR with or without proteinuria after treatment with RAM. The proteinuria group was defined as proteinuria detected at more than 1+ at least once.
Results
Overall, a total of 108 patients were included in this analysis. Thirty-nine patients were classified into a proteinuria group and the remaining 69 patients were classified into the non-proteinuria group. Age, sex, and eGFR before treatment with RAM did not significantly differ between the proteinuria group and non-proteinuria group. There were significant decreases in proteinuria group mean eGFR(-26.7±5.6 ml/min/1.73 m3), which was greater than the non-proteinuria group mean eGFR(-15.0±4.2 ml/min/1.73 m3), compared to eGFR before treatment (p<0.05). The incidence of grade 3 or 4 chronic kidney disease (CKD) was observed in 8 patients (20.5%) in the proteinuria group, but in only 3 patients (4.5%) in the non-proteinuria group (p<0.05). Patients treated over 200 days with RAM had a significant incidence of proteinuria, and in the proteinuria group, the appearance of proteinuria within 28 days from first administration decreased eGFR more than after 28 days.
Conclusions
Proteinuria caused by RAM might be decreased in eGFR, particularly in cases that immediately detected. Renal dysfunction can affect subsequent chemotherapy, and as such, it is important to regularly check proteinuria during treatment with RAM. It is necessary to take particular care for cases in which proteinuria is detected and renal function has already declined.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
393P - Clinical characteristics and prognosis of patients with pulmonary mucoepidermoid carcinoma: A SEER-based analysis
Presenter: Lingxiao Qiu
Session: e-Poster Display Session
394P - Apatinib plus etoposide capsules as third-line or further-line treatment for extensive stage small cell lung cancer patients: A multicenter, single arm, phase II clinical trial
Presenter: Zhen He
Session: e-Poster Display Session
395P - Afatinib in Asian and non-Asian patients (pts) with EGFR mutation positive (EGFRm+) NSCLC harboring major uncommon mutations
Presenter: James Chih-Hsin Yang
Session: e-Poster Display Session
396P - Efficacy and safety of S-1 in elderly patients with advanced non-small cell lung cancer previously treated with platinum-based chemotherapy: A subgroup analysis of the EAST-LC
Presenter: James Chih-Hsin Yang
Session: e-Poster Display Session
397P - A phase I cohort expansion trial of OBI-833 in non-small cell lung cancer patients
Presenter: Ching-Liang Ho
Session: e-Poster Display Session
398P - Real-world mechanism of crizotinib-resistance in MET exon 14 skipping mutations non-small-cell lung cancer using next generation sequencing: A multicenter study
Presenter: Dong Wang
Session: e-Poster Display Session
399P - Real-world insights into patients (pts) with advanced NSCLC and MET alterations
Presenter: Marisa Bittoni
Session: e-Poster Display Session
400P - Sequential afatinib and osimertinib in real-world EGFR mutation positive (EGFRm+) NSCLC: Final analysis of Asian patients in the GioTag study
Presenter: Maximilian J. Hochmair
Session: e-Poster Display Session
401P - A prospective, phase II trial of low-dose afatinib monotherapy for patients with EGFR, mutation-positive, non-small cell lung cancer (TORG1632)
Presenter: Satoshi Igawa
Session: e-Poster Display Session
402P - Efficacy and safety of sintilimab plus docetaxel in patients with previously treated advanced non-small cell lung cancer (NSCLC)
Presenter: Zhehai Wang
Session: e-Poster Display Session