Risk Factors for Acute Kidney Injury During High-dose Chemotherapy and Outcomes for Patients With Relapsed Germ Cell Tumors.


Journal

Clinical genitourinary cancer
ISSN: 1938-0682
Titre abrégé: Clin Genitourin Cancer
Pays: United States
ID NLM: 101260955

Informations de publication

Date de publication:
10 2020
Historique:
received: 13 12 2019
revised: 29 01 2020
accepted: 30 01 2020
pubmed: 17 3 2020
medline: 19 8 2021
entrez: 17 3 2020
Statut: ppublish

Résumé

Patients with relapsed germ cell tumors (GCTs) can be cured with salvage chemotherapy. We evaluated the risk factors and outcomes of patients who had developed acute kidney injury (AKI) during high-dose chemotherapy (HDCT) for relapsed GCT. All patients were scheduled to receive 2 consecutive courses of HDCT per our standard protocol. The characteristics and outcomes of the patients with stage ≥ 3 AKI were analyzed and compared with those without stage ≥ 3 AKI. Of 462 patients, 21 (4.5%) developed stage ≥ 3 AKI. Of these 21 patients, 18 had required hemodialysis during HDCT and 6 had died during HDCT. Of the 15 patients who had survived HDCT, 10 experienced recovery of renal function to baseline. AKI had occurred in the first cycle of HDCT in 18 patients. These patients were also more likely to have received HDCT in a third-line setting or further, to have Eastern Cooperative Oncology Group performance status of 1 or 2, and to have experienced gastrointestinal, hepatic, pulmonary, and infectious grade ≥ 3 toxicities. At a median follow-up of 10 months after HDCT, 5 patients had no evidence of disease, 3 were alive with disease, 6 had died of disease, 6 had died of complications from HDCT, and 1 had been lost to follow-up. Irreversible AKI during HDCT for relapsed GCT is uncommon but is associated with greater rates of infectious, gastrointestinal, hepatic, and pulmonary complications and treatment-related death. These patients were also more heavily pretreated and had a lower baseline performance status. However, most surviving patients had recovered their renal function and 5 of 21 were alive with no evidence of disease.

Sections du résumé

BACKGROUND
Patients with relapsed germ cell tumors (GCTs) can be cured with salvage chemotherapy. We evaluated the risk factors and outcomes of patients who had developed acute kidney injury (AKI) during high-dose chemotherapy (HDCT) for relapsed GCT.
PATIENTS AND METHODS
All patients were scheduled to receive 2 consecutive courses of HDCT per our standard protocol. The characteristics and outcomes of the patients with stage ≥ 3 AKI were analyzed and compared with those without stage ≥ 3 AKI.
RESULTS
Of 462 patients, 21 (4.5%) developed stage ≥ 3 AKI. Of these 21 patients, 18 had required hemodialysis during HDCT and 6 had died during HDCT. Of the 15 patients who had survived HDCT, 10 experienced recovery of renal function to baseline. AKI had occurred in the first cycle of HDCT in 18 patients. These patients were also more likely to have received HDCT in a third-line setting or further, to have Eastern Cooperative Oncology Group performance status of 1 or 2, and to have experienced gastrointestinal, hepatic, pulmonary, and infectious grade ≥ 3 toxicities. At a median follow-up of 10 months after HDCT, 5 patients had no evidence of disease, 3 were alive with disease, 6 had died of disease, 6 had died of complications from HDCT, and 1 had been lost to follow-up.
CONCLUSIONS
Irreversible AKI during HDCT for relapsed GCT is uncommon but is associated with greater rates of infectious, gastrointestinal, hepatic, and pulmonary complications and treatment-related death. These patients were also more heavily pretreated and had a lower baseline performance status. However, most surviving patients had recovered their renal function and 5 of 21 were alive with no evidence of disease.

Identifiants

pubmed: 32173356
pii: S1558-7673(20)30034-3
doi: 10.1016/j.clgc.2020.01.008
pii:
doi:

Substances chimiques

Etoposide 6PLQ3CP4P3

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e585-e587

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Kevin Juan Zhang (KJ)

Department of Internal Medicine, Indiana University School of Medicine, Indianapolis, IN. Electronic address: kevizhan@iu.edu.

Nasser H Hanna (NH)

Division of Hematology and Medical Oncology, Indiana University Melvin and Bren Simon Cancer Center, Indianapolis, IN.

Sandra K Althouse (SK)

Division of Biostatistics, Indiana University School of Medicine, Indianapolis, IN.

Mohammad Abu Zaid (MA)

Division of Hematology and Medical Oncology, Indiana University Melvin and Bren Simon Cancer Center, Indianapolis, IN.

Rafat Abonour (R)

Division of Hematology and Medical Oncology, Indiana University Melvin and Bren Simon Cancer Center, Indianapolis, IN.

Costantine Albany (C)

Division of Hematology and Medical Oncology, Indiana University Melvin and Bren Simon Cancer Center, Indianapolis, IN.

Lawrence H Einhorn (LH)

Division of Hematology and Medical Oncology, Indiana University Melvin and Bren Simon Cancer Center, Indianapolis, IN.

Nabil Adra (N)

Division of Hematology and Medical Oncology, Indiana University Melvin and Bren Simon Cancer Center, Indianapolis, IN.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH