First case report of tumor lysis syndrome after third line systemic therapy with gemcitabine and pazopanib in a patient with lower extremity soft tissue sarcoma.


Journal

Chinese clinical oncology
ISSN: 2304-3873
Titre abrégé: Chin Clin Oncol
Pays: China
ID NLM: 101608375

Informations de publication

Date de publication:
Aug 2023
Historique:
received: 10 11 2022
accepted: 14 06 2023
medline: 14 9 2023
pubmed: 21 8 2023
entrez: 21 8 2023
Statut: ppublish

Résumé

Tumor lysis syndrome (TLS) is recognized as an oncologic disorder with a variable incidence. TLS can cause the rapid destruction of tumor cells in response to oncologic therapy and is characterized by multiple electrolyte disturbances as well as its secondary complications, including death. This disease is common among patients with hematologic neoplasms, but very rare among those with solid tumors, as is the case with sarcomas. Such patients have a poor prognosis and increased risk of mortality. In the patient's particular case, this occurred after initiating third-line systemic therapy with gemcitabine associated with pazopanib, an event not previously described in the literature. We report the case of a patient with a history of high-grade sarcoma of the left lower limb T4N1M0 stage IIIB undergoing surgical management and exhibiting tumor progression with the need for third-line systemic therapy with pazopanib and gemcitabine. The patient presented with pain at the amputation site, inflammatory changes, and a tumor mass of large components on admission. They later developed electrolyte imbalance and acute renal injury compatible with TLS after systemic therapy was initiated. Pharmacological therapy, including rasburicase, was initiated based on the clinical and laboratory findings. Due to the progression of renal involvement, it was necessary to initiate haemodialysis, and during her hospital stay, the patient presented febrile syndrome associated with pancytopenia. The patient showed a favourable clinical response to the proposed antibiotic therapy and recovery of renal function, for which reason therapy was restarted with pazopanib and gemcitabine, the latter with a 20% reduction for the following cycles. Outpatient follow-up continued, completing eight cycles of treatment with good tolerance and partial clinical response; the patient died of respiratory complications eight months after discharge. There is limited evidence for TLS in patients with high-grade sarcoma in the literature related to the oncologic therapy used; this indicates that early risk evaluation along with prompt initiation of effective therapies is required to prevent the appearance of this type of complications in the short and long term.

Sections du résumé

BACKGROUND BACKGROUND
Tumor lysis syndrome (TLS) is recognized as an oncologic disorder with a variable incidence. TLS can cause the rapid destruction of tumor cells in response to oncologic therapy and is characterized by multiple electrolyte disturbances as well as its secondary complications, including death. This disease is common among patients with hematologic neoplasms, but very rare among those with solid tumors, as is the case with sarcomas. Such patients have a poor prognosis and increased risk of mortality. In the patient's particular case, this occurred after initiating third-line systemic therapy with gemcitabine associated with pazopanib, an event not previously described in the literature.
CASE DESCRIPTION METHODS
We report the case of a patient with a history of high-grade sarcoma of the left lower limb T4N1M0 stage IIIB undergoing surgical management and exhibiting tumor progression with the need for third-line systemic therapy with pazopanib and gemcitabine. The patient presented with pain at the amputation site, inflammatory changes, and a tumor mass of large components on admission. They later developed electrolyte imbalance and acute renal injury compatible with TLS after systemic therapy was initiated. Pharmacological therapy, including rasburicase, was initiated based on the clinical and laboratory findings. Due to the progression of renal involvement, it was necessary to initiate haemodialysis, and during her hospital stay, the patient presented febrile syndrome associated with pancytopenia. The patient showed a favourable clinical response to the proposed antibiotic therapy and recovery of renal function, for which reason therapy was restarted with pazopanib and gemcitabine, the latter with a 20% reduction for the following cycles. Outpatient follow-up continued, completing eight cycles of treatment with good tolerance and partial clinical response; the patient died of respiratory complications eight months after discharge.
CONCLUSIONS CONCLUSIONS
There is limited evidence for TLS in patients with high-grade sarcoma in the literature related to the oncologic therapy used; this indicates that early risk evaluation along with prompt initiation of effective therapies is required to prevent the appearance of this type of complications in the short and long term.

Identifiants

pubmed: 37599513
doi: 10.21037/cco-22-111
pii: cco-22-111
doi:

Substances chimiques

pazopanib 7RN5DR86CK
Gemcitabine 0
Electrolytes 0

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Pagination

45

Auteurs

Edith Norela Benitez-Escobar (EN)

Specialization Program in Internal Medicine, School of Health, Universidad Santiago de Cali, Santiago de Cali, Colombia; Research and Education Department, Clínica de Occidente S.A., Santiago de Cali, Colombia; Genetics Physiology and Metabolism Research Group (GEFIME), Universidad Santiago de Cali, Santiago de Cali, Colombia.

Duvan Arley Galindes-Casanova (DA)

Specialization Program in Internal Medicine, School of Health, Universidad Santiago de Cali, Santiago de Cali, Colombia; Research and Education Department, Clínica de Occidente S.A., Santiago de Cali, Colombia; Genetics Physiology and Metabolism Research Group (GEFIME), Universidad Santiago de Cali, Santiago de Cali, Colombia.

Luis Álvaro Melo-Burbano (LÁ)

Specialization Program in Internal Medicine, School of Health, Universidad Santiago de Cali, Santiago de Cali, Colombia; Research and Education Department, Clínica de Occidente S.A., Santiago de Cali, Colombia; Genetics Physiology and Metabolism Research Group (GEFIME), Universidad Santiago de Cali, Santiago de Cali, Colombia.

Diana Marcela Bonilla-Bonilla (DM)

Specialization Program in Internal Medicine, School of Health, Universidad Santiago de Cali, Santiago de Cali, Colombia; Research and Education Department, Clínica de Occidente S.A., Santiago de Cali, Colombia; Genetics Physiology and Metabolism Research Group (GEFIME), Universidad Santiago de Cali, Santiago de Cali, Colombia.

Luis Miguel Osorio-Toro (LM)

Specialization Program in Internal Medicine, School of Health, Universidad Santiago de Cali, Santiago de Cali, Colombia; Research and Education Department, Clínica de Occidente S.A., Santiago de Cali, Colombia; Genetics Physiology and Metabolism Research Group (GEFIME), Universidad Santiago de Cali, Santiago de Cali, Colombia.

Jorge Enrique Daza-Arana (JE)

Specialization Program in Internal Medicine, School of Health, Universidad Santiago de Cali, Santiago de Cali, Colombia.

Santiago Leandro Escobar-Dávila (SL)

Research and Education Department, Clínica de Occidente S.A., Santiago de Cali, Colombia; Comprehensive Cancer Center, Clínica de Occidente S.A., Santiago de Cali, Colombia.

Giovanna Patricia Rivas-Tafurt (GP)

Specialization Program in Internal Medicine, School of Health, Universidad Santiago de Cali, Santiago de Cali, Colombia; Research and Education Department, Clínica de Occidente S.A., Santiago de Cali, Colombia; Comprehensive Cancer Center, Clínica de Occidente S.A., Santiago de Cali, Colombia.

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Classifications MeSH