Cisplatin-based chemotherapy for the treatment of metastatic collecting duct carcinomas: A real-world, retrospective analysis

Collecting duct carcinomas (CDCs) are a particularly rare subtype of kidney cancer, endowed by a particularly poor prognosis. Since no active treatments have been established for CDCs, due to similarities with upper tract urothelial carcinomas, the use of the cisplatin-gemcitabine doublet is usually...

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Main Authors: Mimma Rizzo, Silvia Chiellino, Angela Gernone, Camillo Porta
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-10-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2022.939953/full
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author Mimma Rizzo
Silvia Chiellino
Angela Gernone
Camillo Porta
Camillo Porta
author_facet Mimma Rizzo
Silvia Chiellino
Angela Gernone
Camillo Porta
Camillo Porta
author_sort Mimma Rizzo
collection DOAJ
description Collecting duct carcinomas (CDCs) are a particularly rare subtype of kidney cancer, endowed by a particularly poor prognosis. Since no active treatments have been established for CDCs, due to similarities with upper tract urothelial carcinomas, the use of the cisplatin-gemcitabine doublet is usually recommended. Here we report a retrospective analysis of 36 metastatic CDCs treated, as everyday clinical practice, with either cisplatin-gemcitabine or cisplatin-gemcitabine-paclitaxel from 2005 to 2021. Thirty-three patients received gemcitabine (1000 mg/m2, days 1 and 8) and cisplatin (70 mg/m2, day 1), while 3 were treated with paclitaxel (80 mg/m2, days 1 and 8), gemcitabine (1000 mg/m2, days 1 and 8) and cisplatin (70 mg/m2, day 1), every 21 days for a maximum of 6 cycles. Eight out of 36 patients (22.2%) experienced a partial response, while 9 others (25%) had a disease stabilization. No benefit was observed in the only 3 patients treated with the triplet. Median PFS was just 6 months, while median OS was 8 months. The commonest grade ≥3 treatment-related adverse events were: neutropenia (75%, 11.1% of febrile neutropenia), anemia (50%), thrombocytopenia (38.8%), and vomiting (8.3%). Dose omissions and dose reductions were common, and few frail patients started the treatment with a 25% dose reduction. In conclusion, our real-world experience confirmed the modest activity and relevant toxicity of cisplatin-based chemotherapy for the treatment of CDCs. More translational studies and novel study designs are thus badly needed in these still orphan tumors.
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spelling doaj.art-679390e15bfc42939213cd71cc9b3edd2022-12-22T04:32:05ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2022-10-011210.3389/fonc.2022.939953939953Cisplatin-based chemotherapy for the treatment of metastatic collecting duct carcinomas: A real-world, retrospective analysisMimma Rizzo0Silvia Chiellino1Angela Gernone2Camillo Porta3Camillo Porta4Division of Medical Oncology, Azienda Ospedaliero Universitaria (A.O.U.) Consorziale Policlinico di Bari, Bari, ItalyDivision of Medical Oncology, Istituto di Ricovero e Cura a Carattere Scientifico (I.R.C.C.S.) San Matteo University Hospital, Pavia, ItalyDivision of Medical Oncology, Azienda Ospedaliero Universitaria (A.O.U.) Consorziale Policlinico di Bari, Bari, ItalyDivision of Medical Oncology, Azienda Ospedaliero Universitaria (A.O.U.) Consorziale Policlinico di Bari, Bari, ItalyChair of Oncology, Interdisciplinary Department of Medicine, University of Bari “A. Moro”, Bari, ItalyCollecting duct carcinomas (CDCs) are a particularly rare subtype of kidney cancer, endowed by a particularly poor prognosis. Since no active treatments have been established for CDCs, due to similarities with upper tract urothelial carcinomas, the use of the cisplatin-gemcitabine doublet is usually recommended. Here we report a retrospective analysis of 36 metastatic CDCs treated, as everyday clinical practice, with either cisplatin-gemcitabine or cisplatin-gemcitabine-paclitaxel from 2005 to 2021. Thirty-three patients received gemcitabine (1000 mg/m2, days 1 and 8) and cisplatin (70 mg/m2, day 1), while 3 were treated with paclitaxel (80 mg/m2, days 1 and 8), gemcitabine (1000 mg/m2, days 1 and 8) and cisplatin (70 mg/m2, day 1), every 21 days for a maximum of 6 cycles. Eight out of 36 patients (22.2%) experienced a partial response, while 9 others (25%) had a disease stabilization. No benefit was observed in the only 3 patients treated with the triplet. Median PFS was just 6 months, while median OS was 8 months. The commonest grade ≥3 treatment-related adverse events were: neutropenia (75%, 11.1% of febrile neutropenia), anemia (50%), thrombocytopenia (38.8%), and vomiting (8.3%). Dose omissions and dose reductions were common, and few frail patients started the treatment with a 25% dose reduction. In conclusion, our real-world experience confirmed the modest activity and relevant toxicity of cisplatin-based chemotherapy for the treatment of CDCs. More translational studies and novel study designs are thus badly needed in these still orphan tumors.https://www.frontiersin.org/articles/10.3389/fonc.2022.939953/fullcollecting duct carcinomasnon clear cell renal cell carcinomakidney cancercisplatinchemotherapyretrospective study
spellingShingle Mimma Rizzo
Silvia Chiellino
Angela Gernone
Camillo Porta
Camillo Porta
Cisplatin-based chemotherapy for the treatment of metastatic collecting duct carcinomas: A real-world, retrospective analysis
Frontiers in Oncology
collecting duct carcinomas
non clear cell renal cell carcinoma
kidney cancer
cisplatin
chemotherapy
retrospective study
title Cisplatin-based chemotherapy for the treatment of metastatic collecting duct carcinomas: A real-world, retrospective analysis
title_full Cisplatin-based chemotherapy for the treatment of metastatic collecting duct carcinomas: A real-world, retrospective analysis
title_fullStr Cisplatin-based chemotherapy for the treatment of metastatic collecting duct carcinomas: A real-world, retrospective analysis
title_full_unstemmed Cisplatin-based chemotherapy for the treatment of metastatic collecting duct carcinomas: A real-world, retrospective analysis
title_short Cisplatin-based chemotherapy for the treatment of metastatic collecting duct carcinomas: A real-world, retrospective analysis
title_sort cisplatin based chemotherapy for the treatment of metastatic collecting duct carcinomas a real world retrospective analysis
topic collecting duct carcinomas
non clear cell renal cell carcinoma
kidney cancer
cisplatin
chemotherapy
retrospective study
url https://www.frontiersin.org/articles/10.3389/fonc.2022.939953/full
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AT angelagernone cisplatinbasedchemotherapyforthetreatmentofmetastaticcollectingductcarcinomasarealworldretrospectiveanalysis
AT camilloporta cisplatinbasedchemotherapyforthetreatmentofmetastaticcollectingductcarcinomasarealworldretrospectiveanalysis
AT camilloporta cisplatinbasedchemotherapyforthetreatmentofmetastaticcollectingductcarcinomasarealworldretrospectiveanalysis