The Impact of Cisplatin- or Non-Cisplatin-Containing Chemotherapy on Long-Term and Conditional Survival of Patients with Advanced Urinary Tract Cancer.


Journal

The oncologist
ISSN: 1549-490X
Titre abrégé: Oncologist
Pays: England
ID NLM: 9607837

Informations de publication

Date de publication:
10 2019
Historique:
received: 01 11 2018
accepted: 15 01 2019
pubmed: 3 4 2019
medline: 7 8 2020
entrez: 3 4 2019
Statut: ppublish

Résumé

The impact of cisplatin use on long-term survival of unselected patients with advanced urinary tract cancer (aUTC) has not been adequately investigated. We used a multinational database to study long-term survival and the impact of treatment type in unselected patients with aUTC. A total of 1,333 patients with aUTC (cT4bN0M0, cTanyN+M0, cTanyNanyM+), transitional-cell, squamous, or adenocarcinoma histology who received systemic chemotherapy and had available survival data were selected. Long-term survival was defined as alive at 3 years following initiation of first-line chemotherapy. Conditional overall survival (COS) analysis was employed to study change in prognosis given time survived from initiation of first-line chemotherapy. Median follow-up was 31.7 months. The combination of cisplatin use and cisplatin eligibility accurately predicted long-term survival. Eligible patients treated with cisplatin conferred a 31.6% probability of 3-year survival (95% confidence interval [CI]: 25.1-38.3), and 2-year COS for patients surviving 3 years after initiation of cisplatin-based chemotherapy was 83% (95% CI: 59.7-93.5). The respective probabilities for patients who were ineligible for cisplatin or not treated with cisplatin despite eligibility were 14% (95% CI: 10.8-17.6) and 49.3% (95% CI: 28.2-67.4). Two-year COS remained significantly different between these two groups up to 3 years after chemotherapy initiation. Cisplatin-based therapy was associated with the highest likelihood of long-term survival in patients with aUTC and should be used in patients who fulfill the established eligibility criteria. Novel therapies are necessary to increase long-term survival in cisplatin-ineligible patients. Long-term, disease-free survival is possible in one in four eligible-for-cisplatin patients with advanced urinary tract cancer (aUTC) treated with cisplatin-based combination chemotherapy. Therefore, deviations from eligibility criteria should be avoided. Consolidation surgery should be considered in responders. These data provide benchmarks for the study of novel therapies in aUTC.

Sections du résumé

BACKGROUND
The impact of cisplatin use on long-term survival of unselected patients with advanced urinary tract cancer (aUTC) has not been adequately investigated. We used a multinational database to study long-term survival and the impact of treatment type in unselected patients with aUTC.
MATERIALS AND METHODS
A total of 1,333 patients with aUTC (cT4bN0M0, cTanyN+M0, cTanyNanyM+), transitional-cell, squamous, or adenocarcinoma histology who received systemic chemotherapy and had available survival data were selected. Long-term survival was defined as alive at 3 years following initiation of first-line chemotherapy. Conditional overall survival (COS) analysis was employed to study change in prognosis given time survived from initiation of first-line chemotherapy.
RESULTS
Median follow-up was 31.7 months. The combination of cisplatin use and cisplatin eligibility accurately predicted long-term survival. Eligible patients treated with cisplatin conferred a 31.6% probability of 3-year survival (95% confidence interval [CI]: 25.1-38.3), and 2-year COS for patients surviving 3 years after initiation of cisplatin-based chemotherapy was 83% (95% CI: 59.7-93.5). The respective probabilities for patients who were ineligible for cisplatin or not treated with cisplatin despite eligibility were 14% (95% CI: 10.8-17.6) and 49.3% (95% CI: 28.2-67.4). Two-year COS remained significantly different between these two groups up to 3 years after chemotherapy initiation.
CONCLUSION
Cisplatin-based therapy was associated with the highest likelihood of long-term survival in patients with aUTC and should be used in patients who fulfill the established eligibility criteria. Novel therapies are necessary to increase long-term survival in cisplatin-ineligible patients.
IMPLICATIONS FOR PRACTICE
Long-term, disease-free survival is possible in one in four eligible-for-cisplatin patients with advanced urinary tract cancer (aUTC) treated with cisplatin-based combination chemotherapy. Therefore, deviations from eligibility criteria should be avoided. Consolidation surgery should be considered in responders. These data provide benchmarks for the study of novel therapies in aUTC.

Identifiants

pubmed: 30936379
pii: theoncologist.2018-0739
doi: 10.1634/theoncologist.2018-0739
pmc: PMC6795165
doi:

Substances chimiques

Cisplatin Q20Q21Q62J

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1348-1355

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

Informations de copyright

© AlphaMed Press 2019.

Déclaration de conflit d'intérêts

Disclosures of potential conflicts of interest may be found at the end of this article.

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Auteurs

Aristotelis Bamias (A)

Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece abamias@med.uoa.gr.

Kimon Tzannis (K)

Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.

Christina Bamia (C)

Department of Hygiene and Epidemiology, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.

Lauren C Harshman (LC)

Dana-Farber Cancer Institute, Boston, Massachusetts, USA.

Simon Crabb (S)

University of Southampton, Southampton, United Kingdom.

Elizabeth R Plimack (ER)

Fox Chase Cancer Center, Philadelphia, Pennsylvania, USA.

Sumanta Pal (S)

City of Hope Comprehensive Cancer Center, Duarte, California, USA.

Ugo De Giorgi (U)

IRCCS Istituto Scientifico Romagnolo per lo Studio e la Curadei Tumori, Meldola, Italy.

Sylvain Ladoire (S)

Center Georges-François Leclerc, Dijon, France.

Christine Theodore (C)

Department of Oncology, Hopital Foch, Suresnes, France.

Neeraj Agarwal (N)

University of Utah, Salt Lake City, Utah, USA.

Evan Y Yu (EY)

University of Washington, Seattle, Washington, USA.

Guenter Niegisch (G)

Department of Urology, Medical Faculty, Heinrich-Heine-University, Düsseldorf, Germany.

Cora N Sternberg (CN)

San Camillo Forlanini Hospital, Rome, Italy.

Sandy Srinivas (S)

Stanford University School of Medicine, Stanford, California, USA.

Ulka Vaishampayan (U)

Karmanos Cancer Institute, Detroit, Michigan, USA.

Andrea Necchi (A)

Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Michalis Liontos (M)

Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.

Jonathan E Rosenberg (JE)

Memorial Sloan-Kettering Cancer Center, New York New York, USA.

Thomas Powles (T)

Barts Health and the Royal Free NHS Trust, Queen Mary University of London, London, United Kingdom.

Joaquim Bellmunt (J)

Dana-Farber Cancer Institute, Boston, Massachusetts, USA.

Matthew D Galsky (MD)

Mount Sinai School of Medicine, Tisch Cancer Institute, New York New York, USA.

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