Activity of Platinum-Based Chemotherapy in Patients With Advanced Prostate Cancer With and Without DNA Repair Gene Aberrations

Sabine Schmid; Aurelius Omlin; Celestia Higano; Christopher Sweeney; Nieves Martinez Chanza; Niven Mehra; Malou C P Kuppen; Himisha Beltran; Vincenza Condeduca; Daniel Vargas Pivato de Almeida; Fernando Cotait Maluf; William K Oh; Che-Kai Tsao; Oliver Sartor; Elisa Ledet; Giuseppe Di Lorenzo; Steven M Yip; Kim N Chi; Diletta Bianchini; Ugo De Giorgi; Aaron R Hansen; Tomasz M Beer; Lavaud Pernelle; Rafael Morales-Barrera; Marcello Tucci; Elena Castro; Kostas Karalis; Andries M Bergman; Mo Linh Le; Ursina Zürrer-Härdi; Carmel Pezaro; Hiroyoshi Suzuki; Andrea Zivi; Dirk Klingbiel; Sämi Schär; Silke Gillessen

doi:10.1001/jamanetworkopen.2020.21692

. 2020 Oct 28;3(10):e2021692. doi: 10.1001/jamanetworkopen.2020.21692

Activity of Platinum-Based Chemotherapy in Patients With Advanced Prostate Cancer With and Without DNA Repair Gene Aberrations

Sabine Schmid ^1,^2,^✉, Aurelius Omlin ¹, Celestia Higano ³, Christopher Sweeney ⁴, Nieves Martinez Chanza ⁴, Niven Mehra ⁵, Malou C P Kuppen ^5,⁶, Himisha Beltran ^4,⁷, Vincenza Condeduca ^7,⁸, Daniel Vargas Pivato de Almeida ^9,¹⁰, Fernando Cotait Maluf ^11,¹², William K Oh ¹³, Che-Kai Tsao ¹³, Oliver Sartor ¹⁴, Elisa Ledet ¹⁴, Giuseppe Di Lorenzo ¹⁵, Steven M Yip ¹⁶, Kim N Chi ¹⁶, Diletta Bianchini ^17,¹⁸, Ugo De Giorgi ⁸, Aaron R Hansen ², Tomasz M Beer ¹⁹, Lavaud Pernelle ²⁰, Rafael Morales-Barrera ²¹, Marcello Tucci ²², Elena Castro ²³, Kostas Karalis ²⁴, Andries M Bergman ²⁵, Mo Linh Le ²⁶, Ursina Zürrer-Härdi ²⁷, Carmel Pezaro ²⁸, Hiroyoshi Suzuki ²⁹, Andrea Zivi ^30,³¹, Dirk Klingbiel ³², Sämi Schär ³², Silke Gillessen ^33,³⁴

¹Department of Medical Oncology and Haematology, Cantonal Hospital of St Gallen, St Gallen, Switzerland

²Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, Canada

³Seattle Cancer Care Alliance, University of Washington, Seattle

⁴Department of Medical Oncology, Dana Farber Cancer Institute, Boston, Massachusetts

⁵Radboud University, Medical Center Nijmegen, Utrecht, the Netherlands

⁶Institute for Medical Technology Assessment, Erasmus School of Health Policy and Management, Erasmus University, Rotterdam, the Netherlands

⁷Department of Medical Oncology, Weill Cornell Medicine, New York, New York

⁸Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori IRCCS, Meldola, Italy

⁹Department of Medical Oncology Beneficencia Portuguesa de São Paulo, São Paulo, Brazil

¹⁰Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, New York

¹¹Department of Medical Oncology, Hospital Israelita Albert Einstein, Beneficencia Portuguesa de São Paulo, São Paulo, Brazil

¹²Oncoclinicas Oncology Group, Brasilia, Brazil

¹³Division of Hematology and Medical Oncology, Tisch Cancer Institute, Icahn School of Medicine, Mount Sinai Hospital, New York, New York

¹⁴Tulane Cancer Center, Tulane Medical School, New Orleans, Louisiana

¹⁵Medical Oncology, Department of Medicine and Health Sciences Vincenzo Tiberio, University of Molise, Campobasso, Italy

¹⁶British Columbia Cancer, Vancouver, Canada

¹⁷Division of Clinical Studies, Prostate Cancer Targeted Therapies Group, Institute of Cancer Research, Royal Marsden NHS Foundation Trust, Sutton, United Kingdom

¹⁸Maidstone Hospital, Kent, United Kingdom

¹⁹Oregon Health and Science Knight Cancer Institute, Oregon Health and Science University, Portland

²⁰Department of Cancer Medicine, Gustave Roussy, Cancer Campus, Grand Paris, Université Paris-Sud, Université Paris-Saclay, Villejuif, France

²¹Department of Medical Oncology, Vall d’Hebron University Hospital, Barcelona, Spain

²²Division of Medical Oncology, San Luigi Gonzaga Hospital, Department of Oncology, University of Turin, Orbassano, Turin, Italy

²³Prostate Cancer Clinical Research Unit, Spanish National Cancer Research Centre, Madrid, Spain

²⁴Department of Genitourinary Medical Oncology, Athens Medical Center, Athens, Greece

²⁵Division of Internal Medicine and Oncogenomics, Netherlands Cancer Institute, Amsterdam, the Netherlands

²⁶Guy’s and St Thomas’ Hospital, London, United Kingdom

²⁷Department of Medical Oncology, Cantonal Hospital Winterthur, Winterthur, Switzerland

²⁸Department of Oncology, Eastern Health, Box Hill, Victoria, Australia

²⁹Department of Urology, Toho University Sakura Medical Center, Chiba, Japan

³⁰Department of Medical Oncology, Azienda Ospedaliera Universitaria Integrata di Verona, Verona, Italy

³¹Section of Cancer, Department of Surgery and Cancer, Faculty of Medicine, Imperial College London, London, United Kingdom

³²Coordinating Center, Swiss Group for Clinical Cancer Research, Bern, Switzerland

³³Oncology Institute of Southern Switzerland, Bellinzona, Switzerland

³⁴Faculty of Biomedical Sciences, Università della Svizzera Italiana, Lugano, Switzerland

Accepted for Publication: July 31, 2020.

Published: October 28, 2020. doi:10.1001/jamanetworkopen.2020.21692

^✉

Corresponding Author: Sabine Schmid, MD, Division of Medical Oncology, Princess Margaret Cancer Centre, University Health Network, 610 University Ave, Toronto ON M5G 2M9, Canada (sabine.schmid@uhn.ca).

Author Contributions: Drs Schmid and Omlin had full access to all of the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis. Drs Schmid and Omlin contributed equally.

Concept and design: Schmid, Omlin, Di Lorenzo, Yip, Beer, Tucci, Gillessen.

Acquisition, analysis, or interpretation of data: Schmid, Omlin, Higano, Sweeney, Martinez Chanza, Mehra, Kuppen, Beltran, Conteduca, Vargas Pivato de Almeida, Cotait Maluf, Oh, Tsao, Sartor, Ledet, Di Lorenzo, Yip, Chi, Bianchini, De Giorgi, Hansen, Beer, Pernelle, Morales-Barrera, Castro, Karalis, Bergman, Le, Zürrer-Härdi, Pezaro, Suzuki, Zivi, Klingbiel, Schär, Gillessen.

Drafting of the manuscript: Schmid, Omlin, Sweeney, Sartor, Yip, Beer, Morales-Barrera, Castro, Klingbiel, Schär, Gillessen.

Critical revision of the manuscript for important intellectual content: Schmid, Omlin, Higano, Sweeney, Martinez Chanza, Mehra, Kuppen, Beltran, Conteduca, Vargas Pivato de Almeida, Cotait Maluf, Oh, Tsao, Sartor, Ledet, Di Lorenzo, Yip, Chi, Bianchini, De Giorgi, Hansen, Beer, Pernelle, Tucci, Castro, Karalis, Bergman, Le, Zürrer-Härdi, Pezaro, Suzuki, Zivi, Klingbiel, Schär, Gillessen.

Statistical analysis: Beer, Morales-Barrera, Klingbiel, Schär.

Administrative, technical, or material support: Tsao, Yip, Chi, De Giorgi, Castro, Karalis, Zürrer-Härdi, Suzuki.

Supervision: Omlin, Tsao, Chi, Hansen, Beer, Morales-Barrera, Gillessen.

Conflict of Interest Disclosures: Dr Schmid reported receiving grants from AstraZeneca and Bristol Myers Squibb; receiving travel support and serving on the advisory boards of Merck Sharp and Dohme and Boehringer Ingelheim; and receiving travel support from Takeda outside the submitted work. Dr Omlin reported receiving travel support from and serving in an advisory role for Astellas, Bayer, and Sanofi; receiving travel support and grants and serving in an advisory role for Janssen Pharmaceuticals; serving in an advisory role for AstraZeneca, Merck Sharp and Dohme, Molecular Partners, Roche, and Pfizer; and receiving grants from Teva during the conduct of the study. Dr Higano reported receiving research support from Aragon, Aptevo (Emergent), Astellas, AstraZeneca, Bayer, Clovis Oncology, eFFECTOR Therapeutics, Ferring Pharmaceuticals, Hoffman-LaRoche, Medivation, and Pfizer; receiving personal fees from Astellas, Clovis, Dendreon, Ferring, Genentech, Pfizer, Bayer, Blue Earth Diagnostics, Hinova, Janssen Pharmaceuticals, Merck, Orion, Carrick Therapeutics, and Novartis; and that spouse holds stock and former officer of CTI Biopharma outside the submitted work. Dr Sweeney reported receiving grants from Janssen Pharmaceuticals, Sanofi, Sotio, and Dendreon; grants and personal fees from Astellas, Pfizer, and Bayer; serving in a consulting or advisory role for Sanofi, Janssen Pharmaceuticals, Astellas, Bayer, Genentech, AstraZeneca, Pfizer, and Celgene; and receiving personal fees from Eli Lilly and Co during the conduct of the study; in addition, Dr Sweeney reported having a patent to dimethylaminoparthenolide, a patent to cabozantinib plus abiraterone, and a patent to the tristetraprolin prostate cancer biomarker. Dr Martinez Chanza reported serving in an advisory role for and receiving travel support from Pfizer and Ipsen and serving in an advisory role for Bristol Myers Squibb, Janssen Pharmaceuticals, and Sanofi outside the submitted work. Dr Mehra reported serving in an advisory role for Bristol Myers Squibb and Bayer; receiving grants and personal fees from Roche, Astellas, Janssen Pharmaceuticals, Merck Sharp and Dohme, and AstraZeneca; and receiving grants from Pfizer, Sanofi, and Genzyme outside the submitted work. Dr Kuppen reported receiving grants from Bayer, Sanofi, Janssen Cilag, and Astellas during the conduct of the study and receiving travel support from Ipsen outside the submitted work. Dr Beltran reported receiving grants from Abbvie, Millennium, and Eli Lilly and Co; receiving grants from and serving as a consultant for Janssen Pharmaceuticals and Astellas; and serving as a consultant for Amgen, AstraZeneca, Pfizer, Sanofi, Genzyme, and Merck outside the submitted work. Dr Cotait Maluf reported serving on the advisory boards of Sanofi, Janssen Pharmaceuticals, AstraZeneca, Roche, Astellas, Merck Sharp and Dohme, Bristol Myers Squibb, Novartis, Amgen, and Ferring; receiving research support from Sanofi, Janssen Pharmaceuticals, AstraZeneca, Roche, Astellas, Merck Sharp and Dohme, Bristol Myers Squibb, and Novartis; and serving on the speakers bureau of Sanofi, Janssen Pharmaceuticals, AstraZeneca, Roche, Astellas, Merck Sharp and Dohme, Bristol Myers Squibb, Novartis, Amgen, and Ferring outside the submitted work. Dr Oh reported receiving personal fees from AstraZeneca, Sanofi, Teneobio, Sema4, Astellas, and Bayer outside the submitted work. Dr Tsao reported serving in a consulting or advisory role for Clovis, Pfizer, and Eisai. Dr Sartor reported receiving grants and personal fees from Sanofi, Janssen Pharmaceuticals, Pfizer, and Bayer during the conduct of the study; serving in an advisory role for Advanced Accelerator Applications, Astellas, AstraZeneca, Bayer, Blue Earth Diagnostics, Bavarian Nordic, Novartis, Bristol Myers Squibb, Clovis, Constellation, Dendreon, EMD Serono, Myriad, Noxopharm, Progenics, Janssen Pharmaceuticals, Myovant, Pfizer, and Sanofi; and receiving grants from AstraZeneca, Dendreon, Endocyte, Innocrin, Invitae, Merck, and Sotio outside the submitted work. Dr Yip reported receiving grants from Janssen Pharmaceuticals and Bayer and receiving personal fees from Pfizer, AstraZeneca, Bayer, Bristol Myers Squibb, Hoffman La Roche, Novartis, Pfizer, and Janssen Pharmaceuticals outside the submitted work. Dr Chi reported receiving grants from the Canadian Cancer Society, Prostate Cancer Canada, Janssen Pharmaceuticals, Astellas, and the British Columbia Cancer Foundation during the conduct of the study as well as receiving personal fees from Novartis, AstraZeneca, Roche, Daiichi Sankyo, Pfizer, and Point Biopharma and receiving grants and personal fees from Janssen Pharmaceuticals, Astellas, and Sanofi outside the submitted work. Dr Bianchini reported receiving speaker and travel fees from Janssen Pharmaceuticals outside the submitted work. Dr De Giorgi reported serving in an advisory role for Astellas, Bayer, Bristol Myers Squibb, Janssen Cilag, Merck, Novartis, Ipsen, and Sanofi; receiving institutional research support AstraZeneca, Roche, and Sanofi; and receiving travel support from Bristol Myers Squibb, Ipsen, Janssen Cilag, and Pfizer outside the submitted work. Dr Hansen reported receiving personal fees and research support from GlaxoSmithKline and Merck; receiving research support from Bristol Myers Squibb, AstraZeneca, and Roche; and serving in an advisory role for Genentech/Roche, Merck, GlaxoSmithKline, Bristol Myers Squibb, Novartis, Boston Biomedical, Boehringer-Ingelheim, AstraZeneca, and Medimmune outside the submitted work. Dr Beer reported receiving grants from Alliance Foundation Trials, Corcept Therapeutics, Endocyte, Harpoon Therapeutics, Medivation, Sotio, Theralcone Sciences, and Zenith Epigenetics; receiving consulting fees and stock ownership from Arvinas; receiving grants and personal fees from Astellas, Boehringer Ingelheim, Janssen Pharmaceuticals; receiving consulting fees from AstraZeneca, Bayer, Bristol Myers Squib, Clovis Oncology, GlaxoSmithKline, Merck, Novartis, Pfizer, and Tolera; and having stock ownership in Salarius Pharmaceuticals outside the submitted work. Dr Pernelle reported receiving personal and travel fees from Astellas and AstraZeneca and travel fees from Ipsen, Janssen Pharmaceuticals, and Mundi Pharma outside the submitted work. Dr Morales-Barrera reported serving as a consultant, advisor, or on the speakers bureau for Sanofi, Bayer, Roche, AstraZeneca, Merck Sharp and Dohme, and Asofarma; receiving travel and accommodation expenses from Roche, Sanofi, Astellas, Janssen Pharmaceuticals, Merck Sharp and Dohme, Bayer, Pharmacyclics, Clovis Oncology, and Eli Lilly and Co; and having institutional financial interests in AB Science, Aragon Pharmaceuticals, Arog Pharmaceuticals, Astellas, AstraZeneca, Aveo Pharmaceuticals, Bayer, Blueprint Medicines Corporation, BN Immunotherapeutics, Boehringer Ingelheim, Bristol Myers Squibb, Clovis Oncology, Cougar Biotechnology, Deciphera Pharmaceuticals, Exelixis, Hoffmann La Roche, Genentech, GlaxoSmithKline, Incyte, Janssen Cilag International, Karyopharm Therapeutics, Laboratoires Leurquin Mediolanum, Eli Lilly and Co, Medimmune, Millennium Pharmaceuticals, Nanobiotix, Novartis, Pfizer, Puma Biotechnology, Sanofi, SFJ Pharma, and Teva outside the submitted work. Dr Castro reported receiving personal fees from Astellas, Bayer, Pfizer, Merck Sharp and Dohme, and Clovis; receiving grants and personal fees from AstraZeneca, Bayer, and Janssen Pharmaceuticals; serving on the speaker bureaus of AstraZeneca, Bayer, Janssen Pharmaceuticals, and Pfizer; and receiving travel support from Astellas, AstraZeneca, Bayer, Janssen Pharmaceuticals, and Roche outside the submitted work. Dr Bergman reported serving on the advisory boards of Sanofi, Astellas, Bayer, Janssen Pharmaceuticals, and Amgen and receiving grants from Sanofi, Astellas, and Bayer outside the submitted work. Dr Le reported receiving grants from Ipsen and Novartis outside the submitted work. Dr Zürrer-Härdi reported receiving travel support from Gilead, Eli Lilly and Co, Pfizer, Bayer, Celgene, and Merck Sharp and Dohme outside the submitted work. Dr Pezaro reported receiving personal fees from Astellas, AstraZeneca, Ipsen, Mundi Pharma, and Pfizer; receiving personal fees and travel support from Janssen Pharmaceuticals; and receiving travel support from Bayer outside the submitted work. Dr Suzuki reported receiving personal fees from AstraZeneca, Janssen Pharmaceuticals, and Nihon Medi-Physics and receiving grants and personal fees from Takeda, Sanofi, and Astellas during the conduct of the study as well as receiving grants from Taiho and Kissei; receiving grants and personal fees from Pfizer; serving in a consulting or advisory role for AstraZeneca, Astellas, Bayer, Chugai-Roche, Daiichi Sankyo, Eli Lilly and Co, Janssen Pharmaceuticals Merck Sharp and Dohme, Nihon Mediphysics, and Sanofi; receiving research support from Astellas, Daiichi Sankyo, Kissei, Nihon Kayaku, Ono, Sanofi, Taiho, and Takeda; and serving on the speakers bureau for Astellas, Bayer, Janssen Pharmaceuticals, Pfizer, Sanofi, Merck Sharp and Dohme, and Takeda outside the submitted work. Mr Klingbiel reported being employed by and owning stock in Roche outside the submitted work. Dr Gillessen reported serving on the advisory boards of Advanced Accelerator Applications, Active Biotech, Astellas, Bayer, Bristol Myers Squibb, Clovis, Curevac, Dendreon, Ferring, Innocrin, Janssen Cilag, MaxiVAX, Millennium Pharmaceuticals, Orion, Roche, and Sanofi with compensation; serving on the advisory boards of Astellas Pharma, Bayer, Essa Pharmaceuticals, Nectar, ProteoMediX, and Sanofi without compensation; serving on the speakers bureaus of Janssen Pharmaceuticals and Novartis with compensation; serving on the speakers bureaus of Astellas, Janssen Pharmaceuticals, and Sanofi without compensation; receiving fees to the institution from Astellas, Janssen Pharmaceuticals, Innocrin, Bayer, Clovis Oncology, Menarini Silicon Biosystems, Tolero Pharmaceuticals, and ProteoMediX; and receiving personal fees from Janssen Pharmaceuticals Advanced Accelerator Applications, Roche, Sanofi, and Orion Pharma outside the submitted work; in addition, Dr Gillessen reporting holding a patent to biomarker WO 3752009138392 issued. No other disclosures were reported.

Meeting Presentation: Preliminary data from this study were presented as a poster at the ESMO 2018 Congress; October 19-23, 2018; Munich, Germany.

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Corresponding author.

PMCID: PMC7593810 PMID: 33112397

Key Points

Question

Is there a role for platinum-based treatment in molecularly selected patients with advanced prostate cancer?

Findings

In a case series of 508 patients, platinum-based therapy was associated with antitumor activity, especially among patients with known DNA repair gene aberrations. In patients with DNA repair gene aberrations, nearly half had a decrease in prostate-specific antigen levels of at least 50% and experienced soft tissue responses.

Meaning

In patients with prostate cancer and DNA repair gene aberrations, platinum-based therapy may be considered a treatment option.

This case series characterizes the antitumor activity of platinum-based therapies in men with castration-resistant prostate cancer with or without DNA repair gene alterations.

Abstract

Importance

DNA repair gene aberrations occur in 20% to 30% of patients with castration-resistant prostate cancer (CRPC), and some of these aberrations have been associated with sensitivity to poly(ADP-ribose) polymerase (PARP) inhibition platinum-based treatments. However, previous trials assessing platinum-based treatments in patients with CRPC have mostly included a biomarker-unselected population; therefore, efficacy in these patients is unknown.

Objective

To characterize the antitumor activity of platinum-based therapies in men with CRPC with or without DNA repair gene alterations.

Design, Setting, and Participants

In this case series, data from 508 patients with CRPC treated with platinum-based therapy were collected from 25 academic centers from 12 countries worldwide. Patients were grouped by status of DNA repair gene aberrations (ie, cohort 1, present; cohort 2, not detected; and cohort 3, not tested). Data were collected from January 1986 to December 2018. Data analysis was performed in 2019, with data closure in April 2019.

Exposure

Treatment with platinum-based compounds either as monotherapy or combination therapy.

Main Outcomes and Measures

The primary end points were as follows: (1) antitumor activity of platinum-based therapy, defined as a decrease in prostate-specific antigen (PSA) level of at least 50% and/or radiological soft tissue response in patients with measurable disease and (2) the association of response with the presence or absence of DNA repair gene aberrations.

Results

A total of 508 men with a median (range) age of 61 (27-88) years were included in this analysis. DNA repair gene aberrations were present in 80 patients (14.7%; cohort 1), absent in 98 (19.3%; cohort 2), and not tested in 330 (65.0%; cohort 3). Of 408 patients who received platinum-based combination therapy, 338 patients (82.8%) received docetaxel, paclitaxel, or etoposide, and 70 (17.2%) received platinum-based combination treatment with another partner. A PSA level decrease of at least 50% was seen in 33 patients (47.1%) in cohort 1 and 26 (36.1%) in cohort 2 (P = .20). In evaluable patients, soft tissue responses were documented in 28 of 58 patients (48.3%) in cohort 1 and 21 of 67 (31.3%) in cohort 2 (P = .07). In the subgroup of 44 patients with BRCA2 gene alterations, PSA level decreases of at least 50% were documented in 23 patients (63.9%) and soft tissue responses in 17 of 34 patients (50.0%) with evaluable disease. In cohort 3, PSA level decreases of at least 50% and soft tissue responses were documented in 81 of 284 patients (28.5%) and 38 of 185 patients (20.5%) with evaluable disease, respectively.

Conclusions and Relevance

In this study, platinum-based treatment was associated with relevant antitumor activity in a biomarker-positive population of patients with advanced prostate cancer with DNA repair gene aberrations. The findings of this study suggest that platinum-based treatment may be considered an option for these patients.

Introduction

Despite significant progress in drug development for advanced prostate cancer patients in the past decade, new active compounds, ideally for molecularly selected patients, are urgently needed.^1,2 Platinum-based compounds have been evaluated in clinical trials and used clinically as monotherapy or in combination with other chemotherapy agents mainly in the setting of castration-resistant disease but also in hormone-sensitive disease.^3,4 A phase 3 clinical trial of satraplatin compared with prednisone⁵ demonstrated an improvement in progression-free survival and pain control, but no overall survival benefit was seen in unselected patients.

Platinum chemotherapy activity has been associated with its ability to crosslink with purine bases in DNA, interfering with DNA repair mechanisms and causing DNA damage and apoptosis. In various cancer types, responses are enhanced in the presence of underlying double-strand DNA repair alterations in the tumor, resulting in synthetic lethality.⁶ In triple-negative breast cancer (TNBC), carboplatin is highly effective in patients with known BRCA1 (OMIM 113705) and BRCA2 (OMIM 600185) tumors,⁷ and 2 phase 3 trials have shown benefit of poly(ADP-ribose) polymerase (PARP) inhibitors in patients with TNBC and germline BRCA variations.⁸ The role of these agents in an unselected TBNC population is controversial; however, there is evidence that some patients with variations in homologous recombination genes other than BRCA1 and BRCA1 (germline or somatic) can derive benefit from platinum-based treatment.⁹ On the other hand, alterations in other non–homologous recombination DNA damage response genes, such as PTEN (OMIM 601728), are not associated with response to the same extent.⁹

Genomic aberrations that impair DNA repair genes occur at a frequency of up to 20% to 30% in advanced prostate cancer.^10,11,12 Some of these aberrations, which can either be found as germline or somatic alterations in homologous recombination DNA repair genes or DNA damage checkpoints, have been associated with sensitivity to platinum compounds and/or PARP inhibition in preclinical studies and in clinical trials.^{13,14,15,16,17}

Three published case series,^18,19,20 which included a total of 14 patients with metastatic prostate cancer with DNA repair gene aberrations treated with platinum-based chemotherapy, reported encouraging antitumor activity. The recently presented prospective phase 3 PROFOUND study evaluating the PARP-inhibitor olaparib in molecularly selected patients with advanced prostate cancer harboring DNA repair gene aberrations has shown a significant benefit in radiographic progression-free survival and overall response rate for olaparib compared with the sequential use of abiraterone or enzalutamide, thereby strengthening the previously reported findings of the TOPARP study.^21,22,23 Data from these trials suggest higher antitumor activity in patients with BRCA2 alterations.²²

Through the collaborative efforts of an international consortium, we identified a large series of patients with castration-resistant prostate cancer (CRPC) who were treated with platinum-based chemotherapy. Using these data, we performed a retrospective analysis to characterize the antitumor activity (ie, decrease in prostate-specific antigen [PSA] level, radiographic response, and time receiving treatment) of platinum-based therapies (monotherapy and/or combination) in men with CRPC with or without DNA repair gene alterations.

Methods

Patients

Patients with biochemically or histologically confirmed advanced prostate cancer (metastatic or locally advanced and not amenable to locoregional treatment with curative intent) treated with a platinum compound (cisplatin or carboplatin) either as monotherapy or as part of combination chemotherapy were eligible for this analysis. Patients with primary pure small cell carcinoma of the prostate or insufficient data for analysis of the primary end point were excluded. Clinical data from 25 cancer centers from 12 countries worldwide were collected by local investigators. Investigators were encouraged to include all patients eligible at their site for the analysis. Approval of the local ethics committee was obtained before data collection, and informed consent was obtained depending on local regulations. Clinical data were collected locally at each center and assembled in an electronic master database at the coordinating center. Quality control was assured by queries in cases of nonplausible data and inconsistencies; however, no review of the source documentation was performed. The the reporting guideline for case series was followed.²⁴

The primary outcome measure was evaluation of antitumor activity (decrease in PSA level and soft tissue response) to platinum-based therapy (monotherapy and/or combination therapies) and association of response with the presence or absence of DNA repair gene aberrations in patients with advanced prostate cancer. Local assays for assessment of DNA repair gene aberrations on tumor tissue or circulating DNA (ctDNA) were used. DNA repair gene alterations were defined as deleterious variations, such as protein truncating variations, splice site variations, deleterious missense variation, and homozygous deletions, in genes involved in the repair of DNA damage.

The decrease in PSA level is reported as per Prostate Cancer Working Group Criteria,²⁵ with percentage change from baseline (increase or decrease) at 12 weeks and, separately, the maximal change (increase or decrease) at any time using a waterfall plot. Clinically significant PSA changes are defined as decreases of at least 50%. Soft tissue response was defined according to the Response Evaluation Criteria in the Solid Tumors guidelines version 1.1, with response being defined as an at least 30% decrease in the sum of the longest diameter of all target lesions (maximum of 2 lesions per organ and 5 lesions total), taking the baseline sum as reference. Tumor assessments were performed by local investigators. Time on platinum-based treatment was defined as time from start of platinum-based treatment to progression (defined as the end of treatment for clinical or radiological progressive disease or other reasons) or death; overall survival (OS) was defined as time from start of platinum-based treatment to death or last contact. Patients not experiencing an event were censored at the time of data cutoff (ie, September 24, 2019) or at last contact.

Statistical Analysis

Continuous data were summarized by median, minimum, and maximum values. Categorical data were presented as absolute numbers and percentages. Time to event end points were assessed by the Kaplan-Meier method and are presented as median and interquartile range (IQR). The number of missing data points is given for all analyses. Frequency counts of categorical data in subgroups were statistically compared by Fisher exact tests. Between subgroup comparisons of numerical data were carried out by Kruskal-Wallis tests. Time to event end points were compared between subgroups using the log-rank test. The a priori significance level was P < .05, and all statistical tests were 2 sided. All analyses were done in R version 3.5.0 (R Project for Statistical Computing).

To simultaneously assess several factors that could be associated with OS, we performed a multivariable analysis using a Cox proportional hazards model (SAS version 9.4 [SAS Institute]), including clinically relevant and established prognostic factors, ie, age, presence of visceral metastases, presence or absence of DNA repair gene aberrations, treatment line, and type of platinum-based treatment (combination vs monotherapy) as independent variables.

Results

A total of 508 men who were diagnosed with prostate cancer between 1986 and 2018 were included in the study (median [range] age, 61 [37-88 ] years; baseline median [range] PSA level, 18.5 ng/mL [0.7-7577 ng/mL] [to convert to micrograms per liter, multiply by 1.0]). Overall, 216 (42.5%) had de novo metastatic disease at diagnosis and treated with platinum-based chemotherapy between 1999 and 2019. A total of 178 patients (35.0%) had molecular profiling, with DNA repair gene aberrations detected in 80 patients (15.7%; cohort 1) and no aberrations detected in 98 patients (19.3%; cohort 2). In 330 patients (65.0%), tumor genomic profiling was not performed (cohort 3) (Figure 1).

Patients with known DNA repair gene aberrations, compared with patients without DNA repair gene aberrations, had higher median (range) PSA levels at diagnosis (33.0 [2.1-1759.0] ng/mL vs 17.5 [1.1-1530.0] ng/mL, P = .20), higher rates of de novo metastatic disease (42 [52.5%] vs 40 [40.8%], P = .10) (eTable 1 in the Supplement), and a shorter median (IQR) time from diagnosis of CRPC to start of platinum-based treatment (32.7 [11.8-80.6] months vs 52.5 [20.4-89.2] months; P = .06), although none of the differences were statistically significant. Nearly 70% of patients (341 [67.1%]) had received at least 1 prior line of systemic therapy before platinum-based chemotherapy was started. Of note, a high percentage of patients with visceral metastases (cohort 1, 44 [55.0%]; cohort 2, 57 [58.2%]) at the start of platinum-based therapy were included.

DNA repair gene aberrations were detected by various methods: 27 patients (33.8%), fresh biopsy material; 24 (30.0%), archival tissue; 22 (27.5%), ctDNA; and 7 (8.8%), unknown methods. The most common aberrations included alterations in BRCA2 (44 [55.0%]), ATM (OMIM 607585; 12 [15.0%]), and BRCA1 (3 [3.8%]). These were somatic alterations in 57 patients (71.3%). Germline alterations were found in 23 patients (28.8%) and were mainly BRCA2 (17 [73.9%]), BRCA1 (2 [8.7%]), and ATM (3 [13.0%]). Baseline characteristics depending on type of DNA repair gene aberration are summarized in eTable 2 in the Supplement.

Platinum-based therapy was given as first-line CRPC treatment in 167 patients (32.8%), second-line treatment in 145 patients (28.5%), and third-line treatment in 68 patients (13.4%) (Table 1). The percentage of patients receiving first-line platinum treatment was comparable between all cohorts, and in most cases, combination therapy was chosen (139 [83.2%]). Most patients (408 [80.3%]) received a platinum-combination treatment. Combination chemotherapy drugs used included docetaxel (180 [44.1%]), etoposide (92 [22.5%]), and paclitaxel (66 [16.2%]). Only 100 patients (19.7%) were treated with platinum-based monotherapy (88 [88.0%] with carboplatin); however, the proportion was higher in cohort 1 compared with cohort 2 (31 [38.8%] vs 11 [11.2%]; P < .001).

Table 1. Characteristics of Study Participants at Start of Platinum-Based Chemotherapy.

Characteristic	Patients, No. (%)			P value
Characteristic	Cohort 1, with DNA repair gene aberrations(n = 80)	Cohort 2, no DNA repair gene aberrations (n = 98)	Cohort 3, not assessed (n = 330)	All cohorts	Cohorts 1 vs 2
Baseline characteristics at start of platinum therapy
Age, median (range), y	65 (38-81)	67 (49-86)	67 (42-90)	.006	.02
Missing. No.	0	0	2	.006	.02
PSA level, median (range), ng/mL	120 (0.02-4124)	90.2 (0.05-3030)	136.6 (0.01-9145)	.04	.05
Missing, No.	5	14	16	.04	.05
Alkaline phosphatase level, median (range), U/L	161.5 (44-1661)	159 (30-1260)	140 (12-3870)	.50	.50
Missing, No.	10	15	75	.50	.50
Lactate dehydrogenase level, median (range), U/L	327 (12-2680)	282.5 (9-6714)	330.5 (131-5432)	.20	.30
Missing, No.	18	24	154	.20	.30
Hemoglobin leve, median (range)l, g/dL	11.0 (7.0-15.0)	10.9 (7.5-15.0)	10.9 (6.0-15.6)	.80	.90
Missing, No.	11	13	55	.80	.90
Albumin level, median (range), g/dL	3.4 (1.9-4.3)	3.3 (2.0-4.3)	3.6 (2.0-6.6)	.10	.80
Missing, No.	17	26	125	.10	.80
Opiates
No	26 (41.3)	30 (35.7)	94 (33.3)	.04	.01
Strong opioid	30 (47.6)	35 (41.7)	136 (48.2)
Weak opioid	7 (11.1)	19 (22.6)	52 (18.4)
Missing, No.	17	14	48
Time from diagnosis to platinum based chemotherapy, median (IQR), mo	33 (12-81)	53 (20-89)	65 (28-100)	<.001	.06
Missing, No.	7	0	7	<.001	.06
Distribution of metastases at start of platinum based treatment
Bone metastases	66 (82.5)	89 (90.8)	295 (89.4)	.20	.20
Lymph node metastases	55 (68.8)	55 (56.1)	231 (70)	.02	.09
Visceral metastases	44 (55)	57 (58.2)	173 (52.4)	.70	.80
Missing, No.	1	0	5	NA	NA
Platinum therapy
Platinum monotherapy
Overall	31 (38.8)	11 (11.2)	58 (17.6)	<.001	<.001
Carboplatin, No./total No. (%)	30/31 (96.8)	8/11 (72.7)	50/58 (86.2)
Cisplatin, No./total No. (%)	1/31 (3.2)	3/11 (27.3)	8/58 (13.8)
Platinum combination therapy
Overall	49 (61.3)	87 (88.8)	272 (82.4)	<.001	<.001
Carboplatin, No./total No. (%)	38/49 (77.6)	73/87 (83.9)	252/272 (92.6)
Cisplatin, No./total No. (%)	11/49 (22.4)	14/87 (16.1)	18/272 (6.6)
Oxaliplatin, No./total No. (%)	0	0	2/272 (0.7)
Combination partner
Docetaxel, No./total No. (%)	17/49 (34.7)	24/87 (27.6)	139/272 (51.1)	<.001	.090
Etoposide, No./total No. (%)	13/49 (26.5)	31/87 (35.6)	48/272 (17.6)
Other, No./total No. (%)	16/49 (32.7)	17/87 (19.5)	37/272 (13.6)
Paclitaxel, No./total No. (%)	3/49 (6.1)	15/87 (17.2)	48/272 (17.6)
Prior treatment lines
0	25 (31.2)	36 (36.7)	106 (32.1)	<.001	.80
1	16 (20)	15 (15.3)	114 (34.5)
2	14 (17.5)	18 (18.4)	36 (10.9)
≥3	25 (31.2)	29 (29.6)	74 (22.4)

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Abbreviations: IQR, interquartile range; NA, not applicable; PSA, prostate specific antigen.

SI conversion factors: To convert albumin and hemoglobin to grams per liter, multiply by 10; alkaline phosphatase and lactate dehydrogenase to microkatals per liter, multiply by 0.0167; and PSA to micrograms per liter, multiply by 1.0.

Outcomes of Cohort 1 vs Cohort 2

A PSA level decrease of at least 50% was seen in 33 patients (47.1%) in cohort 1 vs 26 (36.1%) in cohort 2 (P = .20) (Table 2 and Figure 2A). A soft tissue response was seen in 28 patients (48.3%) in cohort 1 vs 21 (31.3%) in cohort 2 (P = .07) (Table 2).

Table 2. Antitumor Activity of Platinum Chemotherapy in Cohorts 1 vs 2 and in Subgroups of Patients With DNA Repair Gene Aberrations.

Outcome	Patients with DNA repair gene aberrations, No. %		P value, cohort 1 vs 2	Patients with DNA repair gene aberrations, No. %				P value, among subgroups
Outcome	Cohort 1, yes (n = 80)	Cohort 2, no (n = 98)	P value, cohort 1 vs 2	BRCA2 (n = 44)	BRCA1 (N = 3)	ATM (N = 12)	Other (N = 21)	P value, among subgroups
PSA level decrease of ≥50% on platinum therapy	33 (47.1)	26 (36.1)	.20	23 (63.9)	0	4 (36.4)	6 (28.6)	.02
Missing, No.	10	26	.20	8	1	1	0	.02
Soft tissue response on platinum therapy	28 (48.3)	21 (31.3)	.07	17 (50.0)	0	2 (28.6)	9 (56.3)	.60
Missing, No.	22	31	.07	10	2	5	5	.60
Time receiving treatment and survival, median (IQR), mo	3.4 (1.6-6)	2.8 (1.7-4.6)	.30	7.1 (3.7-13)	3.2 (0-NA)	4.7 (2.2-10)	2.8 (1.8-NA)	.20
Missing, No.	0	1	.30	0	0	0	0	.20
OS from start of platinum therapy, median (IQR), mo	14 (5.7-34)	9.2 (5.5-19)	.20	15 (10-34)	4.1 (3.8-4.4)	9.3 (6.5-11)	4.9 (3.6-NA)	.04
Missing, No.	0	0	.20	0	0	0	0	.04

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Abbreviations: IQR, interquartile range; OS, overall survival; PSA, prostatic-specific antigen.

Patient groups with different DNA repair gene aberrations had different proportions of PSA level decreases of at least 50% (BRCA2, 23 of 44 [63.9%]; BRCA1, 0 of 3; ATM, 4 of 11 [36.4%]; other, 6 of 21 [28.6%]; P = .02) (Figure 2C); however, no significant difference in soft tissue responses was observed, irrespective of type of DNA repair gene aberration (Table 2). In the 12 patients with ATM alterations, a PSA decline of at least 50% was documented in 4 patients (33.3%) and a soft tissue response in 2 of 7 patients (28.6%) with evaluable disease.

Median (IQR) treatment duration on platinum-based treatment was 3.0 (1.7-4.6) months without relevant differences between cohorts (Table 2; eFigure 1 in the Supplement). Seven patients (8.8%) with known DNA repair alterations had PARP therapy before platinum treatment. Of these patients, only 1 (14.3%) had a documented PSA decrease of at least 50% on platinum-based chemotherapy.

Median (IQR) OS from start of platinum-based therapy was lower in patients without DNA repair gene aberrations compared with patients with known DNA repair gene aberrations (9.2 [5.5-19.5] months vs 14.1 [5.7-33.7] months), although this did not reach statistical significance (P = .20) (Figure 3; Table 2).

Median OS differed significantly in cohorts with different DNA repair gene alterations; namely, median (IQR) OS from start of platinum-based therapy was 15.2 (9.9-33.7) months in patients with BRCA2 alterations, 9.3 (6.5 to 11.0) months in patients with ATM alterations, 4.1 (3.8 to 4.4) months in patients with BRCA1 alterations, and 4.9 (3.6 to not reached) in patients with other alterations (P = .04) (Table 2; eFigure 2 in the Supplement). In a multivariable Cox regression for OS, only type of platinum-treatment remained significant (hazard ratio, 0.52; 95% CI, 0.31-0.90; P = .01) (eTable 3 in the Supplement).

A total of 31 patients (38.8%) with known DNA repair gene aberrations and 11 patients (11.2%) without DNA repair gene aberrations were treated with platinum monotherapy. In patients with known DNA repair gene aberrations, 10 (32.3%) had a PSA level decrease of at least 50%. Soft tissue response was seen in 14 patients (45.2%) in cohort 1 with measurable disease. Response to monotherapy was lower in patients without DNA repair gene aberrations, with PSA level decreases of at least 50% and soft tissue response in 3 patients (27.3%) (eTable 4 in the Supplement). Median (IQR) OS was 6.4 (3.6-15.2) months in patients with known alterations and 6.7 (3.5-15.2) months in patients without alterations (eFigure 3 in the Supplement).

Overall, 49 patients (61.3%) with known DNA repair gene aberrations and 87 patients (88.8%) without DNA repair gene aberrations were treated with platinum-based combination therapy. In patients with known DNA repair gene aberrations, 23 (46.9%) had a decrease in PSA level of at least 50%. Soft tissue response was seen in 14 patients (28.6%) with measurable disease. Response to combination therapy was again lower in patients without DNA repair gene aberrations, with PSA level decreases of at least 50% in 23 patients (26.4%) and soft tissue response in 18 (20.7%) (eTable 4 in the Supplement). Median (IQR) OS was 15.2 (9.9-33.7) months in patients with known alterations and 9.8 (6.1-19.5) months in patients without alterations (eFigure 3 in the Supplement).

Outcomes in Cohort 3

Patients in cohort 3 (ie, those without genomic profiling) had an overall PSA level decrease of at least 50% in 81 of 284 patients (28.5%) (eFigure 4 in the Supplement); soft tissue response was reported in 38 of 185 (20.5%) with evaluable disease. A total of 58 patients (17.6%) were treated with platinum-based monotherapy and 272 (82.4%) with platinum-based combination therapy, and detailed response data are summarized in eTable 5 in the Supplement.

Median (IQR) treatment duration on platinum-based treatment was 3.0 (1.7-4.6) months and comparable with cohorts 1 and 2 (eFigure 5 in the Supplement). Median (IQR) OS from start of platinum therapy was 10.0 (5.7-17.7) months (eFigure 6 in the Supplement).

Discussion

In this multicenter retrospective analysis of 508 patients with CRPC, most of whom had received at least 1 prior line of therapy, we found encouraging antitumor activity for treatment with platinum-based therapies in the cohort of patients with tumors harboring DNA repair gene aberrations. Although we observed numerically higher rates of PSA level decreases and soft tissue responses in patients with DNA repair gene aberrations compared with those without, there was no statistically significant difference and no OS benefit. In the subgroup of 44 patients with BRCA2 gene alterations, PSA level decreases of at least 50% were documented in 23 patients (63.9%) and soft tissue responses in 17 patients (38.6%) with evaluable disease. This series is unique because it is among the largest to date that evaluates patients with identified DNA repair gene aberrations who received a platinum-based chemotherapy, very few of whom had previously received treatment with a PARP inhibitor because use of these agents outside of clinical trials was very limited.

Historically, platinum compounds as monotherapy or combination therapy have been widely studied in prostate cancer.²⁶ Besides the SPARC trial,⁵ the studies were mostly small, recruited a molecularly unselected patient population, and demonstrated only moderate antitumor activity. However, a subgroup of patients seemed to derive benefit,³ namely patients with aggressive variant adenocarcinoma of the prostate (with alterations in at least 2 of the following: TP53 [OMIM 191170], RB1 [OMIM 614041], and PTEN, detected by next-generation sequencing or immunohistochemistry).²⁷ With emerging data of a meaningful prevalence of somatic and germline DNA repair gene aberrations in patients with advanced prostate cancer²⁸ and activity of PARP inhibitors in these patients,¹² interest in platinum-based treatment arose again, with the hypothesis of increased activity in this specific subpopulation of patients with prostate cancer, analogous to data from patients with TNBC. Generally, combination treatment should be recommended; however, monotherapy remains an option, and there is expert consensus from the 2019 advanced prostate cancer consensus conference for carboplatin with target area under the curve (AUC) of 5 to 6 every 3 weeks as a preferred regimen.³³

Response to platinum-based monotherapy in patients with DNA repair gene aberrations in our cohort was comparable with the recently presented trials of PARP monotherapy. In the phase 2 TOPARP-B trial assessing 2 different dosing levels of olaparib in patients with DNA repair alterations,²¹ olaparib at 400 mg and 300 mg was associated with soft tissue response of 24.2% and 16.2% of patients, respectively, and a PSA level decrease of at least 50% in 37.0% and 30.2%, respectively. This is in line with the overall response rate of 43.9% with rucaparib in patients with measurable disease in the phase 2 TRITON trial.²⁹ Even more importantly, the PROFOUND trial, evaluating olaparib vs physician’s choice of enzalutamide or abiraterone in patients with CRPC and known DNA repair gene aberrations progressing on prior new hormonal agent, demonstrated a median OS of 18.5 months with olaparib in the total population, and an objective response rate of 33% was reported for patients with BRCA1, BRCA2, or ATM alterations.^22,23 Olaparib and rucaparib were approved by the US Food and Drug Administration in May 2020 for patients with advanced prostate cancer and germline or somatic homologous recombination repair gene mutations (rucaparib only for BRCA1 or BRCA2).

Response to platinum-based combination treatment in our cohort was more favorable than platinum-based monotherapy, and in most cases, a taxane was chosen as the combination partner, which represents the current standard-of-care chemotherapy in the unselected advanced prostate cancer population. However, it seems that in our data set monotherapy was more often used in patients with known DNA repair gene aberrations, whereas in patients without alterations or unknown molecular status, combination therapy was preferred. Taxanes are widely used in advanced prostate cancer in different treatment settings and the combination of carboplatin and paclitaxel as first-line, second-line, or third-line chemotherapy in patients with CRPC. In 2019, Castro et al³⁰ presented the results of a prospective cohort study investigating the association of germline DNA repair gene aberrations with CRPC outcomes. In their cohort, response to taxanes was not different between variation carriers and noncarriers; however, duration of response was shorter in carriers, and treatment sequencing seemed to be of importance.^30,31 Therefore, activity of the taxane component has to be taken into some account when interpreting our efficacy data in patients receiving combination treatment.

Our results showed consistently higher response rates of platinum-based treatment in molecularly selected patients, even though these patients often received platinum-based monotherapy, which seems to be less active than combination therapy overall. Subgroups for specific types of DNA repair gene aberrations were too small to draw any definitive conclusions, but the response rate (PSA decrease and objective response rate) in patients with BRCA2 alterations was encouraging. These results are in line with the PROFOUND results, in which treatment benefit was more pronounced in patients with BRCA1, BRCA2, and ATM alterations compared with alterations in other gene alterations.²² In the exploratory analysis of gene-by-gene radiographic progression-free survival, benefit in patients with BRCA1 and ATM alterations was less pronounced compared with patients with BRCA2 alterations. In the TRITON phase 2 trial, evaluating rucaparib in patients with DNA repair gene aberrations, radiographic and PSA responses were observed in only 2 of 19 patients (10.5%) with exclusively ATM alterations.³² The antitumor activity of platinum compounds in our small cohort of 12 patients with ATM alterations is noteworthy. Overall, different DNA repair gene aberrations are most likely distinct entities with varying responses to platinum as well as PARP inhibition; therefore, they cannot be collectively addressed. More research with prospective trials in molecular subgroups is needed to better characterize which patients might derive benefit.

Importantly, the activity of platinum-based treatment was also seen in the unselected cohort 3 (ie, patients were not tested for DNA repair gene aberrations). This population is possibly most reflective of the general CRPC population seen in many centers around the world, where testing for DNA repair gene aberrations may not be available in daily clinical practice.

Limitations

Our analysis has several limitations, including the retrospective design and data collection, including missing data in a subset of patients. Furthermore, even though quality control was assured by the coordinating center by queries in the case of nonplausible or inconsistent data, no formal review process of the source documentation of each individual contributing center was performed. Also, there was no control of patients excluded from the database on the center level. The bias was minimized by including all patients treated with a platinum-based chemotherapy and not only patients with known DNA repair gene alteration. Radiographic responses (ie, soft tissue response) were assessed retrospectively by local investigators. Patient selection is also an important limitation because the use of a platinum-based chemotherapy, especially in the first-line CRPC setting, could reflect the availability of treatment options; clinical factors, such as the high rate of de novo metastatic disease; and the presence of visceral metastases and/or molecular features. DNA repair gene aberrations were assessed by local assays and were not standardized; therefore, the number of genes tested differed by center. Many patients received platinum-taxane combination treatment and the contribution of taxane and platinum to the response cannot be measured separately. The high number of first-line platinum-based combination treatments suggests that patients with aggressive features were included; of note, we excluded patients with de novo pure small cell carcinoma from the analysis. Molecular profiling was performed in only 178 patients, of whom 80 had a defect (cohort 1) and 98 patients did not (cohort 2). However, the remaining 330 patients (cohort 3) most likely represent a mixed population, including perhaps some patients with DNA repair gene aberrations, and therefore, the results of this cohort have to be interpreted with caution. Currently, several prospective phase 2 trials (randomized and nonrandomized) evaluating carboplatin alone or in combination with docetaxel in molecularly selected patients with CRPC are recruiting.^34,35,36,37

Conclusions

In this multicenter international case series, platinum-based treatment was associated with promising activity in a biomarker-preselected population of patients with CRPC and DNA repair gene aberrations. These results need prospective validation, which hopefully will be provided from the currently recruiting trials in molecularly selected prostate cancer populations. Based on our analysis, platinum-containing therapy should be considered in patients with DNA repair gene aberrations, especially if access to a PARP inhibitor is not available.

Supplement.

eTable 1. Baseline Characteristics for All Cohorts

eTable 2. Baseline Characteristics, by DNA Repair Defect

eFigure 1. Median Treatment Duration, Cohort 1 vs 2

eFigure 2. OS by DNA Repair Alteration

eTable 3. Multivariable Analysis OS, Cohort 1 and 2

eTable 4. Antitumour Activity of Platinum-Based Combination vs Monotherapy, Cohort 1 and 2

eFigure 3. OS of Combination vs Monotherapy, Cohort 1 vs 2

eFigure 4. Waterfall Plot of PSA Decline, Cohort 3

eTable 5. Antitumour Activity of Platinum-Based Combination vs Monotherapy, Cohort 3

eFigure 5. Median Treatment Duration, All Cohorts

eFigure 6. Median OS, All Cohorts

Click here for additional data file.^{(1.7MB, pdf)}

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35.National Library of Medicine BRcA deficient prostate cancer treated with carboplatin or docetaxel (BRACeD). Updated August 7, 2020. Accessed September 29, 2020. https://clinicaltrials.gov/ct2/show/NCT04038502?term=NCT04038502&draw=2&rank=1
36.National Library of Medicine Docetaxel and carboplatin in treating patients with metastatic, castration resistant prostate cancer containing inactivated genes in the BRCA 1/2 pathway. Updated June 16, 2020. Accessed September 29, 2020. https://clinicaltrials.gov/ct2/show/NCT02598895?term=NCT02598895&draw=2&rank=1
37.National Library of Medicine Trial evaluating the efficacy of carboplatin in metastatic prostate cancer with gene alterations in the homologous recombination pathway (PRO-CARBO). Updated February 17, 2020. Accessed September 29, 2020. https://clinicaltrials.gov/ct2/show/NCT03652493?term=NCT03652493&draw=2&rank=1

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplement.

eTable 1. Baseline Characteristics for All Cohorts

eTable 2. Baseline Characteristics, by DNA Repair Defect

eFigure 1. Median Treatment Duration, Cohort 1 vs 2

eFigure 2. OS by DNA Repair Alteration

eTable 3. Multivariable Analysis OS, Cohort 1 and 2

eTable 4. Antitumour Activity of Platinum-Based Combination vs Monotherapy, Cohort 1 and 2

eFigure 3. OS of Combination vs Monotherapy, Cohort 1 vs 2

eFigure 4. Waterfall Plot of PSA Decline, Cohort 3

eTable 5. Antitumour Activity of Platinum-Based Combination vs Monotherapy, Cohort 3

eFigure 5. Median Treatment Duration, All Cohorts

eFigure 6. Median OS, All Cohorts

Click here for additional data file.^{(1.7MB, pdf)}

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PERMALINK

Activity of Platinum-Based Chemotherapy in Patients With Advanced Prostate Cancer With and Without DNA Repair Gene Aberrations

Sabine Schmid, MD

Aurelius Omlin, MD

Celestia Higano, MD

Christopher Sweeney, MD

Nieves Martinez Chanza, MD

Niven Mehra, MD

Malou C P Kuppen, MD

Himisha Beltran, MD

Vincenza Condeduca, MD

Daniel Vargas Pivato de Almeida, MD

Fernando Cotait Maluf, MD

William K Oh, MD

Che-Kai Tsao, MD

Oliver Sartor, MD

Elisa Ledet, MD

Giuseppe Di Lorenzo, MD

Steven M Yip, MD

Kim N Chi, MD

Diletta Bianchini, MD

Ugo De Giorgi, MD

Aaron R Hansen, MD

Tomasz M Beer, MD

Lavaud Pernelle, MD

Rafael Morales-Barrera, MD

Marcello Tucci, MD

Elena Castro, MD

Kostas Karalis, MD

Andries M Bergman, MD

Mo Linh Le, MD

Ursina Zürrer-Härdi, MD

Carmel Pezaro, MD

Hiroyoshi Suzuki, MD

Andrea Zivi, MD

Dirk Klingbiel, PhD

Sämi Schär, PhD

Silke Gillessen, MD

Key Points

Question

Findings

Meaning

Abstract

Importance

Objective

Design, Setting, and Participants

Exposure

Main Outcomes and Measures

Results

Conclusions and Relevance

Introduction

Methods

Patients

Statistical Analysis

Results

Figure 1. Study Flow Diagram.

Table 1. Characteristics of Study Participants at Start of Platinum-Based Chemotherapy.

Outcomes of Cohort 1 vs Cohort 2

Table 2. Antitumor Activity of Platinum Chemotherapy in Cohorts 1 vs 2 and in Subgroups of Patients With DNA Repair Gene Aberrations.

Figure 2. Prostate-Specific Antigen (PSA) Level Changes From Baseline to Week 12 and Maximal PSA Change to Any Time Point.

Figure 3. Overall Survival Among Patients With and Without DNA Repair Gene Aberrations Receiving Platinum-Based Therapy.

Outcomes in Cohort 3

Discussion

Limitations

Conclusions

References

Associated Data

Supplementary Materials

ACTIONS

PERMALINK

RESOURCES

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