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Biochemical Recurrence Surrogacy for Clinical Outcomes After Radiotherapy for Adenocarcinoma of the Prostate

PURPOSE: The surrogacy of biochemical recurrence (BCR) for overall survival (OS) in localized prostate cancer remains controversial. Herein, we evaluate the surrogacy of BCR using different surrogacy analytic methods. MATERIALS AND METHODS: Individual patient data from 11 trials evaluating radiother...

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Autores principales: Roy, Soumyajit, Romero, Tahmineh, Michalski, Jeff M., Feng, Felix Y., Efstathiou, Jason A., Lawton, Colleen A.F., Bolla, Michel, Maingon, Philippe, de Reijke, Theo, Joseph, David, Ong, Wee Loon, Sydes, Matthew R., Dearnaley, David P., Tree, Alison C., Carrier, Nathalie, Nabid, Abdenour, Souhami, Luis, Incrocci, Luca, Heemsbergen, Wilma D., Pos, Floris J., Zapatero, Almudena, Guerrero, Araceli, Alvarez, Ana, San-Segundo, Carmen Gonzalez, Maldonado, Xavier, Reiter, Robert E., Rettig, Matthew B., Nickols, Nicholas G., Steinberg, Michael L., Valle, Luca F., Ma, T. Martin, Farrell, Matthew J., Neilsen, Beth K., Juarez, Jesus E., Deng, Jie, Vangala, Sitaram, Avril, Norbert, Jia, Angela Y., Zaorsky, Nicholas G., Sun, Yilun, Spratt, Daniel, Kishan, Amar U.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10642893/
https://www.ncbi.nlm.nih.gov/pubmed/37639648
http://dx.doi.org/10.1200/JCO.23.00617
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author Roy, Soumyajit
Romero, Tahmineh
Michalski, Jeff M.
Feng, Felix Y.
Efstathiou, Jason A.
Lawton, Colleen A.F.
Bolla, Michel
Maingon, Philippe
de Reijke, Theo
Joseph, David
Ong, Wee Loon
Sydes, Matthew R.
Dearnaley, David P.
Tree, Alison C.
Carrier, Nathalie
Nabid, Abdenour
Souhami, Luis
Incrocci, Luca
Heemsbergen, Wilma D.
Pos, Floris J.
Zapatero, Almudena
Guerrero, Araceli
Alvarez, Ana
San-Segundo, Carmen Gonzalez
Maldonado, Xavier
Reiter, Robert E.
Rettig, Matthew B.
Nickols, Nicholas G.
Steinberg, Michael L.
Valle, Luca F.
Ma, T. Martin
Farrell, Matthew J.
Neilsen, Beth K.
Juarez, Jesus E.
Deng, Jie
Vangala, Sitaram
Avril, Norbert
Jia, Angela Y.
Zaorsky, Nicholas G.
Sun, Yilun
Spratt, Daniel
Kishan, Amar U.
author_facet Roy, Soumyajit
Romero, Tahmineh
Michalski, Jeff M.
Feng, Felix Y.
Efstathiou, Jason A.
Lawton, Colleen A.F.
Bolla, Michel
Maingon, Philippe
de Reijke, Theo
Joseph, David
Ong, Wee Loon
Sydes, Matthew R.
Dearnaley, David P.
Tree, Alison C.
Carrier, Nathalie
Nabid, Abdenour
Souhami, Luis
Incrocci, Luca
Heemsbergen, Wilma D.
Pos, Floris J.
Zapatero, Almudena
Guerrero, Araceli
Alvarez, Ana
San-Segundo, Carmen Gonzalez
Maldonado, Xavier
Reiter, Robert E.
Rettig, Matthew B.
Nickols, Nicholas G.
Steinberg, Michael L.
Valle, Luca F.
Ma, T. Martin
Farrell, Matthew J.
Neilsen, Beth K.
Juarez, Jesus E.
Deng, Jie
Vangala, Sitaram
Avril, Norbert
Jia, Angela Y.
Zaorsky, Nicholas G.
Sun, Yilun
Spratt, Daniel
Kishan, Amar U.
author_sort Roy, Soumyajit
collection PubMed
description PURPOSE: The surrogacy of biochemical recurrence (BCR) for overall survival (OS) in localized prostate cancer remains controversial. Herein, we evaluate the surrogacy of BCR using different surrogacy analytic methods. MATERIALS AND METHODS: Individual patient data from 11 trials evaluating radiotherapy dose escalation, androgen deprivation therapy (ADT) use, and ADT prolongation were obtained. Surrogate candidacy was assessed using the Prentice criteria (including landmark analyses) and the two-stage meta-analytic approach (estimating Kendall's tau and the R(2)). Biochemical recurrence-free survival (BCRFS, time from random assignment to BCR or any death) and time to BCR (TTBCR, time from random assignment to BCR or cancer-specific deaths censoring for noncancer-related deaths) were assessed. RESULTS: Overall, 10,741 patients were included. Dose escalation, addition of short-term ADT, and prolongation of ADT duration significantly improved BCR (hazard ratio [HR], 0.71 [95% CI, 0.63 to 0.79]; HR, 0.53 [95% CI, 0.48 to 0.59]; and HR, 0.54 [95% CI, 0.48 to 0.61], respectively). Adding short-term ADT (HR, 0.91 [95% CI, 0.84 to 0.99]) and prolonging ADT (HR, 0.86 [95% CI, 0.78 to 0.94]) significantly improved OS, whereas dose escalation did not (HR, 0.98 [95% CI, 0.87 to 1.11]). BCR at 48 months was associated with inferior OS in all three groups (HR, 2.46 [95% CI, 2.08 to 2.92]; HR, 1.51 [95% CI, 1.35 to 1.70]; and HR, 2.31 [95% CI, 2.04 to 2.61], respectively). However, after adjusting for BCR at 48 months, there was no significant treatment effect on OS (HR, 1.10 [95% CI, 0.96 to 1.27]; HR, 0.96 [95% CI, 0.87 to 1.06] and 1.00 [95% CI, 0.90 to 1.12], respectively). The patient-level correlation (Kendall's tau) for BCRFS and OS ranged between 0.59 and 0.69, and that for TTBCR and OS ranged between 0.23 and 0.41. The R(2) values for trial-level correlation of the treatment effect on BCRFS and TTBCR with that on OS were 0.563 and 0.160, respectively. CONCLUSION: BCRFS and TTBCR are prognostic but failed to satisfy all surrogacy criteria. Strength of correlation was greater when noncancer-related deaths were considered events.
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spelling pubmed-106428932023-11-15 Biochemical Recurrence Surrogacy for Clinical Outcomes After Radiotherapy for Adenocarcinoma of the Prostate Roy, Soumyajit Romero, Tahmineh Michalski, Jeff M. Feng, Felix Y. Efstathiou, Jason A. Lawton, Colleen A.F. Bolla, Michel Maingon, Philippe de Reijke, Theo Joseph, David Ong, Wee Loon Sydes, Matthew R. Dearnaley, David P. Tree, Alison C. Carrier, Nathalie Nabid, Abdenour Souhami, Luis Incrocci, Luca Heemsbergen, Wilma D. Pos, Floris J. Zapatero, Almudena Guerrero, Araceli Alvarez, Ana San-Segundo, Carmen Gonzalez Maldonado, Xavier Reiter, Robert E. Rettig, Matthew B. Nickols, Nicholas G. Steinberg, Michael L. Valle, Luca F. Ma, T. Martin Farrell, Matthew J. Neilsen, Beth K. Juarez, Jesus E. Deng, Jie Vangala, Sitaram Avril, Norbert Jia, Angela Y. Zaorsky, Nicholas G. Sun, Yilun Spratt, Daniel Kishan, Amar U. J Clin Oncol ORIGINAL REPORTS PURPOSE: The surrogacy of biochemical recurrence (BCR) for overall survival (OS) in localized prostate cancer remains controversial. Herein, we evaluate the surrogacy of BCR using different surrogacy analytic methods. MATERIALS AND METHODS: Individual patient data from 11 trials evaluating radiotherapy dose escalation, androgen deprivation therapy (ADT) use, and ADT prolongation were obtained. Surrogate candidacy was assessed using the Prentice criteria (including landmark analyses) and the two-stage meta-analytic approach (estimating Kendall's tau and the R(2)). Biochemical recurrence-free survival (BCRFS, time from random assignment to BCR or any death) and time to BCR (TTBCR, time from random assignment to BCR or cancer-specific deaths censoring for noncancer-related deaths) were assessed. RESULTS: Overall, 10,741 patients were included. Dose escalation, addition of short-term ADT, and prolongation of ADT duration significantly improved BCR (hazard ratio [HR], 0.71 [95% CI, 0.63 to 0.79]; HR, 0.53 [95% CI, 0.48 to 0.59]; and HR, 0.54 [95% CI, 0.48 to 0.61], respectively). Adding short-term ADT (HR, 0.91 [95% CI, 0.84 to 0.99]) and prolonging ADT (HR, 0.86 [95% CI, 0.78 to 0.94]) significantly improved OS, whereas dose escalation did not (HR, 0.98 [95% CI, 0.87 to 1.11]). BCR at 48 months was associated with inferior OS in all three groups (HR, 2.46 [95% CI, 2.08 to 2.92]; HR, 1.51 [95% CI, 1.35 to 1.70]; and HR, 2.31 [95% CI, 2.04 to 2.61], respectively). However, after adjusting for BCR at 48 months, there was no significant treatment effect on OS (HR, 1.10 [95% CI, 0.96 to 1.27]; HR, 0.96 [95% CI, 0.87 to 1.06] and 1.00 [95% CI, 0.90 to 1.12], respectively). The patient-level correlation (Kendall's tau) for BCRFS and OS ranged between 0.59 and 0.69, and that for TTBCR and OS ranged between 0.23 and 0.41. The R(2) values for trial-level correlation of the treatment effect on BCRFS and TTBCR with that on OS were 0.563 and 0.160, respectively. CONCLUSION: BCRFS and TTBCR are prognostic but failed to satisfy all surrogacy criteria. Strength of correlation was greater when noncancer-related deaths were considered events. Wolters Kluwer Health 2023-11-10 2023-08-28 /pmc/articles/PMC10642893/ /pubmed/37639648 http://dx.doi.org/10.1200/JCO.23.00617 Text en © 2023 by American Society of Clinical Oncology https://creativecommons.org/licenses/by/4.0/Licensed under the Creative Commons Attribution 4.0 License: https://creativecommons.org/licenses/by/4.0/
spellingShingle ORIGINAL REPORTS
Roy, Soumyajit
Romero, Tahmineh
Michalski, Jeff M.
Feng, Felix Y.
Efstathiou, Jason A.
Lawton, Colleen A.F.
Bolla, Michel
Maingon, Philippe
de Reijke, Theo
Joseph, David
Ong, Wee Loon
Sydes, Matthew R.
Dearnaley, David P.
Tree, Alison C.
Carrier, Nathalie
Nabid, Abdenour
Souhami, Luis
Incrocci, Luca
Heemsbergen, Wilma D.
Pos, Floris J.
Zapatero, Almudena
Guerrero, Araceli
Alvarez, Ana
San-Segundo, Carmen Gonzalez
Maldonado, Xavier
Reiter, Robert E.
Rettig, Matthew B.
Nickols, Nicholas G.
Steinberg, Michael L.
Valle, Luca F.
Ma, T. Martin
Farrell, Matthew J.
Neilsen, Beth K.
Juarez, Jesus E.
Deng, Jie
Vangala, Sitaram
Avril, Norbert
Jia, Angela Y.
Zaorsky, Nicholas G.
Sun, Yilun
Spratt, Daniel
Kishan, Amar U.
Biochemical Recurrence Surrogacy for Clinical Outcomes After Radiotherapy for Adenocarcinoma of the Prostate
title Biochemical Recurrence Surrogacy for Clinical Outcomes After Radiotherapy for Adenocarcinoma of the Prostate
title_full Biochemical Recurrence Surrogacy for Clinical Outcomes After Radiotherapy for Adenocarcinoma of the Prostate
title_fullStr Biochemical Recurrence Surrogacy for Clinical Outcomes After Radiotherapy for Adenocarcinoma of the Prostate
title_full_unstemmed Biochemical Recurrence Surrogacy for Clinical Outcomes After Radiotherapy for Adenocarcinoma of the Prostate
title_short Biochemical Recurrence Surrogacy for Clinical Outcomes After Radiotherapy for Adenocarcinoma of the Prostate
title_sort biochemical recurrence surrogacy for clinical outcomes after radiotherapy for adenocarcinoma of the prostate
topic ORIGINAL REPORTS
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10642893/
https://www.ncbi.nlm.nih.gov/pubmed/37639648
http://dx.doi.org/10.1200/JCO.23.00617
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