Cargando…

Final results of DIADEM, a phase II study to investigate the efficacy and safety of durvalumab in advanced pretreated malignant pleural mesothelioma

BACKGROUND: Malignant pleural mesothelioma (MPM) is a cancer with a high mortality rate and few therapeutic options. After platinum–pemetrexed combination, no further promising drug seems to be effective. Immune checkpoint inhibitors may have some activity in pretreated patients and no data are avai...

Descripción completa

Detalles Bibliográficos
Autores principales: Canova, S., Ceresoli, G.L., Grosso, F., Zucali, P.A., Gelsomino, F., Pasello, G., Mencoboni, M., Rulli, E., Galli, F., De Simone, I., Carlucci, L., De Angelis, A., Belletti, M., Bonomi, M., D’Aveni, A., Perrino, M., Bono, F., Cortinovis, D.L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9808442/
https://www.ncbi.nlm.nih.gov/pubmed/36463732
http://dx.doi.org/10.1016/j.esmoop.2022.100644
_version_ 1784862944015679488
author Canova, S.
Ceresoli, G.L.
Grosso, F.
Zucali, P.A.
Gelsomino, F.
Pasello, G.
Mencoboni, M.
Rulli, E.
Galli, F.
De Simone, I.
Carlucci, L.
De Angelis, A.
Belletti, M.
Bonomi, M.
D’Aveni, A.
Perrino, M.
Bono, F.
Cortinovis, D.L.
author_facet Canova, S.
Ceresoli, G.L.
Grosso, F.
Zucali, P.A.
Gelsomino, F.
Pasello, G.
Mencoboni, M.
Rulli, E.
Galli, F.
De Simone, I.
Carlucci, L.
De Angelis, A.
Belletti, M.
Bonomi, M.
D’Aveni, A.
Perrino, M.
Bono, F.
Cortinovis, D.L.
author_sort Canova, S.
collection PubMed
description BACKGROUND: Malignant pleural mesothelioma (MPM) is a cancer with a high mortality rate and few therapeutic options. After platinum–pemetrexed combination, no further promising drug seems to be effective. Immune checkpoint inhibitors may have some activity in pretreated patients and no data are available in this population about durvalumab. MATERIALS AND METHODS: DIADEM was a multicenter, open-label, single-arm, phase II trial aimed at evaluating the efficacy and safety of durvalumab. Patients with locally advanced/metastatic MPM who progressed after platinum–pemetrexed chemotherapy were enrolled to receive durvalumab (1500 mg, intravenously Q4W) for 12 months or until evidence of disease progression or unacceptable toxicity. The primary endpoint was the proportion of patients alive and free from progression at 16 weeks (PFS(16wks)) calculated from treatment initiation. Secondary endpoints were progression-free survival, overall survival, overall response rate, and safety. RESULTS: Sixty-nine patients with a median age of 69 years (range 44-82 years) were enrolled; 62 patients (89.9%) had epithelioid histotype. As first-line treatment, all patients received platinum derivatives–pemetrexed combination (60.9% with carboplatin and 39.1% with cisplatin). As of March 2021, the median follow-up was 9.2 months (interquartile range 5.2-11.1 months). Six patients (8.7%) completed the 12-month treatment; 60 patients discontinued, of whom 42 for progressive disease, and 4 died. Seventeen patients (28.3%; 95% confidence interval 17.5% to 41.4%) were alive or free from progression at 16 weeks. Eleven patients (18.6%) had a grade 3 or 4 treatment-related adverse event (AE), and one (1.4%) had a grade ≥3 immune-related, treatment-related AE. There was one drug-related death. CONCLUSION: Durvalumab alone in pretreated non-selected MPM did not reach a meaningful clinical activity, showing any new major safety issue signals.
format Online
Article
Text
id pubmed-9808442
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-98084422023-01-04 Final results of DIADEM, a phase II study to investigate the efficacy and safety of durvalumab in advanced pretreated malignant pleural mesothelioma Canova, S. Ceresoli, G.L. Grosso, F. Zucali, P.A. Gelsomino, F. Pasello, G. Mencoboni, M. Rulli, E. Galli, F. De Simone, I. Carlucci, L. De Angelis, A. Belletti, M. Bonomi, M. D’Aveni, A. Perrino, M. Bono, F. Cortinovis, D.L. ESMO Open Original Research BACKGROUND: Malignant pleural mesothelioma (MPM) is a cancer with a high mortality rate and few therapeutic options. After platinum–pemetrexed combination, no further promising drug seems to be effective. Immune checkpoint inhibitors may have some activity in pretreated patients and no data are available in this population about durvalumab. MATERIALS AND METHODS: DIADEM was a multicenter, open-label, single-arm, phase II trial aimed at evaluating the efficacy and safety of durvalumab. Patients with locally advanced/metastatic MPM who progressed after platinum–pemetrexed chemotherapy were enrolled to receive durvalumab (1500 mg, intravenously Q4W) for 12 months or until evidence of disease progression or unacceptable toxicity. The primary endpoint was the proportion of patients alive and free from progression at 16 weeks (PFS(16wks)) calculated from treatment initiation. Secondary endpoints were progression-free survival, overall survival, overall response rate, and safety. RESULTS: Sixty-nine patients with a median age of 69 years (range 44-82 years) were enrolled; 62 patients (89.9%) had epithelioid histotype. As first-line treatment, all patients received platinum derivatives–pemetrexed combination (60.9% with carboplatin and 39.1% with cisplatin). As of March 2021, the median follow-up was 9.2 months (interquartile range 5.2-11.1 months). Six patients (8.7%) completed the 12-month treatment; 60 patients discontinued, of whom 42 for progressive disease, and 4 died. Seventeen patients (28.3%; 95% confidence interval 17.5% to 41.4%) were alive or free from progression at 16 weeks. Eleven patients (18.6%) had a grade 3 or 4 treatment-related adverse event (AE), and one (1.4%) had a grade ≥3 immune-related, treatment-related AE. There was one drug-related death. CONCLUSION: Durvalumab alone in pretreated non-selected MPM did not reach a meaningful clinical activity, showing any new major safety issue signals. Elsevier 2022-12-01 /pmc/articles/PMC9808442/ /pubmed/36463732 http://dx.doi.org/10.1016/j.esmoop.2022.100644 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research
Canova, S.
Ceresoli, G.L.
Grosso, F.
Zucali, P.A.
Gelsomino, F.
Pasello, G.
Mencoboni, M.
Rulli, E.
Galli, F.
De Simone, I.
Carlucci, L.
De Angelis, A.
Belletti, M.
Bonomi, M.
D’Aveni, A.
Perrino, M.
Bono, F.
Cortinovis, D.L.
Final results of DIADEM, a phase II study to investigate the efficacy and safety of durvalumab in advanced pretreated malignant pleural mesothelioma
title Final results of DIADEM, a phase II study to investigate the efficacy and safety of durvalumab in advanced pretreated malignant pleural mesothelioma
title_full Final results of DIADEM, a phase II study to investigate the efficacy and safety of durvalumab in advanced pretreated malignant pleural mesothelioma
title_fullStr Final results of DIADEM, a phase II study to investigate the efficacy and safety of durvalumab in advanced pretreated malignant pleural mesothelioma
title_full_unstemmed Final results of DIADEM, a phase II study to investigate the efficacy and safety of durvalumab in advanced pretreated malignant pleural mesothelioma
title_short Final results of DIADEM, a phase II study to investigate the efficacy and safety of durvalumab in advanced pretreated malignant pleural mesothelioma
title_sort final results of diadem, a phase ii study to investigate the efficacy and safety of durvalumab in advanced pretreated malignant pleural mesothelioma
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9808442/
https://www.ncbi.nlm.nih.gov/pubmed/36463732
http://dx.doi.org/10.1016/j.esmoop.2022.100644
work_keys_str_mv AT canovas finalresultsofdiademaphaseiistudytoinvestigatetheefficacyandsafetyofdurvalumabinadvancedpretreatedmalignantpleuralmesothelioma
AT ceresoligl finalresultsofdiademaphaseiistudytoinvestigatetheefficacyandsafetyofdurvalumabinadvancedpretreatedmalignantpleuralmesothelioma
AT grossof finalresultsofdiademaphaseiistudytoinvestigatetheefficacyandsafetyofdurvalumabinadvancedpretreatedmalignantpleuralmesothelioma
AT zucalipa finalresultsofdiademaphaseiistudytoinvestigatetheefficacyandsafetyofdurvalumabinadvancedpretreatedmalignantpleuralmesothelioma
AT gelsominof finalresultsofdiademaphaseiistudytoinvestigatetheefficacyandsafetyofdurvalumabinadvancedpretreatedmalignantpleuralmesothelioma
AT pasellog finalresultsofdiademaphaseiistudytoinvestigatetheefficacyandsafetyofdurvalumabinadvancedpretreatedmalignantpleuralmesothelioma
AT mencobonim finalresultsofdiademaphaseiistudytoinvestigatetheefficacyandsafetyofdurvalumabinadvancedpretreatedmalignantpleuralmesothelioma
AT rullie finalresultsofdiademaphaseiistudytoinvestigatetheefficacyandsafetyofdurvalumabinadvancedpretreatedmalignantpleuralmesothelioma
AT gallif finalresultsofdiademaphaseiistudytoinvestigatetheefficacyandsafetyofdurvalumabinadvancedpretreatedmalignantpleuralmesothelioma
AT desimonei finalresultsofdiademaphaseiistudytoinvestigatetheefficacyandsafetyofdurvalumabinadvancedpretreatedmalignantpleuralmesothelioma
AT carluccil finalresultsofdiademaphaseiistudytoinvestigatetheefficacyandsafetyofdurvalumabinadvancedpretreatedmalignantpleuralmesothelioma
AT deangelisa finalresultsofdiademaphaseiistudytoinvestigatetheefficacyandsafetyofdurvalumabinadvancedpretreatedmalignantpleuralmesothelioma
AT bellettim finalresultsofdiademaphaseiistudytoinvestigatetheefficacyandsafetyofdurvalumabinadvancedpretreatedmalignantpleuralmesothelioma
AT bonomim finalresultsofdiademaphaseiistudytoinvestigatetheefficacyandsafetyofdurvalumabinadvancedpretreatedmalignantpleuralmesothelioma
AT davenia finalresultsofdiademaphaseiistudytoinvestigatetheefficacyandsafetyofdurvalumabinadvancedpretreatedmalignantpleuralmesothelioma
AT perrinom finalresultsofdiademaphaseiistudytoinvestigatetheefficacyandsafetyofdurvalumabinadvancedpretreatedmalignantpleuralmesothelioma
AT bonof finalresultsofdiademaphaseiistudytoinvestigatetheefficacyandsafetyofdurvalumabinadvancedpretreatedmalignantpleuralmesothelioma
AT cortinovisdl finalresultsofdiademaphaseiistudytoinvestigatetheefficacyandsafetyofdurvalumabinadvancedpretreatedmalignantpleuralmesothelioma
AT finalresultsofdiademaphaseiistudytoinvestigatetheefficacyandsafetyofdurvalumabinadvancedpretreatedmalignantpleuralmesothelioma