A systematic review of salvage therapies in refractory metastatic colorectal cancer.


Journal

International journal of colorectal disease
ISSN: 1432-1262
Titre abrégé: Int J Colorectal Dis
Pays: Germany
ID NLM: 8607899

Informations de publication

Date de publication:
May 2020
Historique:
accepted: 13 03 2020
pubmed: 29 3 2020
medline: 30 1 2021
entrez: 29 3 2020
Statut: ppublish

Résumé

Established that the only approved agents in previously treated metastatic colorectal cancer (CRC) are trifluoridine/tipiracil and regorafenib, we conducted a systematic review of all the published phase 2-3 trials, with the scope to evaluate the benefit of any later-line regimens in refractory metastatic CRC. Phase 2-3 studies that enrolled patients with stage IV disease receiving salvage therapies for refractory CRC were identified using electronic databases (Pubmed, EMBASE, and Cochrane Library). Clinical outcomes were pooled using a point estimates for the weighted values of median overall survival (OS), progression-free survival (PFS), response rate (ORR), stable disease rate (SD), and 6-month and 1-year OS. Overall, 7556 patients were included from 67 studies (n = 70 arms). Overall, the pooled ORR and SD were 15.4% (95% CI 13-18%) and 36.9% (95% CI 33.5-40.6%). Median PFS, 6-month and 1-year OS, and median OS were 3.2 (95% CI 2.9-3.3) months, 65.4% (95% CI 61.9-68.8%), 36% (95% CI 32.3-39.9%) and 8.8 (95% CI 8.3-9.2) months. Overall survival was different in the monochemotherapy, polychemotherapy, chemotherapy + targeted therapy, and targeted therapy alone arms (7.6, 9.5, 10.3, and 7.9 months, respectively, P for difference = 0.01). Median PFS were respectively 2.3, 3.9, 3.8, and 2.6, respectively (P for difference < 0.01). Overall, combination therapy (polychemotherapy with or without targeted agents) is associated with a higher control of disease and better outcome than approved agents. Treatment, if possible, should be personalized according to the patients' conditions, physician preference and molecular profile of disease.

Identifiants

pubmed: 32219509
doi: 10.1007/s00384-020-03571-5
pii: 10.1007/s00384-020-03571-5
doi:

Types de publication

Journal Article Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

783-794

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Auteurs

Fausto Petrelli (F)

Oncology Unit, Medical Sciences Department, ASST Bergamo Ovest, Piazzale Ospedale 1, 24047, Treviglio, BG, Italy. faupe@libero.it.

Gianluca Perego (G)

Pharmacy Unit, San Raffaele Hospital, Milan, Italy.

Antonio Ghidini (A)

Oncology Unit, Casa di Cura Igea, Milan, Italy.

Michele Ghidini (M)

Oncology Unit, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy.

Karen Borgonovo (K)

Oncology Unit, Medical Sciences Department, ASST Bergamo Ovest, Piazzale Ospedale 1, 24047, Treviglio, BG, Italy.

Cinzia Scolari (C)

Pharmacy Unit, ASST Bergamo Ovest, Treviglio, BG, Italy.

Renata Nozza (R)

Pharmacy Unit, ASST Bergamo Ovest, Treviglio, BG, Italy.

Valentina Rampulla (V)

Surgical Oncology Unit, ASST Bergamo Ovest, Treviglio, BG, Italy.

Antonio Costanzo (A)

Surgical Oncology Unit, ASST Bergamo Ovest, Treviglio, BG, Italy.

Antonio Varricchio (A)

Surgical Oncology Unit, ASST Bergamo Ovest, Treviglio, BG, Italy.

Emanuele Rausa (E)

Surgery Unit, ASST Papa Giovanni XXIII, Bergamo, Italy.

Filippo Pietrantonio (F)

Oncology Unit, Fondazione IRCCS Istituto Nazionale Tumori di Milano, Milan, Italy.

Alberto Zaniboni (A)

Oncology Unit, Fondazione Poliambulanza, Brescia, Italy.

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