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      Does neoadjuvant treatment in resectable pancreatic cancer improve overall survival? A systematic review and meta-analysis of randomized controlled trials

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          Abstract

          Background

          Neoadjuvant chemotherapy may improve overall survival (OS) in ‘borderline’ resectable pancreatic cancer (RPC). Whether the results are the same in upfront RPC is unknown.

          Materials and methods

          To evaluate the association of neoadjuvant treatment and survival outcomes in RPC, a systematic literature review was carried out including prospective randomized trials of neoadjuvant treatment versus upfront surgery. Articles indexed in PubMed, Embase and Scopus were evaluated. Data regarding systemic treatment regimens, R0 resection rates, disease-free survival (DFS) and OS were extracted. The outcomes were compared using a random-effects model. The index I 2 and the graphs of funnel plot were used for the interpretation of the data.

          Results

          Of 3229 abstracts, 6 randomized controlled trials were considered eligible with a combined sample size of 805 RPC patients. Among the trials, PACT-15, PREP-02/JSAP-05 and updated long-term results from PREOPANC and NEONAX trials were included. Combining the studies with meta-analysis, we could see that neoadjuvant treatment in RPC does not improve DFS [hazard ratio (HR) 0.71 (0.46-1.09)] or OS [HR 0.76 (0.52-1.11)], without significant heterogeneity. Interestingly, R0 rates improved ∼20% with the neoadjuvant approach [HR 1.2 (1.04-1.37)]. It is important to note that most studies evaluated gemcitabine-based regimens in the neoadjuvant setting.

          Conclusions

          Neoadjuvant chemotherapy or chemoradiation does not improve DFS or OS in RPC compared to upfront surgery followed by adjuvant treatment. Neoadjuvant treatment improves R0 rates by ∼20%. Randomized ongoing trials are eagerly awaited with more active combined regimens including modified FOLFIRINOX.

          Highlights

          • We did a meta-analysis of six randomized trials evaluating neoadjuvant treatment in RPC.

          • R0 resections rates improved by ∼20% with the neoadjuvant approach.

          • However, neoadjuvant treatment did not improve OS or DFS in RPC.

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          Most cited references35

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          Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries

          This article provides an update on the global cancer burden using the GLOBOCAN 2020 estimates of cancer incidence and mortality produced by the International Agency for Research on Cancer. Worldwide, an estimated 19.3 million new cancer cases (18.1 million excluding nonmelanoma skin cancer) and almost 10.0 million cancer deaths (9.9 million excluding nonmelanoma skin cancer) occurred in 2020. Female breast cancer has surpassed lung cancer as the most commonly diagnosed cancer, with an estimated 2.3 million new cases (11.7%), followed by lung (11.4%), colorectal (10.0 %), prostate (7.3%), and stomach (5.6%) cancers. Lung cancer remained the leading cause of cancer death, with an estimated 1.8 million deaths (18%), followed by colorectal (9.4%), liver (8.3%), stomach (7.7%), and female breast (6.9%) cancers. Overall incidence was from 2-fold to 3-fold higher in transitioned versus transitioning countries for both sexes, whereas mortality varied <2-fold for men and little for women. Death rates for female breast and cervical cancers, however, were considerably higher in transitioning versus transitioned countries (15.0 vs 12.8 per 100,000 and 12.4 vs 5.2 per 100,000, respectively). The global cancer burden is expected to be 28.4 million cases in 2040, a 47% rise from 2020, with a larger increase in transitioning (64% to 95%) versus transitioned (32% to 56%) countries due to demographic changes, although this may be further exacerbated by increasing risk factors associated with globalization and a growing economy. Efforts to build a sustainable infrastructure for the dissemination of cancer prevention measures and provision of cancer care in transitioning countries is critical for global cancer control.
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            Measuring inconsistency in meta-analyses.

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              RoB 2: a revised tool for assessing risk of bias in randomised trials

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                Author and article information

                Contributors
                Journal
                ESMO Open
                ESMO Open
                ESMO Open
                Elsevier
                2059-7029
                11 January 2023
                February 2023
                11 January 2023
                : 8
                : 1
                : 100771
                Affiliations
                [1 ]Center for Personalized Medicine, Hospital Israelita Albert Einstein, São Paulo
                [2 ]Hospital Israelita Albert Einstein, São Paulo, Brazil
                [3 ]Mayo Clinic, Phoenix, USA
                Author notes
                [] Correspondence to: Dr Pedro Luiz Serrano Uson Junior, Av Albert Einstein 627, Sao Paulo, Brazil. Tel: +55-11-21511233 pedro.serrano@ 123456einstein.br
                Article
                S2059-7029(22)00405-7 100771
                10.1016/j.esmoop.2022.100771
                10024142
                36638709
                6dc2a82a-3638-40d5-8646-1b1f0bd0b75c
                © 2022 The Authors

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                Categories
                Original Research

                resectable pancreatic cancer,chemotherapy,gemcitabine,neoadjuvant treatment,folfirinox,overall survival

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