Sequential neoadjuvant chemoradiotherapy (CRT) followed by curative surgery vs. primary surgery alone for resectable, non-metastasized pancreatic adenocarcinoma: NEOPA- a randomized multicenter phase III study (NCT01900327, DRKS00003893, ISRCTN82191749).

Abstract:

BACKGROUND:Median OS after surgery in curative intent for non-metastasized pancreas cancer ranges under study conditions from 17.9 months to 23.6 months. Tumor recurrence occurs locally, at distant sites (liver, peritoneum, lungs), or both. Observational and autopsy series report local recurrence rates of up to 87% even after potentially "curative" R0 resection. To achieve better local control, neoadjuvant CRT has been suggested for preoperative tumour downsizing, to elevate the likelihood of curative, margin-negative R0 resection and to increase the OS rate. However, controlled, randomized trials addressing the impact of neoadjuvant CRT survival do not exist. METHODS/DESIGN:The underlying hypothesis of this randomized, two-armed, open-label, multicenter, phase III trial is that neoadjuvant CRT increases the three-year overall survival by 12% compared to patients undergoing upfront surgery for resectable pancreatic cancer. A rigorous, standardized technique of histopathologically handling Whipple specimens will be applied at all participating centers. Overall, 410 patients (n=205 in each study arm) will be enrolled in the trial, taking into regard an expected drop out rate of 7% and allocated either to receive neoadjuvant CRT prior to surgery or to undergo surgery alone. Circumferential resection margin status, i.e. R0 and R1 rates, respectively, surgical resectability rate, local and distant disease-free and global survival, and first site of tumor recurrence constitute further essential endpoints of the trial. DISCUSSION:For the first time, the NEOPA study investigates the impact of neoadjuvant CRT on survival of resectable pancreas head cancer in a prospectively randomized manner. The results of the study have the potential to change substantially the treatment regimen of pancreas cancer. TRIAL REGISTRATION:Clinical Trial gov: NCT01900327, DRKS00003893, ISRCTN82191749.

journal_name

BMC Cancer

journal_title

BMC cancer

authors

Tachezy M,Gebauer F,Petersen C,Arnold D,Trepel M,Wegscheider K,Schafhausen P,Bockhorn M,Izbicki JR,Yekebas E

doi

10.1186/1471-2407-14-411

subject

Has Abstract

pub_date

2014-06-07 00:00:00

pages

411

issn

1471-2407

pii

1471-2407-14-411

journal_volume

14

pub_type

杂志文章,多中心研究,随机对照试验
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    更新日期:2016-08-19 00:00:00

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    doi:10.1186/1471-2407-9-343

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    更新日期:2009-09-25 00:00:00

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    doi:10.1186/1471-2407-10-269

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    doi:10.1186/1471-2407-10-108

    authors: Hicks DG,Janarthanan BR,Vardarajan R,Kulkarni SA,Khoury T,Dim D,Budd GT,Yoder BJ,Tubbs R,Schreeder MT,Estopinal NC,Beck RA,Wang Y,Ring BZ,Seitz RS,Ross DT

    更新日期:2010-03-22 00:00:00

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    authors: Bacopulos S,Amemiya Y,Yang W,Zubovits J,Burger A,Yaffe M,Seth AK

    更新日期:2012-02-08 00:00:00

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    authors: Lyhne JD,Smith A'B,Frostholm L,Fink P,Jensen LH

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    pub_type: 杂志文章,meta分析,评审

    doi:10.1186/1471-2407-12-17

    authors: Zhou Y,Yin X,Ying J,Zhang B

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  • Metastasis-associated in colon cancer-1 and aldehyde dehydrogenase 1 are metastatic and prognostic biomarker for non-small cell lung cancer.

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    doi:10.1186/s12885-016-2903-z

    authors: Zhou L,Yu L,Zhu B,Wu S,Song W,Gong X,Wang D

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  • LAD1 expression is associated with the metastatic potential of colorectal cancer cells.

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    pub_type: 杂志文章

    doi:10.1186/s12885-020-07660-0

    authors: Moon B,Yang SJ,Park SM,Lee SH,Song KS,Jeong EJ,Park M,Kim JS,Yeom YI,Kim JA

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    pub_type: 杂志文章

    doi:10.1186/s12885-018-4376-8

    authors: Rasmussen S,Haastrup PF,Balasubramaniam K,Christensen RD,Søndergaard J,Jarbøl DE

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    journal_title:BMC cancer

    pub_type: 杂志文章,多中心研究,随机对照试验

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    journal_title:BMC cancer

    pub_type: 杂志文章

    doi:10.1186/1471-2407-13-618

    authors: Bezan A,Hohla F,Meissnitzer T,Greil R

    更新日期:2013-12-31 00:00:00

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    pub_type: 杂志文章

    doi:10.1186/s12885-020-6515-2

    authors: Zhou F,Wang D,Wei W,Chen H,Shi H,Zhou N,Wu L,Peng R

    更新日期:2020-01-16 00:00:00

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    journal_title:BMC cancer

    pub_type: 杂志文章

    doi:10.1186/s12885-016-2865-1

    authors: Yu X,Zhang Y,Chen H

    更新日期:2016-11-04 00:00:00

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    journal_title:BMC cancer

    pub_type: 杂志文章

    doi:10.1186/s12885-015-1151-y

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    更新日期:2015-03-15 00:00:00

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    journal_title:BMC cancer

    pub_type: 杂志文章

    doi:10.1186/s12885-015-1996-0

    authors: Mazzone PJ,Wang XF,Lim S,Choi H,Jett J,Vachani A,Zhang Q,Beukemann M,Seeley M,Martino R,Rhodes P

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    doi:10.1186/s12885-019-5951-3

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    journal_title:BMC cancer

    pub_type: 杂志文章,meta分析,评审

    doi:10.1186/1471-2407-14-406

    authors: Park S,Jee SH,Shin HR,Park EH,Shin A,Jung KW,Hwang SS,Cha ES,Yun YH,Park SK,Boniol M,Boffetta P

    更新日期:2014-06-06 00:00:00

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    pub_type: 杂志文章

    doi:10.1186/s12885-020-07293-3

    authors: Xue X,Huang W,Qiu T,Guo L,Ying J,Lv N

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    doi:10.1186/s12885-017-3056-4

    authors: Roininen N,Takala S,Haapasaari KM,Jukkola-Vuorinen A,Mattson J,Heikkilä P,Karihtala P

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    journal_title:BMC cancer

    pub_type: 杂志文章

    doi:10.1186/s12885-016-2749-4

    authors: Itoh A,Sadamori H,Yabushita K,Monden K,Tatsukawa M,Hioki M,Hyodo T,Omonishi K,Ueki T,Ohno S,Sakaguchi K,Takakura N

    更新日期:2016-09-01 00:00:00

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    journal_title:BMC cancer

    pub_type: 杂志文章

    doi:10.1186/s12885-020-07212-6

    authors: Ramelow J,Brooks CD,Gao L,Almiman AA,Williams TM,Villalona-Calero MA,Duan W

    更新日期:2020-08-08 00:00:00

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    journal_title:BMC cancer

    pub_type: 杂志文章

    doi:10.1186/s12885-017-3579-8

    authors: Kinnunen PTT,Murtola TJ,Talala K,Taari K,Tammela TLJ,Auvinen A

    更新日期:2017-08-29 00:00:00

  • Copper compound induces autophagy and apoptosis of glioma cells by reactive oxygen species and JNK activation.

    abstract:BACKGROUND:Glioblastoma multiforme (GBM) is the most aggressive of the primary brain tumors, with a grim prognosis despite intensive treatment. In the past decades, progress in research has not significantly increased overall survival rate. METHODS:The in vitro antineoplastic effect and mechanism of action of Casiopei...

    journal_title:BMC cancer

    pub_type: 杂志文章

    doi:10.1186/1471-2407-12-156

    authors: Trejo-Solís C,Jimenez-Farfan D,Rodriguez-Enriquez S,Fernandez-Valverde F,Cruz-Salgado A,Ruiz-Azuara L,Sotelo J

    更新日期:2012-04-27 00:00:00