PMID- 32208351 OWN - NLM STAT- MEDLINE DCOM- 20201123 LR - 20201123 IS - 1879-0852 (Electronic) IS - 0959-8049 (Linking) VI - 130 DP - 2020 May TI - Older versus younger adults with gastric cancer receiving perioperative treatment: Results from the CRITICS trial. PG - 146-154 LID - S0959-8049(20)30057-5 [pii] LID - 10.1016/j.ejca.2020.02.008 [doi] AB - AIM: To evaluate treatment-related toxicity, treatment compliance, surgical complications and event-free survival (EFS) in older (>/=70 years) versus younger (<70 years) adults who underwent perioperative treatment for gastric cancer. METHODS: In the CRITICS trial, 788 patients with resectable gastric cancer were randomised before start of any treatment and received preoperative chemotherapy (3 cycles of epirubicin, cisplatin or oxaliplatin and capecitabine), followed by surgery, followed by either postoperative chemotherapy or chemoradiotherapy (45Gy + cisplatin + capecitabine). RESULTS: 172 (22%) patients were older adults. During preoperative chemotherapy, 131 (77%) older adults versus 380 (62%) younger adults experienced severe toxicity (p < 0.001); older adults received significantly lower relative dose intensities (RDIs) for all chemotherapeutic drugs. Equal proportions of older versus younger adults underwent curative surgery: 137 (80%) versus 499 (81%), with comparable postoperative complications and postoperative mortality. Postoperative therapy after curative surgery started in 87 (64%) older adults versus 391 (78%) younger adults (p < 0.001). Incidence of severe toxicity during postoperative chemotherapy was 22 (54%) in older adults versus 113 (59%) in younger adults (p = 0.541); older adults received significantly lower RDIs for all chemotherapeutic drugs. Severe toxicity rates for postoperative chemoradiotherapy were 22 (48%) older adults versus 89 (45%) for younger adults (p = 0.703), with comparable chemotherapy RDIs and radiotherapy dose. Two-year EFS was 53% for older adults versus 51% for younger adults. CONCLUSION: Perioperative treatment compliance, especially in the postoperative phase, was poorer in older adults compared with younger adults. As comparable proportions of patients underwent curative surgery, future studies should focus on neo-adjuvant treatment. TRIAL REGISTRATION: ClinicalTrials.gov identifier: NCT00407186. EudraCT number: 2006-00413032. CI - Copyright (c) 2020 The Author(s). Published by Elsevier Ltd.. All rights reserved. FAU - Slagter, Astrid E AU - Slagter AE AD - Department of Radiation Oncology, Netherlands Cancer Institute, Amsterdam, the Netherlands. FAU - Tudela, Benjamin AU - Tudela B AD - Department of Radiation Oncology, Netherlands Cancer Institute, Amsterdam, the Netherlands; Department of Radiation Oncology, Universidad de Valparaiso, Valparaiso, Chile. FAU - van Amelsfoort, Romy M AU - van Amelsfoort RM AD - Department of Radiation Oncology, Netherlands Cancer Institute, Amsterdam, the Netherlands. FAU - Sikorska, Karolina AU - Sikorska K AD - Department of Biometrics, Netherlands Cancer Institute, Amsterdam, the Netherlands. FAU - van Sandick, Johanna W AU - van Sandick JW AD - Department of Surgical Oncology, Netherlands Cancer Institute, Amsterdam, the Netherlands. FAU - van de Velde, Cornelis J H AU - van de Velde CJH AD - Department of Surgical Oncology, Leiden University Medical Center, Leiden, the Netherlands. FAU - van Grieken, Nicole C T AU - van Grieken NCT AD - Department of Pathology, Amsterdam University Medical Centers, Location VUmc, Amsterdam, the Netherlands. FAU - Lind, Pehr AU - Lind P AD - Department of Oncology, Stockholm Soder Hospital, Stockholm, Sweden; Karolinska Institutet, Stockholm, Sweden. FAU - Nordsmark, Marianne AU - Nordsmark M AD - Department of Medical Oncology, Aarhus University, Aarhus, Denmark. FAU - Putter, Hein AU - Putter H AD - Department of Biometrics, Leiden University Medical Center, Leiden, the Netherlands. FAU - Hulshof, Maarten C C M AU - Hulshof MCCM AD - Department of Radiation Oncology, Cancer Center Amsterdam, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, the Netherlands. FAU - van Laarhoven, Hanneke W M AU - van Laarhoven HWM AD - Department of Medical Oncology, Cancer Center Amsterdam, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, the Netherlands. FAU - Grootscholten, Cecile AU - Grootscholten C AD - Department of Gastrointestinal Oncology/Medical Oncology, Netherlands Cancer Institute, Amsterdam, the Netherlands. FAU - Braak, Jeffrey P B M AU - Braak JPBM AD - Department of Surgical Oncology, Leiden University Medical Center, Leiden, the Netherlands. FAU - Meershoek-Klein Kranenbarg, Elma AU - Meershoek-Klein Kranenbarg E AD - Department of Surgical Oncology, Leiden University Medical Center, Leiden, the Netherlands. FAU - Jansen, Edwin P M AU - Jansen EPM AD - Department of Radiation Oncology, Netherlands Cancer Institute, Amsterdam, the Netherlands. FAU - Cats, Annemieke AU - Cats A AD - Department of Gastrointestinal Oncology/Medical Oncology, Netherlands Cancer Institute, Amsterdam, the Netherlands. FAU - Verheij, Marcel AU - Verheij M AD - Department of Radiation Oncology, Netherlands Cancer Institute, Amsterdam, the Netherlands; Department of Radiation Oncology, Radboud University Medical Center, Nijmegen, the Netherlands. Electronic address: Marcel.Verheij@radboudumc.nl. LA - eng SI - ClinicalTrials.gov/NCT00407186 PT - Clinical Trial, Phase III PT - Journal Article PT - Multicenter Study PT - Research Support, Non-U.S. Gov't DEP - 20200321 PL - England TA - Eur J Cancer JT - European journal of cancer (Oxford, England : 1990) JID - 9005373 SB - IM MH - Adult MH - Aged MH - Aged, 80 and over MH - Female MH - Humans MH - Male MH - Middle Aged MH - Perioperative Care/*methods MH - Stomach Neoplasms/surgery/*therapy OTO - NOTNLM OT - Chemoradiotherapy OT - Chemotherapy OT - Older adults OT - Resectable gastric cancer COIS- Conflicts of interest statement N.C.T. van Grieken reported receiving grants from the Dutch Cancer Society and The Netherlands Organisation for Health Research and Development, and serving on an advisory board for Bristol-Myers Squibb and Merck Sharp & Dohme. H.W.M. van Laarhoven reported receiving grants/medication support from Bayer, BMS, Celgene, Janssen, Lilly, Nordic Pharma, Philips, Roche, Servier, and serving on an advisory board for BMS, Lilly, MSD, Nordic Pharma, Novartis, Servier E.P.M. Jansen, A. Cats and M. Verheij reported receiving grants from the Dutch Cancer Society, the Dutch Colorectal Cancer Group and Hoffmann La Roche. All remaining authors have declared no conflicts of interest. EDAT- 2020/03/26 06:00 MHDA- 2020/11/24 06:00 CRDT- 2020/03/26 06:00 PHST- 2019/11/19 00:00 [received] PHST- 2020/02/06 00:00 [revised] PHST- 2020/02/08 00:00 [accepted] PHST- 2020/03/26 06:00 [pubmed] PHST- 2020/11/24 06:00 [medline] PHST- 2020/03/26 06:00 [entrez] AID - S0959-8049(20)30057-5 [pii] AID - 10.1016/j.ejca.2020.02.008 [doi] PST - ppublish SO - Eur J Cancer. 2020 May;130:146-154. doi: 10.1016/j.ejca.2020.02.008. Epub 2020 Mar 21.