Skip to content
← Study library

NCT00407186 · CITED IN SOURCE DOCUMENTS

Randomized Phase III Trial of Adjuvant Chemotherapy or Chemoradiotherapy in Resectable Gastric Cancer (CRITICS)

An NCI or FDA source cites this study. A citation does not establish that it applies to an individual diagnosis.

Phase
PHASE3
Status at capture
UNKNOWN
Registry last update
2017-10-10

The purpose of this study is to evaluate the efficacy and safety of combined chemotherapy and radiotherapy (in comparison to chemotherapy alone) as adjuvant treatment after surgery for gastric cancer. Prior to surgery all patients will receive neo-adjuvant chemotherapy as well.

Open the original ClinicalTrials.gov record → · Download preserved record

What did the study report?

Outcomes, safety and baseline populations are separate source sections. Quality-of-life measures appear under their original outcome titles.

No posted result sections were captured. Registered plans do not establish that a treatment works.

Who could take part
eligibility Criteria
Inclusion Criteria: * Ib-IVa (no distant metastases) gastric cancer (histologically proven); tumor bulk in the stomach * WHO \< 2 * Age ≥18 yrs * Operable gastric cancer * No prior abdominal radiotherapy or chemotherapy * Tumornegative laparoscopy when CT suggests peritoneal carcinomatosis * Start treatment within 10 working days after registration * Written informed consent Exclusion Criteria: * T1N0 disease (endoscopic ultrasound) * Distant metastases * Inoperable patients; due to technical surgery-related factors or general condition * Previous malignancy, except adequately treated non-melanoma skin cancer or in-situ cancer of the cervix uteri. * Solitary functioning kidney that will be within the radiation field * Major surgery within 4 weeks prior to study treatment start, or lack of complete recovery from the effects of major surgery * Uncontrolled (bacterial) infections * Significant cardiac disorders * Continuous use of immunosuppressive agents * Concurrent use of the antiviral agent sorivudine or chemically related analogues * Hearing loss \> CTC grade 1 * Neurotoxicity \> CTC grade 1
healthy Volunteers
false
minimum Age
18 Years
sex
ALL
std Ages
  1. ADULT
  2. OLDER_ADULT
Treatment arms and interventions
arm Groups
  1. description
    5 weeksadjuvant treatment; radiotherapy and concomitant chemotherapy with cisplatin and capecitabine.
    intervention Names
    1. Drug: cisplatin+capecitabine
    2. Radiation: radiotherapy
    label
    1chemoradiotherapy
    type
    EXPERIMENTAL
  2. description
    3 adjuvant courses epirubicin, cisplatin, capecitabine.
    intervention Names
    1. Drug: epirubicin+cisplatin+capecitabine
    label
    2chemotherapy
    type
    ACTIVE_COMPARATOR
interventions
  1. arm Group Labels
    1. 1chemoradiotherapy
    description
    cisplatin 20 mg/m2 (i.v., q 1 w, 5 weeks), capecitabine 575 mg/m2 (b.i.d., oral, on radiotherapy days.
    name
    cisplatin+capecitabine
    type
    DRUG
  2. arm Group Labels
    1. 1chemoradiotherapy
    description
    45 Gy in 25 fracions (5 days/week)
    name
    radiotherapy
    type
    RADIATION
  3. arm Group Labels
    1. 2chemotherapy
    description
    3 courses q 3 w: epirubicin 50 mg/m2 (i.v., day 1), cisplatin 60 mg/m2 (i.v., day 1), capecitabine 1000 mg/m2 (b.i.d., oral, day 1-14)
    name
    epirubicin+cisplatin+capecitabine
    type
    DRUG
Study design
allocation
RANDOMIZED
intervention Model
PARALLEL
masking Info
masking
NONE
primary Purpose
TREATMENT
Enrollment
count
788
type
ACTUAL
Registered outcome plans (not posted results)
primary Outcomes
  1. measure
    overall survival
    time Frame
    study duration
secondary Outcomes
  1. measure
    disease-free survival
    time Frame
    study duration
  2. measure
    toxicity
    time Frame
    study duration
  3. measure
    health-related quality of life
    time Frame
    study duration
Full study description
brief Summary
The purpose of this study is to evaluate the efficacy and safety of combined chemotherapy and radiotherapy (in comparison to chemotherapy alone) as adjuvant treatment after surgery for gastric cancer. Prior to surgery all patients will receive neo-adjuvant chemotherapy as well.
detailed Description
The mainstay of curative treatment of gastric cancer is radical surgical dissection. Because most patients in the Western world present with advanced stages long term survival is found in about 25%, with local recurrences as part of treatment failure in up to 80% of cases. Studies examining the role of more extended lymph node dissections (D1 vs. D2), adjuvant radiotherapy or adjuvant chemotherapy did not result in a clinical relevant improvement of survival. In 2001 results of a South West Oncology group (SWOG) trial that randomized between surgery and surgery with chemoradiotherapy were published. This trial, that was hampered by suboptimal surgery (less than D1 in majority of patients) and radiotherapy (2D radiotherapy; 35% protocol deviations) showed an absolute increase in median survival of 9 months. More recently results of the MAGIC study, which randomized between surgery and surgery plus 6 perioperative courses of ECF chemotherapy, were presented. This regimen resulted in an absolute 5-year survival benefit of 13% and in a 10% higher resectability rate. This phase III prospectively randomized study investigates whether chemoradiotherapy (45 Gy in 5 weeks with daily cisplatin and capecitabine) after preoperative chemotherapy (3x ECC (epirubicin, cisplatin, capecitabine)) and adequate (D1+) surgery leads to improved survival in comparison with postoperative chemotherapy (3x ECC). Furthermore, toxicity of both treatment regimens will be explored.
Source references
references
  1. citation
    Quaas A, Biesma HD, Wagner AD, Verheij M, van Berge Henegouwen MI, Schoemig-Markiefka B, Pamuk A, Zander T, Siemanowski J, Sikorska K, Egthuijsen JMP, Meershoek-Klein Kranenbarg EM, van de Velde CJH, Buettner R, Alakus H, Cats A, Ylstra B, van Laarhoven HWM, van Grieken NCT. Microsatellite instability and sex differences in resectable gastric cancer - A pooled analysis of three European cohorts. Eur J Cancer. 2022 Sep;173:95-104. doi: 10.1016/j.ejca.2022.06.025. Epub 2022 Jul 18.
    pmid
    35863110
    type
    DERIVED
  2. citation
    Slagter AE, Vollebergh MA, Caspers IA, van Sandick JW, Sikorska K, Lind P, Nordsmark M, Putter H, Braak JPBM, Meershoek-Klein Kranenbarg E, van de Velde CJH, Jansen EPM, Cats A, van Laarhoven HWM, van Grieken NCT, Verheij M. Prognostic value of tumor markers and ctDNA in patients with resectable gastric cancer receiving perioperative treatment: results from the CRITICS trial. Gastric Cancer. 2022 Mar;25(2):401-410. doi: 10.1007/s10120-021-01258-6. Epub 2021 Oct 29.
    pmid
    34714423
    type
    DERIVED
  3. citation
    de Steur WO, van Amelsfoort RM, Hartgrink HH, Putter H, Meershoek-Klein Kranenbarg E, van Grieken NCT, van Sandick JW, Claassen YHM, Braak JPBM, Jansen EPM, Sikorska K, van Tinteren H, Walraven I, Lind P, Nordsmark M, van Berge Henegouwen MI, van Laarhoven HWM, Cats A, Verheij M, van de Velde CJH; CRITICS investigators. Adjuvant chemotherapy is superior to chemoradiation after D2 surgery for gastric cancer in the per-protocol analysis of the randomized CRITICS trial. Ann Oncol. 2021 Mar;32(3):360-367. doi: 10.1016/j.annonc.2020.11.004. Epub 2020 Nov 20.
    pmid
    33227408
    type
    DERIVED
  4. citation
    Slagter AE, Sikorska K, Grootscholten C, van Laarhoven HWM, Lind P, Nordsmark M, Meershoek-Klein Kranenbarg E, van de Velde CJH, van Grieken NCT, van Sandick JW, Jansen EPM, Verheij M, Cats A. Venous thromboembolism during preoperative chemotherapy in the CRITICS gastric cancer trial. Cancer Med. 2020 Sep;9(18):6609-6616. doi: 10.1002/cam4.3118. Epub 2020 Jul 31.
    pmid
    32735752
    type
    DERIVED
  5. citation
    Slagter AE, Tudela B, van Amelsfoort RM, Sikorska K, van Sandick JW, van de Velde CJH, van Grieken NCT, Lind P, Nordsmark M, Putter H, Hulshof MCCM, van Laarhoven HWM, Grootscholten C, Braak JPBM, Meershoek-Klein Kranenbarg E, Jansen EPM, Cats A, Verheij M. Older versus younger adults with gastric cancer receiving perioperative treatment: Results from the CRITICS trial. Eur J Cancer. 2020 May;130:146-154. doi: 10.1016/j.ejca.2020.02.008. Epub 2020 Mar 21.
    pmid
    32208351
    type
    DERIVED
  6. citation
    Cats A, Jansen EPM, van Grieken NCT, Sikorska K, Lind P, Nordsmark M, Meershoek-Klein Kranenbarg E, Boot H, Trip AK, Swellengrebel HAM, van Laarhoven HWM, Putter H, van Sandick JW, van Berge Henegouwen MI, Hartgrink HH, van Tinteren H, van de Velde CJH, Verheij M; CRITICS investigators. Chemotherapy versus chemoradiotherapy after surgery and preoperative chemotherapy for resectable gastric cancer (CRITICS): an international, open-label, randomised phase 3 trial. Lancet Oncol. 2018 May;19(5):616-628. doi: 10.1016/S1470-2045(18)30132-3. Epub 2018 Apr 9.
    pmid
    29650363
    type
    DERIVED
  7. citation
    Dikken JL, van Sandick JW, Maurits Swellengrebel HA, Lind PA, Putter H, Jansen EP, Boot H, van Grieken NC, van de Velde CJ, Verheij M, Cats A. Neo-adjuvant chemotherapy followed by surgery and chemotherapy or by surgery and chemoradiotherapy for patients with resectable gastric cancer (CRITICS). BMC Cancer. 2011 Aug 2;11:329. doi: 10.1186/1471-2407-11-329.
    pmid
    21810227
    type
    DERIVED
  8. citation
    Jansen EPM, Boot H, Dubbelman R, Verheij M, Cats A. Postoperative chemoradiotherapy in gastric cancer--a phase I-II study of radiotherapy with dose escalation of weekly cisplatin and daily capecitabine chemotherapy. Ann Oncol. 2010 Mar;21(3):530-534. doi: 10.1093/annonc/mdp345. Epub 2009 Aug 18.
    pmid
    19690058
    type
    DERIVED
see Also Links
  1. label
    Dutch Colorectal Cancer Group
  2. label
    Nederlands Kanker Instituut/Antoni van Leeuwenhoek Ziekenhuis (Netherlands Cancer Institute/Antoni van Leeuwenhoek Hospital)
Source notices and limitations
    Discovery and provenance
    1. release id
      ctgov-registry-7ad944f6deaf1f5cd6122126
      edge id
      nct-edge-5927c284add5abf52f13
      requested nct id
      NCT00407186
      primary nct id
      NCT00407186
      source kind
      nci_explicit_reference_or_link
      source record id
      Source null
      source file sha256
      20f13c5c62ce6ffbb2dafce9a99993b62ee853964501fae15509a2830b8349c2
      payload sha256
      223c83be9c835e0aaddbc5fa1fe9202bd6e267eca727619bcb330037bed6c1ac
      payload
      clinical indication matching status
      not_inferred
      end exclusive
      true
      id
      nct-edge-5927c284add5abf52f13
      link basis
      explicit_NCT_identifier_in_acquired_source
      nct id
      NCT00407186
      occurrences
      1. context exact
        ss="pdq-content-list"><ul id="_548"><li>The 5-year OS rate was 44% in both arms.</li></ul></div> </li><li>In a phase III Dutch trial (<a href="/clinicaltrials/NCT00407186">CRITICS</a> [NCT00407186]), 788 patients with stage IB to stage IVA gastric/gastroesophageal junction adenocarcinoma received preoperative chemotherapy and su
        end
        93572
        exact text
        NCT00407186
        start
        93561
      2. context exact
        id="_548"><li>The 5-year OS rate was 44% in both arms.</li></ul></div> </li><li>In a phase III Dutch trial (<a href="/clinicaltrials/NCT00407186">CRITICS</a> [NCT00407186]), 788 patients with stage IB to stage IVA gastric/gastroesophageal junction adenocarcinoma received preoperative chemotherapy and surgery, and then were rando
        end
        93598
        exact text
        NCT00407186
        start
        93587
      offset unit
      unicode_code_points
      source file
      /tmp/cancer-full-research/nci/raw/b520476df769e6fecd.html
      source file sha256
      20f13c5c62ce6ffbb2dafce9a99993b62ee853964501fae15509a2830b8349c2
      source json pointer
      Source null
      source kind
      nci_explicit_reference_or_link
      source record id
      Source null
      source retrieved at
      2026-09-09T23:22:22.075850+00:00
      source string basis
      UTF-8_text_with_universal_newline_translation
      source string sha256
      93e6df01e9e806a0673bf0152a2eeeb828353c1de1fb5bdf86185aac466f15f4
      source title
      Gastric Cancer Treatment (PDQ®)–Health Professional Version
      source update dates
      1. context
        Updated: February 21, 2025
        datetime
        2025-02-21T12:00:00Z
        display
        February 21, 2025

    Preserved source evidence · Not medical advice