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
- ADULT
- OLDER_ADULT
Treatment arms and interventions
- arm Groups
- description
- 5 weeksadjuvant treatment; radiotherapy and concomitant chemotherapy with cisplatin and capecitabine.
- intervention Names
- Drug: cisplatin+capecitabine
- Radiation: radiotherapy
- label
- 1chemoradiotherapy
- type
- EXPERIMENTAL
- description
- 3 adjuvant courses epirubicin, cisplatin, capecitabine.
- intervention Names
- Drug: epirubicin+cisplatin+capecitabine
- label
- 2chemotherapy
- type
- ACTIVE_COMPARATOR
- interventions
- arm Group Labels
- 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
- arm Group Labels
- 1chemoradiotherapy
- description
- 45 Gy in 25 fracions (5 days/week)
- name
- radiotherapy
- type
- RADIATION
- arm Group Labels
- 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
- measure
- overall survival
- time Frame
- study duration
- secondary Outcomes
- measure
- disease-free survival
- time Frame
- study duration
- measure
- toxicity
- time Frame
- study duration
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- label
- Dutch Colorectal Cancer Group
- label
- Nederlands Kanker Instituut/Antoni van Leeuwenhoek Ziekenhuis (Netherlands Cancer Institute/Antoni van Leeuwenhoek Hospital)
Source notices and limitations
Discovery and provenance
- 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
- 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
- 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
- context
- Updated: February 21, 2025
- datetime
- 2025-02-21T12:00:00Z
- display
- February 21, 2025
Preserved source evidence · Not medical advice
Triangle