- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07584161
MH-ART vs CF-IMRT in Postoperative Cervical/Endometrial Cancer (ARTISAN)
A Multicenter, Non-Inferiority, Phase III Randomized Controlled Trial Comparing Moderately Hypofractionated Online Adaptive Radiotherapy(MH-ART) vs. Conventional Fractionated Intensity-Modulated Radiotherapy(CF-IMRT) in Postoperative Cervical Cancer and Endometrial Cancer
Studieoversikt
Status
Forhold
Detaljert beskrivelse
Randomization:
Intervention Group: Moderately fractionated radiotherapy using online adaptive radiotherapy technology.
Control Group: Conventionally fractionated radiotherapy using image-guided intensity-modulated radiotherapy technology.
Stratification Factors for Randomization:Participating study center; Disease type (Cervical cancer / Endometrial cancer); Receipt of concurrent chemotherapy
Study Objectives:
Primary Endpoint: Acute adverse reactions/toxicity Secondary Endpoints: Late adverse reactions/toxicity, 3-year local control rate, 3-year distant metastasis rate, 3-year progression-free survival (PFS), 3-year overall survival (OS), 3-year disease-free survival (DFS), quality of life, cost-effectiveness analysis related to treatment.
Study Population:
Planned Sample Size: 228 participants
Inclusion Criteria:
- Participants must be fully voluntary and have decision-making capacity, providing written informed consent within 30 days prior to enrollment.
- Age ≥18 years and ≤75 years.
- ECOG performance status of 0-1, and expected to tolerate lying supine for half an hour.
- Have undergone radical surgery for cervical cancer (procedure: radical hysterectomy + pelvic lymphadenectomy ± para-aortic lymphadenectomy) or surgery for endometrial cancer (procedure: total hysterectomy + bilateral salpingo-oophorectomy ± pelvic and/or para-aortic lymph node dissection/sampling or sentinel lymph node biopsy).
- For participants with cervical cancer, the following criteria must be met:
(1)Pathologically diagnosed with cervical squamous cell carcinoma or adenocarcinoma.
(2)Must have at least one of the following high-risk factors; or have other risk factors requiring postoperative radiotherapy: High-risk factors: Pelvic lymph node metastasis, or positive surgical margin, or parametrial invasion.
Other risk factors: Middle or deep one-third stromal invasion, regardless of tumor size and LVSI status; Tumor size ≥4cm, regardless of depth of stromal invasion and LVSI status; Adenocarcinoma: Tumor size ≥2cm, or positive LVSI, regardless of depth of stromal invasion.
6.For participants with endometrial cancer, the following criteria must be met: Endometrioid adenocarcinoma: Grade 3 with superficial myometrial invasion, accompanied by substantial LVSI or age ≥70 years; Grade 2 with deep myometrial invasion, accompanied by substantial LVSI or age ≥60 years; Grade 3 with deep myometrial invasion; FIGO 2009 Stage II-IIIC1.
Non-endometrioid adenocarcinoma: FIGO 2009 Stage I-IIIC1 (serous carcinoma, clear cell carcinoma, mixed type).
7.Participants with high-risk factors may receive a vaginal brachytherapy boost following the completion of external beam radiotherapy.
8.Participants with high-risk cervical cancer must receive concurrent sensitizing chemotherapy for ≥4 cycles.
9.Participants must be eligible to receive sequential or sandwich adjuvant chemotherapy as planned.
Study Duration: September 2025 to September 2030 Participant Involvement Period: Follow-up for over 3 years after radiotherapy
Studietype
Registrering (Antatt)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiekontakt
- Navn: Xiaorong Hou, Professor
- Telefonnummer: +86 18612672203
- E-post: houxr@pumch.cn
Studer Kontakt Backup
- Navn: Zihan Yan
- Telefonnummer: +86 17860628938
- E-post: yanzihan_zora@163.com
Studiesteder
-
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Beijing Municipality
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Beijing, Beijing Municipality, Kina, 100730
- Rekruttering
- Peking Union Medical College Hospital
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Ta kontakt med:
- Xiaorong Hou, Professor
- Telefonnummer: +86 18612672203
- E-post: houxr@pumch.cn
-
Ta kontakt med:
- Zihan Yan
- Telefonnummer: +86 17860628938
- E-post: yanzihan_zora@163.com
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
- Eldre voksen
Tar imot friske frivillige
Beskrivelse
Inclusion Criteria:
- Participants must be fully voluntary and have decision-making capacity, providing written informed consent within 30 days prior to enrollment.
- Age ≥18 years and ≤75 years.
- ECOG performance status of 0-1, and expected to tolerate lying supine for half an hour.
- Have undergone radical surgery for cervical cancer (procedure: radical hysterectomy + pelvic lymphadenectomy ± para-aortic lymphadenectomy) or surgery for endometrial cancer (procedure: total hysterectomy + bilateral salpingo-oophorectomy ± pelvic and/or para-aortic lymph node dissection/sampling or sentinel lymph node biopsy).
- For participants with cervical cancer, the following criteria must be met:
(1)Pathologically diagnosed with cervical squamous cell carcinoma or adenocarcinoma.
(2)Must have at least one of the following high-risk factors; or have other risk factors requiring postoperative radiotherapy: High-risk factors: Pelvic lymph node metastasis, or positive surgical margin, or parametrial invasion.
Other risk factors: Middle or deep one-third stromal invasion, regardless of tumor size and LVSI status; Tumor size ≥4cm, regardless of depth of stromal invasion and LVSI status; Adenocarcinoma: Tumor size ≥2cm, or positive LVSI, regardless of depth of stromal invasion.
6.For participants with endometrial cancer, the following criteria must be met: Endometrioid adenocarcinoma: Grade 3 with superficial myometrial invasion, accompanied by substantial LVSI or age ≥70 years; Grade 2 with deep myometrial invasion, accompanied by substantial LVSI or age ≥60 years; Grade 3 with deep myometrial invasion; FIGO 2009 Stage II-IIIC1.
Non-endometrioid adenocarcinoma: FIGO 2009 Stage I-IIIC1 (serous carcinoma, clear cell carcinoma, mixed type).
7.Participants with high-risk factors may receive a vaginal brachytherapy boost following the completion of external beam radiotherapy.
8.Participants with high-risk cervical cancer must receive concurrent sensitizing chemotherapy for ≥4 cycles.
9.Participants must be eligible to receive sequential or sandwich adjuvant chemotherapy as planned.
Exclusion Criteria:
- Presence of confirmed distant metastasis or para-aortic lymph node metastasis;
- Requirement for extended-field radiotherapy encompassing the para-aortic region;
- Initiation of radiotherapy exceeds the specified time limit after surgery: exceeding 6 months post-surgery if adjuvant chemotherapy was administered, or exceeding 3 months post-surgery if no adjuvant chemotherapy was administered;
- History of previous abdominal or pelvic radiotherapy;
- History of or concurrent secondary primary malignancy (except for non-melanoma skin cancer, papillary/follicular thyroid carcinoma, or carcinoma in situ of the breast);
- History of underlying intestinal diseases such as ulcerative colitis or Crohn's disease;
- Cervical cancer with pathological types such as adenosquamous carcinoma, small cell carcinoma, clear cell carcinoma, or other special types; Endometrial cancer with pathological types such as undifferentiated carcinoma, carcinosarcoma, or other special types;
- Pregnant or lactating women;
- Presence of active infection or fever;
- Other severe comorbidities that may significantly compromise protocol compliance, such as uncontrolled cardiac disease requiring treatment, renal disease, chronic hepatitis, poorly controlled diabetes, psychiatric disorders, etc.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
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Eksperimentell: MH-ART
Moderately fractionated radiotherapy using online adaptive radiotherapy technology.
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Treatment will be delivered using an online adaptive radiotherapy device.
A moderately fractionated regimen will be employed, with a prescribed dose of 40.05 Gy in 15 fractions, administered once daily, five times per week.
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Annen: CF-IMRT
Conventionally fractionated radiotherapy using image-guided intensity-modulated radiotherapy technology.
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Intensity-modulated radiotherapy techniques will be used, including FF-IMRT, VMAT, or TOMO.
A conventionally fractionated regimen will be employed, with a prescribed dose of 45 Gy in 25 fractions, administered once daily, five times per week.
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Incidence of Acute Toxicity
Tidsramme: Within 90 days (inclusive) from the start of radiotherapy
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Toxicities occurring within 90 days (inclusive) from the start of radiotherapy are defined as acute toxicities.
Acute toxicities will be evaluated using the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0.
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Within 90 days (inclusive) from the start of radiotherapy
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Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Incidence of Late Toxicity
Tidsramme: From 90 days after the start of radiotherapy until death from any cause, assessed up to 3 years.
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Toxicities occurring more than 90 days after the start of radiotherapy are defined as late toxicities.
Late toxicities will be evaluated using the RTOG/EORTC Late Radiation Morbidity Scoring Scheme.
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From 90 days after the start of radiotherapy until death from any cause, assessed up to 3 years.
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3 years Local Recurrence Rate
Tidsramme: From the end of radiotherapy until local recurrence or death from any cause, assessed up to 3 years.
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The proportion of subjects who do not experience tumor recurrence or progression within the radiation field within 3 years after the end of radiotherapy.
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From the end of radiotherapy until local recurrence or death from any cause, assessed up to 3 years.
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3 years Distant Metastasis Rate
Tidsramme: From the start of radiotherapy until distant metastasis or death from any cause, assessed up to 3 years.
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The proportion of subjects who develop distant metastasis within 3 years after the start of radiotherapy.
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From the start of radiotherapy until distant metastasis or death from any cause, assessed up to 3 years.
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3 years Progression-Free Survival
Tidsramme: From the start of radiotherapy until the first disease recurrence (local/regional/distant) or death from any cause, assessed up to 3 years.
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The time interval from the start of radiotherapy to the first occurrence of disease recurrence (local, regional, or distant) or death from any cause within 3 years after the start of radiotherapy.
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From the start of radiotherapy until the first disease recurrence (local/regional/distant) or death from any cause, assessed up to 3 years.
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3 years Overall Survival
Tidsramme: From the start of radiotherapy until death from any cause, assessed up to 3 years.
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The time interval from the start of radiotherapy to death from any cause within 3 years after the start of radiotherapy.
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From the start of radiotherapy until death from any cause, assessed up to 3 years.
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3 years Disease-Free Survival
Tidsramme: From the start of radiotherapy until the first local/regional recurrence, distant metastasis, or death from any cause, assessed up to 3 years.
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The time interval from the start of radiotherapy to the first occurrence of local or regional recurrence, distant metastasis, or death from any cause within 3 years after the start of radiotherapy.
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From the start of radiotherapy until the first local/regional recurrence, distant metastasis, or death from any cause, assessed up to 3 years.
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Quality of Life
Tidsramme: Baseline, at the end of radiotherapy, and every 3 months thereafter until 3 years from start of radiotherapy.
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Quality of life will be assessed using the QLQ-C30 questionnaire, in combination with the disease-specific module (QLQ-CX24 for cervical cancer; QLQ-EN24 for endometrial cancer).
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Baseline, at the end of radiotherapy, and every 3 months thereafter until 3 years from start of radiotherapy.
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Treatment-Related Cost-Effectiveness Analysis
Tidsramme: From the start of radiotherapy until death from any cause, assessed up to 3 years.
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The cost assessment should cover both medical costs and non-medical costs.
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From the start of radiotherapy until death from any cause, assessed up to 3 years.
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Samarbeidspartnere og etterforskere
Sponsor
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
- Urogenitale sykdommer
- Kjønnssykdommer
- Urogenitale neoplasmer
- Neoplasmer etter nettsted
- Neoplasmer
- Kvinnelige urogenitale sykdommer
- Kvinnelige urogenitale sykdommer og graviditetskomplikasjoner
- Livmorsykdommer
- Kjønnssykdommer, kvinner
- Genitale neoplasmer, kvinnelige
- Livmor livmorhalssykdommer
- Uterine neoplasmer
- Uterine cervikale neoplasmer
- Endometriale neoplasmer
Andre studie-ID-numre
- ARTISAN
Plan for individuelle deltakerdata (IPD)
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