- ICH GCP
- Yhdysvaltain kliinisten tutkimusten rekisteri
- Kliininen tutkimus NCT07560358
Adebrelimab Combined With Chemoradiotherapy in Patients With Large Bulky Stage III Unresectable Non-Small Cell Lung Cancer
A Randomized Controlled Clinical Study of Adebrelimab Combined With Chemoradiotherapy in Patients With Large Bulky Stage III Unresectable Non-Small Cell Lung Cancer
Tutkimuksen yleiskatsaus
Tila
Opintotyyppi
Ilmoittautuminen (Arvioitu)
Vaihe
- Vaihe 3
Yhteystiedot ja paikat
Opiskeluyhteys
- Nimi: Zhijie Wang, MD
- Puhelinnumero: +86 13466323860
- Sähköposti: jie_969@163.com
Opiskelupaikat
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Beijing Municipality
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Beijing, Beijing Municipality, Kiina, 100021
- National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College
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Osallistumiskriteerit
Kelpoisuusvaatimukset
Opintokelpoiset iät
- Aikuinen
- Vanhempi Aikuinen
Hyväksyy terveitä vapaaehtoisia
Kuvaus
Inclusion Criteria:
- Aged between 18 and 75 years;
- ECOG performance status score of 0 or 1;
- Histologically or cytologically confirmed non-small cell lung cancer (NSCLC);
- Unresectable stage III NSCLC (per AJCC 9th edition staging), with primary tumor diameter T ≥ 5 cm or regional metastatic lymph node short-axis diameter N ≥ 2 cm;
- Expected survival time of at least 3 months;
- No prior anti-tumor treatment before enrollment, including radiotherapy, chemotherapy, surgery and targeted therapy;
- Adequate function of major organs;
- Female subjects must have a negative pregnancy test result and be willing to use effective contraception;
- Subjects voluntarily participate in the study, sign the informed consent form, with good compliance and willingness to complete follow-up.
Exclusion Criteria:
- Subjects with known positive EGFR mutation or positive ALK fusion.
- Histologically or cytologically confirmed mixed SCLC and NSCLC, large cell neuroendocrine carcinoma, and sarcomatoid carcinoma.
- Participation in another clinical trial within 4 weeks prior to the first study dose or within 5 half-lives of the study drug, whichever is shorter.
- Subjects who have received systemic immunosuppressive therapy within 2 weeks before the first dose, or those who are expected to require systemic immunosuppressive drugs during the study treatment period.
- Subjects with congenital or acquired immunodeficiency, such as HIV infection; or with a history of autoimmune diseases.
- Active hepatitis B, hepatitis C, or co-infection with both hepatitis B and hepatitis C.
- Uncontrolled third-space effusions, such as massive pleural effusion, ascites or pericardial effusion.
- History of other malignant tumors (other than NSCLC) within 5 years prior to screening.
- Subjects with prior interstitial lung disease requiring hormone therapy.
- Subjects with severe cardiovascular and cerebrovascular diseases.
- History of severe bleeding events or arterial/venous thromboembolic events.
- Severe infection within 4 weeks before the first dose; evidence of active tuberculosis infection within 1 year prior to the first dose; active fungal, bacterial and/or viral infections requiring systemic treatment.
- Subjects with prior or planned allogeneic bone marrow transplantation or solid organ transplantation.
- History of live attenuated vaccination within 28 days before the first dose, or planned live attenuated vaccination during the study period; pregnant or lactating women; fertile patients who are unwilling or unable to adopt effective contraceptive measures.
- Known hypersensitivity, anaphylactic reaction or intolerance to adebrelimab, chemotherapy agents, or their excipients.
- Subjects with a known history of psychoactive substance abuse, alcoholism or drug addiction.
Opintosuunnitelma
Miten tutkimus on suunniteltu?
Suunnittelun yksityiskohdat
- Ensisijainen käyttötarkoitus: Hoito
- Jako: Satunnaistettu
- Inventiomalli: Rinnakkaistehtävä
- Naamiointi: Ei mitään (avoin tarra)
Aseet ja interventiot
Osallistujaryhmä / Arm |
Interventio / Hoito |
|---|---|
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Kokeellinen: After chemoimmunotherapy induction followed by cCRT/sCRT, then maintenance immunotherapy.
Patients receive adebrelimab(1200 mg iv, q3w) combined with chemotherapy for 2 cycles of induction therapy, followed by sequential/concurrent chemoradiotherapy (sCRT/cCRT), and then undergo adebrelimab monotherapy for consolidation treatment.
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Patients receive adebrelimab combined with chemotherapy for 2 cycles of induction therapy, followed by sequential/concurrent chemoradiotherapy (sCRT/cCRT), and then undergo adebrelimab monotherapy for consolidation treatment. adebrelimab: 1200 mg iv, q3w Radiation therapy: Total dose of 60 Gy ± 10% (range: 54 Gy - 66 Gy). Chemotherapy: Regimens will be administered in accordance with guideline recommendations. Subsequently, patients will receive adebrelimab monotherapy as consolidation treatment, with each treatment cycle lasting 3 weeks. Treatment will be continued until disease recurrence or metastasis, intolerable toxicity, subject's voluntary withdrawal, or investigator's decision to discontinue the subject from the study. |
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Active Comparator: Receive cCRT/sCRT followed by maintenance immunotherapy.
Adebrelimab monotherapy consolidation is administered after sCRT/cCRT.
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Receive cCRT/sCRT followed by maintenance immunotherapy.
adebrelimab: 1200 mg iv, q3w Radiation therapy: Total dose of 60 Gy ± 10% (range: 54 Gy - 66 Gy).
Chemotherapy: Regimens will be administered in accordance with guideline recommendations.
Subsequently, patients will receive adebrelimab monotherapy as consolidation treatment, with each treatment cycle lasting 3 weeks.
Treatment will be continued until disease recurrence or metastasis, intolerable toxicity, subject's voluntary withdrawal, or investigator's decision to discontinue the subject from the study.
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Mitä tutkimuksessa mitataan?
Ensisijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
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Progression-Free Survival (PFS)
Aikaikkuna: From enrollment to the end of monitoring at 1.5 years.
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PFS is defined as the time from the first dose of study treatment to the first documentation of disease progression according to RECIST v1.1 (as assessed by investigators) or death from any cause, whichever occurs first.
Subjects who are alive without progression at the time of analysis will be censored at the date of the last tumor assessment.
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From enrollment to the end of monitoring at 1.5 years.
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Toissijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
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Overall Survival (OS)
Aikaikkuna: From enrollment to the end of monitoring at 1.5 years.
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OS is defined as the time from the first dose of study treatment to death from any cause.
Subjects who are alive at the time of analysis will be censored at the date of last follow-up.
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From enrollment to the end of monitoring at 1.5 years.
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Objective Response Rate (ORR)
Aikaikkuna: From enrollment to the end of monitoring at 1.5 years.
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ORR is defined as the proportion of subjects who achieve a complete response (CR) or partial response (PR) as per RECIST v1.1.
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From enrollment to the end of monitoring at 1.5 years.
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Duration of Response (DoR)
Aikaikkuna: From enrollment to the end of monitoring at 1.5 years.
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DoR is defined as the time from the first documentation of CR or PR to the first documentation of disease progression or death.
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From enrollment to the end of monitoring at 1.5 years.
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The incidence of adverse events
Aikaikkuna: From enrollment to the end of monitoring at 1.5 years
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Incidence, nature, and severity of adverse events (AEs), graded according to NCI-CTCAE v6.0, including immune-related AEs and serious AEs.
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From enrollment to the end of monitoring at 1.5 years
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Time to Death or Distant Metastasis(TTDM)
Aikaikkuna: From enrollment to the end of monitoring at 1.5 years
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From randomization/enrollment to the first occurrence of distant metastasis or death from any cause, whichever occurs first.
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From enrollment to the end of monitoring at 1.5 years
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Muut tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
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Incremental Cost-Utility Ratio (ICUR)
Aikaikkuna: From randomization/enrollment to the end of 1.5-year follow-up.
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The Incremental Cost-Utility Ratio (ICUR) is defined as the incremental total cost divided by the incremental quality-adjusted life years (QALYs) between the experimental treatment group and the control group.
It reflects the additional cost required to gain one additional unit of health utility outcome (per QALY).
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From randomization/enrollment to the end of 1.5-year follow-up.
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Patient Quality of Life (QoL)
Aikaikkuna: From baseline to the end of 1.5-year follow-up.
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Patient Quality of Life (QoL) was assessed using validated patient-reported outcome questionnaires.
Changes in health-related quality of life from baseline to scheduled follow-up time points were analyzed, including physical function, emotional function, social function and disease-related symptom domains.
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From baseline to the end of 1.5-year follow-up.
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Exploratory biomarker analysis
Aikaikkuna: From enrollment to the end of 1.5-year follow-up.
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Exploratory analysis of relevant biomarker characteristics and their correlation with clinical efficacy outcomes.
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From enrollment to the end of 1.5-year follow-up.
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Yhteistyökumppanit ja tutkijat
Opintojen ennätyspäivät
Opi tärkeimmät päivämäärät
Opiskelun aloitus (Arvioitu)
Ensisijainen valmistuminen (Arvioitu)
Opintojen valmistuminen (Arvioitu)
Opintoihin ilmoittautumispäivät
Ensimmäinen lähetetty
Ensimmäinen toimitettu, joka täytti QC-kriteerit
Ensimmäinen Lähetetty (Todellinen)
Tutkimustietojen päivitykset
Viimeisin päivitys julkaistu (Todellinen)
Viimeisin lähetetty päivitys, joka täytti QC-kriteerit
Viimeksi vahvistettu
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