A Prospective Study of Response-adapted Low-dose Radiotherapy Combined With Orelabrutinib for Localized Mucosa-associated Lymphoid Tissue Extranodal Marginal Zone Lymphoma
Studieoversikt
Status
Status
Forhold
Forhold
Intervensjon / Behandling
Intervensjon / Behandling
Studietype
Studietype
Registrering (Antatt)
Registrering
Fase
Fase
- Fase 2
Kontakter og plasseringer
Studiekontakt
Studiekontakt
- Navn: Gang Cai, MD
- Telefonnummer: 602400 +86-021-64370045
- E-post: cg11855@rjh.com.cn
Studer Kontakt Backup
- Navn: Shu-Bei Wang, MD
- Telefonnummer: 602400 +86-021-64370045
- E-post: wangshubei@163.com
Studiesteder
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Shanghai Municipality
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Shanghai, Shanghai Municipality, Kina, 200000
- Xin Hua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine
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Ta kontakt med:
- Jiang-Bo Wan, MD
- Telefonnummer: +86-021-25077999
- E-post: jiangbowan@sina.com
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Shanghai, Shanghai Municipality, Kina
- Fudan University Affiliated Minhang Hospital
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Ta kontakt med:
- Yun-Hua Hou, MD
- Telefonnummer: +86-021-64923400
- E-post: hou_yunhua@fudan.edu.cn
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Shanghai, Shanghai Municipality, Kina
- Huadong Hospital
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Ta kontakt med:
- Jie-Xian Ma, MD
- Telefonnummer: +86-021-62483180
- E-post: jiexianma@hotmail.com
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Deltakelseskriterier
Kvalifikasjonskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
- Eldre voksen
Tar imot friske frivillige
Beskrivelse
Inclusion Criteria:
- Patients must meet all of the following criteria to be eligible for enrollment in this study:
- The patient voluntarily agrees to participate in this study and provides written informed consent;
- Age ≥ 18 years;
- Histopathologically confirmed diagnosis of extranodal marginal zone B-cell lymphoma of the mucosa-associated lymphoid tissue (MALT) type;
- Involved sites include but are not limited to: orbit, parotid gland, thyroid, Helicobacter pylori (H. pylori)-negative gastric MALT (in this study, H. pylori-negative gastric MALT is defined as negative results on both gastric mucosal tissue biopsy and serum H. pylori antibody test within the past 6 months; for patients with unknown prior H. pylori status who have received anti-H. pylori therapy, a positive serum H. pylori antibody test is permissible, provided that a subsequent gastroscopy or urea breath test confirms negativity);
- Lugano stage I-II disease;
- Able to swallow tablets normally;
- Eastern Cooperative Oncology Group performance status (ECOG-PS) score of 0-2;
- No prior radiotherapy, chemotherapy, targeted therapy, or immunotherapy for MALT lymphoma;
- Life expectancy ≥ 12 months;
Adequate major organ function, meeting the following criteria:
- Hematological parameters: absolute neutrophil count ≥ 1.0 × 10⁹/L; platelet count ≥ 50 × 10⁹/L; hemoglobin ≥ 80 g/L;
- Biochemical parameters: total bilirubin < 1.5 × upper limit of normal (ULN); alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 3 × ULN; serum creatinine ≤ 1.5 × ULN or calculated creatinine clearance > 50 mL/min;
- Female patients of childbearing potential must have a negative serum pregnancy test within 72 hours prior to the first dose of study treatment and must agree to use highly effective methods of contraception during the study period and for 120 days after the last dose. Male patients with female partners of childbearing potential must be surgically sterile or agree to use highly effective methods of contraception during the study period and for 120 days after the last dose.
Exclusion Criteria:
- Patients who meet any of the following criteria will be excluded from enrollment in this study:
- Major surgery (excluding diagnostic surgery) within 4 weeks prior to enrollment;
- Previous or concurrent diagnosis of another malignancy, with the exception of adequately treated basal cell carcinoma of the skin, carcinoma in situ of the cervix, or carcinoma in situ of the breast;
- Active chronic hepatitis B infection, defined as detectable HBV DNA;
- Active HIV or syphilis infection;
- Presence of severe concomitant medical conditions or circumstances that may affect the patient's eligibility or safety during the study period;
- Pregnant or breastfeeding women;
- Presence of active psychiatric disorders or other psychological conditions that may impair the patient's ability to provide informed consent or understand the study procedures;
- Patients considered by the investigator to have poor compliance; Pathologically or radiologically confirmed distant metastasis; Other factors that, in the investigator's judgment, may affect the study results or necessitate premature termination of the study, including but not limited to alcohol abuse, drug abuse, other severe diseases (including psychiatric disorders) requiring concomitant treatment, significant laboratory abnormalities, or family/social circumstances that may compromise patient safety.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Enkelt
Antall våpen
Våpen og intervensjoner
Deltakergruppe / ArmDeltakergruppe / Arm |
Intervensjon / BehandlingIntervensjon / Behandling |
|---|---|
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Eksperimentell: research arm
Patients will receive a total dose of 4 Gy, delivered as 2 consecutive daily fractions, encompassing all initially involved disease sites.
Following radiotherapy, patients will then receive oral orelabrutinib at a dose of 150 mg once daily, administered in 4-week cycles for a total of 6 cycles.
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4 Gy in 2 consecutive daily fractions subsequently with orelabrutinib
Andre navn:
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Aktiv komparator: control arm
Patients will receive a total of 24 Gy in 12 fractions comprehensively to all initially involved sites of disease over 12 consecutive business days.
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24 Gy i 12 brøk
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Hva måler studien?
Primære resultatmål
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Complete response rate
Tidsramme: 6 months
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The disappearance of all target lesions and the normalization of tumor marker levels, with no new lesions identified.
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6 months
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Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Frekvens for akutt toksisitet (alle og over grad 3)
Tidsramme: Fra påmelding til 3 måneder etter behandling
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toksisitet i henhold til CTCAE-kriterier
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Fra påmelding til 3 måneder etter behandling
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Hyppighet av sen toksisitet (alle og over grad 3)
Tidsramme: Etter 3 måneders påmelding
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toksisitet i henhold til CTCAE-kriterier
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Etter 3 måneders påmelding
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Objective Response Rate (ORR)
Tidsramme: 6 months
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The proportion of patients who achieve either a complete response (CR) or partial response (PR) as their best overall response, according to predefined response criteria (e.g., Lugano criteria), relative to the total number of evaluable patients.
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6 months
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Duration of Response (DOR)
Tidsramme: 6 months
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The time from the first documented objective response (CR or PR) to the first documented disease progression (PD) or death from any cause, whichever occurs first.
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6 months
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2-year Event-Free Survival (EFS)
Tidsramme: 2 years
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The probability of remaining free from any predefined event (including disease progression, relapse, initiation of new anticancer therapy, or death from any cause) at 2 years from the start of treatment, as estimated by the Kaplan-Meier method.
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2 years
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2-year Overall Survival (OS)
Tidsramme: 2 years
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The probability of remaining alive at 2 years from the start of treatment, regardless of disease status, as estimated by the Kaplan-Meier method.
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2 years
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2-year Local Control Rate
Tidsramme: 2 years
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The probability of the absence of local progression or local recurrence at the irradiated site(s) at 2 years from the start of treatment, as estimated by the Kaplan-Meier method.
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2 years
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2-year Distant Metastasis Rate
Tidsramme: 2 years
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The proportion of patients who develop new lesions outside the initially involved sites or areas of irradiation within 2 years from the start of treatment.
Alternatively, it can be expressed as the cumulative incidence of distant metastasis at 2 years, accounting for competing risks.
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2 years
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Samarbeidspartnere og etterforskere
Sponsor
Sponsor
Etterforskere
Etterforskere
- Hovedetterforsker: Shu-Bei Wang, MD, Ruijin Hospital
Publikasjoner og nyttige lenker
Generelle publikasjoner
- Deng LJ, Zhou KS, Liu LH, Zhang MZ, Li ZM, Ji CY, Xu W, Liu T, Xu B, Wang X, Gao SJ, Zhang HL, Hu Y, Li Y, Cheng Y, Yang HY, Cao JN, Zhu ZM, Hu JD, Zhang W, Jing HM, Ding KY, Zhang XY, Zhao RB, Zhang B, Tian YM, Song YP, Song YQ, Zhu J. Orelabrutinib for the treatment of relapsed or refractory MCL: a phase 1/2, open-label, multicenter, single-arm study. Blood Adv. 2023 Aug 22;7(16):4349-4357. doi: 10.1182/bloodadvances.2022009168.
- Pinnix CC, Dabaja BS, Gunther JR, Fang PQ, Wu SY, Nastoupil LJ, Strati P, Nair R, Ahmed S, Steiner R, Westin J, Neelapu S, Rodriguez MA, Lee HJ, Wang M, Flowers C, Feng L, Esmaeli B. Response-Adapted Ultralow-Dose Radiation Therapy for Orbital Indolent B-Cell Lymphoma: A Phase 2 Nonrandomized Controlled Trial. JAMA Oncol. 2024 Sep 1;10(9):1195-1203. doi: 10.1001/jamaoncol.2024.2112.
Studierekorddatoer
Studer hoveddatoer
Studiestart (Antatt)
Studiestart
Primær fullføring (Antatt)
Primær fullføring
Studiet fullført (Antatt)
Studiet fullført
Datoer for studieregistrering
Først innsendt
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Først lagt ut
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Sist oppdatering lagt ut
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
Andre studie-ID-numre
- 2026255
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