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Chinese Multicenter Registry for Peutz-Jeghers Syndrome

8. listopadu 2026 aktualizováno: Kangyu, First People's Hospital of Hangzhou

This prospective, observational patient registry will enroll approximately 1,000 individuals with a clinical or molecular diagnosis of Peutz-Jeghers syndrome (PJS) at participating hospitals in China. The registry will collect standardized clinical information, existing genetic test reports, family history, and longitudinal outcomes. The primary objective is to estimate the 10-year cumulative incidence of a first invasive malignancy after enrollment among participants without a previous malignancy or an unresolved suspected malignancy at baseline, accounting for death as a competing event. Secondary objectives address organ-specific malignancies, new primary cancers in participants with a cancer history, mortality, major polyp-related complications, and clinical and STK11 variant characteristics. Participants may be followed for up to 20 years. Biospecimen donation, additional baseline sampling, research sequencing, and patient-derived organoid studies are optional and require the corresponding consent. Refusal of an optional component does not preclude participation in the clinical registry. No treatment or clinical surveillance strategy is assigned by the study.

Přehled studie

Postavení

Nábor

Podmínky

Peutz-Jeghersův syndrom

Detailní popis

Peutz-Jeghers syndrome is a rare inherited tumor-predisposition syndrome associated with gastrointestinal hamartomatous polyps, mucocutaneous pigmentation, and increased risks of several malignancies. This multicenter registry will document the clinical course of enrolled patients receiving usual care and will support carefully defined genotype-phenotype and translational research. It is a hospital-based, non-probability sample and is not designed to provide a probability-representative estimate for the entire Chinese PJS population.

The purpose of this study is to establish a nationwide multicenter registry of patients with PJS, integrating standardized clinical information, existing genetic reports, optional biospecimen studies and prospective follow-up. The primary objective is to estimate 10-year cumulative incidence of a first invasive malignancy among participants without previous or unresolved suspected malignancy at baseline. The study will support defined genotype-phenotype and translational analyses; it does not assign treatment or clinical surveillance.

Specific study objectives are listed below:

Establish a standardized PJS clinical database to define the clinical characteristics and natural history of the disease in Chinese patients.
Analyze the landscape of STK11 gene variants and the relationship between genotype and clinical phenotype.
Establish an optional biobank of patients with PJS, using separately consented specimens, to provide resources for approved research.
Establish separately consented patient-derived organoid models to investigate disease mechanisms and in vitro drug responses without directing patient treatment.
Explore the development of a precision management system. The workflow includes consecutive recruitment, diagnostic confirmation, core registry consent, baseline clinical-data abstraction, prospective follow-up and outcome review. Biospecimen collection, research sequencing and organoid studies are optional components; refusal does not preclude enrollment.

The registry will implement standardized baseline clinical-data abstraction, prospective follow-up and outcome review, with historical medical information will be abstracted at baseline and distinguished from prospectively observed events. All eligible, consenting participants contribute to the clinical registry. Participants will be contacted approximately every 12 months through routine visits, telephone, or institution-approved remote methods. Clinical and genetic associations will account for family relationships, recruitment pathway, center, and relevant prespecified covariates. STK11 germline variants will be classified using the ACMG/AMP framework and applicable subsequent guidance, with the reference sequence, testing scope, evidence, and interpretation date documented. Germline and tumor-only findings will be distinguished. Untested participants, participants with limited testing, those with variants of uncertain significance, and those with adequately evaluated negative findings will not be combined into a single wild-type group.

The primary analysis will estimate the cumulative incidence function at 10 years using an Aalen-Johansen approach, with uncertainty accounting for family clustering when supported by the data. Attained-age analyses will use delayed entry at enrollment and will not treat the period before enrollment as prospectively observed person-time. Optional biospecimen studies prioritize clinical residual material. No research-only tissue biopsy or enlargement of a clinical resection is permitted.Research sequencing, multi-omics, and patient-derived organoid or tumor-organoid studies will be performed only in authorized, suitable subsets. Laboratory and analytical methods will distinguish biological participants from repeated specimens or culture wells. Predictive biomarker analyses require pre-outcome specimens and family-separated validation. Research findings will not direct clinical treatment; clinically meaningful findings considered for return require appropriate confirmation, counseling, and the participant's documented preference.

Typ studie

Pozorovací

Zápis (Odhadovaný)

1000

Kontakty a umístění

Tato část poskytuje kontaktní údaje pro ty, kteří studii provádějí, a informace o tom, kde se tato studie provádí.

Studijní kontakt

Jméno: Yu Kang
Telefonní číslo: +86 19560161853
E-mail: kangyu@hospital.westlake.edu.cn

Studijní místa

Čína
- - Beijing, Čína
    - Zatím nenabíráme
    - Peking University Third Hospital
    - Kontakt:
      
      Congrong Liu
      
      Telefonní číslo: +86 13651215671
      
      E-mail: congrong_liu@163.com
  - Shanghai, Čína
    - Zatím nenabíráme
    - Fudan University Shanghai Cancer Center
    - Kontakt:
      
      Yanyun Li
      
      Telefonní číslo: +86 13601903229
      
      E-mail: liyanyun@fudan.edu.cn
  - Shanghai, Čína
    - Zatím nenabíráme
    - Obstetrics & Gynecology Hospital of Fudan University
    - Kontakt:
      
      Jing Xu
      
      Telefonní číslo: +86 18817301819
      
      E-mail: doctor_xj@163.com
  - Tianjin, Čína
    - Zatím nenabíráme
    - The Second Hospital of Tianjin Medical University
    - Kontakt:
      
      Haitao Wang
      
      Telefonní číslo: +86 18630955984
      
      E-mail: peterrock2000@126.com
- Fujian
  - Fuzhou, Fujian, Čína
    - Zatím nenabíráme
    - Fujian Maternity and Child Health Care Hospital
    - Kontakt:
      
      Huan Yi
      
      Telefonní číslo: +86 15960103922
      
      E-mail: yi.huan@fjmu.edu.cn
- Guangdong
  - Guangzhou, Guangdong, Čína
    - Zatím nenabíráme
    - Sun Yat-sen University Cancer Center
    - Kontakt:
      
      Yanling Feng
      
      Telefonní číslo: +86 13925090579
      
      E-mail: fengyl@sysucc.org.cn
- Shandong
  - Jinan, Shandong, Čína
    - Zatím nenabíráme
    - Qilu Hospital of Shandong University
    - Kontakt:
      
      Peng Li
      
      Telefonní číslo: +86 18560082010
      
      E-mail: peng_li2002@163.com
- Zhejiang
  - Hangzhou, Zhejiang, Čína
    - Nábor
    - First People's Hospital of Hangzhou
    - Kontakt:
      
      Yu Kang
      
      Telefonní číslo: +86 19560161853
      
      E-mail: kangyu@hospital.westlake.edu.cn
  - Hangzhou, Zhejiang, Čína
    - Zatím nenabíráme
    - Zhejiang Cancer Hospital
    - Kontakt:
      
      Qiang Wen
      
      Telefonní číslo: +86 13857105097
      
      E-mail: wenqiang@zjcc.org.cn

Kritéria účasti

Výzkumníci hledají lidi, kteří odpovídají určitému popisu, kterému se říká kritéria způsobilosti. Některé příklady těchto kritérií jsou celkový zdravotní stav osoby nebo předchozí léčba.

Kritéria způsobilosti

Věk způsobilý ke studiu

Dítě
Dospělý
Starší dospělý

Přijímá zdravé dobrovolníky

Pohlaví způsobilá ke studiu

Všechno

Metoda odběru vzorků

Vzorek nepravděpodobnosti

Studijní populace

Individuals with a confirmed clinical or molecular diagnosis of PJS who receive care at participating centers in China. Recruitment will be consecutive where feasible. Previous cancer does not preclude registry enrollment. Diagnostically unconfirmed relatives are not independently enrolled under this version. Relatives who independently meet clinical or molecular diagnostic criteria may enroll with separate consent and a unique individual identifier linked to a pedigree.

Popis

Inclusion Criteria:

A clinical diagnosis of PJS meeting at least one of the following: two or more histologically confirmed Peutz-Jeghers polyps; any number of Peutz-Jeghers polyps and a family history of PJS; characteristic mucocutaneous pigmentation and a family history of PJS; or any number of Peutz-Jeghers polyps together with characteristic mucocutaneous pigmentation. Alternatively, a molecular diagnosis established by a confirmed germline pathogenic or likely pathogenic STK11 variant associated with PJS, interpreted by appropriately qualified professionals.
Valid written informed consent for the core clinical registry from the participant or the legally appropriate guardian, with age- and capacity-appropriate information and assent when applicable.
Minimum clinical or genetic documentation sufficient to confirm eligibility and agreement to at least one feasible method of longitudinal contact or record-based follow-up within the approved consent.

Biospecimen donation, availability of all specimen types, and participation in research sequencing or organoid experiments are not required for clinical registry enrollment.

Exclusion Criteria:

Neither the clinical nor molecular diagnostic pathway can be confirmed. A variant of uncertain significance alone does not satisfy molecular eligibility.
Absence of valid consent for the core registry. Duplicate records of the same individual will be merged rather than counted as additional participants. Inability or refusal to undergo an optional sample procedure is not a registry exclusion criterion. Procedure-specific safety restrictions affect that procedure only.

Studijní plán

Tato část poskytuje podrobnosti o studijním plánu, včetně toho, jak je studie navržena a co studie měří.

Jak je studie koncipována?

Detaily designu

Observační modely: COHORT
Časové perspektivy: PROSPECTIVE

Kohorty a intervence

Skupina / kohorta Skupina / kohorta Skupina nebo podskupina účastníků pozorovací studie, která je hodnocena z hlediska biomedicínských nebo zdravotních výsledků.
Peutz-Jeghers syndrome Individuals meeting protocol-defined clinical diagnostic criteria or carrying a confirmed germline pathogenic or likely pathogenic STK11 variant associated with PJS. Participants with and without previous cancer may enroll. Optional biospecimen and genetic components do not determine clinical registry eligibility.

Co je měření studie?

Primární výstupní opatření

Měření výsledku	Popis opatření	Časové okno
10-year cumulative incidence of a first invasive malignancy Časové okno: From enrollment to 10 years after enrollment, first invasive malignancy, death, withdrawal, or last reliable event-free assessment, as applicable.	Time from registry enrollment to the first confirmed invasive malignant neoplasm among participants with no previous malignancy and no unresolved suspected malignancy at baseline. Pathology will be the preferred evidence for solid tumors; hematologic malignancies will follow the relevant diagnostic criteria. Benign lesions, in situ disease, recurrence, progression, and metastases from an existing primary are excluded from this endpoint. The cumulative incidence at 10 years will be estimated with death before malignancy as a competing event. Participants with previous malignancy are not included in this primary risk set.	From enrollment to 10 years after enrollment, first invasive malignancy, death, withdrawal, or last reliable event-free assessment, as applicable.

Sekundární výstupní opatření

Měření výsledku	Popis opatření	Časové okno
Organ-specific cumulative incidence of a new primary invasive malignancy Časové okno: From enrollment up to 20 years; estimates at 5, 10, and 20 years where supported.	First new primary invasive malignancy at each specified organ site, analyzed separately among participants without a previous malignancy at that site and with the relevant organ at risk at baseline. Site and histologic type will be recorded. Death and removal of the at-risk organ without target cancer will be handled according to the prespecified competing-risk or multistate analysis. In situ disease and metastases will not be counted as new primary invasive cancers.	From enrollment up to 20 years; estimates at 5, 10, and 20 years where supported.
Cumulative incidence of a subsequent new primary invasive malignancy in participants with a cancer history Časové okno: From enrollment up to 20 years.	Time from enrollment to the next confirmed new primary invasive malignancy among participants with a malignancy diagnosed before enrollment. New primary disease will be distinguished by clinical review from recurrence, progression, and metastasis of an existing cancer. Death before a subsequent primary cancer is a competing event.	From enrollment up to 20 years.
All-cause mortality Časové okno: From enrollment up to 20 years; summaries at 5, 10, and 20 years where supported.	Time from enrollment to death from any cause among all enrolled participants. Death dates and evidence sources will be recorded. Participants not known to have died will be censored at the last date on which they were known to be alive or the applicable end of follow-up. Survival probabilities and death rates will be reported.	From enrollment up to 20 years; summaries at 5, 10, and 20 years where supported.
Cumulative incidence of cancer-related death Časové okno: From enrollment up to 20 years.	Time from enrollment to death attributed to malignancy, based on available medical records, death documentation, and outcome review. Non-cancer death is a competing event. Deaths of uncertain cause will be recorded separately and included in sensitivity analyses.	From enrollment up to 20 years.
Cumulative incidence of a first major polyp-related complication Časové okno: From enrollment up to 20 years.	Time from enrollment to the first episode of intussusception, bowel obstruction, or gastrointestinal bleeding that results in hospitalization, emergency surgery or endoscopic treatment, or transfusion. Preventive polypectomy without an acute complication is excluded. Repeat episodes and the individual components will also be documented and summarized separately.	From enrollment up to 20 years.
Age at clinical diagnosis of PJS Časové okno: At enrollment, using available historical records.	Age, in years, when the participant first met documented clinical diagnostic criteria for PJS. The evidence source and precision of the date will be recorded. Median, interquartile range, and the number with available information will be reported; molecularly ascertained participants without a clinical diagnosis will be identified separately.	At enrollment, using available historical records.
Baseline gastrointestinal polyp involvement by anatomical site Časové okno: At enrollment, using available historical and baseline records.	Number and proportion of participants with documented PJS-related polyps in each gastrointestinal site before or at baseline, with sites reported separately. Each proportion will use the number with sufficient information for that site as its denominator; unassessed or unknown sites will not be coded as negative.	At enrollment, using available historical and baseline records.
Distribution of documented STK11 germline variant classifications and variant types Časové okno: At enrollment; updated classifications retained separately during follow-up.	Counts and proportions of participants and independent families by STK11 germline variant classification and predefined variant type. Testing method, scope, and interpretation date will be documented. Pathogenic/likely pathogenic findings, variants of uncertain significance, adequately assessed negative findings, limited testing, and no testing will be reported separately. Genotype-phenotype association analyses use the clinical endpoints defined elsewhere and are exploratory.	At enrollment; updated classifications retained separately during follow-up.

Spolupracovníci a vyšetřovatelé

Zde najdete lidi a organizace zapojené do této studie.

Sponzor

First People's Hospital of Hangzhou

Publikace a užitečné odkazy

Osoba odpovědná za zadávání informací o studiu tyto publikace poskytuje dobrovolně. Mohou se týkat čehokoli, co souvisí se studiem.

Obecné publikace

Termíny studijních záznamů

Tato data sledují průběh záznamů studie a předkládání souhrnných výsledků na ClinicalTrials.gov. Záznamy ze studií a hlášené výsledky jsou před zveřejněním na veřejné webové stránce přezkoumány Národní lékařskou knihovnou (NLM), aby se ujistily, že splňují specifické standardy kontroly kvality.

Hlavní termíny studia

Začátek studia (Odhadovaný)

1. listopadu 2026

Primární dokončení (Odhadovaný)

1. října 2046

Dokončení studie (Odhadovaný)

1. října 2056

Termíny zápisu do studia

První předloženo

16. října 2026

První předloženo, které splnilo kritéria kontroly kvality