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Prospective Observation of Failure Patterns in NSCLC Treated With ICIs

29. juli 2020 oppdatert av: Zhengfei Zhu, Fudan University

Prospective Observational Study of Failure Patterns in Non-small Cell Lung Cancer Patients Treated With Immune Checkpoint Inhibitors

By prospectively observing the time to the best therapeutic effect of non-small cell lung cancer after ICI treatment, the characteristics of lesion distribution when the best therapeutic effect is reached, and the phenotype of disease progression after ICI treatment response, the investigators intended to explore the failure pattern of NSCLC after the once effective ICI treatment. The investigators also aim to evaluate the feasibility and clinical value of radiotherapy for the treatment of oligo-progressive lesions after ICI.

Studieoversikt

Status

Har ikke rekruttert ennå

Studietype

Observasjonsmessig

Registrering (Forventet)

320

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studiesteder

    • Shanghai
      • Shanghai, Shanghai, Kina, 200031
        • Fudan University Shanghai Cancer Center
        • Ta kontakt med:

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år til 75 år (Voksen, Eldre voksen)

Tar imot friske frivillige

N/A

Kjønn som er kvalifisert for studier

Alle

Prøvetakingsmetode

Ikke-sannsynlighetsprøve

Studiepopulasjon

stage IV NSCLC developing acquired resistance under ICI treatment.

Beskrivelse

Inclusion Criteria (Part I):

  • Age between 18 and 75 years.
  • ECOG PS 0-1.
  • Pathologically confirmed stage IV NSCLC.
  • Negative for driver genes including EGFR, ALK, and ROS-1.
  • Patients achieved PR or CR after ICI treatment, as defined by RECIST 1.1.
  • Patients with complete radiological information of baseline lesions.
  • Life expectancy of more than 3 months.
  • Ability to understand and willingness to provide the informed consent.

Exclusion Criteria (Part I):

  • Severe autoimmune disease or other contradictions to ICI treatment.
  • Mixed small cell with non-small cell lung cancer histology.
  • Driver gene positive, including EGFR, ALK, and ROS-1.
  • Pregnant or lactating women.
  • History of any other malignancy.
  • Active infection, congestive heart failure, myocardial infarction within the 6 months prior to enrollment, unstable angina pectoris or cardiac arrhythmia.
  • Patients receiving immunosuppressive agents,or other investigational treatment. Long-term corticosteroid users are also excluded.
  • Mental disorders, drug abuse, and social condition that may negatively impact compliance in the opinion of the investigator.

Inclusion Criteria (Part II, patients with OPD):

  • Patients with oligo-progression disease (1-3 progression lesions in 1-2 organs) when developing acquired resistance to ICI.
  • Radiotherapy to at least one of the OPD lesions is indicated in the opinion of the investigator. At least one of the irradiated lesion(s) should be evaluable according to RECIST 1.1.
  • ECOG PS 0-2.
  • Life expectancy of more than 3 months.
  • Complete radiological information of all lesions during the follow-up.
  • Patients with a prior history of surgery are eligible if they have recovered adequately from the toxicity and/or complications of surgery.
  • Adequate bone marrow function within 1 week prior to the enrollment: hemoglobin ≥80g/L, white blood cell (WBC) count ≥ 4.0 * 10 ^ 9/L or neutrophil count ≥ 1.5 * 10 ^ 9/L, and platelet count ≥ 100 * 10 ^ 9/L;
  • Ability to understand and willingness to provide the informed consent.

Exclusion Criteria (Part II):

  • Secondary malignancy.
  • Histology transformation to non-NSCLC.
  • Ineligible for radiotherapy in the opinion of the investigator. Or none of the OPD are evaluable by RECIST 1.1.
  • ECOG PS 3 or worse.
  • Short life expectancy (less than 3 months).
  • Unable to provide complete radiological information of lesions.
  • Inadequate bone marrow function.
  • Cannot understand or unwilling to provide the informed consent.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Oligo-progression disease rate in NSCLC patients developing acquired resistance to ICI treatment.
Tidsramme: at least 2 months after ICI treatment.

Acquired resistance (AR) was defined as disease progression after partial or complete response (PR or CR) to ICI treatment. (by RECIST standard v1.1)

When observing disease progression in ICI treatment, the number and distribution of progression lesions were recorded.

Oligo-progression disease (OPD) was defined as 1-3 progression lesions in 1-2 organs. The OPD rate in all AR cases will be calculated.

at least 2 months after ICI treatment.

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Prosentandel av deltakere med uønskede hendelser
Tidsramme: To år
Behandlingsrelaterte bivirkninger ble vurdert og gradert i henhold til CTCAE v. 5.0.
To år
Overall objective response rate to radiotherapy.
Tidsramme: at least 4 weeks after radiotherapy.
When radiotherapy to at least one of the OPD lesions is indicated in the opinion of the investigator. Overall objective response rate (ORR) to radiotherapy will be recorded. ORR was defined as the proportion of participants with partial response (PR) or complete response (CR) to treatment as defined by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1.
at least 4 weeks after radiotherapy.
Objective response rate in non-irradiated lesion
Tidsramme: at least 4 weeks after radiotherapy.
Objective response rate (ORR) in Non-irradiated Lesion was defined as the proportion of patients with at least 30% reduction from baseline in the longest diameter of any of non-irradiated target lesions defined by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 at any time-point from the date of treatment initiation to the date of last follow-up.
at least 4 weeks after radiotherapy.
Overall Survival since AR development.
Tidsramme: Two years
OS was defined as the time from the date of enrollment until death by any cause. Participants still alive at the time of data analysis were censored at the date of last follow-up.
Two years

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Forventet)

1. september 2020

Primær fullføring (Forventet)

31. august 2023

Studiet fullført (Forventet)

31. august 2025

Datoer for studieregistrering

Først innsendt

27. juli 2020

Først innsendt som oppfylte QC-kriteriene

27. juli 2020

Først lagt ut (Faktiske)

30. juli 2020

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

31. juli 2020

Siste oppdatering sendt inn som oppfylte QC-kriteriene

29. juli 2020

Sist bekreftet

1. juli 2020

Mer informasjon

Begreper knyttet til denne studien

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

produkt produsert i og eksportert fra USA

Nei

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