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A Multicenter Randomized Open-Label Trial Evaluating ctDNA-Guided Interruption Versus Standard of Care Immune-Checkpoint Inhibitor (ICI) Therapy In Patients With Advanced / Metastatic Solid Tumors. (SIGNAL-IO 301)
A Multicenter Randomized Open-Label Trial Evaluating ctDNA-Guided Interruption Versus Standard of Care Continuous Immune-Checkpoint Inhibitor (ICI) Therapy In Patients With Advanced/Metastatic Solid Tumors
Studie Overzicht
Toestand
Conditie
- NSCLC
- Geavanceerde solide tumoren
- Vaste tumoren
- Metastatische solide tumoren
- RCC, niercelkanker
- Gevorderde solide tumoren Kanker
- CRC
- MSI hoge colorectale kanker
- Melanoom (huidkanker)
- DMMR Colorectale Kanker
- RCC
- NSCLC (niet-kleincellige longkanker)
- Melanoom (huid) Stadium IV
- NSCLC (geavanceerde niet-kleincellige longkanker)
- NSCLC (niet-kleincellig longcarcinoom)
Interventie / Behandeling
Gedetailleerde beschrijving
This is a multicenter, open-label, randomized (1:1) trial designed to evaluate whether ctDNA-guided interruption of immune-checkpoint inhibitor (ICI) therapy provides comparable survival to standard of care (SoC) continuous ICI therapy in patients with histologically confirmed advanced/metastatic non-small cell lung cancer (NSCLC), melanoma, microsatellite instability-high (MSI-High)/Deficient Mismatch Repair (dMMR) colorectal cancer (CRC), renal cell carcinoma (RCC) and other solid tumors.
Patients meeting eligibility criteria are randomized into two arms:
Arm A (SoC Continuous ICI): Participants will continue current ICI therapy per SoC.
Arm B (ctDNA-Guided Intermittent ICI): Participants will interrupt ICI therapy upon randomization and pursue monitoring that includes serial ctDNA testing. They will reinitiate the same ICI therapy (monotherapy or dual-ICI therapy as documented at enrollment) if they become ctDNA-positive without evidence of radiographic progression. Following reinitiation, ICI therapy may again be interrupted after achievement of ≥ 2 consecutive ctDNA-negative results and subsequently re-initiated upon recurrence of ctDNA positivity without evidence of radiographic progression. This cycle of ctDNA-guided interruption and reinitiation (maximum of 2 ICI interruptions) may continue until radiographic progression is documented. Upon radiographic progression, treatment will be determined by the treating physician in accordance with SoC.
Participants will be followed prospectively from randomization through the end of the treatment monitoring phase for up to 36 months and then survival follow-up, up to 5 years. Participants in both arms will undergo response assessments including imaging (CT/MRI) (BICR review) and ctDNA testing performed q12 weeks; PRO (QLQ-C30, FACT-ICM, PRO-CTCAE & EQ-5D-5L) data collection (q12 weeks); and continued toxicity assessment reviewed per CTCAE v6.0 at each visit and unscheduled contacts.
All data are collected under a unified electronic data-capture (EDC) system with site entry verified by central data management. Core data streams include clinical visits, imaging, ctDNA testing, safety events, PROs, and healthcare resource consumption.
Digitized slides of tissues (obtained either from commercial Signatera tests or upon confirmatory Signatera testing) may be collected for future research. Imaging data collected as part of study procedures may also be centrally archived for exploratory imaging and radiomic analyses.
Optional biobanking: Two 10 mL Streck blood samples may be collected at enrollment and at confirmed disease progression, defined as radiographic progression (per RECIST 1.1), for exploratory biomarker analyses.
Studietype
Inschrijving (Geschat)
Fase
- Niet toepasbaar
Contacten en locaties
Studiecontact
- Naam: Amanda L Andersen
- Telefoonnummer: 844-778-4700
- E-mail: aandersen@natera.com
Studie Contact Back-up
- Naam: Brooke Cormane
- Telefoonnummer: 844-778-4700
- E-mail: bcormane@natera.com
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Beschrijving
Inclusion Criteria:
General inclusion criteria includes the following selection criteria to be eligible for inclusion in any aspect of the study. Eligibility will be assessed by the investigator:
- Signed Informed consent
- Age ≥ 18 years
- ECOG 0-2.
Histologically confirmed advanced/metastatic solid tumors including:
- Melanoma: Unresectable recurrent, advanced, or metastatic
- NSCLC: Advanced or metastatic
- MSI-High/dMMR CRC: Metastatic
- RCC: Unresectable recurrent, advanced, or metastatic
- Other: Metastatic solid tumors
Received first line ICI monotherapy or dual-ICI therapy (e.g., PD-1/CTLA-4 combination therapy) for a minimum of 12 months (maximum of 15 months) for NSCLC, RCC & other metastatic solid tumors, or for a minimum of 6 months (maximum of 9 months) for melanoma and MSI-High /dMMR CRC. Exceptions permitted:
- For patients with NSCLC: First line platinum-based chemo-ICI regimens if on maintenance ICI +/- pemetrexed.
- For patients with melanoma: nivolumab/relatlimab is permissible.
- Radiographic CR/PR: Participants must have CR or PR at the last assessment performed within 6 weeks before randomization according to RECIST v1.1 using a diagnostic CT and/or MRI. Radiographic assessment must be confirmed by the BICR prior to randomization.
Known ctDNA-negative with a tissue-informed assay
- ≥ 2 consecutive ctDNA-negative results at least 6 weeks apart; last test within 1 month of enrollment.
- Note: A confirmatory Signatera Genome negative test must be completed at enrollment if previous ctDNA testing performed for clinical care was done with a test other than Signatera Genome.
Adequate organ function:
- Hematology: ANC ≥1500/μL; Platelets ≥100000/μL;Hemoglobin ≥9.0g/dL;
- Renal: Serum Cr ≤1.5×ULN or calculated CrCl ≥60 mL/min (using Cock-Gault formula);
- Hepatic: Total bilirubin ≤1.5 ×ULN or, for participants with total bilirubin levels >1.5×ULN, direct bilirubin within normal limits; AST (SGOT) and ALT (SGPT) ≤2.5×ULN;
- Coagulation: INR or PT, activated partial thromboplastin time (APTT) ≤1.5×ULN Note: Laboratory assessments performed as part of standard of care evaluations during immunotherapy treatment administration may be used to satisfy these eligibility criteria, provided they are obtained within 28 days of enrollment.
- Recovery to baseline or ≤ Grade 1 common terminology criteria for adverse events (CTCAE) v6 from AE(s) related to any prior treatments unless AE(s) are deemed clinically non-significant (e.g., Grade 2 alopecia) by the Investigator and/or stable on supportive therapy.
- No prior malignancy, with the exception of basal cell carcinoma of the skin, superficial bladder cancer, squamous cell carcinoma of the skin, or in situ cancer, or has undergone potentially curative therapy with no evidence of that disease recurrence for 5 years since completion of definitive therapy
- Participants must be willing and able to comply with study visits, treatment plans, laboratory tests, and other study procedures
- Women of child-bearing potential (WOCBP) and male participants partnering with WOCBP must agree to use highly effective contraception during the treatment phase and at least 180 days post last dose
- Patients must be willing to discontinue clinically-directed ctDNA testing for treatment response monitoring during the period of clinical trial testing as dictated by the protocol.
Exclusion Criteria
Patients are not eligible for the study if they meet any of the following criteria, as assessed by the investigator:
- Available alternate treatment options with curative intent, e.g. surgery and / or RT and / or Chemotherapy.
- Symptomatic or progressing CNS metastases; or presence of leptomeningeal disease.
- Patient has active autoimmune disease that required systemic treatment in the past 2 years, is immunocompromised in the opinion of the Investigator, or is receiving systemic immunosuppressive treatment. (Note: Participants with splenectomy are allowed.) Replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc) is not considered a form of systemic treatment.
- Patient is receiving systemic steroid therapy ≤3 days prior to enrollment or receiving any other form of immunosuppressive medication with the exception of daily steroid replacement therapy. Note: Use of inhaled corticosteroids, local steroid injection, or steroid eye drops is allowed.
- Had allogeneic tissue/solid organ transplantation.
- Interstitial lung disease or history of pneumonitis that has required oral or IV steroids. Note: Patients with lymphangitic carcinomatosis secondary to NSCLC can be considered as eligible.
- Has received or will receive a live vaccine within 30 days prior to enrollment (seasonal flu vaccines that do not contain live vaccine are permitted).
- Active infection requiring intravenous systemic therapy.
- Known history of human immunodeficiency virus (HIV).
- Known active Hepatitis B or C.
- Pregnant, breastfeeding, or expecting to conceive or father children within the projected duration of the study.
- Currently participating or has participated in a study of an investigational agent or using an investigational device within 4 weeks of enrollment.
- Use of any commercial ctDNA or liquid biopsy monitoring outside of the study protocol during the treatment monitoring phase within the protocol.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: SOC Continuous ICI
Participants will continue the current ICI therapy, per approved product label and / or treating investigator's clinical judgement. Standard infusion visits are maintained for the total of 2 years or until radiographic progression, unacceptable toxicity, or withdrawal of consent. |
The test is used to monitor for disease recurrence.
|
|
Experimenteel: ctDNA-Guided Intermittent ICI
Participants will interrupt ICI therapy upon randomization and pursue monitoring that includes serial ctDNA testing.
They will reinitiate the same ICI therapy (monotherapy or dual-ICI therapy as documented at enrollment) if they become ctDNA-positive without evidence of radiographic progression.
Following reinitiation, ICI therapy may again be interrupted after achievement of ≥ 2 consecutive ctDNA-negative results and subsequently re-initiated upon recurrence of ctDNA positivity without evidence of radiographic progression.
This cycle of ctDNA-guided interruption and reinitiation (maximum of 2 ICI interruptions) may continue until radiographic progression is documented.
Upon radiographic progression, treatment will be determined by the treating physician in accordance with SoC.
|
The test is used to monitor for disease recurrence.
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
|
To demonstrate that ctDNA-guided intermittent ICI therapy results in at least 50% of patients who do not reinitiate systemic therapy prior to 6 months from randomization.
Tijdsspanne: 6 months from randomization
|
6 months from randomization
|
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To demonstrate that ctDNA-guided intermittent ICI therapy is non-inferior to SoC continuous ICI therapy as measured by 36 month OS in advanced/metastatic solid tumor patients.
Tijdsspanne: 3 years from randomization to death from any cause
|
3 years from randomization to death from any cause
|
Secundaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
|
To compare ctDNA-guided intermittent ICI therapy to SoC continuous ICI therapy as measured by 36 month progression-free survival (PFS) (blinded independent central review [BICR] assessed) in advanced/metastatic solid tumor patients.
Tijdsspanne: 3 years from randomization to the first occurrence of disease progression measured by RECIST 1.1 or death from any cause, whichever occurs first
|
3 years from randomization to the first occurrence of disease progression measured by RECIST 1.1 or death from any cause, whichever occurs first
|
|
To compare the tolerability between the ctDNA-guided intermittent ICI therapy and SoC continuous ICI therapy using the Common Terminology Criteria for Adverse Events (CTCAE) v6.0.
Tijdsspanne: From randomization to Year 3
|
From randomization to Year 3
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Medewerkers en onderzoekers
Sponsor
Onderzoekers
- Studie directeur: Caitlin Shonewolf, MD, Natera, Inc.
Publicaties en nuttige links
Algemene publicaties
- Andre T, Shiu KK, Kim TW, Jensen BV, Jensen LH, Punt C, Smith D, Garcia-Carbonero R, Benavides M, Gibbs P, de la Fouchardiere C, Rivera F, Elez E, Bendell J, Le DT, Yoshino T, Van Cutsem E, Yang P, Farooqui MZH, Marinello P, Diaz LA Jr; KEYNOTE-177 Investigators. Pembrolizumab in Microsatellite-Instability-High Advanced Colorectal Cancer. N Engl J Med. 2020 Dec 3;383(23):2207-2218. doi: 10.1056/NEJMoa2017699.
- Eroglu Z, Krinshpun S, Kalashnikova E, Sudhaman S, Ozturk Topcu T, Nichols M, Martin J, Bui KM, Palsuledesai CC, Malhotra M, Olshan P, Markowitz J, Khushalani NI, Tarhini AA, Messina JL, Aleshin A. Circulating tumor DNA-based molecular residual disease detection for treatment monitoring in advanced melanoma patients. Cancer. 2023 Jun 1;129(11):1723-1734. doi: 10.1002/cncr.34716. Epub 2023 Mar 4.
- Zalcman G, Madroszyk A, Guenzi E, Dayen C, Molinier O, Egenod T, Pote N, Debieuvre D, Beaucaire-Danel S, Dixmier A, Pichon E, Galland-Girodet S, Giroux-Leprieur E, Cloarec N, Cadranel J, Otto J, Romand P, Favier L, Martinez S, Mascaux C, Odier L, Cortot A, Audigier-Valette C, Langlais A, Amour E, Morin F, Antoine M, Gounant V, Westeel V, Toffart AC. Four-Year Outcomes of First-Line Nivolumab Plus Ipilimumab for 6 Months Versus Continuation in Patients With Advanced NSCLC: Results of the Randomized IFCT-1701 "DICIPLE" Phase III Trial. J Thorac Oncol. 2026 Jun;21(6):103609. doi: 10.1016/j.jtho.2026.103609. Epub 2026 Feb 12.
- Vokes NI, Pan K, Le X. Efficacy of immunotherapy in oncogene-driven non-small-cell lung cancer. Ther Adv Med Oncol. 2023 Mar 18;15:17588359231161409. doi: 10.1177/17588359231161409. eCollection 2023.
- Vokes N, Gandara D, Sezer A, Kilickap S, Gümüş M, Bondarenko I, Özgüroğlu M, Gogishvili M, Turk HM, Cicin I, Bentsion D. Circulating tumor DNA (ctDNA) dynamics and survival outcomes in patients with advanced NSCLC and high (> 50%) PD-L1 expression, randomized to cemiplimab vs chemotherapy. In ASCO Annual Meeting, Chicago, IL 2023 Jun.
- Sun L, Bleiberg B, Hwang WT, Marmarelis ME, Langer CJ, Singh A, Cohen RB, Mamtani R, Aggarwal C. Association Between Duration of Immunotherapy and Overall Survival in Advanced Non-Small Cell Lung Cancer. JAMA Oncol. 2023 Aug 1;9(8):1075-1082. doi: 10.1001/jamaoncol.2023.1891.
- Nakamura Y, Watanabe J, Akazawa N, Hirata K, Kataoka K, Yokota M, Kato K, Kotaka M, Kagawa Y, Yeh KH, Mishima S, Yukami H, Ando K, Miyo M, Misumi T, Yamazaki K, Ebi H, Okita K, Hamabe A, Sokuoka H, Kobayashi S, Laliotis G, Aushev VN, Sharma S, Jurdi A, Liu MC, Aleshin A, Rabinowitz M, Bando H, Taniguchi H, Takemasa I, Kato T, Kotani D, Mori M, Yoshino T, Oki E. ctDNA-based molecular residual disease and survival in resectable colorectal cancer. Nat Med. 2024 Nov;30(11):3272-3283. doi: 10.1038/s41591-024-03254-6. Epub 2024 Sep 16.
- Martinez-Vila C, Teixido C, Martin R, Aya F, Sudhaman S, Budde GL, Gonzalez-Navarro EA, Alos L, Castrejon N, Ortiz JB, Krainock M, Liu MC, Arance A. Personalized Circulating Tumor DNA Assay to Assess Long-Term Clinical Benefit in Patients with Advanced Melanoma. Cancers (Basel). 2025 Nov 27;17(23):3804. doi: 10.3390/cancers17233804.
- Larkin J, Sileni VC, Marqueste CG, Rutkowski P, Medina TM, Lao CD, Cowey CL, Schadendorf D, Wagstaff J, Dummer R, Queirolo P. LBA43 10-y survival outcomes from the phase III CheckMate 067 trial of nivolumab plus ipilimumab in advanced melanoma. Annals of Oncology. 2024 Sep 1;35:S1234-5.
- Botta GP, Abdelrahim M, Drengler RL, Aushev VN, Esmail A, Laliotis G, Brewer CM, George GV, Abbate SM, Chandana SR, Tejani MA, Malla M, Bansal D, Rivero-Hinojosa S, Spickard E, McCormick N, Cecchini M, Lacy J, Fei N, Kasi PM, Kasi A, Dayyani F, Hanna DL, Sharma S, Malhotra M, Aleshin A, Liu MC, Jurdi A. Association of personalized and tumor-informed ctDNA with patient survival outcomes in pancreatic adenocarcinoma. Oncologist. 2024 Oct 3;29(10):859-869. doi: 10.1093/oncolo/oyae155.
- Bogani G, Cinquini M, Signorelli D, Pizzutilo EG, Romano R, Bersanelli M, Raggi D, Alfieri S, Buti S, Bertolini F, Bonomo P, Marandino L, Rizzo M, Monteforte M, Aiello M, Tralongo AC, Torri V, Di Donato V, Giannatempo P. A systematic review and meta-analysis on the optimal treatment duration of checkpoint inhibitoRS in solid tumors: The OTHERS study. Crit Rev Oncol Hematol. 2023 Jul;187:104016. doi: 10.1016/j.critrevonc.2023.104016. Epub 2023 May 6.
- Ben-David R, Lidagoster S, Geduldig J, Kolanukuduru KP, Elkun Y, Tillu N, Mandel A, Almoflihi M, Kaufmann B, Attalla K, Mehrazin R, Wiklund P, Sfakianos JP. Undetectable pre-radical cystectomy circulating tumour DNA status predicts improved oncological outcomes. BJU Int. 2025 Mar;135(3):473-480. doi: 10.1111/bju.16556. Epub 2024 Oct 16.
- Basu A, Au C, Kommalapati A, Kandala H, Sudhaman S, Mahmood T, Carson C, Pajak N, Dutta P, Calhoun M, Malhotra M, ElNaggar AC, Liu MC, Ferguson Iii J, Peyton C, Rais-Bahrami S, Tan A. Longitudinal Testing of Circulating Tumor DNA in Patients With Metastatic Renal Cell Carcinoma. JCO Precis Oncol. 2024 Dec;8:e2400667. doi: 10.1200/PO-24-00667. Epub 2024 Dec 18.
- Afzal MZ, Corea-Dilbert FE, Wankel B, Palmer JP, Pirruccello JP, Kale S, Sharma A, Lu Z, Ibrahim S, Cao Y, Sarwar T. Utility of circulating tumor DNA as a tool to detect minimal residual disease in patients with metastatic cancer and durable response following treatment with immune checkpoint inhibitors. American Society of Clinical Oncology Annual Meeting. 2023. e21563-e21563.
Studie record data
Bestudeer belangrijke data
Studie start (Geschat)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
- NSCLC
- Niet-kleincellige longkanker
- Melanoma
- Colorectale kanker
- Niercelcarcinoom
- ctDNA
- CRC
- Circulerend tumor-DNA
- Immuun checkpoint-remmer
- Gevorderde solide tumor
- MRD
- Adjuvante therapie
- RCC
- ICI
- Metastatische solide tumoren
- Moleculaire restziekte
- Signatera
- Biomarker-geleide therapie
- Tumor-geïnformeerde test
- Microsatellite Instability-High/deficient Mismatch Repair
- MSI-High/dMMR
Aanvullende relevante MeSH-voorwaarden
- Urogenitale ziekten
- Urogenitale neoplasmata
- Neoplasmata per site
- Neoplasmata
- Mannelijke urogenitale ziekten
- Nier Ziekten
- Urologische ziekten
- Vrouwelijke urogenitale ziekten
- Vrouwelijke urogenitale ziekten en zwangerschapscomplicaties
- Darmziekten
- Ziekten van de luchtwegen
- Neoplasmata per histologisch type
- Gastro-intestinale neoplasmata
- Neoplasmata van het spijsverteringsstelsel
- Ziekten van het spijsverteringsstelsel
- Gastro-intestinale aandoeningen
- Intestinale neoplasmata
- Rectale ziekten
- Longziekten
- Neoplasmata, glandulair en epitheel
- Adenocarcinoom
- Neoplasmata van de luchtwegen
- Thoracale neoplasmata
- Colon Ziekten
- Longneoplasmata
- Huidziektes
- Urologische neoplasmata
- Carcinoom
- Neuro-ectodermale tumoren
- Neoplasmata, kiemcellen en embryonaal
- Neoplasmata, zenuwweefsel
- Nierneoplasmata
- Carcinoom, bronchogeen
- Bronchiale neoplasmata
- Neuro-endocriene tumoren
- Nevi en melanomen
- Huidneoplasmata
- Huid- en bindweefselaandoeningen
- Colorectale neoplasmata
- Carcinoom, niercel
- Carcinoom, niet-kleincellige long
- Melanoma
Andere studie-ID-nummers
- 26-107-NCP
Plan Individuele Deelnemersgegevens (IPD)
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