Combination Immunotherapy in Rare Cancers Under InvesTigation (MOST-CIRCUIT)
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|ClinicalTrials.gov Identifier: NCT04969887|
Recruitment Status : Recruiting
First Posted : July 21, 2021
Last Update Posted : August 1, 2022
The four tumour streams that will be studied in this protocol are based on immunotherapy sensitive rare cancers from CA209-538 which will be further investigated under this protocol and divided into four groups:
- Neuroendocrine cancers: Atypical bronchial carcinoid, neuroendocrine carcinoma and Grade 3 NETs independent of primary site (SCLC excluded)
- Biliary tract cancers: Intrahepatic cholangiocarcinoma and gallbladder carcinoma
- Gynaecological malignancies: Ovarian clear cell carcinoma, uterine clear cell carcinoma, uterine/ovarian carcinosarcoma, uterine leiomyosarcoma and vaginal/vulva squamous cell carcinoma
- Mismatch repair protein deficient (MSI-H) cancers (excluding colorectal carcinoma).
The role of immunotherapy is being defined in more common cancer types, however because of their rarity, the efficacy of immunotherapy for these cancers is poorly defined.
This protocol provides an important opportunity to establish whether the combination of nivolumab & ipilimumab has efficacy in these cancers.
|Condition or disease||Intervention/treatment||Phase|
|Advanced Biliary Tract Cancer Neuroendocrine Tumors Female Reproductive System Neoplasm MSI-H Solid Malignant Tumor||Drug: Ipilimumab Drug: Nivolumab||Phase 2|
This is a phase 2 clinical trial of nivolumab combined with ipilimumab in immunotherapy sensitive rare cancers. This study will allow an evaluation of the clinical benefit, as measured by progression free survival (PFS) >6 months and overall survival (OS), provided by nivolumab combined with ipilimumab.
Study Rationale Clinically advanced rare cancers pose a significant clinical challenge because evidence based treatments are seldom available for patients suffering from these malignancies. Despite little evidence that shows clinical benefit, these patients are often treated with chemotherapeutic agents that are used in patients with more common malignancies that arise from the same anatomical site. Furthermore, because of small numbers, patients are often excluded from clinical trials with newer agents. CA209-538 examined this treatment combination in three 'baskets' of rare cancers: rare upper gastrointestinal, gynaecological and neuroendocrine cancers. The cancers on study all individually had an incidence of <2/100000/year. The cancer specific survival of patients diagnosed with a rare malignancy is significantly lower than with common cancers highlighting the need to improve management and treatment of rare cancer patients. Given the success of cancer immunotherapy with checkpoint regulators such as ipilimumab and nivolumab in a range of different cancer types, it was postulated that these agents could be beneficial in rare cancers and improve the overall outlook of patients with these conditions. CA209-538 enrolled 120 rare cancer patients on study, clinical benefit rate was >30% across all baskets, long term survival follow-up is underway.
This study will enrol 240 participants, across 4 cohorts with histotypes which demonstrated clinical benefit on CA209-538. All participants will receive ipilimumab and nivolumab as combination immunotherapy.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||240 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Masking Description:||This is an open label study, all patients receive the same treatment as per the protocol.|
|Official Title:||Ipilimumab and Nivolumab Combination Therapy in Patients With Selected Immunotherapy Sensitive Advanced Rare Cancers|
|Actual Study Start Date :||August 3, 2021|
|Estimated Primary Completion Date :||June 1, 2024|
|Estimated Study Completion Date :||December 2024|
Experimental: Ipilimumab and Nivolumab
All Subjects will be treated with: Nivolumab at 3 mg/kg and ipilimumab at 1 mg/kg concurrently every 3 weeks for 4 doses followed by nivolumab only at 480mg every 4 weeks until progression (up to 2 years)
CTLA-4 (cytotoxic T-lymphocyte-associated protein 4) is a key regulator of T cell activity. Ipilimumab is a CTLA-4 immune checkpoint inhibitor that blocks T-cell inhibitory signals induced by the CTLA-4 pathway, increasing the number of tumor reactive T effector cells which mobilize to mount a direct T-cell immune attack against tumor cells. CTLA-4 blockade can also reduce T regulatory cell function, which may lead to an increase in anti-tumor immune response.
Other Name: YERVOY ®
A fully human immunoglobulin (Ig) G4 monoclonal antibody directed against the negative immunoregulatory human cell surface receptor programmed cell death-1 (PD-1,PCD-1) with immune checkpoint inhibitory and antineoplastic activities. Nivolumab binds to and blocks the activation of PD-1, an Ig superfamily transmembrane protein, by its ligands programmed cell death ligand 1 (PD-L1), overexpressed on certain cancer cells, and programmed cell death ligand 2 (PD-L2), which is primarily expressed on APCs (antigen presenting cells). This results in the activation of T-cells and cell-mediated immune responses against tumor cells or pathogens. Activated PD-1 negatively regulates T-cell activation and and plays a key role in in tumor evasion from host immunity.
Other Name: Opdivo
- Confirm the clinical efficacy of ipi/nivo in rare cancer histotypes which have demonstrated to be responsive to the regimen in the CA209-538 study. [ Time Frame: At 12 weeks following registration then as assessed by standard care until progression. ]Clinical benefit rate for whole population (CR (complete response)+PR (partial response) assessed by radiographic evidence in accordance with RECIST 1.1 criteria
- Determine the proportion of participants with progression free survival at 6 months [ Time Frame: Enrolment on study until 6 months. ]Progression-free survival based on clinical or radiographic evidence of progressive disease according to RECIST 1.1 criteria at 6 months.
- To confirm the overall survival of participants receiving ipi/nivo in rare cancer histotypes which have demonstrated to be responsive to the regimen [ Time Frame: From date of enrolment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 5 years. ]Quantification of OS.
- To confirm the progression free survival of participants receiving ipi/nivo in rare cancer histotypes which have demonstrated to be responsive to the regimen [ Time Frame: From date of enrolment until the date of first documented progression up to 5 years. ]Quantification of PFS
- Quantification of treatment related toxicities to ipi/nivo according to CTCAE V5.0 [ Time Frame: From 1st dose until 30 days following last dose [up to max 2 years + 30 days]. ]Quantification of treatment related toxicities according to CTCAE V5.0.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04969887
|Contact: Jodie Palmer, PhDemail@example.com|
|Contact: Billy McMahon, PhDfirstname.lastname@example.org|
|Australia, New South Wales|
|Border Medical Oncology Unit||Recruiting|
|Albury, New South Wales, Australia, 2640|
|Contact: Craig Underhill, MBBS|
|Calvary Mater Newcastle||Not yet recruiting|
|Newcastle, New South Wales, Australia|
|Contact: Kim Adler, RNC|
|Principal Investigator: Gaik T Quah, MBBS|
|Orange Health Service||Not yet recruiting|
|Orange, New South Wales, Australia|
|Contact: Stephen Millard, RN|
|Principal Investigator: Robert Zierlinski, MBBS|
|Sydney, New South Wales, Australia, 2145|
|Contact: Matteo Carlino, MBBS|
|Australia, South Australia|
|Royal Adelaide Hospital||Recruiting|
|Adelaide, South Australia, Australia|
|Contact: Michael Brown|
|Principal Investigator: Michael Brown, MBBS, FRACP|
|Bendigo Health Services||Recruiting|
|Bendigo, Victoria, Australia|
|Contact: Sam Harris, MBBS|
|Frankston, Victoria, Australia|
|Contact: Linda Raineri|
|Principal Investigator: Oliver Klein, MBBS|
|Geelong, Victoria, Australia|
|Contact: Chiara Bortolasci|
|Principal Investigator: Zee Wan Wong, MBBS|
|Heidelberg, Victoria, Australia, 3084|
|Contact: Anne-Marie Woods, RN email@example.com|
|Principal Investigator: Damien Kee, MBBS|
|Peter MacCalllum Cancer Centre||Recruiting|
|Parkville, Victoria, Australia|
|Contact: PCCTU Unit|
|Principal Investigator: Michael Michael, MBBS, FRACP|
|South West Healthcare||Recruiting|
|Warrnambool, Victoria, Australia|
|Contact: Ian Collins, MBBS|
|Principal Investigator: Ian Collins, MBBS|
|Australia, Western Australia|
|Fiona Stanley Hospital||Recruiting|
|Perth, Western Australia, Australia|
|Contact: Caroline Stone|
|Principal Investigator: Wei-Sen Lam, MBBS, FRACP|
|Study Chair:||Oliver Klein, MD||ONJCRI and Austin Health|
|Study Chair:||Jonathan Cebon, MD||ONJCRI and Austin Health|