Golcadomide With Pemetrexed, Rituximab, and Dexamethasone for Relapsed and Refractory CNS Lymphomas
Phase I Pilot Trial of Golcadomide With Pemetrexed, Rituximab, and Dexamethasone for Relapsed and Refractory CNS Lymphomas
調査の概要
詳細な説明
People with systemic diffuse large B-cell lymphoma (DLCBL) can either have a a disease that involves the central nervous system or does not involve the central nervous system. The disease could also be only located in the central nervous system. The central nervous system lymphoma includes disease within the brain, meninges, cranial nerves, cerebrospinal fluid, spinal cord, and/or intraocular. For people with disease that involves the CNS it can be difficult to treat. This is because many effective lymphoma treatments do not cross the blood-brain barrier (BBB).
In general there is a large unmet need for effective and feasible therapies for CNS lymphomas. This study addresses these gaps by combining standard of care chemotherapy with Golcadomide.This approach aims to provide a feasible and potentially effective treatment option for a population with historically poor outcomes.
The purpose of this study is to find out the safety and efficacy of Golcadomide in combination with drugs in the standard care chemotherapy. Another goal is to find the recommended phase 2 dose of Golcadomide in combination with standard of care chemotherapy.
研究の種類
入学 (推定)
段階
- フェーズ 1
連絡先と場所
研究連絡先
- 名前:Allison M Winter, MD
- 電話番号:(216) 445-4635
- メール:wintera2@ccf.org
研究場所
-
-
Ohio
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Cleveland、Ohio、アメリカ、44122
- Cleveland Clinic, Case Comprehensive Cancer Center
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主任研究者:
- Allison Winter, MD
-
コンタクト:
- Allison M Winter, MD
- 電話番号:(216) 445-4635
- メール:wintera2@ccf.org
-
-
参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- Participants or their legally acceptable representative must have signed and dated an IRB approved written ICF in accordance with regulatory, local, and institutional guidelines.
- Participants ≥ 18 years of age.
Confirmed histopathological diagnosis of aggressive malignant B-cell lymphoma based upon a representative histology specimen according to the WHO classification. For participants with secondary CNS lymphoma, this can be confirmed by prior systemic biopsy. If a CNS lesion was not amenable for biopsy, imaging (e.g. MRI Brain ± MRI Full Spine) with CSF analysis for cytology may be used to confirm diagnosis, in lieu of a biopsy. Required. Acceptable histologies include:
- Large B-cell lymphoma NOS
- Diffuse large B-cell lymphoma (including GCB and ABC types)
- High-grade B-cell lymphoma with MYC and BCL2 rearrangements (double hit lymphomas)
- High-grade B-cell lymphoma NOS
- T-cell/histiocyte/rich large B-cell lymphoma (THRLBCL)
- EBV + DLBCL
- PMBCL
- Follicular Large B-Cell (previously referred to as Follicular Lymphoma, Grade 3B)
Participants must have active CNS lymphoma for which this trial is planned. Confirmation of the histology in relapsed setting is not required but participants must have measurable disease per the International PCSNL Collaboration Group Criteria (Section 11.1), as evidenced by at least one of the following:
- CNS disease on MRI (brain or spine including parenchymal and leptomeningeal)
- Detectable in the CSF
- Detectable on ophthalmologic exam
- Participants must have received ≥ 1 prior systemic therapy for treatment of their CNS lymphoma. Participants who had systemic lymphoma and then relapsed with secondary CNS lymphoma must have received at least one prior line of therapy to specifically treat the CNS lymphoma.
Participants must have received prior high dose methotrexate as a line of therapy OR have been ineligible for methotrexate therapy based on the investigator's discretion.
- Participants who have received methotrexate as their first line of therapy but are no longer eligible for ongoing methotrexate and have persistent disease are eligible
- ECOG performance status ≤ 0-3. PS 3 is allowed if it is disease related and not due to comorbidities or frailty and PS 4 is allowed if it is from CNS causing motor weakness and not due to comorbidities or frailty. (see Appendix I)
Adequate bone marrow function, defined by the following laboratory parameters:
- Absolute neutrophil ≥ 1.5 x 109/L
Platelet count ≥ 100 x 109/L
- Hemoglobin ≥ 8 g/dL
Adequate organ function, defined by the following laboratory parameters:
- Adequate hepatic function, with transaminases (alanine aminotransferase [ALT], aspartate aminotransferase [AST], and gamma glutamyl transferase [GGT]) ≤ 2.5 times the upper limit of normal
- Bilirubin ≤1.5 x ULN (unless bilirubin rise is due to Gilbert's syndrome or of non-hepatic origin)
- Calculated creatinine clearance > 45 mL/min by the Cockcroft-Gault equation.
Treating investigator must specify at screening:
- If the intent of therapy is a bridge to cellular therapy or to complete all six cycles of therapy. If bridge to cellular therapy is planned, the type of cellular therapy should also be specified at this time.
- If the r/r CNS lymphoma is primary or secondary
For women of childbearing potential: agreement to remain abstinent (refrain from heterosexual intercourse) or use two methods of contraception simultaneously from signing the ICF, at least 28 days before starting golcadomide, throughout the study, for up to 28 days following the last dose of golcadomide, and for 12 months after the last dose of rituximab, whichever is longer.. Two methods of contraception must include one highly effective method and one additional effective (barrier method).
A woman is considered to be of childbearing potential if she is postmenarcheal, has not reached a postmenopausal state (< 12 continuous months of amenorrhea with no identified cause other than menopause), and has not undergone surgical sterilization (removal of ovaries, fallopian tubes, and/or uterus).
- Examples of contraceptive methods include highly effective methods such as oral, injectable, or implantable hormonal contraceptive; tubal ligation; intrauterine device; vasectomized partner and barrier methods with spermicide.
- The reliability of sexual abstinence should be evaluated in relation to the duration of the clinical trial and the preferred and usual lifestyle of the patient. Periodic abstinence (e.g., calendar, ovulation, symptothermal, or postovulation methods) and withdrawal are not acceptable methods of contraception.
- Must agree to pregnancy testing per protocol. This applies even if the participant practices true abstinence from heterosexual contact.
- Agree to abstain from breastfeeding or providing breast milk while on golcadomide and 28 days after discontinuation of golcadomide and according to the approved
- For men: agreement to remain abstinent (refrain from heterosexual intercourse) or use contraceptive measures, and agreement to refrain from donating sperm, as defined below:
- With female partners of childbearing potential, men must remain abstinent or use a condom plus an additional contraceptive method that together result in a failure rate of < 1% per year during the treatment period and for at least 28 days after the last dose of study intervention or 90 days for rituximab, whichever is longer. Men must refrain from donating sperm during this same period.
- With pregnant female partners, men must remain abstinent or use a condom during the treatment period and for at least 28 days after the last dose of study intervention or 90 days for rituximab, whichever is longer.
- The reliability of sexual abstinence should be evaluated in relation to the duration of the clinical trial and the preferred and usual lifestyle of the patient. Periodic abstinence (e.g., calendar, ovulation, symptothermal, or postovulation methods) and withdrawal are not acceptable methods of contraception.
Exclusion Criteria:
- Prior treatment toxicities not resolved to grade < 2 according to NCI CTCAE 6.0 (with the exception of alopecia or grade 2 sensory peripheral neuropathy).
- Participants receiving any other investigational agents.
- History of anaphylactic reactions or severe allergic reactions prohibiting further administration attributed to compounds of similar chemical or biologic composition to rituximab or other agents used in this study.
- Autologous stem cell transplant within 30 days of start of study drug (C1D1).
- CAR T-cell therapy within 90 days of start of study drug (C1D1).
- Previous allogeneic stem cell transplant
- Women who are pregnant or breastfeeding.
- Clinically significant autoimmune disease.
- Known seropositive and requiring anti-viral therapy for human immunodeficiency (HIV) virus.
- Malabsorption syndrome or other conditions that precludes enteral route of administration.
- Chemotherapy or radiation within 2 weeks of the first scheduled study treatment
- Participant is currently receiving warfarin. Participants may begin screening if the plan is to change to an alternative anticoagulant such as a DOAC prior to enrollment.
- Participant has current treatment with strong cytochrome P450 3A4/5 (CYP3A4/5) modulators. The washout period for strong CYP3A4/5 modulators is 7 days or 5 half-lives (whichever is longer) before initiation of golcadomide.
Evidence of other clinically significant uncontrolled condition(s) including, but not limited to:
- Uncontrolled and/or active systemic infection (viral, bacterial or fungal)
- Chronic hepatitis B virus (HBV) or hepatitis C (HCV) requiring treatment. Note: participants with serologic evidence of prior vaccination to HBV (i.e. hepatitis B surface (HBs) antigen negative-, anti-HBs antibody positive and anti-hepatitis B core (HBc) antibody negative) or positive anti-HBc antibody from intravenous immunoglobulins (IVIG) may participate.
- Other uncontrolled conditions including uncontrolled cardiovascular disease or arrhythmia, decompensated diabetes or COPD.
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:Golcadomide + Pemetrexed, Rituximab and Dexamethasone
A 3+3 design will be used to identify the recommended phase 2 dose of Golcadomide in combination with Pemetrexed, Rituximab, and Dexamethasone. 3 participants will be enrolled in the first dose level.
If these participants do not experience any dose limiting toxicities, then 3 more patients will be enrolled in the next dose level.
If one or more participants experience dose limiting toxicities, then this dose will be considered the highest dose administered dose and 3 additional patients will be enrolled in the next lowest dose level.
If 2 or more patients experience dose limiting toxicities, then the dose escalation will be stopped and 3 additional patients will enrolled in the next lowest dose level.
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To be taken orally daily on days 1-7 of the cycle Maximum 3 cycles but participants may received up to 3 additional cycles (for a total of up to 6 cycles) Cycle Length : 21 days Dose Levels:
To be given intravenously (IV) on day 1 of each cycle Maximum 3 cycles but participants may receive up to 3 additional cycles (for a total of up to 6 cycles) Cycle Length: 21 days Dose Level
To be given intravenously on day 1 of each cycle Maximum 3 cycles but participants may receive up to 3 additional cycles (for a total of up to 6 cycles) Cycle Length: 21 days Dose Level
To be given orally on days 1-4 of each cycle Day 1 dose should be given at least 30 minutes before rituximab infusion Maximum 3 cycles but participants may receive up to 3 additional cycles (for a total of up to 6 cycles) Cycle Length: 21 days Dose Level
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Safety of Golcadomide + Pemetrexed, Rituximab and Dexamethasone
時間枠:up to 6 cycles (up to 6 months)
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Safety is defined as rates of adverse events experienced by participants.
Adverse event severity is graded according to the NCI Common Terminology Criteria for Adverse Events (CTCAE), Version 6.0.
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up to 6 cycles (up to 6 months)
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Identify the maximum tolerated dose of Golcadomide + Pemetrexed, Rituximab and Dexamethasone
時間枠:up to 6 cycles (up to 6 months)
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determined by the 3+3 dose escalation design
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up to 6 cycles (up to 6 months)
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Overall response rate (ORR) by International Primary CNS Lymphoma Collaborative Group (IPCG) of Golca + PRD
時間枠:up to 18 months
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ORR includes complete response (CR), Unconfirmed CR (CRu), partial response (PR), & disease control rate (DCR), according to the 2005 IPCG Response Criteria. CR: complete disappearance of abnormalities on gadolinium-enhanced MRI, no contrast enhancement in brain imaging, no corticosteroid dose, normal eye examination & negative Cerebrospinal fluid (CSF) cytology. CRu: fulfilling criteria for CR but with minimum to no contrast enhancement in brain imaging, continuing use of corticosteroid therapy, normal to minor retinal pigment epithelium (RPE) abnormality, & negative CSF cytology. PR: greater than 50% decrease in contrast-enhancing lesion compared to baseline imaging, normal to minor RPE abnormality, negative CSF cytology & no new sites of disease. SD: less than a PR but is not progressive disease. |
up to 18 months
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Disease control rate (DCR) by IPCG
時間枠:18 months
|
DCR is the percentage of participants whose cancer did not get worse after treatment (i.e. the percentage of participants who had CR, PR, or , SD, as defined below), and this will be measured by the IPCG response criteria. CR: complete disappearance of abnormalities on gadolinium-enhanced MRI, no contrast enhancement in brain imaging, no corticosteroid dose, normal eye examination & negative Cerebrospinal fluid (CSF) cytology. CRu: fulfilling criteria for CR but with minimum to no contrast enhancement in brain imaging, continuing use of corticosteroid therapy, normal to minor retinal pigment epithelium (RPE) abnormality, & negative CSF cytology. PR: greater than 50% decrease in contrast-enhancing lesion compared to baseline imaging, normal to minor RPE abnormality, negative CSF cytology & no new sites of disease. SD: less than a PR but is not progressive disease. |
18 months
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Overall survival rate
時間枠:18 months
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Overall survival (OS) is defined as the duration of time from start of treatment to time of death from any cause for participants who complete treatment.
|
18 months
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Progression free survival rate
時間枠:18 months
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Progression-Free Survival (PFS) is defined as the duration of time from start of treatment to time of progression or death, whichever occurs first, for participants who complete treatment.
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18 months
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Proportion of participants designated for cellular therapy who receive cellular therapy
時間枠:18 months
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The number of participants intended for cellular therapy who receive cellular therapy will be described as a proportion.
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18 months
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Proportion of participants who have a successful mobilization of autologous stem cell transplant
時間枠:18 months
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The number of participants who undergo mobilization for collection of autologous stem cell transplant following treatment with Golca + RPD and have successful mobilization will be described as proportion.
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18 months
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協力者と研究者
スポンサー
捜査官
- 主任研究者:Allison M Winter, MD、Cleveland Clinic, Case Comprehensive Cancer Center
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
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その他の研究ID番号
- CASE3425
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