Cutaneous T-Cell Lymphoma RefractoryPhase 1/2NCT07535710
Aclarubicin Plus Cyclophosphamide, Vincristine, and Prednisone (CAOP) in Patients With Previously Treated Cutaneous T-cell Lymphoma
A Phase 1/2 study testing Aclarubicin, Cyclophosphamide and Vincristine in people with Cutaneous T-Cell Lymphoma Refractory and Cutaneous T-Cell Lymphoma, Relapsed, run by Shanghai Jiao Tong University School of Medicine at 2 sites in China.
Trial summary
Cutaneous T-cell lymphomas (CTCL) are a rare and heterogeneous group of extranidal T-cell lymphomas characterized by skin involvement. Current treatment options for CTCL are limited. Although responses have been demonstrated, their duration is often short, especially in patients with advanced stage disease. Read more about this study
- Who is it for?
- Ages 60 years and older
- Conditions the study is for
- Cutaneous T-Cell Lymphoma Refractory, Cutaneous T-Cell Lymphoma, Relapsed, Sezary Syndrome
- What is being tested?
- Aclarubicin, Cyclophosphamide and Vincristine
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 37 participants
- Where
- 2 sitesChina
- Study dates
- 30 Mar 2026to 31 Dec 2028
- Phase
- Phase 1/2
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 60 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Understand and voluntarily sign the informed consent form
- Age ≥ 60 years at enrollment
- Eastern Cooperative Oncology Group (ECOG) performance status ≤ 1
- Histologically confirmed primary cutaneous T-cell lymphoma (CTCL) or Sézary syndrome (SS) (according to the fifth edition of the WHO Classification of Tumors of the Hematopoietic and Lymphoid System)
- Stage II-B, III, or IV (referring to the Olsen criteria of the International Society for Cancer Research (ISCL)/USCC/EORTC, 2022)
- Patients who have failed at least one systemic therapy; psoralen combined with ultraviolet radiation therapy (PUVA) is not considered a systemic therapy
Show all 14Show fewer
- All clinically significant toxicities caused by previous anticancer therapy have resolved to ≤ Grade 1 (according to NCI-CTCAE v5.0 criteria)
- Hematological, renal, and liver function tests meet the following requirements:
- Absolute neutrophil count (ANC) ≥ 1,500 cells/μL
- Platelet count ≥ 100,000 cells/μL
- For patients with known bone marrow involvement, ANC ≥ 1,000 cells/μL and platelets ≥ 75,000 cells/μL
- Total bilirubin ≤ 1.5 times the institutional upper limit of normal (ULN) (except for patients with Gilbert syndrome)
- Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 × ULN; if liver involvement is known in C TCL, ≤ 5.0 × ULN
- Serum creatinine ≤ 1.5 × ULN, or creatinine clearance calculated by the Cockcroft-Gault formula > 50 mL/min
Who cannot join
- Patients diagnosed with a malignancy within the past two years. Exclude the following situation: non-melanoma skin cancer, melanoma in situ, localized prostate cancer (current PSA <0.1 ng/mL), treated thyroid cancer; or cervical carcinoma in situ or breast ductal/lobular carcinoma in situ diagnosed within the past two years, as long as there is no current evidence of active disease.
- Clinical evidence of central nervous system (CNS) infiltration.
- Large cell transformation (LCT). Patients with a history of LCT but no current invasive disease and no evidence of LCT on skin or lymph node pathology may be enrolled.
- Psychiatric illness, disability, or social circumstances that may affect the subject's safety, ability to provide informed consent, or poor compliance.
- Patients with significant uncontrolled comorbidities or infections, as follows:
- Uncontrolled infection requiring intravenous antibiotics
Show all 17Show fewer
- Clinically significant heart disease (New York Heart Association class III or IV), unstable angina
- History of angioplasty, stent implantation, or myocardial infarction within 6 months
- Uncontrolled hypertension despite treatment with two antihypertensive medications (systolic blood pressure >160 mmHg or diastolic blood pressure >100 mmHg, measured on two consecutive occasions, one week apart)
- Clinically significant arrhythmias
- Uncontrolled diabetes mellitus
- Known or tested positive for human immunodeficiency virus (HIV), human T-cell leukemia virus (HTLV-1), hepatitis B, or hepatitis C.
- Active herpes simplex or herpes zoster. Patients who have started antiviral prophylaxis ≥30 days prior to the pretreatment visit, have no signs of active infection, and whose last active infection occurred more than 6 months ago may be enrolled and must continue taking prescribed medications during the study.
- Known active autoimmune disease (e.g., Graves' disease, systemic lupus erythematosus, rheumatoid arthritis, Crohn's disease, psoriasis).
- Allergic reaction to study medications.
- History of allogeneic transplantation.
- Pregnancy (confirmed by β-hCG) or lactation.
Trial locations and contacts
2 sites in 1 country. Contact the study team or a site near you to ask about taking part.
China2 sites
Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai
Shanghai
Yunxiang Zhang, +86-13564516001, zyx12103@rjh.com.cn
Ruijin Hospital Wuxi Branch
Wuxi
Jiong Hu, +8613764313546, hj10709@rjh.com.cn
About this study
Official title: A Multicenter, Open-Label, Phase 1/2 Clinical Study of the Safety and Efficacy of Aclarubicin Plus Cyclophosphamide, Vincristine, and Prednisone (CAOP) in Patients With Previously Treated Cutaneous T-cell Lymphoma
Cutaneous T-cell lymphomas (CTCL) are a rare and heterogeneous group of extranidal T-cell lymphomas characterized by skin involvement. Current treatment options for CTCL are limited. Although responses have been demonstrated, their duration is often short, especially in patients with advanced stage disease. Additional treatment options are needed which demonstrate activity in cutaneous and extracutaneous sites. The traditional CHOP regimen (Cyclophosphamide, Hydroxydaunorubicin, Vincristine and Prednisone) has some efficacy for CTCL patients, but due to the cardiotoxicity of anthracyclines, patients can only receive a limited course of treatment. After stopping the regimen, most patients will experience relapse.
Aclarubicin, also known as aclacinomycin A, is an anthracycline type of antibiotic with significant anti-cancer properties. Previous studies have shown that aclarubicin only induces histone eviction without causing DNA damage, and it stands out in pre-clinical models and clinical studies, as it potently kills AML cells. Meanwhile, aclarubicin lacks cardiotoxicity, and can be safely administered even after the maximum cumulative dose of either doxorubicin or idarubicin has been reached. Aclarubicin's treatment indications include malignant lymphoma, but actual clinical application experience is limited.
The purpose of this study is to determine the maximum tolerated dose, safety and efficacy of aclarubicin combined with cyclophosphamide, vincristine, and prednisone (CAOP) for subjects with relapsed or refractory CTCL.
Read the detailed description
The estimated incidence of CTCL in China is 6.9 per million, accounting for 75% to 80% of primary cutaneous lymphomas. CTCL has diverse subtypes, stages, and clinical manifestations, with mycosis fungoides (MF) being the most common subtype. The etiology of CTCL remains unclear, but it may be related to DNA damage, epigenetic regulation, programmed cell death, and abnormalities in the T-cell receptor (TCR) signaling pathway.
The diagnosis and classification of CTCL primarily refer to the 5th edition of the World Health Organization (WHO) Classification of Hematopoietic and Lymphoid Neoplasms. A definitive diagnosis requires a comprehensive assessment of the patient's clinical presentation, histopathological findings, immunohistochemical staining, and TCR gene rearrangement testing. Sézary syndrome (SS) is no longer classified as CTCL in 5th edition of the WHO Classification. However, due to its close association with MF, current treatment recommendations still do not separate SS from MF. Early skin manifestations of CTCL include patchy or plaque-like lesions. Advanced stages may develop tumors or erythroderma. Extracutaneous involvement may also occur, often with regional lymph node involvement and the presence of atypical lymphocytes in the peripheral blood. Prognostic factors for CTCL include the presence of extracutaneous involvement, the body surface area of affected skin, the type of skin lesion, and the pathological type. Currently, disease staging and treatment efficacy assessment are primarily based on the 2022 ISCL/USCC/EORTC recommended criteria.
Commonly used systemic therapies for CTCL include interferon α, oral retinoids, histone deacetylase inhibitors, CD30 antibody-drug conjugates (velutuximab), and CCR4 monoclonal antibodies (moglizumab). The global Phase III MAVORIC study of moglizumab demonstrated a median progression-free survival (PFS) of 7.7 months and a median time to next treatment (TTNT) of 11 months in adult patients with relapsed/refractory SS or stage III-IV MF. The objective response rate (ORR) in hematology was 68%, and the ORR in skin reached 42%. However, due to cost and accessibility, clinical application in China remains limited. For patients who have failed these systemic therapies, existing combination chemotherapy regimens, while effective, are limited by patient tolerance, toxicity, and comorbidities, making continued use difficult.
Aclarubicin (Acla) is an anthracycline anticancer drug. In vitro, Acla has demonstrated potent cytotoxicity against various lymphoma and T-lymphocytic leukemia cell lines. Mechanistic studies of anthracyclines have revealed that doxorubicin, epirubicin, daunorubicin, and idarubicin all induce tumor cell apoptosis through two mechanisms: 1. DNA damage: through inhibition of topoisomerase II (Topo II), leading to DNA double-strand breaks (DSBs); and 2. Chromatin damage: through histone removal, causing chromatin alterations at specific genomic loci. However, these dual mechanisms also lead to dose-dependent, irreversible cardiotoxicity. Compared with classic anthracyclines (such as doxorubicin and daunorubicin), Acla does not cause DNA damage and accumulates significantly in lymphoid tissues (spleen, thymus, and lymph nodes), with poor distribution to other tissues. Consequently, its cardiotoxicity is significantly reduced. Even at high cumulative doses, it is less likely to cause cardiac dysfunction. Therefore, Acla may offer a safer option for elderly patients or those with concomitant heart disease. Previous studies have shown that the combination of Acla and cytarabine (such as the CAG regimen) has some efficacy and is well tolerated in relapsed/refractory and elderly patients with acute myeloid leukemia. In the 1980s and 1990s, studies explored the use of Acla in chemotherapy regimens for non-Hodgkin's lymphoma and Hodgkin's lymphoma, demonstrating some activity. Small studies have shown that Acla monotherapy can achieve a response rate of approximately 30% in patients with advanced non-hedging lymphoma, without compromising cardiac function. Japanese researchers have found that combination chemotherapy regimens containing Acla in T-cell lymphomas exhibit superior efficacy.
In this study, the investigators will replace doxorubicin in the traditional CHOP regimen with aclarubicin, a drug with proven efficacy and low cardiotoxicity, to create a novel aclarubicin, cyclophosphamide, vincristine, and prednisone (CAOP) regimen for patients with relapsed/refractory CTCL and SS who have received at least one prior systemic therapy. This combination chemotherapy regimen may improve efficacy while balancing tolerability and safety, providing a new treatment option for elderly patients with CTCL.
- Conditions
- Cutaneous T-Cell Lymphoma Refractory, Cutaneous T-Cell Lymphoma, Relapsed, Sezary Syndrome, Cutaneous T Cell Lymphoma (CTCL)
- Being tested
- Aclarubicin, Cyclophosphamide, Vincristine, Prednisone
- Keywords
- Aclarubicin, CTCL, Sezary Syndrome, systemic therapy
- Medical subject headings
- Lymphoma, T-Cell, Cutaneous, Recurrence, Sezary Syndrome
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
AclarubicinDrug
Cycle 1-6:
Phase I starting dose 20mg/m^2/D, D1-2 (dose group 1), D1-3 (dose group 2), D1-4 (dose group 3), QD, ivgtt The Phase II dose was determined based on the Phase I results
Cycle 7-10:
Phase I starting dose 20mg/ m^2/D, D1-2 (dose group 1), D1-3 (dose group 2), D1-4 (dose group 3), QD, ivgtt The Phase II dose was determined based on the Phase I results
CyclophosphamideDrug
Cycle 1-6 750 mg/m^2, D1, QD, ivgtt Cycle 7-10 750 mg/m^2, D1, QD, ivgtt
VincristineDrug
Cycle 1-6 1.4 mg/m^2, D1 (maximum 2mg/d), QD, iv Cycle 7-10 1.4 mg/m^2, D1 (maximum 2mg/d), QD, iv
PrednisoneDrug
Cycle 1-6 60 mg/m^2, D1-5 (maximum 100mg/d), QD, Po
Cycle 7-10 60 mg/m^2, D1-5 (maximum 100mg/d), QD, Po
| Study group | Role | What they receive |
|---|---|---|
| CAOP | Experimental | Aclarubicin will be used in a dose escalation and dose expansion approach. Cyclophosphamide, Vincristine and Prednisone will be used in a fixed dose throughout the phases.
Phase I dose-escalation: a standard "3+3" approach for aclarubicin. Phase II dose expansion: enroll patients same as in phase I, and aclarubicin will be used at the dose determined by the dose escalation.
The whole treatment includes induction and maintenance. Induction treatment includes 3 week cycles for 6 cycles of CAOP or until progression.
Maintenance treatment includes 6 week cycles for 4 cycles of CAOP or until progression. Receives: Drug: Aclarubicin; Drug: Cyclophosphamide; Drug: Vincristine; Drug: Prednisone |
What is being measured
The primary outcome is the main question the study is designed to answer.
Maximum tolerated dose (MTD)
MTD for aclarubicin (primary outcome measure of phase I)
Measured: 28 days after first dose of aclarubicin
Recommended Phase 2 Dose (RP2D)
RP2D for aclarubicin (primary outcome measure of phase I)
Measured: 28 days after first dose of aclarubicin
Objective response rate (ORR)
Proportion of patients who achieved complete remission (CR) or partial remission (PR) after treatment (primary outcome measure of phase II)
Measured: At the end of induction cycle 6 (each cycle is about 28 days)
Secondary outcomes (6)
Objective response rate (ORR)
Proportion of patients who achieved complete remission (CR) or partial remission (PR) after treatment (secondary outcome measure of phase I)
Measured: At the end of induction cycle 6 (each cycle is about 28 days)
Progression Free Survival
Time from enrollment to confirmation of disease progression or death from any cause (secondary outcome measure of phase II)
Measured: All enrolled patients were followed up for at least 12 months or had an event
Time to Next Treatment (TTNT)
The interval from commencement of one treatment to initiation of the next line of therapy (secondary outcome measure of phase II)
Measured: All enrolled patients were followed up for at least 12 months or had an event
Adverse Events
Adverse Events (CTCAE v6.0), Vital Signs and Physical Examination, ECOG, Clinical Laboratory Tests, Electrocardiogram (ECG), Echocardiography, Cardiac Enzyme Profile
Measured: From enrollment to 28 days after the end of treatment
Change in quality of life as measured by the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30 (EORTC QLQ-C30) global health status score
Quality of life will be assessed using the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30 (EORTC QLQ-C30).
The global health status score ranges from 0 to 100, with higher scores indicating better quality of life. Scores will be calculated according to the EORTC scoring manual and summarized as change from baseline.
Measured: From enrollment to 28 days after the end of treatment
Cancer-related fatigue as measured by the Patient-Reported Outcomes Measurement Information System (PROMIS) Fatigue score
Cancer-related fatigue will be assessed using the Patient-Reported Outcomes Measurement Information System (PROMIS) Fatigue questionnaire.
Scores are reported as T-scores standardized to a reference population, with higher scores indicating greater fatigue (worse outcome). Changes from baseline will be summarized.
Measured: From enrollment to 28 days after the end of treatment
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 Apr 2026
- Study start30 Mar 2026 (estimated)
- Primary completion31 Dec 2027 (estimated)
- Study completion31 Dec 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Cutaneous T-Cell Lymphoma RefractoryStudies of the same condition, open and under way.
- More trials run by Shanghai Jiao Tong University School of MedicineThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 1/2
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Model description
- Phase I Primary Objectives: to evaluate the safety and tolerability of the CAOP regimen in patients with relapsed/refractory cutaneous T-cell lymphoma; to determine the maximum tolerated dose (MTD) based on dose-limiting toxicities (DLTs) and to determine the recommended Acla dose for the dose-expansion phase. Phase II Primary Objectives: to evaluate the efficacy of the CAOP regimen in patients with relapsed/refractory cutaneous T-cell lymphoma; the primary endpoint is objective response rate (ORR).
- Masking
- None (open label)
- Enrolment
- 37 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Shanghai Jiao Tong University School of Medicine
- Sponsor type
- University, hospital or other
- Collaborators
- Leiden University Medical Center
- Responsible party
- Principal investigator, Junmin Li, Shanghai Jiao Tong University School of Medicine
- Investigators
- Junmin Li, Professor, Principal investigator, Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07535710
- Sponsor's protocol ID
- Acla-CTCL
- Status last verified
- Apr 2026
- First submitted
- 20 Mar 2026
- Last updated
- 17 Apr 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 17 Apr 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Multicenter, Open-Label, Phase 1/2 Clinical Study of the Safety and Efficacy of Aclarubicin Plus Cyclophosphamide, Vincristine, and Prednisone (CAOP) in Patients With Previously Treated Cutaneous T-cell Lymphoma
- ClinicalTrials.gov ID
- NCT07535710
- Acronym / sponsor ID
- Acla-CTCL
- Conditions
- Cutaneous T-Cell Lymphoma Refractory, Cutaneous T-Cell Lymphoma, Relapsed, Sezary Syndrome, Cutaneous T Cell Lymphoma (CTCL)
- Keywords
- Aclarubicin, CTCL, Sezary Syndrome, systemic therapy
- Phase
- Phase 1/2
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 37 participants (estimated)
- Lead sponsor
- Shanghai Jiao Tong University School of MedicineUniversity, hospital or other
- Collaborators
- Leiden University Medical Center
- Study start
- 30 Mar 2026 (estimated)
- Primary completion
- 31 Dec 2027 (estimated)
- Study completion
- 31 Dec 2028 (estimated)
- First posted
- 17 Apr 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Cutaneous T-cell lymphomas (CTCL) are a rare and heterogeneous group of extranidal T-cell lymphomas characterized by skin involvement. Current treatment options for CTCL are limited. Although responses have been demonstrated, their duration is often short, especially in patients with advanced stage disease. Additional treatment options are needed which demonstrate activity in cutaneous and extracutaneous sites. The traditional CHOP regimen (Cyclophosphamide, Hydroxydaunorubicin, Vincristine and Prednisone) has some efficacy for CTCL patients, but due to the cardiotoxicity of anthracyclines, patients can only receive a limited course of treatment. After stopping the regimen, most patients will experience relapse.
Aclarubicin, also known as aclacinomycin A, is an anthracycline type of antibiotic with significant anti-cancer properties. Previous studies have shown that aclarubicin only induces histone eviction without causing DNA damage, and it stands out in pre-clinical models and clinical studies, as it potently kills AML cells. Meanwhile, aclarubicin lacks cardiotoxicity, and can be safely administered even after the maximum cumulative dose of either doxorubicin or idarubicin has been reached. Aclarubicin's treatment indications include malignant lymphoma, but actual clinical application experience is limited.
The purpose of this study is to determine the maximum tolerated dose, safety and efficacy of aclarubicin combined with cyclophosphamide, vincristine, and prednisone (CAOP) for subjects with relapsed or refractory CTCL.
Detailed description
The estimated incidence of CTCL in China is 6.9 per million, accounting for 75% to 80% of primary cutaneous lymphomas. CTCL has diverse subtypes, stages, and clinical manifestations, with mycosis fungoides (MF) being the most common subtype. The etiology of CTCL remains unclear, but it may be related to DNA damage, epigenetic regulation, programmed cell death, and abnormalities in the T-cell receptor (TCR) signaling pathway.
The diagnosis and classification of CTCL primarily refer to the 5th edition of the World Health Organization (WHO) Classification of Hematopoietic and Lymphoid Neoplasms. A definitive diagnosis requires a comprehensive assessment of the patient's clinical presentation, histopathological findings, immunohistochemical staining, and TCR gene rearrangement testing. Sézary syndrome (SS) is no longer classified as CTCL in 5th edition of the WHO Classification. However, due to its close association with MF, current treatment recommendations still do not separate SS from MF. Early skin manifestations of CTCL include patchy or plaque-like lesions. Advanced stages may develop tumors or erythroderma. Extracutaneous involvement may also occur, often with regional lymph node involvement and the presence of atypical lymphocytes in the peripheral blood. Prognostic factors for CTCL include the presence of extracutaneous involvement, the body surface area of affected skin, the type of skin lesion, and the pathological type. Currently, disease staging and treatment efficacy assessment are primarily based on the 2022 ISCL/USCC/EORTC recommended criteria.
Commonly used systemic therapies for CTCL include interferon α, oral retinoids, histone deacetylase inhibitors, CD30 antibody-drug conjugates (velutuximab), and CCR4 monoclonal antibodies (moglizumab). The global Phase III MAVORIC study of moglizumab demonstrated a median progression-free survival (PFS) of 7.7 months and a median time to next treatment (TTNT) of 11 months in adult patients with relapsed/refractory SS or stage III-IV MF. The objective response rate (ORR) in hematology was 68%, and the ORR in skin reached 42%. However, due to cost and accessibility, clinical application in China remains limited. For patients who have failed these systemic therapies, existing combination chemotherapy regimens, while effective, are limited by patient tolerance, toxicity, and comorbidities, making continued use difficult.
Aclarubicin (Acla) is an anthracycline anticancer drug. In vitro, Acla has demonstrated potent cytotoxicity against various lymphoma and T-lymphocytic leukemia cell lines. Mechanistic studies of anthracyclines have revealed that doxorubicin, epirubicin, daunorubicin, and idarubicin all induce tumor cell apoptosis through two mechanisms: 1. DNA damage: through inhibition of topoisomerase II (Topo II), leading to DNA double-strand breaks (DSBs); and 2. Chromatin damage: through histone removal, causing chromatin alterations at specific genomic loci. However, these dual mechanisms also lead to dose-dependent, irreversible cardiotoxicity. Compared with classic anthracyclines (such as doxorubicin and daunorubicin), Acla does not cause DNA damage and accumulates significantly in lymphoid tissues (spleen, thymus, and lymph nodes), with poor distribution to other tissues. Consequently, its cardiotoxicity is significantly reduced. Even at high cumulative doses, it is less likely to cause cardiac dysfunction. Therefore, Acla may offer a safer option for elderly patients or those with concomitant heart disease. Previous studies have shown that the combination of Acla and cytarabine (such as the CAG regimen) has some efficacy and is well tolerated in relapsed/refractory and elderly patients with acute myeloid leukemia. In the 1980s and 1990s, studies explored the use of Acla in chemotherapy regimens for non-Hodgkin's lymphoma and Hodgkin's lymphoma, demonstrating some activity. Small studies have shown that Acla monotherapy can achieve a response rate of approximately 30% in patients with advanced non-hedging lymphoma, without compromising cardiac function. Japanese researchers have found that combination chemotherapy regimens containing Acla in T-cell lymphomas exhibit superior efficacy.
In this study, the investigators will replace doxorubicin in the traditional CHOP regimen with aclarubicin, a drug with proven efficacy and low cardiotoxicity, to create a novel aclarubicin, cyclophosphamide, vincristine, and prednisone (CAOP) regimen for patients with relapsed/refractory CTCL and SS who have received at least one prior systemic therapy. This combination chemotherapy regimen may improve efficacy while balancing tolerability and safety, providing a new treatment option for elderly patients with CTCL.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
- Model description
- Phase I Primary Objectives: to evaluate the safety and tolerability of the CAOP regimen in patients with relapsed/refractory cutaneous T-cell lymphoma; to determine the maximum tolerated dose (MTD) based on dose-limiting toxicities (DLTs) and to determine the recommended Acla dose for the dose-expansion phase. Phase II Primary Objectives: to evaluate the efficacy of the CAOP regimen in patients with relapsed/refractory cutaneous T-cell lymphoma; the primary endpoint is objective response rate (ORR).
| Arm | Type | Receives |
|---|---|---|
| CAOP | Experimental | Drug: Aclarubicin, Drug: Cyclophosphamide, Drug: Vincristine, Drug: PrednisoneAclarubicin will be used in a dose escalation and dose expansion approach. Cyclophosphamide, Vincristine and Prednisone will be used in a fixed dose throughout the phases. Phase I dose-escalation: a standard "3+3" approach for aclarubicin. Phase II dose expansion: enroll patients same as in phase I, and aclarubicin will be used at the dose determined by the dose escalation. The whole treatment includes induction and maintenance. Induction treatment includes 3 week cycles for 6 cycles of CAOP or until progression. Maintenance treatment includes 6 week cycles for 4 cycles of CAOP or until progression. |
Who may qualify
- Ages
- 60 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (14 listed)
- Understand and voluntarily sign the informed consent form
- Age ≥ 60 years at enrollment
- Eastern Cooperative Oncology Group (ECOG) performance status ≤ 1
- Histologically confirmed primary cutaneous T-cell lymphoma (CTCL) or Sézary syndrome (SS) (according to the fifth edition of the WHO Classification of Tumors of the Hematopoietic and Lymphoid System)
- Stage II-B, III, or IV (referring to the Olsen criteria of the International Society for Cancer Research (ISCL)/USCC/EORTC, 2022)
Key exclusion criteria (17 listed)
- Patients diagnosed with a malignancy within the past two years. Exclude the following situation: non-melanoma skin cancer, melanoma in situ, localized prostate cancer (current PSA <0.1 ng/mL), treated thyroid cancer; or cervical carcinoma in situ or breast ductal/lobular carcinoma in situ diagnosed within the past two years, as long as there is no current evidence of active disease.
- Clinical evidence of central nervous system (CNS) infiltration.
- Large cell transformation (LCT). Patients with a history of LCT but no current invasive disease and no evidence of LCT on skin or lymph node pathology may be enrolled.
- Psychiatric illness, disability, or social circumstances that may affect the subject's safety, ability to provide informed consent, or poor compliance.
- Patients with significant uncontrolled comorbidities or infections, as follows:
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| AclarubicinCycle 1-6: Phase I starting dose 20mg/m^2/D, D1-2 (dose group 1), D1-3 (dose group 2), D1-4 (dose group 3), QD, ivgtt The Phase II dose was determined based on the Phase I results Cycle 7-10: Phase I starting dose 20mg/ m^2/D, D1-2 (dose group 1), D1-3 (dose group 2), D1-4 (dose group 3), QD, ivgtt The Phase II dose was determined based on the Phase I results | Drug | CAOP |
| CyclophosphamideCycle 1-6 750 mg/m^2, D1, QD, ivgtt Cycle 7-10 750 mg/m^2, D1, QD, ivgtt | Drug | CAOP |
| VincristineCycle 1-6 1.4 mg/m^2, D1 (maximum 2mg/d), QD, iv Cycle 7-10 1.4 mg/m^2, D1 (maximum 2mg/d), QD, iv | Drug | CAOP |
| PrednisoneCycle 1-6 60 mg/m^2, D1-5 (maximum 100mg/d), QD, Po Cycle 7-10 60 mg/m^2, D1-5 (maximum 100mg/d), QD, Po | Drug | CAOP |
Primary outcome
Maximum tolerated dose (MTD)
Time frame: 28 days after first dose of aclarubicin
MTD for aclarubicin (primary outcome measure of phase I)
Recommended Phase 2 Dose (RP2D)
Time frame: 28 days after first dose of aclarubicin
RP2D for aclarubicin (primary outcome measure of phase I)
Objective response rate (ORR)
Time frame: At the end of induction cycle 6 (each cycle is about 28 days)
Proportion of patients who achieved complete remission (CR) or partial remission (PR) after treatment (primary outcome measure of phase II)
6 secondary outcomes
Objective response rate (ORR)
Time frame: At the end of induction cycle 6 (each cycle is about 28 days)
Progression Free Survival
Time frame: All enrolled patients were followed up for at least 12 months or had an event
Time to Next Treatment (TTNT)
Time frame: All enrolled patients were followed up for at least 12 months or had an event
Adverse Events
Time frame: From enrollment to 28 days after the end of treatment
Change in quality of life as measured by the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30 (EORTC QLQ-C30) global health status score
Time frame: From enrollment to 28 days after the end of treatment
Cancer-related fatigue as measured by the Patient-Reported Outcomes Measurement Information System (PROMIS) Fatigue score
Time frame: From enrollment to 28 days after the end of treatment
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 17 Apr 2026.
- Individual participant dataSharing planned: No
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Hematologic Malignancy, Leukemia
RecruitingObservational study
Tissue, Blood, and Body Fluid Sample Collection From Patients With Hematologic Cancer
Chronic Myeloproliferative Disorders, Leukemia
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Junmin Li, Professor principal investigator
Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 1/2 study testing Aclarubicin, Cyclophosphamide and Vincristine in people with Cutaneous T-Cell Lymphoma Refractory and Cutaneous T-Cell Lymphoma, Relapsed, run by Shanghai Jiao Tong University School of Medicine at 2 sites in China.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 14 inclusion and 17 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 17 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in China. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this combined phase mean?
Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Jiong Hu (86-13764313546, hj10709@rjh.com.cn), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Maximum tolerated dose (MTD) (time frame: 28 days after first dose of aclarubicin). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Apr 2026.