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临床试验/NCT02409576
NCT02409576Unknown1 期

Pilot Study of Expanded , Activated Haploidentical Natural Killer Cell Infusions for Sarcomas

National University Hospital, Singapore2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2015年2月最近更新:
适应症
干预措施

试验速览

阶段
1 期
入组人数
20
试验地点
2
主要终点
Disease response after expanded activated NK cell infusion

研究概览

简要总结

Progress in the treatment of children with leukemia and lymphoma results in high cure rates but progress in the treatment of children and adolescents with solid tumors has been slow. Despite aggressive therapy with multimodality treatment involving surgery, radiation and chemotherapy, about two thirds of the patients with metastatic Ewing sarcoma (EWS), and intermediate and high risk rhabdomyosarcoma (RMS) will relapse. The available second line therapies for relapse are limited and often not effective. There is a dire need to look for treatment options beyond conventional means for the treatment of these patients.

Infusions of allogeneic natural killer (NK) cells in leukemia patients have shown to be tolerated well without inducing graft versus host disease (GVHD). There is also mounting evidence that NK cells have activity against solid tumors.

In the lab the investigators tested NK cell activity against cell lines from different paediatric solid tumors. Among paediatric solid tumors, EWS and RMS are exquisitely sensitive to killing by expanded NK cells; NK cells also have activity against OS cells. Preliminary clinical data suggest that donor NK cells may exert antitumor activity in children with solid tumors undergoing allogeneic hematopoietic stem cell transplantation.

Taking into account the safety of adaptive NK cell infusion, and their efficacy against EWS, RMS and OS, NK cells could be a powerful new tool in the treatment of paediatric solid tumors.

The great anti-tumor activity of expanded and activated NK cells, together with the feasibility of infusing haploidentical NK cells in a non-transplant setting form a compelling rationale for the clinical testing of these NK cells in patients with sarcoma.

详细描述

Adoptive transfer of allogeneic NK cells has been shown to be safe in patients with leukemia.

The patients enrolled on this will receive lymphodepleting chemotherapy with cyclophosphamide (1 day) followed by fludarabine (5 days) Each patient will receive IL-2 on alternate days starting 1 day before infusion of NK cells for a total of 6 doses.

Patient will undergo imaging MRI or PET or CT scan one month after the infusion to assess response to the NK cell infusion.

In our study we aim to determine the feasibility, safety and efficacy of expanded, activated NK cells in patients with EWS and RMS .

We will also study the persistence and phenotype of expanded NK cells in research participants with EWS and RMS .

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
— 至 80 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • A ) NK cell Recipient:
  • Age 0 months to 80 years old.
  • Patients with metastatic, progressive or relapsed EWS, RMS after completing standard of care therapy who are at high risk of relapse even if they do not have any evidence of residual disease.
  • a) For patients without residual disease at the point of study entry, response to NK cells will be measured by their incidence of relapse as indicated by their 5-year event free survival. Only patients at high risk of relapse > 70% will be enrolled if there is no evidence of residual disease.
  • Shortening fraction greater than or equal to 25%. Left ventricular ejection fraction (LVEF) greater than or equal to 40%
  • Glomerular filtration rate greater than or equal to 60 ml/min/1.73 m
  • Pulse oximetry greater than or equal to 92% on room air.
  • Direct bilirubin less than or equal to 3.0 mg/dL (50 mmol/L).
  • Alanine aminotransferase (ALT) is no more than 2 times the upper limit of normal.
  • Aspartate transaminases (AST) is no more than 2 times the upper limit of normal.
  • Karnofsky or Lansky performance score of greater than or equal to
  • Does not have a current pleural or pericardial effusion.
  • Has a suitable adult family member donor available for NK cell donation.
  • Has recovered from all acute NCI Common Terminology Criteria for Adverse Events (CTCAE) grade II-IV non-hematologic acute toxicities resulting from prior therapy per the judgment of the PI.
  • At least two weeks since receipt of any biological therapy, systemic chemotherapy, and/or radiation therapy.
  • Is not receiving more than the equivalent of prednisone 10 mg daily.
  • Not pregnant (negative serum or urine pregnancy test to be conducted within 7 days prior to enrollment).
  • Not lactating.
  • B) NK cell Donor:
  • First and second degree relative acceptable.
  • 18 years of age or above.
  • Not lactating.
  • Greater than or equal to 3 of 6 HLA match to recipient.
  • Meets eligibility and suitability criteria for hematopoietic cells donation as per institutional guidelines.
  • Not pregnant (negative serum or urine pregnancy test to be conducted within 7 days prior to enrollment).
  • HIV negative. Negative results must be within 60 days prior to enrolment.

排除标准

  • Failure to meet any of the inclusion criteria.

研究组 & 干预措施

Expanded, activated NK Cells(NKEXPSARC)

Experimental

Intravenous infusion of expanded, activated NK Cells Donor cell will be expanded and activated in the cGMP compliant TECT lab for 10 to 12 days prior to infusion into the patient.

干预措施: Expanded , Activated NK cells (Biological)

结局指标

主要结局

Disease response after expanded activated NK cell infusion

时间窗: 1 month post-NK cell infusion (and at regular intervals thereafter till a year post-NK cell infusion)

Radiological response will be measured based on PET or MRI or CT scan whichever is appropriate imaging for the tumor type and location.

次要结局

  • Acute and Chronic GVHD(Initiation of conditioning until 1 month ( 30 days) post- last dose of IL-2)
  • Persistence and phenotype of expanded NK cells in research participants with EWS, RMS and OS.(1 month ( 30 days) post- NK cell infusion)
  • Toxicity of NK cells infusion (NCI toxicity criteria CTC version 4.0)(1 month ( 30 days) post- NK cell infusion)
  • Performance status will be assessed by age-dependent Performances Scores ( Lansky scale or Karnofsky performance scale)(Initiation of conditioning till 30 days post-NK cell infusion)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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