Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID05646576

Defining the Role of Palliative Care for Patients With Hematologic Malignancies Undergoing Adoptive Cellular Therapy: The PEACE Study

Led by Massachusetts General Hospital · Updated on 2026-04-21

90

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

Sponsors

M

Massachusetts General Hospital

Lead Sponsor

C

Conquer Cancer Foundation

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating whether a palliative care intervention called PEACE can improve the quality of life and experiences of adults with hematologic malignancies such as lymphoma, leukemia, or multiple myeloma who are receiving adoptive cellular therapy (ACT). This study involves a randomized controlled design following an initial open pilot phase. The goal is to understand if adding this specialized palliative care improves outcomes compared to usual oncology care. Around 90 participants are expected to take part, with the study lasting up to two years. Participants first join an open pilot where 10 individuals receive the PEACE palliative care intervention throughout their treatment. After refining the approach, about 80 participants will be randomly assigned to one of two groups: one receiving the PEACE palliative care plus usual oncology care, and the other receiving standard oncology care alone. The PEACE intervention involves regular meetings with palliative care clinicians starting within one week of T-cell collection and frequent follow-ups during hospitalization and for up to one year post-randomization. During the study, participants will attend scheduled assessments, which can be completed remotely or on paper, to monitor various outcomes. These include quality of life, anxiety, depression, PTSD symptoms, physical symptom burden, coping, prognostic understanding, and communication about end-of-life care. Safety and feasibility will also be tracked, with some participants completing exit interviews in the pilot phase. The study is supported by the American Society of Clinical Oncology and conducted at a single center.

CONDITIONS

Brief Title

Defining the Role of Palliative carE for Patients With Hematologic Malignancies Undergoing Adoptive CEllular Therapy

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Ability to complete surveys in English or with assistance of an interpreter
  • Diagnosis of a hematologic malignancy such as lymphoma, leukemia, or multiple myeloma
  • Receiving autologous adoptive cellular therapy (ACT) at Massachusetts General Hospital with an FDA approved cellular therapy product
Not Eligible

You will not qualify if you...

  • Impaired cognition or uncontrolled mental illness that prevents study participation based on oncology clinician assessment
  • Currently receiving palliative care services

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - Up to 2 years

Participants receive adoptive cellular therapy (ACT) and are assigned to either palliative care intervention plus usual oncology care or usual oncology care alone. Those in the palliative care group meet with a palliative care clinician before and during hospitalization for ACT.

Multiple visits including at least 2 visits per week during hospitalization for ACT and regular follow-up visits up to one year after enrollment

Follow-up

Duration - Up to 90 days

Participants complete follow-up assessments on pre-determined days up to 90 days post-treatment and may complete exit interviews in the open pilot phase.

Assessments completed remotely or via paper on scheduled days

Trial Site Locations

Total: 1 location

1

Massachusetts General Hospital Cancer Center

Boston, Massachusetts, United States, 02215

Actively Recruiting

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Research Team

P

Patrick C Johnson

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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