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NCT01156259CompletedPhase 3

30Gy Versus 40Gy Radiotherapy for Localized Diffuse Large B Cell Lymphoma Achieving CR After Chemotherapy

30 Gy Versus 40 Gy Consolidative Radiotherapy for Early-stage Diffuse Large B-cell Lymphoma After Complete Response to Chemotherapy: a Multicentre, Randomised, Phase 3, Non-inferiority Trial

Source: ClinicalTrials.gov · Last updated 28 Oct 2026

Brief summary (registry, in English)

The purpose of this study is to determine whether 30Gy radiotherapy is as effective as 40Gy in the treatment of localized Diffused Large B cell Lymphoma (DLBCL) when completing CR after chemotherapy.

Status (registry)
Completed
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
432 (actual)
First submitted
29 Jun 2010
Start date
Jul 2010
Primary completion date
Jul 2025
Lead sponsor
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
NCT number
NCT01156259

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 432
  • From Jul 2010 to the primary completion date, Jul 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Any concurrent condition precluding protocol treatment.
  • Chemotherapy or radiotherapy before trial enrolment.

Other illness

  • HIV seropositivity.
  • Previous malignancy other than cervical carcinoma in situ.
  • Hepatic or cardiac failure.

Other

  • Primary lymphoma of the central nervous system, skin, or testis.
  • Transformation from another indolent lymphoma.
  • Pregnancy or breastfeeding.

Who the study is looking for

  • Written informed consent obtained before any trial-specific procedure.
  • Age 15 years or older.
  • Newly diagnosed, histologically confirmed DLBCL or primary mediastinal B-cell lymphoma (PMBL).
  • Ann Arbor stage I or II disease.
  • Complete response after chemotherapy, defined as the absence of clinical or imaging evidence of active disease, or a Deauville score of 1-3 on PET/CT.
  • An interval of less than 90 days between completion of chemotherapy and radiotherapy.
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0-2.
  • Able to receive conformal radiotherapy and to complete the required follow-up.

Age in the registry: 15 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Department of Radiation Oncology, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College
Coordinator of this site? Confirm its status
BeijingChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.