The final report regarding allogeneic stem cell transplantation (ASCT) in aggressive B-cell non-Hodgkin's lymphoma (B-NHL) and in T-cell non-Hodgkin's lymphoma (T-NHL) was published by the Institute for Quality and Efficiency in Health Care in July

29

Aug 2018

On the 4th of July of 2018, the Institute for Quality and Efficiency in Health Care (IQWiG) has published a final report regarding allogeneic stem cell transplantation (ASCT) in aggressive B-cell non-Hodgkin's lymphoma (B-NHL) and in T-cell non-Hodgkin's lymphoma (T-NHL). The following aims were outlined in the scope of this report:

  • The benefit assessment of ASCT in adults with aggressive B-cell lymphoma (excluding primary CNS lymphomas) with:
    • progression or relapse after high-dose chemotherapy and ASCT in comparison to patients treated without curative intent (B-NHL/post-auto-SCT);
    • absence of progression or relapse after therapy without stem cell transplantation compared to a high dose chemotherapy and ASCT (B-NHL/naïve SCT);
  • The benefit assessment of ASCT as a first-line therapy in adults with T-cell lymphoma (except cutaneous T-cell lymphomas) and the need for systemic drug therapy in comparison to systemic drug therapy alone or in combination with high-dose chemotherapy and ASCT (T-NHL/first line);
  • The benefit assessment of ASCT as a first-line therapy in adults with T-cell lymphoma (except cutaneous T-cell lymphomas) with progression or relapse after systemic drug therapy compared to patients treated without curative intent (T-NHL/high-grade).

The following conclusions were provided:

  • Overall, the benefit of allogeneic stem cell transplantation in B-NHL and T-NHL is unclear, as no meaningful studies are available;
  • Allogeneic stem cell transplantation is currently associated with the risk of graft-versus-host disease, so the potential risks and benefits of the allogeneic stem cell transplantation should be considered before its use;
  • No studies have assessed a quality of life of the patients.

See full details in German here.

Subscribe to our newsletter delivered every second week not to miss important reimbursement information.

The latest related news

22

Mar 2022

On February 17, 2022, the Federal Joint Committee (G-BA) has decided to include the method of matrix-associated autologous chondrocyte implantation (M-ACI) on the knee joint in the case of symptomatic cartilage damage in the lists of reimbursed procedures in the hospital and ambulatory settings.

Read more

09

Mar 2022

On February 16, 2022, the Innovation Committee at the Federal Joint Committee (G-BA) has published the decisions which recommended the transfer to standard care for three completed projects. The projects relate to the prevention of antibiotic resistance, improvement of healthcare in socially disadvantaged areas, and misuse of control colonoscopies in Germany.

Read more

03

Mar 2022

In February 2022, two more health apps were introduced in the Directory of digital health applications (DiGAs) at the Federal Office for Drugs and Medical Devices (BfArM) and thus became reimbursable. These apps can be prescribed by physicians and psychotherapists and will be reimbursed by health insurers. In total, thirty health apps are now available at the DiGA Directory.

Read more

14

Feb 2022

On January 28, 2022, the Institute for the Hospital Remuneration System (InEK) has published the list of the requests for innovation funding (NUB) that were submitted by the hospitals in 2021. The medical technologies belonging to the cardiovascular, ENT, eHealth, gastrointestinal, neuromodulation, neurovascular, orthopedic, and other technology groups obtained positive status 1.

Read more

07

Feb 2022

On January 20, 2022, the Federal Joint Committee (G-BA) has initiated an evaluation procedure for early benefit assessment for the use of a stent retriever (pRELAX by femtos) to treat vasospasm of cerebral arteries after subarachnoid hemorrhage.

Read more