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Hematopoietic Cell Transplantation for Non-Hodgkin Lymphomas

For individuals with non-Hodgkin lymphoma (NHL) B-cell subtypes considered aggressive (except mantle cell lymphoma), either allogeneic hematopoietic cell transplantation (HCT) using a myeloablative conditioning regimen or autologous HCT may be considered medically necessary:

as salvage therapy for individuals who do not achieve a complete remission (CR) after first-line treatment (induction) with a full course of standard-dose chemotherapy;

to achieve or consolidate a CR for those in a chemosensitive first or subsequent relapse; or

to consolidate a first CR in individuals with diffuse large B-cell lymphoma, with an age-adjusted International Prognostic Index score that predicts a high- or high-intermediate risk of relapse.

For individuals with mantle cell lymphoma:

Autologous HCT may be considered medically necessary to consolidate a first remission.

Allogeneic HCT, with myeloablative or reduced-intensity conditioning, may be considered medically necessary as salvage therapy.

Autologous HCT is considered investigational as salvage therapy.

Allogeneic HCT is considered investigational to consolidate a first remission.

For individuals with NHL B-cell subtypes considered indolent, either allogeneic HCT using a myeloablative conditioning regimen or autologous HCT may be considered medically necessary:

as salvage therapy for individuals who do not achieve CR after first-line treatment (induction) with a full course of standard-dose chemotherapy; or

to achieve or consolidate CR for those in a first or subsequent chemosensitive relapse, whether or not their lymphoma has transformed to a higher grade.

Either autologous HCT or allogeneic HCT is considered investigational:

as initial therapy (ie, without a full course of standard-dose induction chemotherapy) for any NHL;

to consolidate a first CR for individuals with diffuse large B-cell lymphoma and an International Prognostic Index score that predicts a low- or low-intermediate risk of relapse;

to consolidate a first CR for those with indolent NHL B-cell subtypes.

For individuals with mature T-cell or natural killer cell (peripheral T-cell) neoplasms:

Autologous HCT may be considered medically necessary to consolidate a first CR in high-risk subtypes (see Policy Guidelines section).

Autologous or allogeneic HCT (with myeloablative or reduced-intensity conditioning) may be considered medically necessary as salvage therapy.

Allogeneic HCT is considered investigational to consolidate a first remission.

For individuals with hepatosplenic T-cell lymphoma:

Allogenic HCT may be considered medically necessary to consolidate a first CR or partial response.

Autologous HCT may be considered medically necessary to consolidate a first response if a suitable donor is not available or for individuals who are ineligible for allogeneic HCT.

Autologous or allogeneic HCT as initial therapy (i.e., without a full course of standard-dose induction chemotherapy) is considered investigational.

Reduced-intensity conditioning with allogeneic HCT may be considered medically necessary as a treatment of NHL in individuals who meet criteria for an allogeneic HCT but who do not qualify for a myeloablative allogeneic HCT (see Policy Guidelines section).

Tandem transplants are considered investigational to treat patients with any stage, grade, or subtype of NHL.

Note: Small lymphocytic lymphoma may be considered a node-based variant of chronic lymphocytic leukemia. Therefore, small lymphocytic lymphoma is considered along with chronic lymphocytic leukemia in evidence review 08.001.047. Lymphoplasmacytic lymphoma/Waldenström macroglobulinemia is considered in evidence review 08.001.054.

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