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Low Grade NH Lymphoma SACT Regimens

Low Grade NH Lymphoma (General NHL, FL, WM)

cycloPHOSphamide, DOXOrubicin, vinCRIStine and prednisoLONE (CHOP) Therapy– 21 days

Regimen

Indication

00841a

Treatment of Non-Hodgkin lymphoma (NHL)

Chlorambucil 10mg/m2 Therapy

Regimen

Indication

00411a

Treatment of patients with low grade lymphoma.

riTUXimab and Bendamustine Therapy

Regimen

Indication

00345a

Treatment of patients with previously untreated indolent CD20-positive, stage III-IV Non-Hodgkin lymphoma (NHL).

R-CEOP Therapy -21 days

Regimen

Indication

00510a

Treatment of Non Hodgkin CD20 positive Lymphoma for patients not suitable for anthracycline therapy

(*riTUXimab) cycloPHOSphamide, DOXOrubicin, vinCRIStine and prednisoLONE (*R)-CHOP Therapy– 14 days

Regimen

Indication

00409a

Treatment of Non-Hodgkin Lymphoma (NHL)*

*riTUXimab to be included in CD20 positive patients

(*riTUXimab) cycloPHOSphamide, DOXOrubicin, VinCRIStine and prednisoLONE (*R)-CHOP) Therapy– 21 days

Regimen

Indication

00307a

Treatment of Non-Hodgkin Lymphoma (NHL).*

*riTUXimab to be included in CD20 positive patients.

riTUXimab S/C, cycloPHOSphamide, DOXOrubicin, vinCRIStine and prednisoLONE (R-CHOP) Therapy – 21 Days

Regimen

Indication

00667a

Treatment of Non-Hodgkin Lymphoma (NHL)

(R**)- miniCHOP Therapy – 21 days

Regimen

Indication

00436a

Treatment of Non-Hodgkin Lymphoma in patients aged greater than 80 or with significant co-morbidities.

* riTUXimab to be included in all CD20 positive patients.

(R*)-ICE ((riTUXimab*), Ifosfamide, CARBOplatin and Etoposide) Therapy - Outpatient

Regimen

Indication

00751a

Treatment of relapsed/refractory Non-Hodgkin Lymphoma (NHL)*

(R*)-ESHAP Therapy

Regimen

Indication

00394a

Treatment of relapsed Non-Hodgkin Lymphoma

riTUXimab** Gemcitabine and CISplatin ((R**)-GDP) Therapy

Regimen

Indication

00441a

Treatment of relapsed Non-Hodgkin Lymphoma

(R**)-ICE ((riTUXimab), Ifosfamide, CARBOplatin and Etoposide) Therapy

Regimen

Indication

00397a

Treatment of relapsed/refractory Non-Hodgkin Lymphoma**

**riTUXimab to be included in CD20 positive patients.

ICE (Ifosfamide, CARBOplatin and Etoposide) Therapy

Regimen

Indication

00842a

Treatment of relapsed/refractory Non-Hodgkin Lymphoma

(*riTUXimab) CycloPHOSphamide and prednisoLONE (R*)-CVP ) Therapy-21 days

Regimen

Indication

00293b

Treatment of patients with relapsed/refractory low grade B cell Non-Hodgkin lymphoma (NHL)*

*riTUXimab to be included in CD20 positive patients.

riTUXimab 375 mg/m2 Maintenance Therapy-84 day

Regimen

Indication

00540a

Maintenance therapy for the treatment of relapsed/refractory follicular CD20 positive, B-cell Non-Hodgkin Lymphoma (NHL) in patients who have responded to induction therapy

riTUXimab 375 mg/m2 Maintenance Therapy- 56 day

Regimen

Indication

00543a

Maintenance therapy for the treatment of previously untreated follicular CD20 positive, B-cell Non-Hodgkin Lymphoma patients responding to induction therapy

riTUXimab (S/C 1400mg) Maintenance Therapy-84 day

Regimen

Indication

00599a

Maintenance therapy for the treatment of relapsed/refractory follicular CD20 positive, B-cell Non-Hodgkin Lymphoma (NHL) in patients who have responded to induction therapy

riTUXimab (S/C 1400mg) Maintenance Therapy- 56 day

Regimen

Indication

00600a

Maintenance therapy for the treatment of previously untreated follicular CD20 positive, B-cell Non-Hodgkin Lymphoma patients responding to induction therapy

ESHAP Therapy

Regimen

Indication

00838a

Treatment of relapsed Non-Hodgkin Lymphoma

Idelalisib Monotherapy

Regimen

Indication

00291a

Monotherapy for the treatment of adult patients with follicular lymphoma (FL) that is refractory to two prior lines of treatment.

Obinutuzumab Maintenance Therapy - 56 day

Regimen

Indication

00425a

Obinutuzumab maintenance therapy is indicated in patients with follicular lymphoma (FL) who have responded to induction treatment with obinutuzumab and chemotherapy (CHOP, CVP or bendamustine) or have stable disease.

Obinutuzumab and Bendamustine Therapy

Regimen

Indication

00424a

Obinutuzumab in combination with bendamustine is indicated for the treatment of patients with follicular lymphoma (FL) who did not respond or who progressed during or up to 6 months after treatment with riTUXimab or a riTUXimab-containing regimen.

00424b

Obinutuzumab in combination with bendamustine is indicated for the treatment of patients with previously untreated advanced follicular lymphoma.

Obinutuzumab cycloPHOSphamide vinCRIStine and prednisoLONE (O- CVP) Therapy– 21 days

Regimen

Indication

00550a

Obinutuzumab in combination with CVP chemotherapy is indicated for the treatment of patients with previously untreated advanced follicular lymphoma.

Obinutuzumab and cycloPHOSphamide, DOXOrubicin, vinCRIStine and prednisoLONE (O-CHOP) Therapy – 21 day

Regimen

Indication

00549a

Obinutuzumab in combination with CHOP chemotherapy is indicated for the treatment of patients with previously untreated advanced follicular lymphoma.

riTUXimab 375 mg/m2 Therapy-7 day

Regimen

Indication

00541a

First line treatment of follicular lymphoma

00541b

As monotherapy for induction treatment for adult patients with stage
III-IV follicular lymphoma who are chemoresistant or are in their second
or subsequent relapse after chemotherapy

00541c

As monotherapy for retreatment of patients who have responded to
previous treatment with riTUXimab monotherapy for
relapsed/refractory follicular lymphoma

riTUXimab 375 mg/m2 Combination Therapy-21 day

Regimen

Indication

00542a

In combination with chemotherapy for induction treatment of
previously untreated or relapsed/ refractory CD 20 positive patients
with follicular lymphoma

(*riTUXimab) cycloPHOSphamide and prednisoLONE (R*)-CVP ) Therapy-21 days

Regimen

Indication

00293a

First line treatment for patients with stage 3/4 follicular lymphoma

dexAMETHasone, riTUXimab and cycloPHOSphamide (DRC) Therapy

Regimen

Indication

00532a

Treatment of symptomatic treatment naive or relapsed/refractory Waldenstrom’s macroglobulinaemia

Ibrutinib Therapy-CLL Waldenström’s macroglobulinaemia

Regimen

Indication

00296c

As a single agent for the treatment of adult patients with Waldenström’s macroglobulinaemia (WM) who have received at least one prior therapy, or in first line treatment for patients unsuitable for chemo-immunotherapy.

Zanubrutinib Therapy

Regimen

Indication

00708a

As monotherapy for the treatment of adult patients with Waldenström’s macroglobulinaemia (WM), who have received at least one prior therapy or as first line treatment for patients unsuitable for chemo-immunotherapy