Indolent non hodgkins lymphoma

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Transcript of Indolent non hodgkins lymphoma

Indolent non Hodgkin lymphomas

Dr. Rajib BhattacharjeeJunior Resident

IPGMER, Kolkata

WHO classification 2008

Most common types of NHL encountered in clinical practice

types of NHL Incidence DLBCL 33%

Follicular Lymphoma 22%

Marginal Zone Lymphoma 10%

PTCL 10%

SLL/CLL 7%

Mantle cell lymphoma 7%

Types of NHL based on aggressiveness

Low grade Intermediate grade high grade

Follicular lymphoma

Marginal zone lymphoma

SLL/CLL

DLBCL

PTCL

Burkitt’s lymphoma

Lymphoblastic lymphoma

New ticket day… in the OPD…

Our patient enters…. A man in his 60s

•Median age at presentation – 55-65 years

•Males are affected more than females

I started to listen to his clinical history..

He complained of a painless swelling in his neck..

2/3rd of NHL patients present with asymptomatic lymph node swelling (nodal disease)Common in FL,MCL & SLLSites- Neck 70%Groin 60%Axilla 50%

Any extranodal disease…

• I asked him,” Do you have any problem during swallowing or do you get full with little food?”

1/3rd of NHL patients may present with extranodal disease.Common in DLBCL & MZLSite-GIT - 25-35%Waldayers ring – 18-23%

B Symptoms

I asked 3 questions:-1. Did you suffer from fever in the last few

months?2. Have you lost a lot of weight lately?3. Do you change your shirt often due to night

sweats?Then I asked… did you find any cause to these or

were they unexplained?

Exam time..

• Lymph node examination• Head and neck – waldeyer’s ring• Chest – Sternal/2nd ICS percussion Pleural effusion• Abdomen- Organomegally, Lump, Ascites Testes• Skin - Nodules

Investigations ..

Lab investigations• CBC, KFT, LFT, Electrolytes• Ca2+

• LDH, Uric acid• HBsAg, IgM HBc• HIV I & II

Imaging• Chest X-Ray• CT Thorax, abdomen & pelvis• PET CT• Tc-99m Bone Scan• MUGA/ Echocardiography

Endoscopy • Upper GI

• Bone marrow biopsy A must for all NHL patients (SLL, mantle cell lymphoma – 70% FL – 50% , DLBCL – 15%)

• CSF Cytology Only in suspected leptomeningeal

involvement

Histopathological examination

The cervical lymph node must go for biopsy….

A medium sized accessible lymph node is preferred for excision.Cervical lymph node if palpable, is preffered

Which stage is the disease..???

X = Bulky disease• Clinically diameter > 10cm• CXR PA- Mediastinal mass ratio(MMR) = Max width of mass__ > 0.33

Max intrathoracic dia = Max width of mass >0.35 Intrathoracic dia @ T5 - T6

Possible histologies for our discussion

Follicular Lymphoma

5Y OS

70.7%

50.9%

35.5%

How do I treat this patient if he has localised FL – Stage I & II?

Gr 1-2, non bulky, asymptomatic

IFRT (30Gy)

Gr 3, bulky, B symptoms

IFRT(30Gy) RCHOP (4 cycles)

Boost (upto 40 Gy) IFRT to the bulky site (30Gy)

How do I treat this patient if he has advanced FL – Stage III & IV?

Asymptomatic

Observation or Rituximab

Symptomatic, B symptoms, cytopenias, compromised end organ function

RCVP/RCHOP (6 cycles)

Gr 3 RCHOP (6 cycles)

Important studies study Conclusion

BNLI Study 2003 Observation is a good initial approach in asymptomatic stage III & IV FL

GLSG Trial 2005 & Marcus et al Rituximab with both CVP & CHOP produce enhanced OS

SWOG Trial Anthracyclins fail to improve OS in indolent lymphoma

Bendamustine in 1st line

indolent/mantle cell

R-B R R-CHOP 69.5mo PFS 31.2mo

toxicity

Maintenance Rituximab

Follicular lymphoma RCHOP/RCVP/RFCM

mRituximab R Obv

75% PFS 58%

72% CR 52%

Progressive disease

• Elderly, asymptomatic – Obv• 2nd line chemotherapy – Bendamustine FCM• Radioimmunotherapy – Zavaline, Baxxar• mTOR inhibitors – NVP-BEZ235• Proteasome inhibitors• Stem cell transplant

Marginal zone lymphoma

Three entities• Nodal • Extranodal - MALToma• Splenic

StomachSmall intestineOccularSkinParotidThyroid

How to treat…Extranodal disease• Symptomatic local tumor – RT• Generalized disease Asymptomatic – Obv Symptomatic - CT (Chlorambucil)

Nodal disease – R-CHOP

Splenic disease – Splenectomy or Splenic RT

Gastric MALToma• C/F- abdominal fullness, loss of appetite,

waight loss, B symptoms, pain, bleeding• Diagnosis- Endoscopic biopsy• H. pylori association in 92% (# Isaacson et al)• Antibiotics and PPI (even in H.pylori –ve cases) CRR-75% 5Y FFS-50% OS>90%• Endoscopy after 3 months• Lymphoma persist- *deep invasion *t(11:18)• Antibiotic failure T/t – RT(24-30Gy)• Not suitable for RT – Rituximab monotherapy

SLL

• Localized disease – IFRT (30Gy)

• Advanced disease – Chemoimmunotherapy

Age>70, co-morbidities Age<70, medically fit Relapse

•Obinutuzumab + Chlorambucil•Rituximab + Chlorambucil•Bendamustine + Rituximab

•FCR (Fludarabine + Cyclofosfamide + Rituximib)

•Ibrutinib

IFRT

Fallow up

• Physical exam & labwork - 3-6 months for 1st 5 years then annually.

• CT scan every 6 months for 2 years then annually.

THANK YOU