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Treatment of Hodgkin
Lymphoma
Treatment of Hodgkin lymphoma
 Selection of initial treatment for
HL is usually based upon
presenting stage and prognostic
factors.
 An important issue during any
form of therapy is monitoring for
extent of disease.
Early stage HL (stage I-II)
 Divided into favorable and unfavorable prognosis .
 The two most commonly used definitions of
favorable disease are the European Organization
for the Research and Treatment of Cancer (EORTC)
and the German Hodgkin Study Group (GHSG).
Early stage HL (stage I-II)
 The EORTC defines favorable prognostic group as
patients age 50 or under , without large mediastinal
adenopathy , with an ESR of less than 50 , and no B
symptoms (or with an ESR of less than 30 in those who
have B symptoms), and disease limited to three or
fewer regions of involvement.
 The GHSG defines favorable prognostic group as
patients with no more than two sites of disease , no
extranodal extension, no mediastinal mass measuring
one-third the maximum thoracic diameter or greater;
and ESR less than 50 (less than 30 if B symptoms
present).
Favorable prognosis - Early stage HL
(stage I-II)
 ABVD(doxorubicin, bleomycin, vinblastine, dacarbazi
ne) for three - four cycles, followed by involved field
irradiation to 30 Gy with fields encompassing the
initially involved lymph node site , This approach has
the lowest relapse rate.
 ABVD for four to six cycles without radiation therapy.
This is an emerging option for patients at risk of long-
term complications from radiotherapy. Disease control
with combined therapy is superior compared with
chemotherapy alone , but this must be weighed
against the risks of radiotherapy.
Unfavorable prognosis - Early stage
HL (stage I-II)
 ABVD(doxorubicin, bleomycin, vinblastine,
and dacarbazine) remains the "gold standard"
chemotherapy for these patients .
 For most patients, ABVD plus radiation therapy.
Advanced stage HL (stage III-IV)
 ABVD (doxorubicin, bleomycin, vinblastine, and dacarbazine)
has been the standard regimen .
 BEACOPP(bleomycin, etoposide, doxorubicin, cyclophosphamide
, vincristine, procarbazine, and prednisone) incorporate
radiation therapy for most patients and have shown advantages
in freedom from progression but not overall survival when
compared with ABVD in three randomized trials.
 advantages with this more intense regimen is a reasonable
alternative to ABVD for patients with the highest risk of relapse .
 BEACOPP is associated with higher rates of toxicity including
reversible bone marrow suppression, secondary malignancies,
sterility, and rare cases of fatal sepsis.
 Toxicities are particularly severe in the elderly, making it
inappropriate in this population.
Advanced stage HL (stage III-IV)
 StanfordV(doxorubicin, vinblastine, mechloretha
mine, vincristine, bleomycin, etoposide,
and prednisone) incorporates radiation therapy for
all patients and may be preferred in some settings
because of its short administration schedule and
decreased pulmonary toxicity.
 It may have advantages for certain patients,
particularly those for whom radiation will be part
of their planned therapy. Randomized trials have
demonstrated no advantage over ABVD.

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Treatment of hodgkin lymphoma

  • 2. Treatment of Hodgkin lymphoma  Selection of initial treatment for HL is usually based upon presenting stage and prognostic factors.  An important issue during any form of therapy is monitoring for extent of disease.
  • 3.
  • 4. Early stage HL (stage I-II)  Divided into favorable and unfavorable prognosis .  The two most commonly used definitions of favorable disease are the European Organization for the Research and Treatment of Cancer (EORTC) and the German Hodgkin Study Group (GHSG).
  • 5. Early stage HL (stage I-II)  The EORTC defines favorable prognostic group as patients age 50 or under , without large mediastinal adenopathy , with an ESR of less than 50 , and no B symptoms (or with an ESR of less than 30 in those who have B symptoms), and disease limited to three or fewer regions of involvement.  The GHSG defines favorable prognostic group as patients with no more than two sites of disease , no extranodal extension, no mediastinal mass measuring one-third the maximum thoracic diameter or greater; and ESR less than 50 (less than 30 if B symptoms present).
  • 6. Favorable prognosis - Early stage HL (stage I-II)  ABVD(doxorubicin, bleomycin, vinblastine, dacarbazi ne) for three - four cycles, followed by involved field irradiation to 30 Gy with fields encompassing the initially involved lymph node site , This approach has the lowest relapse rate.  ABVD for four to six cycles without radiation therapy. This is an emerging option for patients at risk of long- term complications from radiotherapy. Disease control with combined therapy is superior compared with chemotherapy alone , but this must be weighed against the risks of radiotherapy.
  • 7. Unfavorable prognosis - Early stage HL (stage I-II)  ABVD(doxorubicin, bleomycin, vinblastine, and dacarbazine) remains the "gold standard" chemotherapy for these patients .  For most patients, ABVD plus radiation therapy.
  • 8. Advanced stage HL (stage III-IV)  ABVD (doxorubicin, bleomycin, vinblastine, and dacarbazine) has been the standard regimen .  BEACOPP(bleomycin, etoposide, doxorubicin, cyclophosphamide , vincristine, procarbazine, and prednisone) incorporate radiation therapy for most patients and have shown advantages in freedom from progression but not overall survival when compared with ABVD in three randomized trials.  advantages with this more intense regimen is a reasonable alternative to ABVD for patients with the highest risk of relapse .  BEACOPP is associated with higher rates of toxicity including reversible bone marrow suppression, secondary malignancies, sterility, and rare cases of fatal sepsis.  Toxicities are particularly severe in the elderly, making it inappropriate in this population.
  • 9. Advanced stage HL (stage III-IV)  StanfordV(doxorubicin, vinblastine, mechloretha mine, vincristine, bleomycin, etoposide, and prednisone) incorporates radiation therapy for all patients and may be preferred in some settings because of its short administration schedule and decreased pulmonary toxicity.  It may have advantages for certain patients, particularly those for whom radiation will be part of their planned therapy. Randomized trials have demonstrated no advantage over ABVD.