In recent
years there has been an unprecedented increase in the incidence
of non-Hodgkin's lymphoma in Singapore, mirroring that in
Western societies. In 1997, it was the 8th commonest tumour
in males, but with about 150 new cases every year the incidence
is fast rising. No certain aetiological link is known, although
speculation abounds regarding environmental and infectious
factors. However, much progress has been made in the classification
and treatment of lymphomas.
Lymphomas
are one of the few cancers that can be cured, in that after
treatment the median survival of a patient could be similar
to that of anyone of the same age. This optimistic outlook
has been made possible by the success of combination chemotherapy
and more recently by the addition of "smart-bomb" immunotherapy
and radio-immuno-conjugates. Genetic signatures and immune
targets have been best studied in this cancer and have enabled
the development of antibody therapy, such as Rituximab (an
antibody to CD-20 for treatment of B-cell lymphoma), and
genetic tools for precise diagnosis.
Unlike
most cancers, for which surgery is the mainstay for removal
and cure of early-stage tumours, in lymphomas non-surgical
treatment is the cornerstone while surgery has a role in
the diagnosis and management of selected complications such
as bleeding or obstruction of viscera. Yet, overall the
treatment approach is truly multidisciplinary, with radiation
playing an important part.
This
tumour offers a glimmer of hope in cancer medicine, with
cure rates as high as 60% even for advanced-stage disease.
This high curability requires proper identification and
management of the cancer. Hence it is very important that
all physicians understand the management of this entity.
Nevertheless, proper understanding is somehow restricted,
one difficulty being that there are over 20 histological
types of cancers of this one organ system (lymphatic system).
In this issue of Cancer Update we hope to present a simple
overview to aid understanding of this important and curable
malignant tumour. We also hope to educate readers about
the common procedures that a patient with lymphoma has to
go through. Our aim is that all physicians will become more
comfortable in diagnosing and managing or referring future
lymphoma patients.
Dr Sandeep
K Rajan
Editor