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Abstract Non-Hodgkin’s lymphoma is one of the common malignant diseases world wide. In 1995, more than 45,000 new cases were diagnosed in the USA. In Egypt, MHLs represent 11% of malignant cases presenting to the National Cancer institute (Ibrahim, 1997). Over the last 20 years, diagnosis and management ofNHL at the National Cancer Institute, Cairo University have passed into different trial generations. . The first generation regimen included the use of non-anthracycline • containing regimens e.g. COP, C-MOPP, and other simple combinations or single agents, as well as anthracycline containing CHOP regimen. The second generation regimens started with the use of standard BECQP regimen and its dose intensified versions. These modified versions included giving BECOP with the same doses every 3 weeks instead of 4 weeks, or achieving further increase in the dose intensity by 25% dose increase of the 2 most active agents in the combination i.e. cyclophophamide and epidoxorubicin together with growth factors support. The third generation regimens included the use of either continuous infusion chemotherapy e.g. EPOCH regimen, other third generation combinations e.g. m-BACOD, COP-BLAM, or the use of interferon as a maintenance therapy after induction therapy. In the current study a trial has been made to evaluate the clinicopathologic profile, end results of treatment, and the impact of the various prognostic factors on treatment response, and survival of most ofNHL -89- -~-----_.~-~~~- patients presenting to the National Cancer Institute, Cairo University during a five years period (1995-1999). In Egypt, diffuse aggressive lymphomas (intermediate and high grades ofworking fonnulation) Predominate and in one series (Tawfik et at, 1984) diffuse aggressive lymphomas represented by 68.3% of their patients respectively and Nearly similar results were reported by Mokhta, (1991) 83.3%. In our series and like other Egyptian servies aggressive and Indolent NHL represented by 68.4% and 3 I.5% respectively. In contrast to Egyptian data most western studies reported an incidence of 40% of aggressive NHL (Anderson et al., 1982). Malignant Jymphom~ in Egyptian patients present special unmvourable features, which are distinctly different from those reported in the western Jiterature.Thus, in addition to the predominance of diffuse aggressive pathologic subtypes as previously mentioned; the patients usually present at advanced stages, with 85% of cases in stages III and IV of Ann Arbor classification. They also present with bulky disease, higher incidence of primary extranoda1lymphomas (34%) and high serum levels ofLDH (Abou Rabia, and Khaletl, 1994; EI Bolkainy et aL, 1984). In accordance with these observations and other published data reported by £l-Bokainy et al; (1984); Tawfik et al, (1984) and Mokihtar (1991) and the data of our series. Systemic B-symptoms were present in 66% of our cases (52% in Abou rabia and Khaled’s Series, 1994). Stages III and IV were observed in 47.6% and extra nodal affection was encountered in 43% of our patients included in this series. -JO.. For along period of time, the standard staging system for NHL than HD, and that it does not conelate well with prognosis so, many clinical features has been identified as being of influence on response to treatment and on survival. On applying this international index to the present retrospective series of patients presented to the National Cancer Institute clinics during the period 1995-1999, where at that time, the prognostic index was not yet developed, we found that it is very difficult to guarantee that the 5 prognostic constituents of this index have been looked for. So, we presented our data in an approximate way by ensuring that at least 1.2,3.~.etc of the factors are present in each patient. This means that for each case, the index category could be more than that presented due to some missed one or more of the international index constituent factor (s) put it cannot be less than that scored for each case. In view of this and applying this international index on our patients. About half of our patients belonged to the high risk categories i.e. presence of more than 2 risk factors. In a study by Shipp et al., (1993), 35% of their cases were of low risk (0-1 factor), 27% low intermediate (2 factors), 22% high intermediate (3 factors), and 16%were of the high risk category, (4-5 factors). Although, our data are incomplete due to the known nature of any retrospective study, and thus its evaluation in relation to other studies would be difficult but our study revealed 15% of our cases were low risk (0-1 factor), 37% low intermediate (2 factors), 27.6% high intermediate (3 factor), and 20.5% were of the high risk category (4-5 factors). ..91- -~-.-.-----------. __ ._------- For further and more comprehensive analysis of our patients according to the international index, we have also individually compared the five pretreatment characteristics which determine the international index of our cases reported by SI,ipp et al., (1993). While those patients whose age was > 60 years represented 20% of our series, 41% of the patients in Shipp’$ study belonged to the old age group. Tumour stage III and IV among our Patients was 47.6%, while it was 66% in Shipp’s predictive model. Extranodal involvement to of more than one site was encountered In 55% vs 30% among our patients and those of Shipp’s study respectively. Performance status of the patients in the present study was 51.5%, 38.3%, 8.6% and 1.6% for PS 1,2,3, and 4 respectively, while it was 27%, 34%, 12%, 4%, and 2% for PS 0, J , 12,3, and 4 in SIIIPP’s series. The serum LDH was high in 58.3% vs 40%. Most of our patient (50.7%) received chop chemotherapy and (25%) received other lines of chemotherapy and (24.2%) did not receive any chemotherapy but the majority of these patient; weren’t regular in receiving therapy and didn’t complete their planned treatment. These alarming observations of treatment irregularity and incomplete therapy for the majority of patients analysed in this series may be partially explained by the known mutual reluctancy of both the patient and the physician to aggressively treat low grade NIll.. due to its long natural history and lack of curative therapy specially in advanced cases. However, several other factors can explain this observation. These factors are multifactorial and include those related to the patient, meidcal ~----_ ..~----- ----- profession, the hospital, social workers, nature of the disease and its treatment, and the general environment of our society. Patients may be irregular in their follow up and in treatment due to several reasons. These reasons include poverty and fmancial problems specially if they are living far from Cairo, unawareness of the impact of their disease and its fatal sequalae if untreated, fear of coming to a hospital where ”cancer” is treated, or of receiving chemotherapy or its •side effects, and other social problems. In addition, apparent and deceiving initial remission that may occur in cases sensitive to chemotherapy may give the patient a false belief that he is cured, and there is no need to continue therapy. Regarding medical profession, many factors may be responsible for this lack of information and regular follow up of patients. Inaccuracy and reluctance to report and record the clinical data and follow up notes in patients. Inaccuracy and reluctance to report and record the clinical data and follow up notes in patients files is one factor. Also, relative lack of unified treatment stratigies and protocols, irregular attendance in the clinic, and the psychological relation of the patient to a special doctor and his wish not to be examined by another one, all those may contribute to this high incidence of irregular follow up and treatment. On the other hand, factors related to the hospital and health care facilities include the following (1) : the presence of increasing number of patients in the clinics with the relative deficiency of doctors and other health care profession, (2) relative lack of enough beds in the inpatient department, (3) unavailability of regular supply of some chemotherapeutic agents and other medications due to financial or -93- --------_ ..__ ._._------_ .._--._---._- -._--. - ...._-_._- administrative causes, (4) unavoidable delay in getting the result of the different laboratory and radiological investigations of some cases due to the large number of patients treated at the hospital, (5) loss offiles of some patients due to inadequate,filing system, (6) lack of cooperation in certain instances between the different service and clinical departments, and (7) suboptimal social services. |