Pm. Mauch et al., 2ND MALIGNANCIES AFTER TREATMENT FOR LAPAROTOMY STAGED IA-IIIB HODGKINS-DISEASE - LONG-TERM ANALYSIS OF RISK-FACTORS AND OUTCOME, Blood, 87(9), 1996, pp. 3625-3632
The survival of patients with Hodgkin's disease has dramatically impro
ved over the past 30 years because of advances in treatment. However,
concern for the risk of long-term complications has resulted in a numb
er of trials to evaluate reduction of therapy. The consequences of the
se trials on recurrence, development of long-term complications, and s
urvival remain unknown. One major consequence of successful treatment
of Hodgkin's disease is the development of second malignant neoplasms.
We sought to determine the factors most important for development of
second tumors in pathologically staged and treated Hodgkin's disease p
atients followed for long intervals to provide background information
for future clinical trials and guidelines for routine patient follow-u
p. Between April 1969 and December 1988, 794 patients with laparotomy
staged (PS) IA-IIIB Hodgkin's disease were treated with radiation ther
apy (RT) alone or combined radiation therapy and chemotherapy (CT). Th
ere were 8,500 person-years of follow-up (average of 10.7 person-years
per patient). Age and gender-specific incidence rates were multiplied
by corresponding person-years of observation to obtain expected numbe
rs of events. Observed to expected results were calculated by type of
treatment, age at treatment, sex, and time after Hodgkin's disease. Ab
solute (excess) risk was expressed as number of excess cases per 10,00
0 person-years. Seventy-two patients have developed a second malignant
neoplasm. Eight patients developed acute leukemia, 10 had non-Hodgkin
's lymphoma (NHL), and 53 patients developed solid tumors at a median
time of 5 years, 7.25 years, and 12.2 years, respectively, after Hodgk
in's disease. One patient developed multiple myeloma 16.5 years after
Hodgkin's disease. The relative risk (RR) of developing a second malig
nancy was 5.6. The absolute excess risk per 10,000 person-years (AR) o
f developing a second malignancy was 69.6 (7.0% excess risk per person
per decade of follow-up). The highest RR occurred for the development
of leukemia (RR = 66.2), however because of the low expected risk, th
e AR was only 9.3. The RR of solid tumors after Hodgkin's disease was
lower (4.7); however, the AR was greater (49) than for acute leukemia.
Among the solid tumors, breast, gastrointestinal, lung, and soft tiss
ue cancers had the highest absolute excess risks. The risk for develop
ing breast cancer after Hodgkin's disease was greatest in women who we
re under the age of 25 at treatment. The most significant risk factor
for the development of both leukemia and solid tumors was the combined
use of radiation therapy and chemotherapy. The RR following RT alone
was 4.1 (AR = 51.1); for RT + CT (initially or at relapse) the RR was
9.75 (P < 0.05, nonoverlapping confidence limits, AR = 123.9). Surviva
l following development of a second malignancy was poor in patients wi
th leukemia, gastrointestinal tumors, lung cancer, and sarcoma. Surviv
al from other malignancies including NHL and breast cancer was more en
couraging. Second malignant neoplasms are a major cause of late morbid
ity and mortality following treatment for Hodgkin's disease. The most
significant risk factor for the development of second tumors is the ex
tent of treatment for Hodgkin's disease, Recommendations are presented
for both prevention and early detection of these tumors. (C) 1996 by
The American Society of Hematology.