Clinical characteristics and prognosis of patients with therapy-related myelodysplastic syndrome and acute myeloid leukemia arising from malignant tumors / 中华血液学杂志

Objective: To investigate the clinical characteristics, cytogenetics, molecular biology, treatment, and prognosis of patients with therapy-related myelodysplastic syndrome and acute myeloid leukemia (t-MDS/AML) secondary to malignancies. Methods: The clinical data of 86 patients with t-MDS/AML in West China Hospital of Sichuan University between January 2010 and April 2023 were retrospectively analyzed. The clinical characteristics, primary tumor types, and tumor-related therapies were analyzed. Results: The study enrolled a total of 86 patients with t-MDS/AML, including 67 patients with t-AML, including 1 patient with M(0), 6 with M(1), 27 with M(2), 9 with M(3), 12 with M(4), 10 with M(5), 1 with M(6), and 1 with M(7). Sixty-two patients could be genetically stratified, with a median overall survival (OS) of 36 (95% CI 22-52) months for 20 (29.9%) patients in the low-risk group and 6 (95% CI 3-9) months for 10 (14.9%) in the intermediate-risk group. The median OS time was 8 (95% CI 1-15) months in 32 (47.8%) patients in the high-risk group. For patients with non-acute promyelocytic leukemia (APL) and AML, the median OS of the low-risk group was 27 (95% CI 18-36) months, which was significantly longer than that of the non-low-risk group (χ(2)=5.534, P=0.019). All 9 APL cases were treated according to the initial treatment, and the median OS was not reached, and the 1-, 2-, and 3-year OS rates were 100.0%, (75.0±6.2) %, and (75.0±6.2) % respectively. Of the 58 patients with non-APL t-AML (89.7%), 52 received chemotherapy, and 16 achieved complete remission (30.8%) after the first induction chemotherapy. The 1-, 2-, and 3-year OS rates of the non-APL t-AML group were (42.0 ± 6.6) %, (22.9±5.7) %, and (13.4±4.7) %, respectively. The median OS of patients who achieved remission was 24 (95% CI 18-30) months, and the median OS of those who did not achieve remission was 6 (95% CI 3-9) months (χ(2)=10.170, P=0.001). Bone marrow CR was achieved in 7 (53.8%) of 13 patients treated with vineclar-containing chemotherapy, with a median OS of 12 (95% CI 9-15) months, which was not significantly different from that of vineclar-containing chemotherapy (χ(2)=0.600, P=0.437). In 19 patients with t-MDS, the 1-, 2-, and 3-year OS rates were (46.8±11.6) %, (17.5±9.1) %, and (11.7±9.1) % with a median OS of 12 (95% CI 7-17) months, which was not significantly different from that in t-AML (χ(2)=0.232, P=0.630) . Conclusions: Breast cancer, bowel cancer, and other primary tumors are common in patients with t-MDS/AML, which have a higher risk of adverse genetics. Patients with APL had a high induction remission rate and a good long-term prognosis, whereas patients without APL had a low remission rate and a poor long-term prognosis.

Development of Acute Megakaryoblastic Leukemia with Isochromosome (12p) after a Primary Mediastinal Germ Cell Tumor in Korea

The association of hematological malignancies with a mediastinal germ cell tumor (GCT) is very rare. We report one case of a young adult male with primary mediastinal GCT who subsequently developed acute megakaryoblastic leukemia involving isochromosome (12p). A 25-yr-old man had been diagnosed with a mediastinal GCT and underwent surgical resection and adjuvant chemotherapy. At 1 week after the last cycle of chemotherapy, his peripheral blood showed leukocytosis with blasts. A bone marrow study confirmed the acute megakaryoblastic leukemia. A cytogenetic study revealed a complex karyotype with i(12p). Although additional chemotherapy was administered, the patient could not attain remission and died of septic shock. This case was definitely distinct from therapy-related secondary leukemia in terms of clinical, morphologic, and cytogenetic features. To our knowledge, this is the first case report of a patient with mediastinal GCT subsequently developing acute megakaryoblastic leukemia involving i(12p) in Korea.

Two Lung Masses with Different Responses to Pemetrexed

We described here a patient who had two lung masses. Although the two masses had the same histology and a similar good response to initial chemotherapy with gemcitabine and carboplatin, the response to pemetrexed as a second-line treatment was different after re-growth of the tumors. These two lung masses could have originated from different clones or they could have progressed through different paths of molecular pathogenesis after metastasis, which would lead to different tumor characteristics, including their chemosensitivity. Regardless of their pathogenetic mechanisms, it seems important to recognize that tumors with the same histology that develop in one patient can have different responses to drugs.

Segundos cánceres primarios / Second primary cancers

Los Segundos Cánceres Primarios (SCP) pueden ocurrir con frecuencia. Según datos de la SEER (Surveillance, Epidemiology and End Results) pueden constituir hasta un 16 por ciento de la incidencia total de cáncer. Se reporta una serie de casos conformada por 11 pacientes (2 hombres y 9 mujeres) con edad promedio de 61 años. En esta serie se presentaron 3 casos de cánceres sincrónicos y 8 metacrónicos, con un intervalo entre ambos de 2 a 72 meses. Se analizan diversos aspectos del tema como la quimioprevención y los aspectos relacionados con los SCP asociados a terapias (quimioterapia y radioterapia). Se describen aspectos particulares de los pacientes fumadores que constituyen un grupo especial de riesgo, debido al tipo de carcinógeno al que se ven expuestos. Finalmente se revisa el concepto de cancerización de campo que los afecta mayoritariamente.

Abordagem atual dos pacientes com doença de Hodgkin / Current approach to patients with Hodgkin's disease

Nos últimos anos, houve um progresso substancial na abordagem do paciente com doença de Hodgkin. Uma nova classificação histopatológica foi adotada, e fatores prognósticos reprodutíveis foram identificados. Os pacientes são tratados de acordo com o estádio clínico e, no caso de pacientes com doença localizada, também de acordo com os fatores prognósticos. Uma consistente série de estudos em pacientes com doença localizada tornou obsoleta a realização de laparotomia e a abordagem radioterápica isolada. Nos pacientes com doença avançada, o ABVD emergiu como o regime com a melhor relação risco/benefício após uma dura seqüência de comparações com o MOPP e combinações de MOPP e ABVD. Dois regimes inovadores estão em testes, o Stanford V e o BEACOPP. Entretanto, o avanço dos resultados terapêuticos depende da redução da toxicidade nos pacientes de baixo risco e da melhora do controle da doença nos pacientes de alto risco.

Tumores segundos primarios de cabeza y cuello / Second primary tumors of head and neck

Se presentan 3 casos (1,11 por ciento) de tumores segundos primarios y un caso (0,37 por ciento) de tercer primario de cavidad bucofaringolaríngea estudiados entre enero de 1982 y abril de 1991 en el consultorio externo de patología de cabeza y cuello del Hospital P. Piñero, sobre un total de 270 consultas por patología bucofaringolaríngea. Se destaca la importancia de los factores predisponentes tales como tabaco, alcohol y mala higiene dental. La terapéutica adoptada en dichos casos fue encarada como si se tratara de un tumor primario en todos los casos, y con un período libre de enfermedad entre primario y secundario de 3,8 años.