Multiple myeloma in association with second malignancy.
J Grudeva-Popova1, I Nenova, M Spasova
1Department of Oncology and Hematology, University Multiprofile Hospital for Active Treatment "Sv. Georgi", Plovdiv, Bulgaria.
Summary
The frequency of second primary malignancies in multiple myeloma (MM) patients is comparable to other cancers. Second primary malignancies are uncommon in MM, often occurring years after initial diagnosis, and are associated with longer survival.
Area of Science:
- Hematology
- Oncology
- Epidemiology
Background:
- Multiple myeloma (MM) is a hematologic malignancy.
- Understanding the incidence of second primary malignancies (SECMAL) in MM patients is crucial for comprehensive cancer care.
- Previous research has explored SECMAL in various cancers, but specific data for MM requires further investigation.
Purpose of the Study:
- To determine the frequency of second primary malignancies (SECMAL) in patients diagnosed with multiple myeloma (MM).
- To compare the incidence of SECMAL in MM patients with that in patients with solid tumors.
Main Methods:
- Retrospective analysis of medical records for 332 MM patients diagnosed between 1990-2010.
- Inclusion of a control group of 21,768 patients with solid tumors and SECMAL.
- Comparison of SECMAL incidence and timing between MM and solid tumor cohorts.
Main Results:
- SECMAL occurred in 4.52% of MM patients versus 5.09% in the solid tumor control group (p>0.05).
- In MM patients with SECMAL, the primary solid tumor diagnosis preceded MM in 66.67% of cases.
- Breast and gastric cancers were the most common SECMALs in MM patients (26.67% each).
- Median survival was significantly longer for MM patients with SECMAL (77.2 months) compared to the overall MM cohort (38.6 months; p<0.05).
Conclusions:
- The rate of SECMAL in multiple myeloma patients is comparable to that observed in other lymphoproliferative disorders and solid tumors.
- SECMAL is an infrequent event during the clinical course of multiple myeloma.
- The occurrence of SECMAL in MM is more likely in patients with longer survival.
Related Concept Videos
Multiple Sclerosis l: Introduction
Multiple sclerosis is a chronic autoimmune disease of the central nervous system (CNS) that affects the brain, spinal cord, and optic nerves. It is an inflammatory demyelinating disorder and a leading cause of neurological disability in young adults.EpidemiologyMS commonly begins between 20 and 40 years of age and is twice as common in women. Its exact cause remains unclear, but genetic susceptibility contributes, with higher risk in first-degree relatives and identical twins. A greater...
Tumor Progression
Tumor progression is a phenomenon where the pre-formed tumor acquires successive mutations to become clinically more aggressive and malignant. In the 1950s, Foulds first described the stepwise progression of cancer cells through successive stages.
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...
Metastasis
Metastasis is the spread of cancer cells from the original site to distant locations in the body. Cancer cells can spread via blood vessels (hematogenous) as well as lymph vessels in the body.
Epithelial-to-Mesenchymal Transition
The epithelial-to-mesenchymal transition or EMT is a developmental process commonly observed in wound healing, embryogenesis, and cancer metastasis. EMT is induced by transforming growth factor-beta (TGF-β) or receptor tyrosine kinase (RTK) ligands, which further...
Epithelial-to-Mesenchymal Transition
The epithelial-to-mesenchymal transition or EMT is a developmental process commonly observed in wound healing, embryogenesis, and cancer metastasis. EMT is induced by transforming growth factor-beta (TGF-β) or receptor tyrosine kinase (RTK) ligands, which further...

