Long-term Outcome of Soft Tissue Sarcomas Treated with Mesna-Doxorubicin-Ifosfamid-Dacarbazine regimen (MAID): A Retrospective Study from a Single Institution
Öz
Objective
Soft tissue sarcomas (STSs) account 1% of adult cancers. Essential treatment is surgery but chemotherapy and/or radiotherapy are frequently used due to aggressive behaviour or incomplete surgery. Doxorubicin-based regimens are the most frequently used chemotherapy combinations but real life data with these agents are relatively limited in our country. Here we wanted to present clinico-demographic and prognostic features of STS sarcoma cases treated by MAID regimen containing mesna-doxorubicin-ifosfamide-dacarbazin.
Material and Method
Forty five cases with STS treated with MAID regimen as initial therapy and followed between 2007-2016 in Cukurova University Medical Faculty Department of Medical Oncology were analyzed retrospectively. Associations between clinical and histopathological parameters with overall survival (OS) and progression free survival (PFS) were analyzed using Kaplan- Meier curves and compared by the log-rank test. Univariate and multivariate analyses were used to assess their prognostic values for PFS and OS.
Results
The median age of our patients was 49 and the most common subtypes were undifferentiated pleomorphic carcinoma (37.8%) followed by liposarcoma (17.8%), leiomyosarcoma (13.3%) and 62.2% of the cases were found in the extremity localization. According to their AJCC TNM stages, 15.6% were stage 1-2, 53.3% were stage 3 and 31.1% were stage 4. The median PFS and OS were 17 months and 39 months, and the 5-year PFS and OS rates were 14% and 32.5%. Prognostic significance of age, sex, and grade was not determined, but univariate analyzes indicated that mitosis, necrosis, AJCC TNM stage and surgery were prognostic for both PFS and OS. However, according to multivariate analyzes, only the AJCC TNM stage is an independent prognostic factor for both PFS and OS.
Conclusion
AJCC TNM is the only
independent prognostic factor for both PFS and OS in patients with STS
receiving MAID chemotherapy as initial therapy
Anahtar Kelimeler
Kaynakça
- 1. Siegel RL, Miller KD, Jemal A. Cancer statistics, 2018. CA Cancer J Clin. 2018;68(1):7-30
- 2. Ducimetière F, Lurkin A, Ranchère-Vince D, Decouvelaere AV, Péoc'h M, Istier L, et al. Incidence of sarcoma histotypes and molecular subtypes in a prospective epidemiological study with central pathology review and molecular testing. PloS one. 2011;6(8):e20294.
- 3. Borden EC, Baker LH, Bell RS, Bramwell V, Demetri GD, Eisenberg BL, et al. Soft tissue sarcomas of adults: state of the translational science. Clin Cancer Res. 2003;9(6): 1941-1956.
- 4. Colombo C, Randall RL, Andtbacka RHI, Gronchi A. Surgery in soft tissue sarcoma: more conservative in extremities, more extended in the retroperitoneum. Expert Rev Anticancer Ther. 2012;12(8):1079–1087.
- 5. Crago AM, Brennan MF. Principles in management of soft tissue sarcoma. Adv Surg. 2015;49:107–122
- 6. Koliou P, Karavasilis V, Theochari M, Pollack SM, Jones RL, Thway K. Advances in the treatment of soft tissue sarcoma: Focus on eribulin. Cancer Manag Res. 2018;10:207-216
- 7. Jain A, Sajeevan KV, Babu KG, Lakshmaiah KC. Chemotherapy in adult soft tissue sarcoma. Indian J Cancer. 2009;46(4):274-87
- 8. Ratan R, Patel SR. Chemotherapy for soft tissue sarcoma. Cancer. 2016;122(19), 2952-2960.
Ayrıntılar
Birincil Dil
İngilizce
Konular
-
Bölüm
Araştırma Makalesi
Yazarlar
Cem Mirili
*
0000-0002-5986-5493
Türkiye
Semra Paydas
0000-0003-4642-3693
Türkiye
Mert Tohumcuoglu
Bu kişi benim
Türkiye
Abdullah Evren Yetisir
Bu kişi benim
Türkiye
Yayımlanma Tarihi
18 Aralık 2019
Gönderilme Tarihi
17 Haziran 2019
Kabul Tarihi
13 Ekim 2019
Yayımlandığı Sayı
Yıl 2019 Cilt: 7 Sayı: 3