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Prostate Cancer Patients With Unmanaged Diabetes or Receiving Insulin Experience Inferior Outcomes and Toxicities After Treatment With Radiation Therapy.
Zaorsky, Nicholas G; Shaikh, Talha; Ruth, Karen; Sharda, Pankaj; Hayes, Shelly B; Sobczak, Mark L; Hallman, Mark A; Smaldone, Marc C; Chen, David Y T; Horwitz, Eric M.
Afiliação
  • Zaorsky NG; Department of Radiation Oncology, Fox Chase Cancer Center, Philadelphia, PA. Electronic address: nicholaszaorsky@gmail.com.
  • Shaikh T; Department of Radiation Oncology, Fox Chase Cancer Center, Philadelphia, PA.
  • Ruth K; Biostatistics and Bioinformatics Facility, Fox Chase Cancer Center, Philadelphia, PA.
  • Sharda P; Department of Endocrinology, Fox Chase Cancer Center, Philadelphia, PA.
  • Hayes SB; Department of Radiation Oncology, Fox Chase Cancer Center, Philadelphia, PA.
  • Sobczak ML; Department of Radiation Oncology, Fox Chase Cancer Center, Philadelphia, PA.
  • Hallman MA; Department of Radiation Oncology, Fox Chase Cancer Center, Philadelphia, PA.
  • Smaldone MC; Department of Surgical Oncology, Fox Chase Cancer Center, Philadelphia, PA.
  • Chen DY; Department of Surgical Oncology, Fox Chase Cancer Center, Philadelphia, PA.
  • Horwitz EM; Department of Radiation Oncology, Fox Chase Cancer Center, Philadelphia, PA.
Clin Genitourin Cancer ; 15(2): 326-335.e3, 2017 04.
Article em En | MEDLINE | ID: mdl-27789181
ABSTRACT

BACKGROUND:

The purpose of the study was to determine the effect of type 2 diabetes mellitus (T2DM) on outcomes and toxicities among men with localized prostate cancer receiving definitive radiation therapy. PATIENTS AND

METHODS:

We performed a retrospective review of 3217 patients, from 1998 to 2013, subdivided into 5 subgroups (I) no T2DM; (II) T2DM receiving oral antihyperglycemic agent that contains metformin, no insulin; (III) T2DM receiving nonmetformin oral agent alone, no insulin; (IV) T2DM receiving any insulin; and (V) T2DM not receiving medication. Outcome measures were overall survival, freedom from biochemical failure (BF), freedom from distant metastasis, cancer-specific survival, and toxicities. Kaplan-Meier analysis, log rank tests, Fine and Gray competing risk regression (to adjust for patient and lifestyle factors), Cox models, and subdistribution hazard ratios (sHRs) were used.

RESULTS:

Of the 3217 patients, 1295 (40%) were low-risk, 1192 (37%) were intermediate-risk, and 652 (20%) were high risk. The group I to V distribution was 81%, 8%, 5%, 3%, and 4%. The median dose was 78 Gy, and the median follow-up time was 50 (range, 1-190) months. Group V had increased mortality (sHR, 2.1; 95% confidence interval [CI], 0.66-1.54), BF (sHR, 2.14; 0.88-1.83), and cause-specific mortality (sHR, 3.87; 95% CI, 1.31-11). Acute toxicities were higher in group IV versus group I (genitourinary 38% vs. 26%; P = .01; gastrointestinal 21% vs. 5%; P = 001). Late toxicities were higher in groups IV and V versus group I (12%-14% vs. 2%-6%; P < .01).

CONCLUSION:

Men with T2DM not receiving medication and men with T2DM receiving insulin had worse outcomes and toxicities compared to other patients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Diabetes Mellitus Tipo 2 / Hipoglicemiantes / Insulina Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Diabetes Mellitus Tipo 2 / Hipoglicemiantes / Insulina Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article