2020
DOI: 10.1016/j.suc.2020.02.009
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Peritoneal Cancers and Hyperthermic Intraperitoneal Chemotherapy

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Cited by 22 publications
(19 citation statements)
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“…Furthermore the choice of drugs under hyperthermic conditions is important because suitable hyperthermia can accelerate velocity of drug permeability into tumor tissue. So optimization of therapy regimen can increase cytotoxicity at the peritoneal lesions without an increase in systemic (especially bone marrow) toxicity [15,16]. Docetaxel is a semisynthetic taxane, which is widely used for NSCLC, breast cancer,gastric cancer,ovarian cancer,et al [17].…”
Section: Discussionmentioning
confidence: 99%
“…Furthermore the choice of drugs under hyperthermic conditions is important because suitable hyperthermia can accelerate velocity of drug permeability into tumor tissue. So optimization of therapy regimen can increase cytotoxicity at the peritoneal lesions without an increase in systemic (especially bone marrow) toxicity [15,16]. Docetaxel is a semisynthetic taxane, which is widely used for NSCLC, breast cancer,gastric cancer,ovarian cancer,et al [17].…”
Section: Discussionmentioning
confidence: 99%
“…It is unclear if the IP administration, the heat, or the additional dose of chemotherapy is responsible for the benefit as all three interventions were utilized. These results are encouraging; however, further studies are needed before there is widespread adoption of this technique, which requires additional technical expertise [31,32].…”
Section: Surgical Managementmentioning
confidence: 95%
“…Although primary peritoneal malignancies are rare, the peritoneum is a common site of metastases or peritoneal carcinomatosis (PC) for organs within the peritoneal cavity. Most commonly, PC arises from appendiceal, colorectal, ovarian, and gastric malignancies [ 1 , 2 , 3 ]. While less frequent, PC can also arise from gastrointestinal (GI) malignancies from other abdominal organs, including the small bowel, pancreas, gallbladder, and rarely from non-GI and extra-abdominal organs, such as breast, lung, and melanoma [ 1 , 2 , 3 , 4 ].…”
Section: Introductionmentioning
confidence: 99%
“…Most commonly, PC arises from appendiceal, colorectal, ovarian, and gastric malignancies [ 1 , 2 , 3 ]. While less frequent, PC can also arise from gastrointestinal (GI) malignancies from other abdominal organs, including the small bowel, pancreas, gallbladder, and rarely from non-GI and extra-abdominal organs, such as breast, lung, and melanoma [ 1 , 2 , 3 , 4 ]. PC is so common with many GI malignancies that it is present at the time of diagnosis in approximately 5–10% of colorectal and 40–70% of appendiceal cancers [ 5 , 6 ].…”
Section: Introductionmentioning
confidence: 99%