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1.
J Oncol Pharm Pract ; 30(2): 400-403, 2024 Mar.
Article in English | MEDLINE | ID: mdl-37787402

ABSTRACT

INTRODUCTION: Uterine leiomyosarcoma is a rare gynecological malignancy, the limited literature indicated that doxorubicin alone or gemcitabine/docetaxel combination is the preferred chemotherapy regimen. Given the rarity of the disease and the lack of high-level clinical evidence, there is no consensus on the best treatment. CASE REPORT: We report a case of a patient with uterine leiomyosarcoma who recurred after adjustment treatment with doxorubicin, gemcitabine, docetaxel, and anlotinib; and required a new chemotherapy regimen. MANAGEMENT AND OUTCOMES: The follow-up chemotherapy regimen was doxorubicin-liposome 40 mg/m2 on one day in combination with dacarbazine 250 mg/m2 on one to five days of intravenous infusion every 21 days. We monitored adverse effects during chemotherapy and the process was smooth. DISCUSSION: It is important to comprehensively consider the patient's condition, and fully consider the efficacy, dosage, and adverse reactions of the chemotherapy regimen to determine the appropriate plan, in order to achieve the best therapeutic benefits for patients.


Subject(s)
Leiomyosarcoma , Pelvic Neoplasms , Uterine Neoplasms , Female , Humans , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Disease-Free Survival , Docetaxel/therapeutic use , Doxorubicin/therapeutic use , Gemcitabine , Leiomyosarcoma/drug therapy , Neoplasm Recurrence, Local/drug therapy , Pelvic Neoplasms/drug therapy , Uterine Neoplasms/drug therapy , Uterine Neoplasms/pathology
2.
Biomed Pharmacother ; 154: 113632, 2022 Oct.
Article in English | MEDLINE | ID: mdl-36063646

ABSTRACT

Local recurrence of colorectal cancer (CRC) can occur in patients after curative resection, and additional surgical resection may therefore be required; however, this is a significant burden for patients, because additional surgical resection may necessitate the resection of other organs such as the bladder, prostate, uterus, or sacral bone. Therefore, there is a need for alternative therapeutic strategies. We focused on boron neutron capture therapy (BNCT) as a treatment modality that can selectively target tumor cells without excessive damage to normal tissues. The usefulness of BNCT to pelvic CRC remains unknown. This study investigated the anti-cancer effect of boronophenylalanine (BPA)-mediated BNCT in a previously established mouse model of pelvic recurrence of CRC. Uptake of BPA in CRC was observed both in vitro and in vivo, and the concentrations were sufficient for BNCT. Our results are the first to show that BPA-mediated BNCT prolonged the survival of experimental mice with pelvic tumors; moreover, it did not cause any obvious severe side effects in the treated animals. In conclusion, BPA-mediated BNCT could contribute to treating local recurrence of pelvic CRC.


Subject(s)
Boron Neutron Capture Therapy , Colorectal Neoplasms , Mouth Neoplasms , Pelvic Neoplasms , Animals , Boron Compounds/therapeutic use , Boron Neutron Capture Therapy/adverse effects , Boron Neutron Capture Therapy/methods , Colorectal Neoplasms/drug therapy , Disease Models, Animal , Female , Humans , Male , Mice , Mouth Neoplasms/pathology , Pelvic Neoplasms/drug therapy , Pelvic Neoplasms/etiology
4.
J Cancer Res Ther ; 16(5): 1020-1026, 2020 Sep.
Article in English | MEDLINE | ID: mdl-33004743

ABSTRACT

BACKGROUND: There are no standardized treatments for giant cell tumors of the bone (GCTB) in rare locations such as the spine and pelvis or for those that are inoperable and recurrent, let alone for multicentric GCTB. This study reports a novel case of multicentric GCTB treated with a promising antiangiogenic drug, apatinib, a small-molecule tyrosine kinase inhibitor. The efficacy of apatinib in the treatment of GCTB has not been reported previously. PATIENTS AND METHODS: A 27-year-old female presented with two giant cell tumors of the spine and sacrum-ilium diagnosed on December 15, 2016. Surgery and selective arterial embolization (SAE) were not reasonable options for this patient, and denosumab was unavailable; therefore, the antiangiogenic drug apatinib and the osteoclast inhibitor zoledronic acid were administered. Apatinib was initially administered at a dose of 850 mg daily, which was decreased to 425 mg daily after 7 months, and then increased again to 635 mg after 11 months. The patient was prescribed a maintenance dose of 500 mg daily after 16 months. The patient reported side effects of Grades I-III nausea, vomiting, and Grades II-III hand-foot syndrome. The patient underwent SAE at 26 months, and at that time, she was switched to denosumab instead of zoledronic acid. RESULTS: The patient showed noticeable symptomatic improvement and visibly reduced tumor size after the first month of treatment. Computed tomography in the 4th month identified a partial response based on the RECIST criteria. The patient has achieved an objective reduction in tumor size at 32 months. CONCLUSIONS: Comprehensive treatment including apatinib represents a potential new treatment strategy for inoperable GCTB, with tolerable side effects. However, further clinical trials are now necessary to confirm an effective dose and determine the efficacy and safety of apatinib in the treatment of GCTB.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Bone Neoplasms/drug therapy , Giant Cell Tumor of Bone/drug therapy , Pelvic Neoplasms/drug therapy , Spinal Neoplasms/drug therapy , Tomography, X-Ray Computed/methods , Adult , Bone Neoplasms/pathology , Female , Giant Cell Tumor of Bone/pathology , Humans , Pelvic Neoplasms/pathology , Pyridines/administration & dosage , Spinal Neoplasms/pathology , Treatment Outcome , Zoledronic Acid/administration & dosage
5.
JAMA Netw Open ; 3(10): e2013929, 2020 10 01.
Article in English | MEDLINE | ID: mdl-33006617

ABSTRACT

Importance: The association of radiation and chemotherapy with the development of secondary sarcoma is known, but the contemporary risk has not been well characterized for patients with cancers of the abdomen and pelvis. Objective: To compare the risk of secondary sarcoma among patients treated with combinations of surgery, radiation, or chemotherapy with patients treated with surgery alone and the general population. Design, Setting, and Participants: This population-based cohort study included 173 580 patients in Ontario, Canada, with nonmetastatic cancer of the prostate, bladder, colon, rectum or anus, cervix, uterus, or testis. Patients were enrolled from January 1, 2002, to January 31, 2017. Data analysis was conducted from March 1, 2019, to January 31, 2020. Exposures: Treatment combinations of radiation, chemotherapy, and surgery. Main Outcome and Measures: Diagnosis of sarcoma based on histologic codes from the Ontario Cancer Registry. Time to sarcoma was compared using a cause-specific proportional hazard model. Results: Of 173 580 patients, most were men (125 080 [72.1%]), and the largest group was aged between 60 and 69 years (58 346 [33.6%]). Most patients had genitourinary cancer (86 235 [51.4%]) or colorectal cancer (69 241 [39.9%]). Overall, 64 301 (37.1%) received surgery alone, 51 220 (29.5%) received radiation alone, 15 624 (9.0%) were treated with radiation and chemotherapy, 15 252 (8.8%) received radiation with surgery, and 11 822 (6.8%) received all 3 treatments. A total of 332 patients (0.2%) had sarcomas develop during a median (interquartile range) follow-up of 5.7 (2.2-8.9) years. The incidence of sarcoma was 0.3% among those who underwent radiation alone (138 of 51 220) and radiation with chemotherapy (40 of 15 624), 0.2% among those who received radiation and surgery (36 of 15 252) and all 3 modalities (25 of 11 822), and 0.1% among those who received surgery with chemotherapy (13 of 14 861) and surgery alone (80 of 64 801). Compared with a reference group of patients who had surgery alone, the greatest risk of sarcoma was found among patients who underwent a combination of radiation and chemotherapy (cause-specific relative hazard [csRH], 4.07; 95% CI, 2.75-6.01; P < .001), followed by patients who had radiation alone (csRH, 2.35; 95% CI, 1.77-3.12; P < .001), radiation with surgery (csRH, 2.33; 95% CI, 1.57-3.46; P < .001), and all 3 modalities (csRH, 2.27; 95% CI, 1.44-3.58; P < .001). In the general population, 7987 events occurred during 46 554 803 person-years (17.2 events per 100 000 person-years). The standardized incidence ratio for sarcoma among patients treated with radiation compared with the general population was 2.41 (95% CI, 1.57-3.69; 41.3 events per 100 000 person-years). The annual number of cases of sarcoma increased from 2009 (15 per 100 000 persons) to 2016 (32 per 100 000 persons), but the annual rate did not change during the study period. Conclusions and Relevance: In this cohort study, patients treated with radiation or chemotherapy for abdominopelvic cancers had an increased rate of sarcoma. Although the absolute rate is low, patients and physicians should be aware of this increased risk of developing sarcoma.


Subject(s)
Abdominal Neoplasms/drug therapy , Abdominal Neoplasms/radiotherapy , Abdominal Neoplasms/surgery , Neoplasms, Second Primary/etiology , Pelvic Neoplasms/drug therapy , Pelvic Neoplasms/radiotherapy , Pelvic Neoplasms/surgery , Sarcoma/etiology , Abdominal Neoplasms/complications , Adolescent , Adult , Aged , Aged, 80 and over , Cohort Studies , Female , Humans , Incidence , Male , Middle Aged , Ontario/epidemiology , Pelvic Neoplasms/complications , Proportional Hazards Models , Retrospective Studies , Risk Factors , Young Adult
6.
Clin Nucl Med ; 45(7): 547-548, 2020 Jul.
Article in English | MEDLINE | ID: mdl-32404703

ABSTRACT

The pelvis is a rare site for the origin of soft tissue sarcomas, and leiomyosarcoma remains the most common soft tissue sarcoma arising in the pelvis. Pelvic leiomyosarcomas are frequently aggressive tumors, and metastatic recurrence rates are high, with the lung, peritoneum, bone, and liver being the most frequent sites. We describe the findings of serial F-FDG PET/CT in a 53-year-old woman having pelvic leiomyosarcoma with uncommon site of metastasis, emphasizing the role of F-FDG PET/CT in response assessment.


Subject(s)
Fluorodeoxyglucose F18 , Leiomyosarcoma/diagnostic imaging , Leiomyosarcoma/pathology , Pelvic Neoplasms/diagnostic imaging , Pelvic Neoplasms/pathology , Positron Emission Tomography Computed Tomography , Splenic Neoplasms/secondary , Female , Humans , Leiomyosarcoma/drug therapy , Middle Aged , Pelvic Neoplasms/drug therapy , Treatment Outcome
7.
Immunotherapy ; 12(4): 229-234, 2020 03.
Article in English | MEDLINE | ID: mdl-32172642

ABSTRACT

Metastatic colorectal cancer with BRAF mutation is a type of highly invasive malignant tumor with poor prognosis and few treatment options. Here, we report a case of a BRAF-mutant and DNA mismatch-repair deficiency colorectal cancer patient with postoperative recurrence as well as abdominal cavity and pelvic metastasis, whose condition was relieved continuously after treatment with a new anti-PD-1 antibody, BGB-A317.


Subject(s)
Antibodies, Monoclonal, Humanized/therapeutic use , Colorectal Neoplasms/drug therapy , Colorectal Neoplasms/pathology , DNA Mismatch Repair/genetics , Immune Checkpoint Inhibitors/therapeutic use , Proto-Oncogene Proteins B-raf/genetics , Abdominal Neoplasms/drug therapy , Abdominal Neoplasms/genetics , Abdominal Neoplasms/secondary , Adenocarcinoma/drug therapy , Adenocarcinoma/genetics , Adenocarcinoma/secondary , Aged , Biomarkers, Tumor/genetics , Colorectal Neoplasms/genetics , Female , Humans , Immunotherapy , Microsatellite Instability , Mutation , Pelvic Neoplasms/drug therapy , Pelvic Neoplasms/genetics , Pelvic Neoplasms/secondary , Treatment Outcome
8.
Anticancer Drugs ; 31(5): 533-535, 2020 06.
Article in English | MEDLINE | ID: mdl-31743134

ABSTRACT

Although giant cell tumor of bone has been considered as a disease with benign course, it can lead to bone destruction and serious morbidity. A 19-year-old case was presented with hip pain. There was a recurrence after 9 months of curative surgical resection and zoledronic acid use, and as surgical morbidity would be high, antiosteoclastic receptor activator of nuclear factor kappa B ligand inhibitor denosumab treatment was administered. She had a complete remission after 18 months of denosumab treatment. The important point in the present case is that it has been followed up without recurrence after around 42 months of denosumab use and 11 months of follow-up after the cessation of drug. In recurrent cases in which nonmetastatic surgery is not suitable, the use of denosumab decreases tumor progression. The duration of use in unresectable and advanced cases still remains unclear.


Subject(s)
Bone Density Conservation Agents/therapeutic use , Bone Neoplasms/drug therapy , Denosumab/therapeutic use , Giant Cell Tumor of Bone/drug therapy , Pelvic Neoplasms/drug therapy , Adult , Bone Neoplasms/pathology , Female , Giant Cell Tumor of Bone/pathology , Humans , Pelvic Neoplasms/pathology , Prognosis , Remission Induction , Time Factors , Young Adult
9.
Support Care Cancer ; 27(11): 4327-4330, 2019 Nov.
Article in English | MEDLINE | ID: mdl-30880371

ABSTRACT

BACKGROUND: Visceral pain conducted by sympathetic fibers with pelvic and perineal origin can be treated using ganglion impar (GIB) or Walters' block in a simple and effective manner. This article aims to evaluate the effectiveness, security, and performance difficulty of GIB in patients with pelvic and perineal oncological pain. METHODS: A retrospective study between January 2016 and August 2017. Patients with poorly controlled pelvic oncological pain and patients experimenting opioid side effects in which GIB was performed ambulatory were included. Prognostic GIB was performed, under echographic and fluoroscopic control, with local anesthetic and corticoid. The neurolytic block was performed under fluoroscopic guidance. The technique was performed by the same anesthetist with pain management competence. For statistical analysis, Microsoft Excel 2013® and IBM SPSS Statistics version 22.0 were used. RESULTS: Fifteen patients were included. One patient was excluded. A statistical significant basal pain score reduction was observed ((median of the verbal numerical scale (VNS) 7 (p25 = 7; p75 = 8)) compared with 72 h median VNS 4 ((p25 = 3; p75 = 5.3) p = 0.001, and 3 months (median VNS 4 (p25 = 3, p75 = 7)) p = 0.003 after the procedure. Regarding morphine consumption, a statistically significant reduction was observed 3 months after GIB performance (p = 0.012). DISCUSSION/CONCLUSION: GIB is a safe and easy-to-perform technique achieving satisfactory and statistically significant results, regarding pain control improvement and opioid consumption reduction in patients which meet selection criteria. Prospective, randomized studies with more patients are needed for further conclusions.


Subject(s)
Cancer Pain/drug therapy , Ganglia, Sympathetic/drug effects , Pain Management/methods , Pelvic Neoplasms/complications , Pelvic Neoplasms/drug therapy , Female , Humans , Male , Pelvic Neoplasms/pathology , Retrospective Studies
10.
J Oncol Pharm Pract ; 25(6): 1301-1304, 2019 Sep.
Article in English | MEDLINE | ID: mdl-29945534

ABSTRACT

BACKGROUND: Patients with locally advanced, recurrent or metastatic solitary fibrous tumour are often treated with bevacizumab and temozolomide based on the clinical efficacy reported in a case series of 14 patients. Given the rarity of solitary fibrous tumour, large trials are not feasible. We report the efficacy of this regimen based on a population-based analysis. METHODS: This was a population-based retrospective, multi-centre analysis using patient data from a provincial cancer registry and treatment database. Cases from June 2006 through October 2016 were identified for patients receiving bevacizumab and temozolomide for locally advanced, recurrent or metastatic solitary fibrous tumour or hemangiopericytoma, which is sometimes used to describe tumours arising from the meninges. The primary outcome was overall response rate. Secondary outcomes included time to response, progression free survival and overall survival estimated using the Kaplan-Meier method. RESULTS: Fourteen patients were identified: median age 59 (range 44-70), male 78.6%. Diagnoses were solitary fibrous tumour in 10 (71.4%) and hemangiopericytoma in four (28.6%), with metastatic disease in 10 (72.7%) patients. The most common primary sites were meninges in four (28.6%) and pelvis in three (21.4%) patients. The median follow-up was 15.5 months, with median treatment of four months. Overall response rate was 21.4% (no complete response, 3 partial response), with median time to response of four months. Median progression free survival, six-month progression free survival and overall survival were 17 months, 65.0%, and 45 months, respectively. CONCLUSIONS: Efficacy of bevacizumab and temozolomide in solitary fibrous tumour appeared to be similar to that previously reported. Our findings confirmed that bevacizumab and temozolomide is an effective and tolerated treatment for this patient population.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Hemangiopericytoma/drug therapy , Meningeal Neoplasms/drug therapy , Neoplasm Recurrence, Local/drug therapy , Pelvic Neoplasms/drug therapy , Solitary Fibrous Tumors/drug therapy , Solitary Fibrous Tumors/pathology , Adult , Aged , Bevacizumab/administration & dosage , Female , Humans , Male , Middle Aged , Progression-Free Survival , Registries , Remission Induction , Retrospective Studies , Survival Rate , Temozolomide/administration & dosage , Treatment Outcome
11.
Benef Microbes ; 9(6): 899-916, 2018 Dec 07.
Article in English | MEDLINE | ID: mdl-30232908

ABSTRACT

Chemotherapy and radiotherapy treatment regimens for gastrointestinal, peritoneal and pelvic tumours can disrupt the intestinal microbiome and intestinal epithelia. Such disturbances can provoke symptoms such as diarrhoea, nausea and vomiting. Chemotherapy and radiotherapy induced gastrointestinal toxicity aggravating intestinal microbiome dysbiosis is postulated to adversely alter the intestinal microbiome, with a consequent induced pro-inflammatory effect that disrupts the intestinal microbiome-epithelia-mucosal immunity axis. Although not widely recognised, the intestinal mucosa is the largest and most densely and dynamically populated immune-environment. Cancer treatment adverse effects that affect intestinal and mucosal cells inadvertently target and disrupt resident intestinal macrophages, the cells that marshal immune activity in the intestinal mucosa by shaping pro-inflammatory and anti-inflammatory activities to control and eradicate infectious insults and maintain local homeostasis. Pathobionts (bacteria capable of pathogenic pro-inflammatory activity) and noxious environmental and bacterial antigens use the intestinal epithelia and gap junctions as a point of entry into the systemic circulation. This translocation movement promotes toxic sequelae that obstruct intestinal macrophage functions resulting in uncontrolled local and systemic pro-inflammatory activity, loss of phagocytic function and loss of expression of tight junction proteins. Probiotic bacteria as an adjunctive treatment shows efficacy in ameliorating enteropathies such as mucositis/diarrhoea resulting from chemotherapy or radiotherapy regimens. As such we posit that an important benefit that warrants a further focused research effort is the administration of adjuvant probiotics to help reduce the incidence of febrile neutropenia.


Subject(s)
Antineoplastic Agents/adverse effects , Bacterial Translocation , Dysbiosis/prevention & control , Probiotics/administration & dosage , Radiotherapy/adverse effects , Antineoplastic Agents/administration & dosage , Dysbiosis/complications , Gastrointestinal Neoplasms/complications , Gastrointestinal Neoplasms/drug therapy , Gastrointestinal Neoplasms/radiotherapy , Humans , Incidence , Pelvic Neoplasms/complications , Pelvic Neoplasms/drug therapy , Pelvic Neoplasms/radiotherapy , Peritoneal Neoplasms/complications , Peritoneal Neoplasms/drug therapy , Peritoneal Neoplasms/radiotherapy , Treatment Outcome
12.
J Coll Physicians Surg Pak ; 28(6): 445-447, 2018 Jun.
Article in English | MEDLINE | ID: mdl-29848420

ABSTRACT

OBJECTIVE: To evaluate the outcomes of patients undergoing radiotherapy for primary local control of pelvic ewing sarcoma (ES). STUDY DESIGN: Case series. PLACE AND DURATION OF STUDY: Shaukat Khanum Memorial Cancer Hospital, Lahore, from January 2010 to October 2015. METHODOLOGY: Patients with primary pelvic ES were included in the analysis and all other primary disease sites were excluded. All of them were treated with radiotherapy and followed the EuroEwing-99 chemotherapy protocol. Tumor volume, relapse and metastases were noted. RESULTS: There were 13 patients with pelvic ES. The median age at the time of diagnosis was 15 years with IQR of 7 years (range 2-19 years). Tumor volume was more than 400ml in more than 50% of the patients. Eight patients (61.5%) had local relapses and 5 patients (38.5%) had combined local and distant disease metastases. CONCLUSION: These results showed poor local control and overall survival in local pelvic ES cases in children and adolescents. Intensity modulated radiotherapy (IMRT) can be used to deliver higher doses of radiation. Compressed cycles of chemotherapy should be evaluated in local setting.


Subject(s)
Pelvic Neoplasms/radiotherapy , Sarcoma, Ewing/radiotherapy , Adolescent , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Child , Combined Modality Therapy , Female , Humans , Infant , Male , Neoplasm Metastasis , Neoplasm Recurrence, Local , Pelvic Neoplasms/drug therapy , Pelvic Neoplasms/pathology , Pelvic Neoplasms/surgery , Retrospective Studies , Sarcoma, Ewing/drug therapy , Sarcoma, Ewing/pathology , Sarcoma, Ewing/surgery , Survival Rate , Treatment Outcome , Tumor Burden , Young Adult
13.
Cell Mol Biol (Noisy-le-grand) ; 64(6): 110-113, 2018 May 15.
Article in English | MEDLINE | ID: mdl-29808809

ABSTRACT

Aggressive angiomyxoma (AA) is a distinctive soft tissue tumor with a high risk of local recurrence. Clinicians must be aware of this rare tumor pre-operatively. Excision is the preferred method of AA treatment. The case report presents a case of a 36-year-old woman who was difficulty in walking due to a non-painful tumor in the abdomen and perineum. She was misdiagnosed as abdomen neurofibroma for more than 10 years, and an operation was performed in 1997. However, the tumor was incompletely resected because its huge volume accompanies with extensive infiltration and bleeding. The tumors in her abdomen and perineum were growing gradually, and the latter became a large lump which impeded her daily life. In 2008, the perineal tumor was incompletely resected, which weighed 10725 g. The severe hemorrhage had been ceased by Gonadotropin-Releasing Hormone treatment. She is alive till now. Details of the history and operative procedures are presented. An AA diagnosis was made by microscopy immunohistochemically. Long-time misdiagnosis and improper treatment are the important reasons for making it impossible to be radically resected. Pathological and immunohistochemical examination are important for avoiding misdiagnosis. For this case, there is a remaining tumor in her abdomen. A special project including further follow-up and treatment will be taken out.


Subject(s)
Abdominal Neoplasms/diagnosis , Diagnostic Errors , Myxoma/diagnosis , Neurofibroma/diagnosis , Pelvic Neoplasms/diagnosis , Perineum , Abdominal Neoplasms/drug therapy , Abdominal Neoplasms/pathology , Abdominal Neoplasms/surgery , Adult , Antineoplastic Agents, Hormonal/therapeutic use , Combined Modality Therapy , Cystotomy , Disease Progression , Female , Goserelin/therapeutic use , Hemorrhage/etiology , Humans , Laparotomy , Magnetic Resonance Imaging , Mobility Limitation , Myxoma/drug therapy , Myxoma/pathology , Myxoma/surgery , Neoplasm Invasiveness/pathology , Pelvic Neoplasms/drug therapy , Pelvic Neoplasms/pathology , Pelvic Neoplasms/surgery , Perineum/pathology , Perineum/surgery , Tumor Burden , Ureterostomy
14.
Gulf J Oncolog ; 1(26): 75-78, 2018 Jan.
Article in English | MEDLINE | ID: mdl-29607829

ABSTRACT

Desmoid tumors are rare benign neoplasms with an aggressive local growth. In children, intra-abdominal localization is less frequent and few reports exist in the literature about the management of DTs in those special patients. In our report, we describe a case of a 13-year old patient with a bifocal intra-abdominal DT, treated unsuccessfully with tamoxifene, and we discuss briefly the existing literature data.


Subject(s)
Antineoplastic Agents, Hormonal/adverse effects , Fibromatosis, Aggressive/drug therapy , Neoplasm Recurrence, Local/chemically induced , Pelvic Neoplasms/drug therapy , Tamoxifen/adverse effects , Adolescent , Fatal Outcome , Female , Fibromatosis, Aggressive/pathology , Humans , Pelvic Neoplasms/pathology
15.
Am J Clin Oncol ; 41(8): 792-796, 2018 08.
Article in English | MEDLINE | ID: mdl-28225446

ABSTRACT

BACKGROUND: Adjuvant therapy choice for women with FIGO stage III endometrial carcinoma (EC) is controversial. We investigate the comparative benefit of adjuvant chemotherapy (CT) alone, radiation therapy alone (RT) or in combination (chemotherapy and radiation therapy [CRT]) with respect to recurrence-free survival (RFS) and overall survival (OS) in women with pelvis-limited (PL) EC (stage IIIA, IIIB, and IIIC1). MATERIALS AND METHODS: A multi-institutional database of 270 surgically staged women with PLEC was analyzed. Univariate log-rank analyses and Cox regression multivariate analyses (MVA) were performed to identify factors associated with RFS and OS. RESULTS: Median RFS and OS were 112 and 130 months, respectively, for the full cohort. Adjuvant treatment was CT in 21%, RT in 27%, and CRT in 47%. Age, year of treatment, grade, histology, and adjuvant treatment were significantly associated with RFS and OS on univariate analysis. PLEC patients receiving CT alone fared worse in terms of RFS (P=0.07 relative to RT and <0.01 relative to CRT). On MVA, CRT retained significantly improved RFS relative to CT (hazard ratio for recurrence 0.38, P<0.01). PLEC patients receiving RT or CRT had improved OS compared with CT, P<0.01 and 0.03, respectively. On MVA, both RT only and CRT retained association with improved OS relative to CT alone (hazard ratio for death, 0.43, P=0.02 and 0.40, P<0.01, respectively). CONCLUSIONS: For surgically staged PL stage III EC, treatment regimens incorporating RT were associated with improved survival endpoints relative to CT alone. As such, RT should be considered an important component in the adjuvant management of stage III PLEC.


Subject(s)
Chemoradiotherapy, Adjuvant/mortality , Chemotherapy, Adjuvant/mortality , Endometrial Neoplasms/mortality , Pelvic Neoplasms/mortality , Radiotherapy, Adjuvant/mortality , Adult , Aged , Aged, 80 and over , Endometrial Neoplasms/drug therapy , Endometrial Neoplasms/pathology , Endometrial Neoplasms/radiotherapy , Female , Follow-Up Studies , Humans , Middle Aged , Pelvic Neoplasms/drug therapy , Pelvic Neoplasms/pathology , Pelvic Neoplasms/radiotherapy , Prognosis , Retrospective Studies , Survival Rate , Young Adult
17.
Int J Mol Sci ; 18(11)2017 Nov 09.
Article in English | MEDLINE | ID: mdl-29120401

ABSTRACT

Pelvic Melanoma relapse occurs in 15% of patients with loco regional metastases, and 25% of cases do not respond to new target-therapy and/or immunotherapy. Melphalan hypoxic pelvic perfusion may, therefore, be an option for these non-responsive patients. Overall median survival time (MST), stratified for variables, including BRAF V600E mutation and eligibility for treatments with new immunotherapy drugs, was retrospectively assessed in 41 patients with pelvic melanoma loco regional metastases. They had received a total of 175 treatments with Melphalan hypoxic perfusion and cytoreductive excision. Among the 41 patients, 22 (53.7%) patients exhibited a wild-type BRAF genotype, 11 of which were not eligible for immunotherapy. The first treatment resulted in a 97.5% response-rate in the full cohort and a 100% response-rate in the 22 wild-type BRAF patients. MST was 18 months in the full sample, 20 months for the 22 wild-type BRAF patients and 21 months for the 11 wild-type BRAF patients not eligible for immunotherapy. Melphalan hypoxic perfusion is a potentially effective treatment for patients with pelvic melanoma loco regional metastases that requires confirmation in a larger multicenter study.


Subject(s)
Antineoplastic Agents, Alkylating/therapeutic use , Chemotherapy, Cancer, Regional Perfusion/methods , Melanoma/drug therapy , Melphalan/therapeutic use , Neoplasm Recurrence, Local/drug therapy , Pelvic Neoplasms/drug therapy , Aged , Cohort Studies , Female , Humans , Male , Melanoma/pathology , Middle Aged , Neoplasm Metastasis , Neoplasm Staging , Pelvic Neoplasms/pathology , Pelvis/pathology , Proto-Oncogene Proteins B-raf/genetics , Retrospective Studies , Survival Analysis
18.
Int J Radiat Oncol Biol Phys ; 99(4): 1039-1047, 2017 11 15.
Article in English | MEDLINE | ID: mdl-28870786

ABSTRACT

BACKGROUND: Adequate tumor temperatures during hyperthermia are essential for good clinical response, but excessive heating of normal tissue should be avoided. This makes locoregional heating using phased array systems technically challenging. Online application of hyperthermia treatment planning could help to improve the heating quality. The aim of this study was to evaluate the clinical benefit of online treatment planning during treatment of pelvic tumors heated with the AMC-8 locoregional hyperthermia system. METHODS: For online adaptive hyperthermia treatment planning, a graphical user interface was developed. Electric fields were calculated in a preprocessing step using our in-house-developed finite-difference-based treatment planning system. This allows instant calculation of the temperature distribution for user-selected phase-amplitude settings during treatment and projection onto the patient's computed tomographic scan for online visualization. Online treatment planning was used for 14 treatment sessions in 8 patients to reduce the patients' reports of hot spots while maintaining the same level of tumor heating. The predicted decrease in hot spot temperature should be at least 0.5°C, and the tumor temperature should decrease less than 0.2°C. These predictions were compared with clinical data: patient feedback about the hot spot and temperature measurements in the tumor region. RESULTS: In total, 17 hot spot reports occurred during the 14 sessions, and the alternative settings predicted the hot spot temperature to decrease by at least 0.5°C, which was confirmed by the disappearance of all 17 hot spot reports. At the same time, the average tumor temperature was predicted to change on average -0.01°C (range, -0.19°C to 0.34°C). The measured tumor temperature change was on average only -0.02°C (range, -0.26°C to 0.31°C). In only 2 cases the temperature decrease was slightly larger than 0.2°C, but at most it was 0.26°C. CONCLUSIONS: Online application of hyperthermia treatment planning is reliable and very useful to reduce hot spots without affecting tumor temperatures.


Subject(s)
Hot Temperature , Hyperthermia, Induced/methods , Melanoma/therapy , Pelvic Neoplasms/therapy , Radiotherapy Planning, Computer-Assisted/methods , Therapy, Computer-Assisted/methods , Urinary Bladder Neoplasms/therapy , Uterine Cervical Neoplasms/therapy , Female , Humans , Hyperthermia, Induced/adverse effects , Hyperthermia, Induced/instrumentation , Melanoma/diagnostic imaging , Melanoma/drug therapy , Melanoma/radiotherapy , Pelvic Neoplasms/diagnostic imaging , Pelvic Neoplasms/drug therapy , Pelvic Neoplasms/radiotherapy , Urinary Bladder Neoplasms/diagnostic imaging , Urinary Bladder Neoplasms/drug therapy , Urinary Bladder Neoplasms/radiotherapy , Uterine Cervical Neoplasms/diagnostic imaging , Uterine Cervical Neoplasms/drug therapy , Uterine Cervical Neoplasms/radiotherapy
19.
BMC Res Notes ; 10(1): 411, 2017 Aug 15.
Article in English | MEDLINE | ID: mdl-28810925

ABSTRACT

BACKGROUND: Isolated pelvic perfusion (IPP) can be used to treat unresectable melanoma metastases of the pelvis. IPP can be performed either by surgical or percutaneous approaches, using different balloon catheters. The aim of this study was to examine whether the surgical and percutaneous approaches were comparable with respect to tumor drug exposure in the pelvis. METHODS: A pharmacokinetic study was performed in 5 melanoma patients treated with surgical IPP and five with percutaneous IPP. Both groups received melphalan at the dose of 30 mg/m2. Melphalan pharmacokinetic analyses were performed and the main parameter used to evaluate pelvic tumor drug-exposure was the ratio of areas under the melphalan plasma concentration curves in the pelvis and the systemic compartment, during the perfusion time (AUC0 to 20). Non-parametric Mann-Whitney tests were employed for statistical comparisons. RESULTS: The median and interquartile range (IQR) values of the ratios between melphalan AUC0 to 20 in pelvic and systemic compartments were 7.9 (IQR 7.2 to 9.9) and 5 (IQR 4 to 7.9) for surgical and percutaneous IPPs, respectively (p = 0.209). CONCLUSIONS: Tumor exposure to drug using these two methods did not statistically differ and both methods, therefore, can be adopted interchangeably, utilizing a perfusion blood flow rate of approximately 120 ml/min. The small sample size is a limitation of this study but our preliminary results can be used to calculate the effect size of a larger trial. Trial Registration Clinical Trials.gov Identifier NCT01920516; date of trial registration: August 6, 2013.


Subject(s)
Antineoplastic Agents, Alkylating/pharmacokinetics , Chemotherapy, Cancer, Regional Perfusion/methods , Melanoma/drug therapy , Melphalan/pharmacokinetics , Pelvic Neoplasms/drug therapy , Surgical Procedures, Operative/methods , Aged , Antineoplastic Agents, Alkylating/blood , Antineoplastic Agents, Alkylating/pharmacology , Area Under Curve , Female , Humans , Male , Melanoma/blood supply , Melanoma/pathology , Melanoma/surgery , Melphalan/blood , Melphalan/pharmacology , Middle Aged , Pelvic Neoplasms/blood supply , Pelvic Neoplasms/pathology , Pelvic Neoplasms/surgery , Pelvis/blood supply , Pelvis/pathology , Pelvis/surgery , Pilot Projects , Statistics, Nonparametric
20.
J Obstet Gynaecol Res ; 43(9): 1489-1492, 2017 Sep.
Article in English | MEDLINE | ID: mdl-28691239

ABSTRACT

Leiomyomatosis peritonealis disseminata is a rare disease characterized by pelvic smooth-muscle nodules of various sizes. It is sometimes misdiagnosed as ovarian or peritoneal carcinoma metastasis; therefore, surgical excision for pathological diagnosis is required. Treatment options include bilateral salpingo-oophorectomy (BSO), gonadotrophin-releasing hormone agonist therapy, and aromatase inhibitor therapy. All of these suppress estrogen levels, but a standard treatment has not been established. A 40-year-old woman had multiple pelvic tumors, suspicious for ovarian cancer. She underwent laparotomy, where frozen sections of the nodules revealed leiomyomatosis peritonealis disseminata. After she completed gonadotrophin-releasing hormone agonist therapy, we performed a total abdominal hysterectomy and BSO with residual-nodule resection, but the nodules recurred 6 months after surgery. We then started letrozole, and 3 years have now elapsed without nodule enlargement or development of new lesions. The long-term use of aromatase inhibitor therapy is thought to be effective and safe for patients with recurrence after BSO.


Subject(s)
Aromatase Inhibitors/pharmacology , Leiomyomatosis/drug therapy , Neoplasm Recurrence, Local/drug therapy , Nitriles/pharmacology , Pelvic Neoplasms/drug therapy , Peritoneal Cavity/pathology , Triazoles/pharmacology , Adult , Aromatase Inhibitors/administration & dosage , Aromatase Inhibitors/adverse effects , Female , Humans , Leiomyomatosis/surgery , Letrozole , Neoplasm Recurrence, Local/surgery , Nitriles/administration & dosage , Nitriles/adverse effects , Pelvic Neoplasms/surgery , Peritoneal Cavity/surgery , Triazoles/administration & dosage , Triazoles/adverse effects
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