Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 85
Filter
1.
Indian J Med Sci ; 2019 Mar; 71(2): 88-92
Article | IMSEAR | ID: sea-196522

ABSTRACT

This article in the MEDic LAWgic series focussed on the meaning and implications of workplace insubordination. It describes why it is considered as misconduct. It also explains how gross subordination can lead to restraining order under section 144 of Indian criminal procedure code and can become a permanent part of service records of the perpetrator, affecting their career.

2.
Indian J Med Sci ; 2018 SEP; 70(3): 43-47
Article | IMSEAR | ID: sea-196507

ABSTRACT

Introduction: We came across patients inquiring with oncologists about cheap copy medicines. These were of recently licensedinnovator drugs that should have been available from original company holding their patents. In fact these copy medicines weremanufactured in our neighboring countries and made available in India. We investigated further and this manuscript puts together thestartling information that we were able to find regarding the thriving grey market for fake generic medicines.

3.
Indian J Cancer ; 2014 Oct-Dec; 51(4): 410-413
Article in English | IMSEAR | ID: sea-172427

ABSTRACT

Leptomeningeal metastasis is a common problem in advanced solid tumor malignancies. A significant number of patients have underlying lung cancer. With the advent of better therapies, the management of leptomeningeal metastasis is gained more importance to improve survival and quality of live. This review article focuses on the epidemiology, clinical features, diagnostics and the recent management strategies directed towards leotomeningela metastasis from solid tumor, esp lung cancer.

5.
Indian J Cancer ; 2014 Apr-Jun; 51(2): 113-116
Article in English | IMSEAR | ID: sea-154307

ABSTRACT

The office of the Drugs Controller General (India) vide order dated 19th November 2013 has made audio visual (AV) recording of the informed consent mandatory for the conduct of all clinical trials in India. We therefore developed a standard operating procedure (SOP) to ensure that this is performed in compliance with the regulatory requirements, internationally accepted ethical standards and that the recording is stored as well as archived in an appropriate manner. The SOP was developed keeping in mind all relevant orders, regulations, laws and guidelines and have been made available online. Since, we are faced with unique legal and regulatory requirements that are unprecedented globally, this SOP will allow the AV recording of the informed consent to be performed, archived and retrieved to demonstrate ethical, legal and regulatory compliance. We also compared this to the draft guidelines for AV recording dated 9th January 2014 developed by Central Drugs Standard Control Organization. Our future efforts will include regular testing, feedback and update of the SOP.


Subject(s)
Clinical Trials as Topic/legislation & jurisprudence , Clinical Trials as Topic/standards , Humans , India , Informed Consent/legislation & jurisprudence , Informed Consent/standards , Video Recording/legislation & jurisprudence , Video Recording/standards
6.
Indian J Cancer ; 2014 Feb; 51(6_Suppl): s1
Article in English | IMSEAR | ID: sea-156774
7.
Indian J Cancer ; 2014 Jan-Mar; 51(1): 73-79
Article in English | IMSEAR | ID: sea-154291

ABSTRACT

The management of hormone receptor‑positive Her2‑negative breast cancer patients with advanced or metastatic disease is a common problem in India and other countries in this region. This expert group used data from published literature, practical experience, and opinion of a large group of academic oncologists, to arrive at practical consensus recommendations for use by the community oncologists.


Subject(s)
Breast Neoplasms/metabolism , Breast Neoplasms/secondary , Breast Neoplasms/therapy , Combined Modality Therapy , Consensus , Disease Management , Female , Humans , Practice Guidelines as Topic , Receptor, ErbB-2/metabolism , Receptors, Estrogen/metabolism , Receptors, Progesterone/metabolism , Societies, Medical
8.
Indian J Cancer ; 2013 Jan-Mar; 50(1): 31-40
Article in English | IMSEAR | ID: sea-147317

ABSTRACT

The availability of imatinib followed by other tyrosine kinase inhibitors (TKIs) has dramatically altered the outcome of gastrointestinal stromal tumor (GIST). Patients with advanced or poor risk disease can now expect survival measured in years instead of months. An experienced multi disciplinary team (MDT) will be able to personalize therapy to ensure maximum benefit. This review will provide the updated information and finer points regarding state of the art management of GIST with the use of imatinib and other TKIs.


Subject(s)
Antineoplastic Agents/therapeutic use , Benzamides/therapeutic use , Female , Gastrointestinal Neoplasms/drug therapy , Gastrointestinal Stromal Tumors/drug therapy , Humans , Precision Medicine , Male , Molecular Targeted Therapy , Patient Care Team , Piperazines/therapeutic use , Practice Guidelines as Topic , Protein Kinase Inhibitors/therapeutic use , Pyrimidines/therapeutic use , Treatment Outcome
9.
Indian J Cancer ; 2012 Jan-Mar; 49(1): 107-113
Article in English | IMSEAR | ID: sea-144560

ABSTRACT

Background: In patients with persistent fever and netropenia, amphotericin B is administered empirically for early treatment and prevention of systemic fungal infections. Despite this treatment, there are chances of breakthrough fungal infections and drug is also toxic. Materials and Methods: A multicentric, randomized, controlled clinical trial was conducted to compare liposomal amphotericin B two doses with conventional amphotericin B as empirical antifungal therapy. Results: The average body weight of patients was 26.4±14.8 (n=22), 32.9±19.4 (n=23) and 37.9±20.0 (n=20) kg in 1 mg, 3 mg Fungisome (liposomal amphotericin B) and 1 mg/kg/day conventional amphotericin B group, respectively. The mean age was 16.2±13.4, 16.0±10.9 and 22.7±16.2 yrs in 1 and 3 mg/kg/day Fungisome and 1 mg/kg/day conventional AMP B group, respectively. The average duration of treatment with 1 mg and 3 mg/kg/day Fungisome and 1 mg/kg/day conventional amphotericin B was 17±9.8, 16.2±8.3, and 14.7±10.7 days, respectively. The time to resolve fever was 13.3±10.2, 10.9±7.1, 10.1±6.7 days, and for absolute neutrophil count (ANC) to be above 500 cells per microliter, it took 13.4±9.6, 10.6±7.6 and 7.3±3.4 days, respectively. Liposomal formulations were well-tolerated compared to conventional amphotericin B. Conclusions: This small randomized study showed that the indigenous liposomal formulation Fungisome TM appears to be equally efficacious and safer than conventional amphotericin B. Also, the lower dose Fungisome (1 mg/kg/day) appears to be equally efficacious and was well-tolerated as compared to higher dose Fungisome (3 mg/kg/day). Treatment cost would be a major factor for limiting use of higher dose of Fungisome.


Subject(s)
Adolescent , Adult , Amphotericin B/administration & dosage , Amphotericin B/adverse effects , Antifungal Agents/administration & dosage , Antifungal Agents/adverse effects , Child , Child, Preschool , Dose-Response Relationship, Drug , Female , Humans , India , Male , Middle Aged , Mycoses/drug therapy , Neutropenia/drug therapy , Neutropenia/pathology , Safety , Treatment Outcome
10.
Indian J Cancer ; 2011 Apr-Jun; 48(2): 158-164
Article in English | IMSEAR | ID: sea-144445

ABSTRACT

Background: In order to document the understanding of current evidence for the management of triple negative breast cancer and application of this knowledge in daily practice, we conducted an interactive survey of practicing Indian oncologists. Materials and Methods: A core group of academic oncologists devised two hypothetical triple negative cases (metastatic and early breast cancer, respectively) and multiple choice options under different clinical circumstances. The respondents were practicing oncologists in different Indian cities who participated in either an online survey or a meeting. The participants electronically chose their preferred option based on their everyday practice. Results: A total of 152 oncologists participated. Just over half (53.8%) preferred taxane based chemotherapy as first-line chemotherapy in the metastatic setting. In the adjuvant setting, a taxane regimen was chosen by 61%. Over half of respondents (52.6%) underestimated the baseline survival of a patient with node positive triple-negative tumor and 18.9% overestimated this survival compared to the estimate of the Adjuvant! program. Discussion: This data offers insight into the perceptions and practice of a diverse cross-section of practicing oncologists in India with respect to their therapeutic choices in metastatic and adjuvant settings in triple negative breast cancer.


Subject(s)
Adult , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Breast Neoplasms/drug therapy , Breast Neoplasms/pathology , Chemotherapy, Adjuvant , Cyclophosphamide/administration & dosage , Doxorubicin/administration & dosage , Female , Humans , India , Lung Neoplasms/drug therapy , Lung Neoplasms/secondary , Lymphatic Metastasis , Medical Oncology , Middle Aged , Practice Patterns, Physicians' , Receptor, ErbB-2/metabolism , Receptors, Estrogen/metabolism , Survival Rate , Taxoids/administration & dosage , Treatment Outcome
12.
Indian J Cancer ; 2011 Jan-Mar; 48(1): 11-17
Article in English | IMSEAR | ID: sea-144405

ABSTRACT

Glioblastoma is a rapidly progressive and extremely fatal form of brain tumor with poor prognosis. It is the most common type of primary brain tumor. Even with the most aggressive conventional treatment that comprises surgery followed by radiotherapy and chemotherapy, most patients die within a year of diagnosis. Developments in molecular and cell biology have led to better understanding of tumor development, leading to novel treatment strategies including biological therapy and immunotherapy to combat the deadly disease. Targeted drug delivery strategies to circumvent the blood-brain barrier have shown efficiency in clinical trials. Gliadel wafer is a new approach to the treatment of glioblastoma, which involves controlled release delivery of carmustine from biodegradable polymer wafers. It has shown promising results and provides a silver lining for glioblastoma patients.


Subject(s)
Antineoplastic Agents, Alkylating/therapeutic use , Brain Neoplasms/drug therapy , Carmustine/therapeutic use , Delayed-Action Preparations , Humans
13.
Indian J Cancer ; 2011 Jan-Mar; 48(1): 1-10
Article in English | IMSEAR | ID: sea-144404

ABSTRACT

This review article provides the current recommendations and evidence for the correct management of anemia in cancer patients. The various options available include transfusions, iron and erythropoiesis stimulation. The indications, pros and cons of each option are discussed.


Subject(s)
Anemia/drug therapy , Anemia/etiology , Humans , Neoplasms/complications , Neoplasms/drug therapy
19.
Indian J Cancer ; 2008 Oct-Dec; 45(4): 142-8
Article in English | IMSEAR | ID: sea-50672

ABSTRACT

Therapeutic management of multiple myeloma (MM) for the last several decades has mainly involved regimens based on use of glucocorticoids and cytotoxic chemotherapeutics. Despite progress in delineating the activity of such regimens, at either conventional or high doses, MM has remained an incurable disease. This has sparked major interest in the development of novel therapies that in part capitalize on recent advances in our understanding of the biology of MM, including the molecular mechanisms by which MM cell-host bone marrow (BM) interactions regulate tumor-cell growth, survival, and drug resistance in the BM milieu. Herein, we review the latest progress in the development of these novel anti-MM therapies, with major focus on therapies which have translated from preclinical evaluation to clinical application, including thalidomide and its more potent immunomodulatory derivatives (IMiD), the first-in-class proteasome inhibitor bortezomib (formerly known as PS-341). Search strategy included Medline using the terms 'Myeloma and Newer Drugs' citations relevant to treatment guidelines issued in 1999 and 2008 were screened.


Subject(s)
Antineoplastic Agents/therapeutic use , Biological Therapy , Boronic Acids/therapeutic use , Humans , Multiple Myeloma/metabolism , Pyrazines/therapeutic use , Thalidomide/therapeutic use
20.
Article in English | IMSEAR | ID: sea-118386

ABSTRACT

BACKGROUND: Fludarabine has been reported to be an effective drug for the treatment of chronic lymphocytic leukaemia (CLL) and indolent lymphomas. However, its safety and efficacy in Indian patients has not been studied. We retrospectively analysed our experience with fludarabine in low grade lymphomas and CLL. METHODS: The records of all patients with low grade lymphoma or CLL who received fludarabine between April 1999 and November 2006 were analysed. Response evaluation was done as per the National Cancer Institute-Working Group guidelines for CLL and International Workshop criteria for non-Hodgkin lymphomas, respectively, in those patients who received at least 3 cycles of fludarabine. Toxicity was graded as per the common terminology criteria for adverse events, version 3.0. Median event-free survival was obtained using Kaplan-Meier survival analysis. RESULTS: Forty-seven patients were included in the study and 189 cycles were administered (median: 4 cycles per patient). Sixteen patients had a treatment delay, 14 due to myelosuppression. Twenty-five patients had low grade lymphoma and 22 had CLL. The response was evaluable in 22 patients with low grade lymphoma and 20 with CLL. The overall response rate for CLL was 100% in those treated upfront (n=9) and 55% in those with relapsed disease (n=11). The overall response rate for low grade lymphoma was 88% (63% complete remission) in untreated patients and 79% (43% complete remission) in those with relapsed disease. Common adverse events were myelosuppression and infection. Two patients died of sepsis and 4 due to disease progression on treatment. Median event-free survival for patients treated upfront with fludarabine was 31.4 months. CONCLUSION: In our patient population, response to fludarabine is similar to that in the published literature. Our patients had a higher frequency of haematological toxicity.


Subject(s)
Adult , Aged , Antineoplastic Agents/adverse effects , Female , Humans , Leukemia, Lymphoid/drug therapy , Lymphoma/drug therapy , Male , Middle Aged , Retrospective Studies , Survival Analysis , Vidarabine/adverse effects
SELECTION OF CITATIONS
SEARCH DETAIL