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Dive into the research topics where Mukund S. Didolkar is active.

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Featured researches published by Mukund S. Didolkar.


American Journal of Surgery | 1974

Evaluation of the risk in pulmonary resection for bronchogenic carcinoma

Mukund S. Didolkar; Robert H. Moore; Hiroshi Takita

Abstract Preoperative pulmonary function test results in 258 patients who underwent pulmonary resection for bronchogenic carcinoma were studied in relation to postoperative mortality from cardiopulmonary complications. Poor outcome of surgery was related to the maximal breathing capacity value below 59 per cent of the predicted normal, age over sixty-nine years, and abnormal electrocardiographic findings. Combinations of these factors were associated with a very high mortality (56 per cent). This group of patients needs further evaluation on an individual basis to identify the risk of pulmonary resection. A formula to predict the risk of surgery based on the maximal breathing capacity value is suggested. Values for one second forced expiratory volume and vital capacity were of no use in predicting the outcome of surgery.


American Journal of Surgery | 1989

Prognostic factors in squamous cell carcinoma of the larynx

Jason D. Eiband; E.George Elias; Charles M. Suter; William C. Gray; Mukund S. Didolkar

One hundred fifty-two patients with squamous cell carcinoma of the larynx were studied. The disease-free survival and overall survival rates were correlated to 12 variables. Seven of them seemed to affect survival. Poor prognosis was related to (1) advanced stage of disease at diagnosis, (2) cord fixation and massive local invasion, (3) ulceration of the primary tumor, (4) lymph node metastases at diagnosis, (5) glottic lesions had a poorer prognosis than supraglottic ones, (6) locoregional recurrences, and (7) male gender. However, most of these significant differences were in disease-free survival, and only primary tumor staging; lymph node status; and locoregional recurrences affected overall survival. On the other hand, the other five variables showed no effect on either disease-free or overall survival rates. These included age, race, cell differentiation, type of recurrence, and the initial definitive therapeutic modality.


Cancer | 1986

Toxicity and complications of vascular isolation and hyperthermic perfusion with lmidazole carboxamide (DTIC) in melanoma

Mukund S. Didolkar; J. Lawrence Fitzpatrick; Andre J. Jackson; Gerald S. Johnston

The authors have used imidazole carboxamide (DTIC) in vascular isolation and hyperthermic perfusion for melanoma. The regional and systemic toxicity and complications of this procedure were studied in 40 cases with Stage 111 (15) and Stage I (25) melanoma. Technetium 99m‐labelled serum albumin crossover and pharmacokinetic studies were done simultaneously to see if these correlate with toxicity. Local toxicity on muscles, nerves, skin, and arteries was conspicuously absent despite using dosages of 2 g/m2 (40‐45 mg/kg) for the lower extremity and 1.2 g/m2 (24‐28 mg/kg) for the upper extremity. Skin and core temperature were raised to 39°C to 40°C. Deep vein thrombosis was noted in three patients. No death or gangrene of the extremities occurred. Local infection was noted in only one patient. Fourteen patients (35%) manifested bone marrow toxicity (leukocyte count of 4000/mm3 or platelets of 100,000/mm3) in the second or third week after perfusion. Severe hematologic toxicity was seen in two instances. Dosages of DTIC greater than 40 mg/kg were associated with toxicity in 65% of the patients. No bleeding complications occurred in seven patients with thrombocytopenia. Measurement of crossover and recovery of radionuclide were not reliable indicators of subsequent systemic toxicity. Perfusion fluid balance data also were of no predictive value. Forty‐seven percent of the administered DTIC was recovered in washout fluid. Of this, less than 2% was converted to its metabolites, thot is aminoimidazole carboxamide and 2‐azahypoxanthine. Thirty‐five of 40 patients experienced mild nausea and vomiting. Transient and mild hepatotoxicity was noted in seven patients. It appears that DTIC hyperthermic isolation perfusion is a safe procedure, however, the total dosage should be below 40 mg/kg to avoid hematologic toxicity. Cancer 57:1961‐1966, 1986.


American Journal of Surgery | 1980

Biologic behavior of ocular malignant melanoma and comparison with melanoma of the head and neck

Mukund S. Didolkar; E.George Elias; Nathaniel A. Barber; Robert H. Moore

Ocular melanoma is the most common malignant tumor of the eye and accounts for 70 to 80 percent of all extracutaneous melanomas. Its biologic behavior differs from that of its cutaneous counterpart. To elucidate this, 62 patients with histologically proven melanoma of eye (58 uveal tract and 4 conjuntiva) at Roswell Park Memorial Institute from 1945 to 1977 were studied. The prominent contradistinctions from other head and neck melanomas were (1) a very high percentage of patients had either locally advanced or systemic disease at diagnosis, although the eye is the most sensitive organ; (2) regional lymph node involvement was absent even in the late stages of disease; (3) hematogenous spread involved single organs, most commonly the liver and the lung; (4) local recurrence was rare; (5) most recurrences occurred evenly in first 10 years after treatment; (6) regional resection, chemotherapy or both are advocated for distant metastases since they are confined to a single organ and are amenable to it; and (7) despite hematogenous spread and advanced disease at diagnosis, the overall prognosis of ocular melanoma is comparable to that of cutaneous melanoma.


American Journal of Surgery | 1991

Long-term results of a combined modality approach in treating inflammatory carcinoma of the breast

E.George Elias; Debra A. Vachon; Mukund S. Didolkar; Joseph Aisner

Twenty-eight patients with inflammatory carcinoma of the breast were managed initially by induction chemotherapy consisting of 3 courses of a combination of cyclophosphamide, doxorubicin hydrochloride, and 5-fluorouracil. Twenty-two showed a partial response, and 21 underwent mastectomies. Histopathologic examination of the surgical specimens revealed no residual tumor in 2 breasts, but all 21 patients had residual metastases in their axillary lymph nodes. Postoperatively, they received the same chemotherapy. The other six patients who failed to respond to induction chemotherapy received radical radiation therapy followed by a combination chemotherapy regimen that consisted of cyclophosphamide, methotrexate, 5-fluorouracil, vincristine, and prednisone. Any patient in whom chemotherapy failed during the follow-up period was treated by radiation therapy and/or a combination of mitomycin-C and vinblastine as necessary. At the time of diagnosis, 17 patients who had no evidence of distant metastasis, i.e., stage III B disease, had disease-free survival ranging from 5 to more than 84 months, with a median of 30 months, and an overall survival of 7 to more than 120 months with a median of 32 months. The 5-year survival rate was 18%. The other 11 patients who had distant metastases, i.e., stage IV disease, had an overall survival ranging from 4 to 14 months. The results of this approach of initial systemic chemotherapy followed by local-regional cytoreductive therapy, then systemic therapy, might suggest some survival benefits in patients with stage III disease.


American Journal of Surgery | 1989

Flow cytometric DNA analysis of primary and concurrent metastatic squamous cell carcinoma of the head and neck

Julian A. Kim; Valerie L. Moore; Mukund S. Didolkar; Jose V. Ordonez; Robert A. Van Wesep; Charles M. Suter

Adequate flow cytometric DNA analysis comparing primary and concurrent metastatic squamous cell carcinoma of the head and neck has not been done in the past. The purpose of this study was to define any differences between the primary and concurrent metastasis of each patient with respect to flow cytometric parameters and histologic grade. Paraffin-embedded archival specimens from 28 patients with primary and metastatic tumors were prepared into nuclei and analyzed by flow cytometry using human lymphocyte standards. The mean DNA index was 0.82 for primary tumors and 0.83 for the metastases. Aneuploidy was found in 68 percent of primary tumors and in 82 percent of metastases. The percentage of cells in the proliferative fraction was 40.4 in the primary tumors and 24.5 in the metastases. A direct correlation was found between the differentiation of the primary and metastatic tumors. No survival difference was discovered among the flow cytometric parameters and histologic grade. We conclude that there is no difference between the primary and concurrent metastasis in squamous cell carcinoma of the head and neck with regard to DNA index, aneuploidy, or histologic grade.


Journal of Surgical Oncology | 1996

Pharmacokinetics of dacarbazine in the regional perfusion of extremities with melanoma

Mukund S. Didolkar; Andre J. Jackson; Lawrence J. Lesko; J. Lawrence Fitzpatrick; Barbara S. Buda; Gerald S. Johnston; Loren A. Zech

The pharmacokinetics of dacarbazine (DTIC), which has been shown to be an effective therapeutic agent against metastatic melanoma, has not been extensively studied. However, to improve the clinical use of the drug, more information on the kinetics is required.


Cancer | 1991

A protocol for the safe administration of debrisoquine in biochemical epidemiologic research protocols for hospitalized patients

Laureen Green-Gallo; Daina M. Buivys; Karen L. Fisher; Wayne J. Ivusich; James H. Resau; Neil Caporaso; Robert G. Slawson; E.George Elias; Mukund S. Didolkar

The genetically determined ability to metabolize the antihypertensive drug debrisoquine has been proposed as a genetic risk factor for primary carcinomas of the lung. To test this hypothesis, the metabolism of the drug was evaluated in a case control study. The subjects were characterized by their ability to metabolize debrisoquine after receiving a test dose of the drug followed by the collection of an 8‐hour urine sample. They were classified by laboratory analysis into one of the following three groups: extensive, intermediate, and poor metabolizers. Poor metabolizers comprise 10% of the population and are unable to hydroxylate the drug. This group was expected to be at highest risk for deleterious effects from this medication. A protocol was created that included patient education and blood pressure monitoring to administer this medication safely to a group of patients with cancer who were already compromised. Although poor metabolizers showed a small decrease in systolic and diastolic blood pressure, no significant hypotensive episodes or clinical sequelae were observed in any of the groups. These data suggest that debrisoquine can be administered safely in a controlled clinical setting and will be useful for the characterization of lung cancer patients in biochemical epidemiology studies.


Surgery gynecology & obstetrics | 1989

Risk factors before hepatectomy, hepatic function after hepatectomy and computed tomographic changes as indicators of mortality from hepatic failure.

Mukund S. Didolkar; Fitzpatrick Jl; Elias Eg; Whitley No; Keramati B; Suter Cm; Sally D. Brown


Cancer Research | 1987

Hepatic Drug-metabolizing Enzymes in Primary and Secondary Tumors of Human Liver

Mohamed El Mouelhi; Mukund S. Didolkar; E. George Elias; F. Peter Guengerich; Frederick C. Kauffman

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Andre J. Jackson

Food and Drug Administration

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Elias Eg

University of Maryland

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Alonzo P. Walker

Medical College of Wisconsin

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E.George Elias

University of Maryland Medical Center

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Charles M. Suter

University of Maryland Medical Center

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