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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1294674 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type/ b$ r. {' j* k1 r
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
+ z3 M6 I8 n: R+ Author Affiliations
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7 a* b5 \1 V  Y5 L1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan ; G7 K2 d; B% }' v8 L0 e0 E/ z
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan * v0 r! C! D& o  V% b$ T  e- Q
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 5 u0 x1 H. {# ?- a: P
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
  [  @, h6 A9 o/ W# V0 P7 w5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
  H8 O% n+ C% i5 h- P1 [  |6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
/ @2 B3 g: e+ L( q1 x+ ^7Kinki University School of Medicine, Osaka 589-8511, Japan
3 x% p- f  L  A+ b* Q) V1 e% {3 P8Izumi Municipal Hospital, Osaka 594-0071, Japan
: q' K9 M- W" B* k+ ?  P# Y5 q( k9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
9 o9 A( j! d7 R9 M: Q- u& ^Correspondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp / d, M1 O* V7 G2 h
AbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type. 6 H; g, H( q' }# P/ p: p& L" F

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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type
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% _" n/ y! }2 x& `- RAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato ' s) v2 |8 h& |5 G

# b' O& B8 b( ]" W: }: U3 SAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
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Published online on: Thursday, December 1, 2011 6 u7 u0 P% p) {# z

% x, ?0 i8 N) _6 LDoi: 10.3892/ol.2011.507
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Pages: 405-410 ' `, l" C0 u* ~7 \( H* K# k& h
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Abstract:
: D# G( u& t% ?8 |& w$ w3 }% D3 f9 ]7 dS-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population! Z1 ]  z$ S! z( D% n
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 ' I4 _5 _$ u2 J
+ Author Affiliations
! [( J' g+ C2 k- Q5 b& q* ~# _' i& j" R1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu / \' A8 l: F& Z2 i' }
2Department of Thoracic Surgery, Kyoto University, Kyoto
( T, J5 }. A$ F/ m3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan . [) |' L- D( p" N* [  _- N
&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp
! k; }1 ~  r  X6 {6 QReceived September 3, 2010. 4 h2 u$ V. n7 A5 j& n
Revision received November 11, 2010. ! a/ H4 J. i/ _( c6 z  ]
Accepted November 17, 2010.
/ R; |% E0 d' Q6 W# d, u- gAbstract) d7 f5 Z1 L; o+ l6 p  e
Background: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed. ) S+ d1 F1 P1 h: H' e
Patients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes. + b8 H% O+ S+ O1 v: ]
Results: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression. 1 R+ i/ c) b( W! u# Q
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.
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个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。& J# l/ V) H. ]- }+ z+ D" T
今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?
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老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy# A  V, ^5 d- b4 u0 O- h( c
http://clinicaltrials.gov/ct2/show/NCT015235870 t& B/ U% b& {& G' ^8 u

- n, a" j3 U% b2 {9 m4 [8 p2 ^  C7 [  ?9 zBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
5 q8 c! T: w. i- Z) c' `http://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑 ( Y3 W: W* H: |" Y6 L( `6 H
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从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
2 R' n! U/ }6 l至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
老马 发表于 2012-4-29 20:53 ; M2 k  e3 I  ?3 K+ M& e
从4月24日开始到4月28日,打了5天的打了5天舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
) x& |7 \6 V$ \- I8 U4 I) h) J( C# A至今为止,未出 ...
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没有副作用是第一追求,效果显著是第二追求。
5 C- N. x9 V6 `/ v: A0 m( @不错。

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