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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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1093082 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
8 y) [" b% b. y. ^0 h3 xNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 ' a) m7 r! \. O! T
+ Author Affiliations- c5 j+ X% I9 j) Q# C
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
& ?1 F4 Z) S1 L0 g7 e8 I7 H4 ^2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 6 E; w- e3 d' s; J6 E+ n% n
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
0 ~( b, l+ z  r% M5 p' p3 u' v4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan / o; Z  I5 Z% p: X. H$ ?4 i, Z
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
/ A$ z7 g5 {4 D: b& Q7 z, [0 @6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
* M2 x6 G/ h9 i0 i6 y7Kinki University School of Medicine, Osaka 589-8511, Japan , b# x) M4 N) a8 k
8Izumi Municipal Hospital, Osaka 594-0071, Japan
' ^/ a) }6 p: w  ]9 i; O9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
. b, l5 b3 Z6 i5 d6 d' M( KCorrespondence 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 - U- K& |! D: N3 e7 V
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. , [" F' [/ _9 D5 _+ L6 ]
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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 8 D. Q0 z& y% }* t

# r2 N# ^! O2 _. d* i; gAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato ' f1 R; n5 e9 d! a3 j* r4 U

$ Q2 x: `' \# p6 Y, @Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  " \1 F7 w# y3 n  f$ o" M/ V
1 l2 B+ N' i7 _8 v$ Y) J! O' q8 g0 e
Published online on: Thursday, December 1, 2011
& Y% m3 N. u$ _/ q9 e
: V$ N0 |. Z7 J- t  ^Doi: 10.3892/ol.2011.507 ) |& O9 z$ v5 T( L- X4 K( ]( d
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Pages: 405-410
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Abstract:
5 w' I+ x7 }  k! q- u8 cS-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
0 L  B6 f& Q, X8 j) w7 l1 AF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
6 w1 I3 W  C' o: w$ {. E+ Author Affiliations, e/ J+ T2 r) \6 A$ B/ ~; {; O
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu ! ^. `/ h( z% ^+ L% z- |
2Department of Thoracic Surgery, Kyoto University, Kyoto " o$ S3 k$ c5 V
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
# ?, D0 _5 y* k* m( e&#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
$ B; o! l$ z8 ~$ h, \2 ^: qReceived September 3, 2010. ) p. o  _' N$ _& e0 `8 e
Revision received November 11, 2010. ) D6 Z0 l. l& _4 {9 |( l
Accepted November 17, 2010.
3 ?: U, B& z  sAbstract3 e, |4 u" x/ M
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. 9 X4 \1 @5 X) t* P2 X, I
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. 2 M& H) I  q/ B; F* R# Y( ?! z+ q) Y
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 h, H/ `6 y7 D' O
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. ) e9 k1 r% `! D
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。2 r' \$ o- E) |
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 Chemotherapy7 o; e& ^- q7 K9 }7 _/ t4 `3 N
http://clinicaltrials.gov/ct2/show/NCT01523587# a- U0 o4 A' ^5 z* B; Y
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
  X" _" |! D& l' `9 h1 y! [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 + }' O$ z1 Q* F4 B/ E) `- L: e. P) s
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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。$ m$ U" @  Q7 y) L1 N
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
2 `* }; `$ c. Y7 z4 m$ n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。
: n7 m) M& P3 p9 D* K( R% L至今为止,未出 ...

1 f8 T. D& t4 ^% ~没有副作用是第一追求,效果显著是第二追求。5 U* }1 o4 E& t" p1 a$ F8 ]$ P
不错。

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